Any feedback?
Please rate this page
(sequences.php)
(0/150)

BRENDA support

Sequence of DGUOK_HUMAN

EC Number:2.7.1.76

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
2'-deoxyadenosine kinase
Q16854
Homo sapiens
277
32056
Reaction
ATP + 2'-deoxyadenosine = ADP + dAMP
Other sequences found for EC No. 2.7.1.76

EC Number:2.7.1.113

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
deoxyguanosine kinase
Q16854
Homo sapiens
277
32056
Reaction
ATP + deoxyguanosine = ADP + dGMP
Other sequences found for EC No. 2.7.1.113

General information:

Sequence
show sequence in fasta format
  0 MAAGRLFLSR LRAPFSSMAK SPLEGVSSSR GLHAGRGPRR LSIEGNIAVG KSTFVKLLTK
 60 TYPEWHVATE PVATWQNIQA AGTQKACTAQ SLGNLLDMMY REPARWSYTF QTFSFLSRLK
120 VQLEPFPEKL LQARKPVQIF ERSVYSDRYI FAKNLFENGS LSDIEWHIYQ DWHSFLLWEF
180 ASRITLHGFI YLQASPQVCL KRLYQRAREE EKGIELAYLE QLHGQHEAWL IHKTTKLHFE
240 ALMNIPVLVL DVNDDFSEEