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Information on EC 2.7.10.2 - non-specific protein-tyrosine kinase and Organism(s) Homo sapiens and UniProt Accession P43403

for references in articles please use BRENDA:EC2.7.10.2

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IUBMB Comments

Unlike EC 2.7.10.1, receptor protein-tyrosine kinase, this protein-tyrosine kinase does not have a transmembrane domain. In the human genome, 32 non-specific protein-tyrosine kinases have been identified and these can be divided into ten families .

The taxonomic range for the selected organisms is: Homo sapiens
The enzyme appears in selected viruses and cellular organisms

Synonyms
bcr-abl, focal adhesion kinase, c-abl, zap-70, src kinase, janus kinase, v-src, ephb4, p56lck, bruton's tyrosine kinase, more

SYNONYM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
tyrosine-protein kinase ZAP-70
-
70 kDa zeta-associated protein
-
-
-
-
A-Raf proto-oncogene serine/threonine-protein kinase
-
Abelson murine leukemia viral homolog (1) protein
-
-
Abelson tyrosine kinase
-
-
Abl kinase
Abl nonreceptor tyrosine kinase
-
-
Abl protein tyrosine kinase
Abl tyrosine kinase
ABL1 tyrosine kinase
-
ABL2
-
-
ABL2/ARG tyrosine kinase
-
-
activated Cdc42-associated tyrosine kinase 1
-
activin receptor type I
-
activin receptor type II
-
ACTR-IIB
-
-
-
-
ACTRIIA
-
-
-
-
Agammaglobulinaemia tyrosine kinase
-
-
-
-
Amylovoran biosynthesis membrane-associated protein amsA
-
-
-
-
anti-mullerian hormone type II receptor
-
ATK
-
-
-
-
B cell progenitor kinase
-
-
-
-
B lymphocyte kinase
-
-
-
-
B-cell/myeloid kinase
-
-
-
-
B-Raf proto-oncogene serine/threonine-protein kinase
-
BCR-Abl
-
-
Bcr-Abl kinase
-
BCR-ABL tyrosine kinase
BCR/ABL kinase
-
-
Blk kinase
-
BMK
-
-
-
-
BMP type II receptor
-
-
-
-
BMP-2/BMP-4 receptor
-
-
-
-
Bmx tyrosine kinase
-
Bone marrow kinase BMX
-
-
-
-
bone morphogenetic protein receptor type IA
-
bone morphogenetic protein receptor type IB
-
BPK
-
-
-
-
Breast tumor kinase
breast tumour kinase
-
Bruton tyrosine kinase
-
Bruton's tyrosine kinase
Bruton's tyrosine kinase PH domain
-
Brutons tyrosine kinase
Bruton’s tyrosine kinase
-
-
Btk tyrosine kinase
-
-
c-ABL
c-Abl tyrosine kinase
c-FER
-
-
-
-
C-FES
-
-
-
-
c-Fes protein-tyrosine kinase
-
-
c-Fes tyrosine kinase
-
-
C-SRC
C-SRC kinase
c-Src nonreceptor tyrosine kinase
-
-
c-Src protein tyrosine kinase
-
-
c-Src tyrosine kinase
C-terminal Src kinase
-
-
C-YES
CADTK
-
-
-
-
CAK beta
-
-
-
-
Calcium-dependent tyrosine kinase
-
-
-
-
CARD-containing interleukin-1 beta converting enzyme associated kinase
-
Cell adhesion kinase beta
-
-
-
-
Chk tyrosine kinase
-
-
Chk1
-
-
Csk homologous kinase
-
-
Csk protein-tyrosine kinase
-
-
CSK-homologous kinase
-
-
cytoplasmic protein tyrosine kinase
-
-
cytoplasmic tyrosine-protein kinase BMX
-
D-ash
-
-
-
-
DFer
-
-
-
-
Dsrc28C
-
-
-
-
ectoprotein kinase
-
-
-
-
Epithelial and endothelial tyrosine kinase
-
-
-
-
EPS I polysaccharide export protein epsB
-
-
-
-
FADK1
-
-
FADK2
-
-
FAK2
-
-
FER tyrosine kinase
-
Fes tyrosine kinase
-
-
Fgr kinase
-
focal adhesion kinase 1
-
-
-
-
focal adhesion protein tyrosine
-
-
Frk kinase
-
Fyn kinase
-
-
Fyn tyrosine kinase
-
-
fyn-related kinase
-
gene lck protein kinase
-
-
-
-
gene lck tyrosine kinase
-
-
-
-
Hck kinase
-
Hematopoietic consensus tyrosine-lacking kinase
Hemopoietic cell kinase
-
-
-
-
IL-1R-associated kinase
-
IL-2-inducible T-cell kinase
-
-
-
-
integrin-linked protein kinase 1
-
integrin-linked protein kinase 76
-
interleukin-1 receptor-associated kinase 1
-
interleukin-1 receptor-associated kinase-81
-
JAK protein tyrosine kinase
-
-
-
-
Jak tyrosine kinase
-
-
Jak2 protein
-
JAK2 tyrosine kinase
-
-
Janus family kinase JAK3
-
Janus kinase
Janus kinase 1
-
-
Janus kinase 2
just another kinase
-
-
Kinase EMB
-
-
-
-
Kinase EMT
-
-
-
-
Kinase TLK
-
-
-
-
kinase, protein (phosphorylating tyrosine)
-
-
-
-
kinase, protein p56lck (phosphorylating)
-
-
-
-
L-JAK
-
-
-
-
Lck kinase
-
Lck Tyrosine kinase
-
-
-
-
Leukocyte janus kinase
LIM domain kinase 2
-
LSK
-
-
-
-
lymphocyte-specific protein tyrosine kinase
-
-
Lyn tyrosine kinase
-
megakaryocyte-associated tyrosine-protein kinase
-
MIS type II receptor
-
non-receptor protein tyrosine kinase
-
-
non-receptor protein-tyrosine kinase
-
-
non-receptor PTK
-
-
non-receptor tyrosine kinase
-
-
non-receptor tyrosine kinase ABL
-
non-receptor tyrosine kinase brk
-
non-receptor tyrosine-protein kinase TYK2
-
nonreceptor protein tyrosine kinase
-
-
-
-
nonreceptor tyrosine kinase
nonreceptor tyrosine kinase c-Abl
-
nonreceptor tyrosine kinase Fes
-
nonreceptor tyrosine kinase SYK
-
nonreceptor tyrosine kinase Tec
-
NRTK
-
-
NTK38
-
-
-
-
Nuclear tyrosine protein kinase RAK
-
-
-
-
ORF6
-
-
-
-
p135tyk2 tyrosine kinase
-
p150
-
-
-
-
p55-BLK
-
-
-
-
P55-FGR
-
-
-
-
p56-HCK
-
-
-
-
p56-HCK/p59-HCK
-
-
-
-
P56-LCK
-
-
-
-
p56lck kinase
-
-
-
-
p56lck protein kinase
-
-
-
-
p56lck protein tyrosine kinase
-
-
-
-
p56lck tyrosine kinase
-
-
-
-
P57-STK
-
-
-
-
P59-FYN
-
-
-
-
p59-HCK/p60-HCK
-
-
-
-
P60-SRC
-
-
-
-
p60-YRK
-
-
-
-
P61-YES
-
-
-
-
p94-FER
-
-
-
-
phosphotyrosyl-protein kinase
-
-
-
-
PP125FAK
proline-rich tyrosin ekinase 2
-
-
proline-rich tyrosine kinase 2
proline-rich tyrosine kinase-2
-
-
Protein kinase (tyrosine-phosphorylating)
-
-
-
-
protein kinase A
-
-
-
-
Protein kinase BATK
-
-
-
-
Protein kinase HYL
-
-
-
-
Protein kinase Lck
-
-
-
-
Protein kinase NTK
-
-
-
-
Protein kinase p56-LCK
-
-
-
-
Protein kinase p56lck
-
-
-
-
Protein p56c-lck kinase
-
-
-
-
Protein p56lck tyrosine kinase
-
-
-
-
Protein tyrosine kinase
protein tyrosine kinase 2
-
-
protein tyrosine kinase 2beta
-
-
-
-
protein tyrosine kinase 6
-
protein tyrosine kinase 70
-
protein tyrosine kinase focal adhesion kinase
-
-
Protein tyrosine kinase lck
-
-
-
-
Protein tyrosine kinase p56lck
-
-
-
-
Protein tyrosine kinase pp56lck
-
-
-
-
protein-tyrosine kinase
-
-
protein-tyrosine kinase Brk
-
Protein-tyrosine kinase C-TKL
-
-
-
-
Protein-tyrosine kinase CYL
-
-
-
-
Protein-tyrosine kinase Syk
-
-
proto-oncogene serine/threonine-protein kinase mos
-
proto-oncogene tyrosine-protein kinase ABL1
-
proto-oncogene tyrosine-protein kinase FER
-
proto-oncogene tyrosine-protein kinase FES/FPS
-
proto-oncogene tyrosine-protein kinase FYN
-
proto-oncogene tyrosine-protein kinase LCK
-
proto-oncogene tyrosine-protein kinase SRC
-
proto-oncogene tyrosine-protein kinase YES
-
PTK-RL-18
-
-
-
-
PTK6/Sik
-
-
PTK70
Pyk-2
-
-
Quek1
-
-
-
-
RAF proto-oncogene serine/threonine-protein kinase
-
Raf-1 protein kinase
-
Rak tyrosine kinase
-
receptor interacting protein 3
-
receptor-associated kinase JAK2
-
receptor-interacting serine/threonine protein kinase 2
Related adhesion focal tyrosine kinase
-
-
-
-
Resting lymphocyte kinase
-
-
-
-
Rlk/Txk
-
-
-
-
S-domain receptor-like protein kinase
-
-
-
-
serine/threonine-protein kinase receptor R2
-
serine/threonine-protein kinase receptor R3
-
SLK
-
-
-
-
Spleen tyrosine kinase
Src family kinase
-
-
Src kinase
Src protein tyrosine kinase
-
-
src protein tyrosine kinase p56Lck
-
-
Src protein-tyrosine kinase
-
-
Src tyrosine kinase
Src-family protein tyrosine kinase
-
-
src-kinase
-
-
-
-
SRC-related intestinal kinase
-
-
-
-
Syk kinase
-
-
Syk-related tyrosine kinase
-
-
-
-
SYN
-
-
-
-
T cell-specific protein-tyrosine kinase
-
-
-
-
T-cell-specific kinase
-
-
-
-
Tec family tyrosine kinase
-
-
Tec kinase
-
-
testis-specific protein kinase 1
-
testis-specific protein kinase 2
-
TGF-beta receptor type I
-
TGF-beta receptor type II
-
TGF-beta RII
-
transforming growth factor beta type II receptor
-
transforming growth factor-beta type I receptor 7
-
Tyrosine kinase
-
-
-
-
tyrosine kinase 2
-
tyrosine kinase Abl
-
-
Tyrosine kinase ARG
-
-
-
-
tyrosine kinase c-Src
-
-
tyrosine kinase cyl
-
tyrosine kinase Fyn
-
Tyrosine kinase lck
-
-
-
-
Tyrosine kinase p56lck
-
-
-
-
tyrosine kinase p60c-src
-
-
tyrosine kinase PTK6
-
tyrosine kinase Src
-
-
tyrosine kinases src
-
tyrosine kinases yes
-
Tyrosine phosphokinase
-
-
-
-
Tyrosine protein kinase
-
-
-
-
Tyrosine protein kinase p56lck
-
-
-
-
tyrosine-protein kinase 6
-
tyrosine-protein kinase ABL2
-
tyrosine-protein kinase BLK
-
Tyrosine-protein kinase brk
-
-
-
-
tyrosine-protein kinase BTK
-
tyrosine-protein kinase CSK
-
Tyrosine-protein kinase CTK
-
-
-
-
tyrosine-protein kinase FRK
-
tyrosine-protein kinase HCK
-
tyrosine-protein kinase ITK/TSK
-
tyrosine-protein kinase JAK1
-
tyrosine-protein kinase JAK2
-
tyrosine-protein kinase JAK3
-
Tyrosine-protein kinase Lyk
-
-
-
-
tyrosine-protein kinase LYN
-
tyrosine-protein kinase SYK
-
tyrosine-protein kinase Tec
-
tyrosine-protein kinase TXK
-
Tyrosine-protein kinase TYRO 10
-
-
-
-
Tyrosine-specific protein kinase
-
-
-
-
Tyrosylprotein kinase
-
-
-
-
v-fps Protein-tyrosine kinase
-
-
-
-
WEE1hu
YES related kinase
-
-
-
-
ZAP-70
-
-
additional information
REACTION
REACTION DIAGRAM
COMMENTARY hide
ORGANISM
UNIPROT
LITERATURE
ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate
show the reaction diagram
REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
phospho group transfer
SYSTEMATIC NAME
IUBMB Comments
ATP:[protein]-L-tyrosine O-phosphotransferase (non-specific)
Unlike EC 2.7.10.1, receptor protein-tyrosine kinase, this protein-tyrosine kinase does not have a transmembrane domain. In the human genome, 32 non-specific protein-tyrosine kinases have been identified and these can be divided into ten families [1].
CAS REGISTRY NUMBER
COMMENTARY hide
114051-78-4
p56lck protein kinase
80449-02-1
protein-tyrosine kinase
9026-43-1
this CAS Reg. No. encompasses a great variety of protein kinases including the serine/threonine specific kinases
SUBSTRATE
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
LITERATURE
COMMENTARY hide
Reversibility
r=reversible
ir=irreversible
?=not specified
ATP + a protein
ADP + a phosphoprotein
show the reaction diagram
ATP + a [homeodomain-interacting protein kinase 2]-L-tyrosine
ADP + a [homeodomain-interacting protein kinase 2]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + a [peptide]-L-tyrosine
ADP + a [peptide]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + a [protein]-L-tyrosine
ADP + a [protein]-L-tyrosine phosphate
show the reaction diagram
ATP + a [Tyr-2 peptide]-L-tyrosine
ADP + a [Tyr-2 peptide]-L-tyrosine phosphate
show the reaction diagram
Substrates: -
Products: -
?
ATP + A-kinase anchor protein 8
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Abl
ADP + phospho-L-tyrosinyl-Abl
show the reaction diagram
ATP + arsenate resistance protein ARS2
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + ataxin 2 related protein
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Bad protein
ADP + phosphotyrosinyl Bad protein
show the reaction diagram
-
Substrates: substrate of Akt
Products: -
?
ATP + Bcl-2-associated transcription factor 1
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + beta 1-integrin cytoplasmic domain peptide
ADP + ?
show the reaction diagram
Substrates: -
Products: -
?
ATP + beta-catenin
ADP + phospho-tyrosinyl-beta-catenin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + biotin-GGEAIYAAPFKK-amide
ADP + phosphorylated biotin-GGEAIYAAPFKK-amide
show the reaction diagram
-
Substrates: a peptide with the preferred c-Abl substrate sequence carrying an Nterminal biotin
Products: -
?
ATP + c-Src
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + calponin 3
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Cas protein
ADP + phospho-tyrosinyl-Cas protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cdc2(6-20) peptide
?
show the reaction diagram
-
Substrates: i.e. KVEKIGEGTYGVVYK, substrate of Src family kinases
Products: -
?
ATP + chromosome 20 open reading frame 77
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cleavage and polyadenylation specific factor 5
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cofilin
ADP + phosphorylated cofilin
show the reaction diagram
Substrates: phosphorylation specifically at Ser-3
Products: -
?
ATP + cortactin
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cortactin
ADP + phospho-tyrosinyl-cortactin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cyclin-associated cyclin-dependent kinase
ADP + phosphorylated cyclin-associated cyclin-dependent kinase
show the reaction diagram
ATP + EEEEY
ADP + EEEE(phospho)Y
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + EEEEYIQ[dP]-8-hydroxy-5-(N,N-dimethylsulfonamido)-2-methylquinoline-G
ADP + EEEEYIQ[dP]-8-hydroxy-5-(N,N-dimethylsulfonamido)-2-methylquinoline-G phosphate
show the reaction diagram
-
Substrates: Y7 Sox-based substrate, kinetic assay
Products: -
?
ATP + epidermal growth factor receptor
ADP + phospho-L-tyrosinyl-epidermal growth factor receptor
show the reaction diagram
ATP + EQEDEPEGDYFEWLE
ADP + EQEDEPEGDpYFEWLE
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + eukaryotic translation initiation factor 3, subunit 4
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + ewing sarcoma breakpoint region 1
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + ezrin
ADP + phospho-tyrosinyl-ezrin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + F peptide
ADP + phospho-L-tyrosinyl-F peptide
show the reaction diagram
-
Substrates: i.e. biotin-Aca-AAAEEIFGEI-NH2
Products: -
?
ATP + FAK
ADP + phospho-tyrosinyl-FAK
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + FUS interacting protein (serine/arginine rich) 1
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + FUS/TLS oncogene
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + FUSE binding protein
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + FUSE binding protein 2
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + GAPEVIYATPGAKKK
ADP + GAPEVI-phosphotyrosinyl-ATPGAKKK
show the reaction diagram
-
Substrates: consensus substrate
Products: -
?
ATP + GGEAIYAAPFKK
ADP + GGEAIYAAPFKK phosphate
show the reaction diagram
-
Substrates: kinase assay using biotinylated model substrate peptide
Products: -
?
ATP + glycogen synthase kinase 3beta
ADP + phosphotyrosinyl glycogen synthase kinase 3beta
show the reaction diagram
-
Substrates: substrate of Akt
Products: -
?
ATP + heterogeneous nuclear ribonucleoprotein A3
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + heterogeneous nuclear ribonucleoprotein AB
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + heterogeneous nuclear ribonucleoprotein D-like
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + heterogeneous nuclear ribonucleoprotein K
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + histone
ADP + phosphorylated histone
show the reaction diagram
Substrates: serine/threonine-specific kinase activity
Products: -
?
ATP + homeobox prox 1
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + IkappaBalpha-L-tyrosine
ADP + IkappaBalpha-L-tyrosine phosphate
show the reaction diagram
ATP + KVEKIGEGTYGVVYK
ADP + ?
show the reaction diagram
-
Substrates: synthetic peptide substrate
Products: -
?
ATP + lysozyme-L-tyrosine
ADP + lysozyme-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate of Src, low activity with Csk or Chk
Products: -
?
ATP + myelin basic protein
ADP + ?
show the reaction diagram
Substrates: -
Products: -
?
ATP + myelin basic protein
ADP + phosphorylated myelin basic protein
show the reaction diagram
ATP + NaV1.2 channel
ADP + phospho-L-tyrosinyl-NaV1.2 channel
show the reaction diagram
-
Substrates: Y66 and Y1893, which are in consensus sequences appropriate for binding to the Fyn SH2 domain after phosphorylation, are both required for optimal binding and regulation by Fyn. Y730, which is located near the SH3-binding motif in LI-II, and Y1497 and Y1498 in the inactivation gate in LIII-IV, are also required for optimal regulation, but phosphorylation of these sites likely promotes fast inactivation
Products: -
?
ATP + NEFA-interacting nuclear protein
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + NICE-4
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + P1 peptide
ADP + phospho-L-tyrosinyl-P1 peptide
show the reaction diagram
-
Substrates: i.e. biotin-Aca-AAAEEIpYGEI-NH2
Products: -
?
ATP + p120 protein
ADP + phospho-tyrosinyl-p120 protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + p190 GTPase
ADP + phospho-tyrosinyl-p190 GTPase
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + p34cdc2
ADP + phosphorylated p34cdc2
show the reaction diagram
ATP + PAK1
ADP + phospho-L-tyrosinyl-PAK1
show the reaction diagram
ATP + paxillin
ADP + phospho-tyrosinyl-Shc paxillin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + PIKE-A
ADP + phosphotyrosinyl-PIKE-A
show the reaction diagram
ATP + plakoglobin
ADP + phospho-tyrosinyl-plakoglobin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + poly(Glu,Tyr)
? + ADP
show the reaction diagram
Substrates: substrate used in the tyrosine kinase asssay
Products: -
?
ATP + poly(Glu-Tyr)
? + ADP
show the reaction diagram
-
Substrates: substrate used in the activity assay
Products: -
?
ATP + poly(Glu4-Tyr)
ADP + poly(Glu4-Tyr)-L-tyrosine phosphate
show the reaction diagram
ATP + proteasome activator subunit 3
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + protein
?
show the reaction diagram
Substrates: CSK phosphorylates other members of the src-family of tyrosine kinases at their regulatory carboxy-terminus. By regulating the activity of these kinases, CSK may play an important role in cell growth and development
Products: -
?
ATP + protein
ADP + protein tyrosine phosphate
show the reaction diagram
Substrates: CSK phosphorylates other members of the src-family of tyrosine kinases at their regulatory carboxy-terminus
Products: -
?
ATP + protein tyrosine
ADP + protein tyrosine phosphate
show the reaction diagram
ATP + protein tyrosine kinase Yes
ADP + phospho-L-tyrosinyl Yes
show the reaction diagram
-
Substrates: Csk inactivates the enzyme substrate
Products: -
?
ATP + RasGAP SH3-domain binding protein
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + recombinant GST/beta3 integrin cytoplasmic tail peptide
ADP + ?
show the reaction diagram
Substrates: -
Products: -
?
ATP + Rho protein
ADP + phospho-tyrosinyl-Rho protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + RNA binding motif protein 10
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + RNA binding motif protein 4B
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + S1 peptide
ADP + phospho-L-tyrosinyl-S1 peptide
show the reaction diagram
-
Substrates: i.e. biotin-Aca-AAAEEIYGEI-NH2
Products: -
?
ATP + Shc protein
ADP + phospho-tyrosinyl-Shc protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + signal transducer and activator of transcription
ADP + phospho-L-tyrosinyl-signal transducer and activator of transcription
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + similar to zinc finger CCCH-type domain-containing protein 6
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + splicing factor proline/glutamine-rich
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + splicing factor, arginine/serine-rich9
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Src
ADP + phospho-L-tyrosinyl Src family kinase
show the reaction diagram
-
Substrates: wild-type Src and catalytically inactive mutant Src K295M, terminal Src kinase Csk specifically phosphorylates Src family kinases on a C-terminal Tyr residue, which down-regulates their activities, identification of the docking determinants in Src recognized by the Csk substrate-docking site, Glu510 of Src interacts with Arg283 of Csk in Csk-Src recognition, activity with Src fragments, overview
Products: -
?
ATP + Src family kinase
?
show the reaction diagram
-
Substrates: substrate of the protein kinases CSK and CHK, which specifically phosphorylate a tyrosine residue at the C-terminus forming intramolecular bonds to the SH2 domain and inhibiting the Src family kinase, overview
Products: -
?
ATP + Src family kinase
ADP + phospho-L-tyrosinyl Src family kinase
show the reaction diagram
-
Substrates: terminal Src kinase Csk specifically phosphorylates Src family kinases on a C-terminal Tyr residue, which down-regulates their activities, identification of the docking determinants in Src recognized by the Csk substrate-docking site
Products: -
?
ATP + Src protein
ADP + Src protein phosphate
show the reaction diagram
Substrates: MATK can phosphorylate the carboxyl-terminal conserved tyrosine of the Src protein
Products: -
?
ATP + STAT3
ADP + phospho-L-tyrosinyl-STAT3
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + STAT3
ADP + phospho-tyrosinyl-STAT3
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Tc10/Cdc42 GTPase-activating protein
ADP + phospho-L-tyrosinyl-Tc10/Cdc42 GTPase-activating protein
show the reaction diagram
ATP + thyroid hormone receptor associated protein 3
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + TRK-fused gene
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Tyr267 of Vav1
ADP + phosphorylated Tyr267 of Vav1
show the reaction diagram
-
Substrates: -
Products: isoform c-Abl kinase probably regulates the activity of Rho guanine exchange factor Vav1 by direct phosphorylation at Tyr267 in the Dbl homology domain. The C-terminal SH3-SH2-SH3 domain and proline-rich region of Vav1 are required for its interaction with c-Abl kinase
?
ATP + zinc finger, CCHC domain containing protein 8
?
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [Abi1]-L-tyrosine
ADP + [Abi1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: c-Abl phosphorylates Y213 of Abi1
Products: -
?
ATP + [actin-stabilizing adapter protein HS1]-L-tyrosine
ADP + [actin-stabilizing adapter protein HS1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: c-Abl binds to phospho-HS1 via its SH2 domains and is required for full tyrosine phosphorylation of HS1 during T-cell activation
Products: -
?
ATP + [androgen receptor]-L-tyrosine
ADP + [androgen receptor]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [aryl hydrocarbon receptor]-L-tyrosine
ADP + [aryl hydrocarbon receptor]-L-tyrosine phosphate
show the reaction diagram
ATP + [c-Cbl]-L-tyrosine
ADP + [c-Cbl]-L-tyrosine phosphate
show the reaction diagram
ATP + [carrier protein-intein-CAEEEIYGEFEA]-L-tyrosine
ADP + [carrier protein-intein-CAEEEIYGEFEA]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CAEEEIYGEFEA derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGKYGVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGKYGVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGKYGVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTFGVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTFGVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTFGVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTpYGVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTpYGVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTpYGVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTYFVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTYFVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTYFVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTYGVEYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTYGVEYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTYGVEYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTYGVVFK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTYGVVFK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTYGVVFK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGEGTYGVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGEGTYGVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGEGTYGVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [carrier protein-intein-CIGKGTYGVVYK]-L-tyrosine
ADP + [carrier protein-intein-CIGKGTYGVVYK]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate is synthesized by fusing a 27 kDa carrier protein to intein which is linked to the peptide CIGKGTYGVVYK derived from human cyclin-dependent kinase harboring a phosphorylation site for Src kinase
Products: -
?
ATP + [estrogen receptor alpha]-L-tyrosine
ADP + [estrogen receptor alpha]-L-tyrosine phosphate
show the reaction diagram
ATP + [fibroblast growth factor receptor FGFR2]-L-tyrosine
ADP + [fibroblast growth factor receptor FGFR2]-L-tyrosine phosphate
show the reaction diagram
ATP + [fibroblast growth factor receptor FGFR3]-L-tyrosine
ADP + [fibroblast growth factor receptor FGFR3]-L-tyrosine phosphate
show the reaction diagram
ATP + [hyperpolarization-activated, cyclic nucleotide-gated 4 channel]-L-tyrosine
ADP + [hyperpolarization-activated, cyclic nucleotide-gated 4 channel]-L-tyrosine phosphate
show the reaction diagram
Substrates: substrate HCN4, tyrosine 531 is phosphorylated
Products: -
?
ATP + [kdSrc kinase]-L-tyrosine
ADP + [kdSrc kinase]-L-tyrosine phosphate
show the reaction diagram
ATP + [P-110]-L-tyrosine
ADP + [P-110]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p110 catalytic subunit of PI 3-kinase]-L-tyrosine
ADP + [p110 catalytic subunit of PI 3-kinase]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p21Cip1]-L-tyrosine
ADP + [p21Cip1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p27Kip1]-L-tyrosine
ADP + [p27Kip1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p57Kip2]-L-tyrosine
ADP + [p57Kip2]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [parkin]-Tyr143
ADP + [parkin]-phospho-Tyr143
show the reaction diagram
-
Substrates: -
Products: nonreceptor tyrosine kinase c-Abl phosphorylates tyrosine 143 of parkin, which encodes a ubiquitin E3 ligase, related to autosomal recessive Parkinson disease. Phosphorylation inhibits parkin's ubiquitin E3 ligase activity and protective function
?
ATP + [protein]-L-tyrosine
ADP + [protein]-L-tyrosine phosphate
show the reaction diagram
ATP + [Runx1]-L-tyrosine
ADP + [Runx1]-L-tyrosine phosphate
show the reaction diagram
ATP + [Sam68]-L-tyrosine
ADP + [Sam68]-L-tyrosine phosphate
show the reaction diagram
ATP + [Signal Transducer and Activation of Transcription (STAT) protein]-L-tyrosine
ADP + [Signal Transducer and Activation of Transcription (STAT) protein]-L-tyrosine phosphate
show the reaction diagram
Substrates: -
Products: -
?
ATP + [Src-family protein tyrosine kinase]-L-tyrosine
ADP + [Src-family protein tyrosine kinase]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: i.e. SFK, substrate of protein tyrosine kinases Csk and Chk, phosphorylation at the regulatory tyrosine leading to inhibition of the SFK
Products: -
?
ATP + [Stat5B]-L-tyrosine
ADP + [Stat5B]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: activation by non-receptor tyrosine kinase Pyk2
Products: -
?
ATP + [transmembrane adaptor protein LAT]-L-tyrosine
ADP + [transmembrane adaptor protein LAT]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate of ZAP-70
Products: -
?
ATP + [tubulin]-L-tyrosine
ADP + [tubulin]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: highly active with c-Fes, which also catalyzes tubulin polymerization in vitro
Products: -
?
ATP + [vimentin]-L-tyrosine
ADP + [vimentin]-L-tyrosine phosphate
show the reaction diagram
Substrates: -
Products: -
?
ATP + [ZAP-70]-L-tyrosine
ADP + [ZAP-70]-L-tyrosine phosphate
show the reaction diagram
ATP + [[Lys19]Cdc2-(6-20) peptide]-L-tyrosine
?
show the reaction diagram
-
Substrates: i.e. KVEKIGEGTYGVVKK
Products: -
?
gelsolin + ATP
phospho-tyrosinyl gelsolin + ADP
show the reaction diagram
p130Cas + ATP
phospho-tyrosinyl p130Cas + ADP
show the reaction diagram
-
Substrates: phosphorylation of the Crk and Nck adaptor protein by Fak
Products: -
?
paxillin + ATP
phospho-tyrosinyl paxillin + ADP
show the reaction diagram
STAT transcription activator protein + ATP
phosphorylated STAT transcription activator protein + ADP
show the reaction diagram
Wiskott-Aldrich syndrome protein + ATP
phospho-tyrosinyl Wiskott-Aldrich syndrome protein + ADP
show the reaction diagram
-
Substrates: i.e. WASP, phosphorylation by Fak
Products: -
?
additional information
?
-
NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
LITERATURE
COMMENTARY hide
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
ATP + a protein
ADP + a phosphoprotein
show the reaction diagram
ATP + a [homeodomain-interacting protein kinase 2]-L-tyrosine
ADP + a [homeodomain-interacting protein kinase 2]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + a [protein]-L-tyrosine
ADP + a [protein]-L-tyrosine phosphate
show the reaction diagram
ATP + Abl
ADP + phospho-L-tyrosinyl-Abl
show the reaction diagram
-
Substrates: Abl is an important substrate for Src signalling in normal cells
Products: -
?
ATP + Bad protein
ADP + phosphotyrosinyl Bad protein
show the reaction diagram
-
Substrates: substrate of Akt
Products: -
?
ATP + beta-catenin
ADP + phospho-tyrosinyl-beta-catenin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Cas protein
ADP + phospho-tyrosinyl-Cas protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cortactin
ADP + phospho-tyrosinyl-cortactin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + cyclin-associated cyclin-dependent kinase
ADP + phosphorylated cyclin-associated cyclin-dependent kinase
show the reaction diagram
Substrates: Wee1 negatively regulates cyclin-dependent kinases by phosphorylation on Y15
Products: -
?
ATP + epidermal growth factor receptor
ADP + phospho-L-tyrosinyl-epidermal growth factor receptor
show the reaction diagram
-
Substrates: the activated Abl tyrosine kinase negaively regulates endocytosis of the epidermal growth factor, e.g. in NR6 cells, overview, Abl allows the ligand-activated EGFR to escape Cbl-dependent down-regulation by inhibiting the accumulation of Cbl at the plasma membrane in response to epidermal growth factor stimulation and disrupting the formation of the EGFR-Cbl complex without affecting Cbl protein stability
Products: -
?
ATP + ezrin
ADP + phospho-tyrosinyl-ezrin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + FAK
ADP + phospho-tyrosinyl-FAK
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + glycogen synthase kinase 3beta
ADP + phosphotyrosinyl glycogen synthase kinase 3beta
show the reaction diagram
-
Substrates: substrate of Akt
Products: -
?
ATP + IkappaBalpha-L-tyrosine
ADP + IkappaBalpha-L-tyrosine phosphate
show the reaction diagram
-
Substrates: p56lck regulates cell motility and nuclear factor kappaB-mediated secretion of urokinase type plasminogen activator through tyrosine phosphorylation of IkappaBalpha following hypoxia/reoxygenation, molecular mechanism, physiological role
Products: -
?
ATP + NaV1.2 channel
ADP + phospho-L-tyrosinyl-NaV1.2 channel
show the reaction diagram
-
Substrates: Y66 and Y1893, which are in consensus sequences appropriate for binding to the Fyn SH2 domain after phosphorylation, are both required for optimal binding and regulation by Fyn. Y730, which is located near the SH3-binding motif in LI-II, and Y1497 and Y1498 in the inactivation gate in LIII-IV, are also required for optimal regulation, but phosphorylation of these sites likely promotes fast inactivation
Products: -
?
ATP + p120 protein
ADP + phospho-tyrosinyl-p120 protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + p190 GTPase
ADP + phospho-tyrosinyl-p190 GTPase
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + p34cdc2
ADP + phosphorylated p34cdc2
show the reaction diagram
Substrates: Wee1 kinase inhibits mitosis by directly phosphorylating p34cdc2 on Y15
Products: -
?
ATP + PAK1
ADP + phospho-L-tyrosinyl-PAK1
show the reaction diagram
-
Substrates: Jak2 is involved in the regulation of serine-threonine kinase PAK1, maximal cell motility is required for tyrosyl phosphorylation of PAK1
Products: -
?
ATP + paxillin
ADP + phospho-tyrosinyl-Shc paxillin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + PIKE-A
ADP + phosphotyrosinyl-PIKE-A
show the reaction diagram
-
Substrates: i.e. phosphatidylinositol 3-kinase enhancer-activating Akt, phosphorylation by fyn is essential for PIKE-A complex formation and apoptotic cleavage, overview
Products: -
?
ATP + plakoglobin
ADP + phospho-tyrosinyl-plakoglobin
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + protein
?
show the reaction diagram
Substrates: CSK phosphorylates other members of the src-family of tyrosine kinases at their regulatory carboxy-terminus. By regulating the activity of these kinases, CSK may play an important role in cell growth and development
Products: -
?
ATP + protein
ADP + protein tyrosine phosphate
show the reaction diagram
Substrates: CSK phosphorylates other members of the src-family of tyrosine kinases at their regulatory carboxy-terminus
Products: -
?
ATP + protein tyrosine
ADP + protein tyrosine phosphate
show the reaction diagram
Substrates: p135tyk2 tyrosine kinase directly binds and tyrosine phosphorylates alpha subunit of the type I IFN receptor, IFN-R
Products: -
?
ATP + protein tyrosine kinase Yes
ADP + phospho-L-tyrosinyl Yes
show the reaction diagram
-
Substrates: Csk inactivates the enzyme substrate
Products: -
?
ATP + Rho protein
ADP + phospho-tyrosinyl-Rho protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Shc protein
ADP + phospho-tyrosinyl-Shc protein
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Src family kinase
?
show the reaction diagram
-
Substrates: substrate of the protein kinases CSK and CHK, which specifically phosphorylate a tyrosine residue at the C-terminus forming intramolecular bonds to the SH2 domain and inhibiting the Src family kinase, overview
Products: -
?
ATP + Src family kinase
ADP + phospho-L-tyrosinyl Src family kinase
show the reaction diagram
-
Substrates: terminal Src kinase Csk specifically phosphorylates Src family kinases on a C-terminal Tyr residue, which down-regulates their activities, identification of the docking determinants in Src recognized by the Csk substrate-docking site
Products: -
?
ATP + Src protein
ADP + Src protein phosphate
show the reaction diagram
Substrates: MATK can phosphorylate the carboxyl-terminal conserved tyrosine of the Src protein
Products: -
?
ATP + STAT3
ADP + phospho-tyrosinyl-STAT3
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + Tc10/Cdc42 GTPase-activating protein
ADP + phospho-L-tyrosinyl-Tc10/Cdc42 GTPase-activating protein
show the reaction diagram
-
Substrates: physical and functional interaction of Fyn with the brain-enriched Rho GTPase-activating protein Tc10/Cdc42 GTPase-activating protein, i.e. TCGAP, TCGAP is involved in Fyn-mediated regulation of axon and dendrite outgrowth
Products: -
?
ATP + [androgen receptor]-L-tyrosine
ADP + [androgen receptor]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [aryl hydrocarbon receptor]-L-tyrosine
ADP + [aryl hydrocarbon receptor]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: Src tyrosine kinases are involved in a signaling transduction pathway activating aryl hydrocarbon receptor AhR-mediated signalling by omeprazole or 2,3,7,8-tetrachlorodibenzo-4-dioxin TCDD ligand-binding, AhR phosphorylation at Tyr320, the omeprazole-dependent mechanism probably involves S318 and K316
Products: -
?
ATP + [c-Cbl]-L-tyrosine
ADP + [c-Cbl]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: proto-oncogenic PTK protein substrate
Products: -
?
ATP + [estrogen receptor alpha]-L-tyrosine
ADP + [estrogen receptor alpha]-L-tyrosine phosphate
show the reaction diagram
Substrates: -
Products: estrogen receptor alpha associates with c-Abl nonreceptor tyrosine kinase. The direct interaction is mediated by two PXXP motifs of estrogen receptor alpha and the c-Abl SH3 domain. Estrogen receptor alpha can be phosphorylated on residues Y52 and Y219. Phosphorylation by c-Abl stabilizes estrogen recptor alpha, resulting in enhanced estrogen receptor alpha transcriptional activity and increased expression of endogenous target genes. Phosphorylation at the Y219 site affects DNA binding and dimerization by estrogen receptor alpha. c-Abl kinase activity is required for regulation of the estrogen receptor alpha function, and a Y52F/Y219F mutant estrogen receptor leads to reduced breast cancer cell growth and invasion
?
ATP + [fibroblast growth factor receptor FGFR2]-L-tyrosine
ADP + [fibroblast growth factor receptor FGFR2]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: activation by non-receptor tyrosine kinase Pyk2, interaction via the FGFR juxtamembrane and the Pyk2 kinase domain, activation is antagonized by tyrosine phosphatase Shp2
Products: -
?
ATP + [fibroblast growth factor receptor FGFR3]-L-tyrosine
ADP + [fibroblast growth factor receptor FGFR3]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: activation by non-receptor tyrosine kinase Pyk2, interaction via the FGFR juxtamembrane and the Pyk2 kinase domain, activation is antagonized by tyrosine phosphatase Shp2
Products: -
?
ATP + [P-110]-L-tyrosine
ADP + [P-110]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p110 catalytic subunit of PI 3-kinase]-L-tyrosine
ADP + [p110 catalytic subunit of PI 3-kinase]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p21Cip1]-L-tyrosine
ADP + [p21Cip1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p27Kip1]-L-tyrosine
ADP + [p27Kip1]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [p57Kip2]-L-tyrosine
ADP + [p57Kip2]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: -
Products: -
?
ATP + [parkin]-Tyr143
ADP + [parkin]-phospho-Tyr143
show the reaction diagram
-
Substrates: -
Products: nonreceptor tyrosine kinase c-Abl phosphorylates tyrosine 143 of parkin, which encodes a ubiquitin E3 ligase, related to autosomal recessive Parkinson disease. Phosphorylation inhibits parkin's ubiquitin E3 ligase activity and protective function
?
ATP + [protein]-L-tyrosine
ADP + [protein]-L-tyrosine phosphate
show the reaction diagram
ATP + [Runx1]-L-tyrosine
ADP + [Runx1]-L-tyrosine phosphate
show the reaction diagram
Substrates: the enzyme phosphorylates transcription factor Runx1 and regulates Runx1-mediated megakaryocyte maturation
Products: -
?
ATP + [Sam68]-L-tyrosine
ADP + [Sam68]-L-tyrosine phosphate
show the reaction diagram
ATP + [Src-family protein tyrosine kinase]-L-tyrosine
ADP + [Src-family protein tyrosine kinase]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: i.e. SFK, substrate of protein tyrosine kinases Csk and Chk, phosphorylation at the regulatory tyrosine leading to inhibition of the SFK
Products: -
?
ATP + [Stat5B]-L-tyrosine
ADP + [Stat5B]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: activation by non-receptor tyrosine kinase Pyk2
Products: -
?
ATP + [transmembrane adaptor protein LAT]-L-tyrosine
ADP + [transmembrane adaptor protein LAT]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate of ZAP-70
Products: -
?
ATP + [ZAP-70]-L-tyrosine
ADP + [ZAP-70]-L-tyrosine phosphate
show the reaction diagram
-
Substrates: substrate of Lck, Fyn, and c-Abl, leads to ZAP-70 activation, mechanism
Products: -
?
gelsolin + ATP
phospho-tyrosinyl gelsolin + ADP
show the reaction diagram
-
Substrates: phosphorylation by PYK2 increases the binding of gelsolin to phosphoatidylinositol lipids and actin polymerization at the fibroblastic cell periphery
Products: -
?
p130Cas + ATP
phospho-tyrosinyl p130Cas + ADP
show the reaction diagram
-
Substrates: phosphorylation of the Crk and Nck adaptor protein by Fak
Products: -
?
paxillin + ATP
phospho-tyrosinyl paxillin + ADP
show the reaction diagram
-
Substrates: phosphorylation at Tyr31 and Tyr118 by Fak plays a role in tumor cell motility inhibition
Products: -
?
STAT transcription activator protein + ATP
phosphorylated STAT transcription activator protein + ADP
show the reaction diagram
-
Substrates: activation of STAT by phosphorylation is required for translocation to the nucleus, the enzyme regulates the cytokine expression via STAT, overview
Products: -
?
Wiskott-Aldrich syndrome protein + ATP
phospho-tyrosinyl Wiskott-Aldrich syndrome protein + ADP
show the reaction diagram
-
Substrates: i.e. WASP, phosphorylation by Fak
Products: -
?
additional information
?
-
COFACTOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
METALS and IONS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
Fe3+
-
when Lyn or Hck kinases, which have been stabilised in the inactive state by phosphorylation of the C-terminal regulatory tyrosine, are incubated with Fe3+ ions, a significant enhancement of kinase activity is observed
additional information
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(2-[2-[(3,5-dimethylphenyl)amino]pyrimidin-4-yl]-1,3-thiazol-4-yl)methanol
-
-
(2-[2-[(3,5-dimethylphenyl)amino]pyrimidin-4-yl]-1,3-thiazol-5-yl)methanol
-
-
(2E)-3-(6-bromopyridin-2-yl)-2-cyano-N-[(1S)-1-phenylethyl]prop-2-enamide
-
WP1066
(2E)-N-benzyl-2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enamide
-
LS104
(2E,4E)-N-benzyl-2-cyano-5-(3,4-dihydroxyphenyl)penta-2,4-dienamide
-
AG490, potent JAK2 inhibitor
1-(4-((5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) amino)piperidin-1-yl)ethan-1-one
100 nM, 70.5% inhibition. 28°C, pH not specified in the publication
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)ethan-1-one
100 nM, 66.2% inhibition. 28°C, pH not specified in the publication
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)pentane-1,4-dione
100 nM, 56.4% inhibition. 28°C, pH not specified in the publication
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)propan-1-one
100 nM, 73.4% inhibition. 28°C, pH not specified in the publication
1-(4-acetylphenyl)-3-(1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)azetidin-3-yl)urea
100 nM, 21.9% inhibition. 28°C, pH not specified in the publication
1-(4-acetylphenyl)-3-(1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)pyrrolidin-3-yl)urea
100 nM, 57.4% inhibition. 28°C, pH not specified in the publication
1-(4-[5-(4-ethoxybenzoyl)-6-[(propan-2-yl)amino]pyrimidin-4-yl]piperazin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 24.04%
1-(4-[5-(4-phenoxybenzoyl)-6-[(propan-2-yl)amino]pyrimidin-4-yl]piperazin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 48.54%
1-(4-[6-[(5-cyclopropyl-1H-pyrazol-3-yl)amino]-2-methylpyrimidin-4-yl]piperazin-1-yl)-3-(1-nonadecyl-1H-1,2,3-triazol-4-yl)propan-1-one
-
1-(4-[[5-(4-ethoxybenzoyl)-6-(ethylamino)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 6.81%
1-(4-[[5-(4-ethoxybenzoyl)-6-(methylamino)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is %
1-(4-[[6-(dimethylamino)-5-(4-ethoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 9.8%
1-(4-[[6-(ethylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is %
1-(4-[[6-(methylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 10.61%
1-(4-[[6-amino-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl)prop-2-en-1-one
inhibitory rate at 0.01 mM is 78.13%
1-azaanthraquinones
-
-
-
1-methyl-emodin
-
inhibition of p56lck and c-Src
1-[(3R)-3-([5-(4-phenoxybenzoyl)-6-[(propan-2-yl)amino]pyrimidin-4-yl]amino)piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 14.56%
1-[(3R)-3-[[5-(4-ethoxybenzoyl)-6-(methylamino)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 10.27%
1-[(3R)-3-[[5-(4-phenoxybenzoyl)-6-(piperidin-1-yl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 15.67%
1-[(3R)-3-[[6-(dimethylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 11.42%
1-[(3R)-3-[[6-(ethylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 18.24%
1-[(3R)-3-[[6-(methylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 6.66%
1-[(3R)-3-[[6-amino-5-(4-ethoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 52.88%
1-[(3R)-3-[[6-amino-5-(4-phenoxybenzoyl)pyrimidin-4-yl]amino]piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 100%
1-[4-([5-(4-ethoxybenzoyl)-6-[(propan-2-yl)amino]pyrimidin-4-yl]amino)piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 8.69%
1-[4-([5-(4-phenoxybenzoyl)-6-[(propan-2-yl)amino]pyrimidin-4-yl]amino)piperidin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 1.2%
1-[4-[5-(4-ethoxybenzoyl)-6-(ethylamino)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 6.43%
1-[4-[5-(4-ethoxybenzoyl)-6-(methylamino)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 11-87%
1-[4-[6-(ethylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 17.53%
1-[4-[6-(methylamino)-5-(4-phenoxybenzoyl)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 8.14%
1-[4-[6-amino-5-(4-ethoxybenzoyl)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 87.67 %
1-[4-[6-amino-5-(4-phenoxybenzoyl)pyrimidin-4-yl]piperazin-1-yl]prop-2-en-1-one
inhibitory rate at 0.01 mM is 93.21%
2,5-dihydroxy-3-(3,4-dihydroxyphenyl)-6-phenyl-1,4-benzoquinone
-
secondary metabolite isolated from fungus Stilbella sp. strain 1586
2,5-dihydroxy-3-phenyl-6-(3,4,5-trihydroxyphenyl)-1,4-benzoquinone
-
secondary metabolite isolated from fungus Stilbella sp. strain 1586
2,7,8-trihydroxy-3-phenyl-1,4-dibenzofurandione
-
secondary metabolite isolated from fungus Stilbella sp. strain 1586
2-(1,1-dimethylethyl)-9-fluoro-3,6-dihydro-7H-benz[h]-imidaz[4,5-f]isoquinolin-7-one
-
i.e. JAK inhibitor-I
2-(2-[2-[(3,5-dimethylphenyl)amino]pyrimidin-4-yl]-4-methyl-1,3-thiazol-5-yl)ethanol
-
-
2-(4-acetylphenyl)-1-(4-(2-((4-morpholinophenyl)amino)thieno[3,2-d]pyrimidin-4-yl)piperazin-1-yl)ethan-1-one
100 nM, 44% inhibition. 28°C, pH not specified in the publication
2-chloro-N-[5-[(3-chlorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
2-chloro-N-[5-[(3-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
2-chloro-N-[5-[(4-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
2-chloro-N-[5-[(4-methoxybenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
2-chloro-N-[5-[(4-nitrobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
2-chloro-omega-hydroxy-emodin
-
inhibition of p56lck and c-Src
2-cyclopentyl-9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-9H-purin-6-amine
-
2-tert-butyl-9-fluoro-3,6-dihydro-7H-benz[h]-imidaz[4,5-f]isoquinoline-7-one
-
potent pan-JAK inhibitor
2-[2-[(3,5-dimethylphenyl)amino]pyrimidin-4-yl]-N-[(1R)-2-hydroxy-1-methylethyl]-4-methyl-1,3-thiazole-5-carboxamide
-
-
2-[2-[(3,5-dimethylphenyl)amino]pyrimidin-4-yl]-N-[(1S)-2-hydroxy-1-methylethyl]-4-methyl-1,3-thiazole-5-carboxamide
-
-
2-[4-methyl-2-(2-[[3-methyl-5-(trifluoromethyl)phenyl]amino]pyrimidin-4-yl)-1,3-thiazol-5-yl]ethanol
-
-
3-(9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-6-[[4-(dimethylphosphoryl)phenyl]amino]-9H-purin-2-yl)propanenitrile
-
3-([4-[4-(hydroxymethyl)-1,3-thiazol-2-yl]pyrimidin-2-yl]amino)-5-(trifluoromethyl)phenol
-
-
3-amino-5-((2R)-3-methylbutan-2-yl)-7-[5-(morpholin-4-yl)-pyridin-2-yl]-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-((2S)-3-methylbutan-2-yl)-7-(1-methyl-1H-pyrazol-3-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-((2S)-3-methylbutan-2-yl)-7-[1-methyl-5-(morpholin-4-yl)-1H-pyrazol-3-yl]-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-((2S)-3-methylbutan-2-yl)-7-[1-methyl-5-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-3-yl]-1,5-dihydro-4H-pyrazolo[4,3-c]-pyridin-4-one
-
3-amino-5-((2S)-3-methylbutan-2-yl)-7-[5-(morpholin-4-yl)-pyridin-2-yl]-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-(2-methylpentan-3-yl)-7-(1-methyl-1H-pyrazol-3-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-(3-methylbutan-2-yl)-7-(1-methyl-1H-pyrazol-3-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-(3-methylbutan-2-yl)-7-[5-(morpholin-4-yl)pyridin-2-yl]-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-isobutyl-7-(1-methyl-1H-pyrazol-3-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-5-sec-butyl-7-(1-methyl-1H-pyrazol-3-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-7-[5-(1,1-dioxidothiomorpholin-4-yl)-1-methyl-1H-pyrazol-3-yl]-5-((2S)-3-methylbutan-2-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
-
3-amino-7-[5-(2-hydroxypropan-2-yl)-1-methyl-1H-pyrazol-3-yl]-5-((2S)-3-methylbutan-2-yl)-1,5-dihydro-4H-pyrazolo[4,3-c]pyridin-4-one
3-[(3R,4R)-4-methyl-3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]piperidin-1-yl]-3-oxopropanenitrile
-
CP-690,550 JAK3-specific inhibitor
3-[3-[[4-(1,3-thiazol-2-yl)pyrimidin-2-yl]amino]-5-(trifluoromethyl)phenoxy]propan-1-ol
-
-
3-[[4-(1,3-thiazol-2-yl)pyrimidin-2-yl]amino]-5-(trifluoromethyl)phenol
-
-
4-(2,4-dichloro-5-methoxyanilino)-6-methoxy-7-[3-(4-methylpiperazin-1-yl)propoxy]quinoline-3-carbonitrile
-
inhibitor of Src and Abl
4-(2-(4-(2-((4-morpholinophenyl)amino)thieno[3,2-d]pyrimidin-4-yl)piperazin-1-yl)-2-oxoethyl)benzonitrile
100 nM, 17.6% inhibition. 28°C, pH not specified in the publication
4-(4-(cyclopropylsulfonyl)piperazin-1-yl)-5-methyl-N-(4-morpholinophenyl)pyrimidin-2-amine
100 nM, 76.2% inhibition. 28°C, pH not specified in the publication
4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine
PP2, AG-1897
4-amino-5-(4-chlorophenyl)-7-(tert-butyl)pyrazolo[3,4-d] pyrimidine
4-amino-5-(4-chlorophenyl)-7-(tert-butyl)pyrazolo[3,4-d]pyrimidine
4-amino-5-(4-methylphenyl)-7-(tert-butyl)pyrazolo[3,4-d] pyrimidine
4-amino-5-(4-methylphenyl)-7-(tert-butyl)pyrazolo[3,4-d]pyrimidine
-
i.e. pp1, inhibits Src family members like Lyn, no inhibition of Syk
4-chloro-N-[5-[(3-chlorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-chloro-N-[5-[(3-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-chloro-N-[5-[(4-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-chloro-N-[5-[(4-methoxybenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-chloro-N-[5-[(4-nitrobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-fluoro-N-[5-[(3-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-fluoro-N-[5-[(4-fluorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-fluoro-N-[5-[(4-methoxybenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-fluoro-N-[5-[(4-nitrobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]benzamide
-
4-methyl-3-[[3-(pyrimidin-4-yl)pyridin-2-yl]amino]-N-[3-(trifluoromethyl)phenyl]benzamide
-
-
4-methyl-N-(3-methylphenyl)-6-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
4-[4-([[3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazol-5-yl]carbamoyl]amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide
inhibitor binds to residues Arg386/Glu282 that isoform ABL1 uses to switch between inactive and active conformations. It potently inhibits both unphosphorylated and phosphorylated ABL1 by inducing a type II inactive conformation, and retains efficacy against the majority of clinically relevant chronic myeloid leukemia resistance mutants, including T315I. The compound inhibits isoform BCR-ABL1T315I-expressing cell lines, prolongs survival in mouse models of T315I-mutant chronic myeloid leukemia and B-lymphoblastic leukemia, and inhibits primary patient leukemia cells expressing mutation T315I in vitro and in vivo
5-methyl-4-(4-(methylsulfonyl)piperazin-1-yl)-N-(4-morpholinophenyl)pyrimidin-2-amine
100 nM, 1.0% inhibition. 28°C, pH not specified in the publication
8-(1-acetylpiperidin-4-yl)-2-((4-morpholinophenyl)amino)pteridin-7(8H)-one
100 nM, 3.5% inhibition. 28°C, pH not specified in the publication
8-methyl-emodin
-
inhibition of p56lck and c-Src
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(1-methylethoxy)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(1-methylethyl)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(1-methylpiperidin-4-yl)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(1H-imidazol-1-yl)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(2-methoxyethoxy)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(4-methylpiperazin-1-yl)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-(pyrrolidin-3-yloxy)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-methoxy-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-morpholin-4-yl-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-2-pyrrolidin-1-yl-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dipropylphosphoryl)phenyl]-2-(1-methylethyl)-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dipropylphosphoryl)phenyl]-9H-purin-6-amine
-
9-[(E)-2-(2,6-dimethylphenyl)ethenyl]-N6-[4-(dimethylphosphoryl)phenyl]-N2,N2-dimethyl-9H-purine-2,6-diamine
-
9-[(E)-2-(2-chloro-6-methylphenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-9H-purin-6-amine
-
9-[(E)-2-(2-chlorophenyl)ethenyl]-N-[4-(dimethylphosphoryl)phenyl]-9H-purin-6-amine
-
9-[(Z)-2-(2,6-dimethylphenyl)ethenyl]-N-[4-(dipropylphosphoryl)phenyl]-2-(1-methylethyl)-9H-purin-6-amine
-
A-419259
-
-
acacetin
-
inhibition of p56lck
AcpYEEI
ATP-phosphopeptide conjugate
ADP
-
competitive versus ATP, noncompetitive versus S1 peptide
AG-490
-
inhibits JAK2 tyrosine kinase
AG1024
-
-
AG490
alsterpaullone
-
at 0.01 mM: 66% inhibition of CHK, 81% inhibition of LCK, and 10% inhibition of CSK
AMN107
-
a specific BCR-ABL tyrosine kinase inhibitor, Abl binding structure, in vivo inhibition study in chronic myeloid leukemia, CML, overview
AP23464
apigenin
-
inhibition of p56lck
AST-487
-
-
ATP-1,13-Trioxa-SA-phospho-Tyr-g-p-azido-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-1,13-Trioxa-Suc-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-1,8-Diam-Suc-1,8-Diam-Suc-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-11-Aund-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-6-Ahex-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-8-Aoct-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-beta-Ala-phospho-Tyr-Glu-Glu-Ile-OH
inhibition of SH2 domain tyrosine protein kinases
ATP-gamma-S
-
AZ960
potent and selective ATP competitive inhibitor of JAK2 enzyme activity
AZD-1480
-
Jak2 inhibitor
AZM 475271
-
-
BAY61-3606
-
-
Bcr protein
-
negative regulator
-
bengamide A
-
c-Src from bengamide A-treated cells retains its N-terminal methionine and suffers a decrease in N-terminal myristoylation, which is accompanied by a shift of its subcellular distribution from the plasma membrane to the cytosol, and decreased tyrosine kinase activities of c-Src both in vitro and in vivo and eventually delayed cell-cycle progression through G2/M, overview, bengamide A reduced tyrosine phosphorylation on a few proteins, and is not a general tyrosine kinase inhibitor
BGB324
i.e. Bemcentinib
bisindolylmaleimide I
-
blocks alboaggregin-A activation of Fyn
bosutinib
C-terminal Src kinase
-
i.e. CSK, an inhibitor which inactivates Src family of protein kinases by phosphorylating a consensus tyrosine YT near the C terminus, phosphorylated YT then intramolecularly binds to the enzyme's SH2 domain, pYT/SH2 interaction, together with binding between the SH2 kinase linker and the SH3 domain, stabilizes the enzyme in a closed inactive conformation, preparation of recombinant SH2 and SH3 domains by expression in Escherichia coli, overview
-
catenarin
-
i.e. 4-hydroxy-emodin, inhibition of p56lck and c-Src
caveolin
-
a non-catalytic inhibitor of SFKs, transient inhibition
-
CGP 76030
-
-
CGP 77675
-
-
CGP76030
-
growth-inhibitory in vivo
Chk
-
i.e. Csk-homologous kinase, a catalytic inhibitor of SFKs phosphorylating the regulatory tyrosine residue of SFK which leads to inhibition of SFK, Chk is also a 'non-catalytic inhibitor' binding directly to the SFK forming stable complexes and inhibiting it, mechanism, overview
-
chrysin
-
inhibition of p56lck
CMP6
-
i.e. 2-tert-butyl-9-fluoro-3,6-dihydro-7H-benz[h]-imidaz[4,5-f]isoquinoline-7-1, specific for JAK2, kinase domain binding structure and mechanism
CP-690 550
-
Jak3 and Jak2 inhibitor
CP-690,550
CP690,550
-
targeting Jak3
Csk
-
i.e. C-terminal Src kinase, a catalytic inhibitor of SFKs phosphorylating the regulatory tyrosine residue of SFK which leads to inhibition of SFK, mechanism, overview
-
CSK-homologous kinase
-
i.e. CHK, an inhibitor which inactivates Src family of protein kinases by phosphorylating a consensus tyrosine YT near the C terminus, phosphorylated YT then intramolecularly binds to the enzyme's SH2 domain, pYT/SH2 interaction, together with binding between the SH2 kinase linker and the SH3 domain, stabilizes the enzyme in a closed inactive conformation, a second non-catalytic inhibitory mechanism involves tight binding of CHK to the enzyme's SFKs. The binding alone is sufficient to inhibit SFKs inhibition, preparation of recombinant SH2 and SH3 domains by expression in Escherichia coli, overview
-
curcumin
cyclopropyl(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazin-1-yl)methanone
100 nM, 77.0% inhibition. 28°C, pH not specified in the publication
damnacanthal
-
an anthraquinone, strong and selective inhibition of p56lck
dasatinib
datiscetin
-
inhibition of p56lck
emodic acid
-
inhibition of p56lck and c-Src
emodin
emodin derivatives
-
synthetic analogues, inhibition of p56lck and Src, overview
-
endocrocin
-
inhibition of p56lck and c-Src
epihematoxylol
-
F-actin
-
negative regulator
-
Fe3+
-
Lyn or Hck kinases in the unphosphorylated active state are significantly inhibited by Fe3+ ion
fisetin
-
inhibition of p56lck
flavone derivatives
-
inhibition of p56lck, overview
-
Fus1 protein
-
negative regulator
-
galangin
-
inhibition of p56lck
genistein
genkwanin
-
inhibition of p56lck
Gleevec
also known as STI-571 or imatinib
haematoxylene
-
haematoxylone
-
hematoxylin
-
Hg2+
-
at PO2 of about 20 mM
ibrutinib
-
iclusig
-
potent inhibitor of Abl
imatinib
imatinib mesylate
INCB018424
INCB16562
-
selective, and orally bioavailable small-molecule inhibitor of JAK1 and JAK2 markedly selective over JAK3
INCB18424
INCB20
-
potently inhibits all members of the JAK family with a 100-1000fold selectivity for JAKs over more than 70 other kinases, potent and specific Pan-JAK inhibitor
-
indirubin-3'-monoxime
-
at 0.01 mM: 62% inhibition of CHK, 89% inhibition of LCK, but no inhibition of CSK
INNO-406
-
previously NS-187, inhibits ABL1
interdomain B
-
connects the enzyme's catalytic kinase domain with its SH2 domain, is responsible for regulatory autoinhibition of ZAP-70 involving Tyr315 and Tyr319, deletion of the interdomain B preserves enzyme function, the regulation mechanism is similar to receptor protein tyrosine kinase EphB2, EC 2.7.10.1, overview
-
ITF2357
-
Jak2 inhibitor
JAK-inhibitor I
40% JAK2 residual activity in the presence of 0.002 mM JAK-inhibitor I and 0.02 mM ATP
-
kaempferide
-
inhibition of p56lck
kaempferol
-
inhibition of p56lck
kaempferol-3-O-arabinoside
-
slight inhibition of p56lck
kaempferol-3-O-rhamnoside
-
slight inhibition of p56lck
kenpaullone
-
at 0.01 mM: 35% inhibition of CHK, 85% inhibition of LCK, and 14% inhibition of CSK
lestaurtinib
LFM-A13
-
significantly impairs CXCL12-induced human B lymphoma cell line, and blocks Akt activation, homing of transferred B cells to peripheral lymph nodes is impaired, LFM-A13 significantly reduces the CXCL12-induced increases in Ca2+, overview
LS104
luteolin
-
inhibition of p56lck
M 475271
-
-
methyl 2,5-dihydroxycinnamate
-
i.e. DHC, inhibition of Syk and Lyn
MK-0457
-
Jak2 inhibitor
Mn2+
-
inhibitory above 1 mM
morin
-
inhibition of p56lck
myricetin
-
inhibition of p56lck
N,N-dimethyl-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 63.4% inhibition. 28°C, pH not specified in the publication
N-(3,5-dimethoxyphenyl)-4-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3,5-dimethylphenyl)-4-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3,5-dimethylphenyl)-4-(4-methyl-1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3,5-dimethylphenyl)-4-(5-methyl-1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3-methylphenyl)-4-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3-phenoxyphenyl)-4-(thiazol-2-yl)pyrimidin-2-amine
-
-
N-(3-[2-[4-(2-acetamidoethoxy)anilino]quinazolin-6-yl]-4-methylphenyl)-3-(trifluoromethyl)benzamide
-
-
N-(4-acetylphenyl)-1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperidine-4-carboxamide
100 nM, 74.3% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-3-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)azetidine-1-carboxamide
100 nM, 8.1% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-3-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)pyrrolidine-1-carboxamide
100 nM, 69.3% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)piperidine-1-carboxamide
100 nM, 80.5% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-5-(trifluoromethyl)pyr-imidin-4-yl)piperazine-1-carboxamide
100 nM, 74.6% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-5-nitropyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 68.4% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-7-oxopteridin-8(7H)-yl)piperidine-1-carboxamide
100 nM, 2.3% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)quinazolin-4-yl)piperazine-1-carboxamide
100 nM, 3.2% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(5-amino-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 22.8% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(5-chloro-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 99.4% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(5-fluoro-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 93.5% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperazine-1-sulfonamide
100 nM, 82.4 % inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide
2.9 nM, 81.8% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-(6-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 15.6% inhibition. 28°C, pH not specified in the publication
N-(4-acetylphenyl)-4-[2-[4-(morpholin-4-yl)anilino]pyrimidin-4-yl]piperazine-1-carboxamide
27 nM, 86.7% inhibition. 28°C, pH not specified in the publication
N-(4-cyanophenyl)-1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperidine-4-carboxamide
100 nM, 72.8% inhibition. 28°C, pH not specified in the publication
N-(4-cyanophenyl)-4-(2-((4-morpholinophenyl)amino)quinazolin-4-yl)piperazine-1-carboxamide
100 nM, 9.7% inhibition. 28°C, pH not specified in the publication
N-(4-cyanophenyl)-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 88.5% inhibition. 28°C, pH not specified in the publication
N-(4-cyanophenyl)-4-(6-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide
100 nM, 8.9% inhibition. 28°C, pH not specified in the publication
N-(4-methyl-3-[[3-(pyrimidin-4-yl)pyridin-2-yl]amino]phenyl)-3-(trifluoromethyl)benzamide
-
-
N-([[N2-(1-[4-[3-(4-[6-[(5-cyclopropyl-1H-pyrazol-3-yl)amino]-2-methylpyrimidin-4-yl]piperazin-1-yl)-3-oxopropyl]-1H-1,2,3-triazol-1-yl]-28,32-dioxo-3,6,9,12,15,18,21,24,30-nonaoxa-27-azadotriacontan-32-yl)-L-glutaminyl]amino][4-(phosphonooxy)phenyl]acetyl)-L-alpha-glutamyl-alpha-glutamyl-L-isoleucinamide
-
N-tert-butyl-3-([5-methyl-2-[(4-piperazin-1-ylphenyl)amino]pyrimidin-4-yl]amino)benzenesulfonamide
-
TG101209
N-tert-butyl-3-[(5-methyl-2-[[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino]pyrimidin-4-yl)amino]benzenesulfonamide
-
TG101348, JAK2-specific inhibitor
N-[3-([3-[4-(4-methoxyanilino)-1,3,5-triazin-2-yl]pyridin-2-yl]amino)-4-methylphenyl]-3-(trifluoromethyl)benzamide
-
-
N-[3-methoxy-5-(trifluoromethyl)phenyl]-4-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-[3-methoxy-5-(trifluoromethyl)phenyl]-4-(5-methyl-1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-[3-methyl-5-(trifluoromethyl)phenyl]-4-(1,3-thiazol-2-yl)pyrimidin-2-amine
-
-
N-[3-[2-(cyclopropylamino)quinazolin-6-yl]-4-methylphenyl]-3-(trifluoromethyl)benzamide
-
-
N-[4-(dimethylphosphoryl)phenyl]-9-[(E)-2-(1H-indazol-4-yl)ethenyl]-9H-purin-6-amine
-
N-[4-(dimethylphosphoryl)phenyl]-9-[(E)-2-(1H-indol-4-yl)ethenyl]-9H-purin-6-amine
-
N-[4-(dimethylphosphoryl)phenyl]-9-[(E)-2-(5-methyl-1H-indazol-4-yl)ethenyl]-9H-purin-6-amine
-
N-[4-(dipropylphosphoryl)phenyl]-2-(1-methylethyl)-9-[(E)-2-phenylethenyl]-9H-purin-6-amine
-
N-[4-(dipropylphosphoryl)phenyl]-2-(1-methylethyl)-9-[(Z)-2-phenylethenyl]-9H-purin-6-amine
-
N-[4-methyl-3-([3-[2-(methylamino)pyrimidin-4-yl]pyridin-2-yl]amino)phenyl]-3-(trifluoromethyl)benzamide
-
-
N-[4-methyl-3-([3-[6-(methylamino)pyrimidin-4-yl]pyridin-2-yl]amino)phenyl]-3-(trifluoromethyl)benzamide
-
-
N-[4-[4-amino-1-(propan-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]phenyl]-N'-[3-(trifluoromethyl)phenyl]urea
-
-
N-[5-(benzylsulfanyl)-1,3,4-thiadiazol-2-yl]-2-chlorobenzamide
-
N-[5-(benzylsulfanyl)-1,3,4-thiadiazol-2-yl]-4-chlorobenzamide
-
N-[5-[(3-chlorobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]-4-fluorobenzamide
-
N-[5-[(4-bromobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]-2-chlorobenzamide
-
N-[5-[(4-bromobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]-4-chlorobenzamide
-
N-[5-[(4-bromobenzyl)sulfanyl]-1,3,4-thiadiazol-2-yl]-4-fluorobenzamide
-
nevadensin
-
inhibition of p56lck
nilotinib
NS-187
-
a specific dual ABL-LYN inhibitor
ON012380
-
inhibits wild-type and mutant Abls, substrate-competitive, ATP-incompetitive
paeciloquinone A
-
inhibition of p56lck and c-Src
Paeciloquinone B
-
inhibition of p56lck and c-Src
paeciloquinone C
-
inhibition of p56lck and c-Src
paeciloquinone D
-
inhibition of p56lck and c-Src
PAG protein
-
negative regulator
-
PD166326
PD173955
-
-
PD180970
-
-
peroxiredoxin 1
-
inhibits ABL1 intracellularly
-
phosphoinositide
-
negative regulator
piceatannol
PIP2
-
inhibits ABL1 intracellularly
PNU156804
-
Jak3 inhibitor
protein tyrosine phosphatases
-
e.g. T-cell protein tyrosine phosphatase, catalytic inhibitor of SFKs dephosphorylating the autoactivation tyrosine residue of SFK which leads to inhibition of SFK
-
purpurin
-
inhibition of p56lck and c-Src
purvalanol
-
at 0.01 mM: 22% inhibition of CHK, 80% inhibition of LCK and CSK
Pyk2-specific siRNA
-
-
-
quercetin
-
inhibition of p56lck
R112
-
-
R406
-
-
RACK1
-
a non-catalytic inhibitor of SFKs, transient inhibition
-
rebastinib
-
potent inhibitor of Abl
resokaempferol
-
inhibition of p56lck
resveratrol
-
inhibition of p56lck
RNAi
knockdown of Btk results in decreased tumor necrosis factor-alpha
-
saracatinib
-
inhibitor of Src and Abl
SB1518
-
Jak2 inhibitor
siRNA
-
SKI-1
-
-
SKI-606
staurosporine
stilbene derivatives
-
inhibition of p56lck, overview
-
SU-6656
-
-
SU6656
syringetin
-
inhibition of p56lck
T47
-
57% inhibition of Syk at 0.1 mM
TG101209
TG101348
tyrophostin A25
-
-
tyrphostin 25
-
p38 MAP kinase inhibitor SB203580 and protein tyrosine kinase inhibitor tyrphostin 25 combined can be used for inhibition of matrix metalloproteinase-9 expression, overview
tyrphostin A23
-
broad-spectrum PTK inhibitor, slight inhibition of Src
tyrphostin A25
-
broad-spectrum PTK inhibitor, slight inhibition of Src
tyrphostin A9
-
-
tyrphostin AG490
-
Jak3 inhibitor
WASP
-
a non-catalytic inhibitor of SFKs, e.g. c-Src, mechanism, transient inhibition
-
WHI-P131
-
Jak3 inhibitor
WHI-P154
-
Jak3 inhibitor
Wortmannin
-
-
WP1066
-
-
XL019
YM193306
-
-
[2-(2-[[3-methoxy-5-(trifluoromethyl)phenyl]amino]pyrimidin-4-yl)-1,3-thiazol-4-yl]methanol
-
-
[2-(2-[[3-methyl-5-(trifluoromethyl)phenyl]amino]pyrimidin-4-yl)-1,3-thiazol-4-yl]methanol
-
-
additional information
-
ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
alboaggregin-A
-
Trimeresurus albolabris venom, activates Fyn activity and translocation
-
AMpYSSV
-
CBP-based phosphopeptide, activates
angiotensin subtype 1 receptor
-
AT-1 receptor
-
Ca2+
G-protein coupled receptor PAC1 regulates the tyrosine phosphorylation of isoform PYK2 in NCI-H838 nonsmall cell lung cancer cells. PYK2 phosphorylation is dependent upon Ca2+. The ability of PAC1 to regulate PYK2 is dependent on phospholipase and Src, and partially dependent on proteinkinase C
CD45
-
transmembrane receptor-like protein tyrosine phosphatase activating the SFK by dephosphorylation of the regulatory tyrosine residue
-
CXCL12
-
-
-
cytokine receptors
-
-
-
Epidermal growth factor
epidermal growth factor receptor
-
the Abl nonreceptor tyrosine kinase is activated by ligand-stimulated EGFR
-
epithelial growth factor receptor
-
-
-
EPQYEEIPIYL
-
a src kinase activating peptide, binds to the SH2 domain of the src-kinase and activates it, activation of endogenous src-PTKs does not inhibit Kv1.3 channels in T lymphocytes, overview
insulin-like growth factor 1 receptor
-
-
-
interleukin 5
-
activates Janus kinases JAK1 and JAK2
-
lipopolysaccharide
Lyn kinase
as part of the activation process Lyn phosphorylates Btk in Tyr551, which is subsequently autophosphorylated in Tyr223
-
lysophosphatidic acid
-
activates fyn
macrophage antigen-1
-
i.e. Mac1, a beta2-integrin activates Src PTKs Hck and Lyn, interaction of both requires Mn2+
-
NGF
rapidly stimulates both Ser and Thr phosphorylation in vivo and autophosphorylation activity in vitro of the B-Raf protein
-
pervanadate
activation of isoform Fer by reactive oxygen species causes increased phosphorylation of RhoGDIalpha, regulator of the small GTPase Rac, and pervanadate treatment further augmented this
platelet-derived growth factor
-
PDGF
-
platelet-derived growth factor receptor
-
-
-
prolactin
-
activates Jak2
-
pseudolaric acid B
-
pseudolaric acid B, PAB, activates PTK to induce apoptosis
reactive oxygen species
activation of isoform Fer by reactive oxygen species causes increased phosphorylation of RhoGDIalpha, regulator of the small GTPase Rac, and pervanadate treatment further augmented this
-
sphingosylphosphorylcholine
-
activates fyn
Src
-
activated Src kinase in aggressive breast cancer cell lines can activate c-Abl kinase
-
transforming growth factor beta receptor
-
TGF-beta receptor
-
tyrosine growth factor
-
the enzyme is activated by the tyrosine growth factor and seven transmembrane-spanning receptors
-
additional information
-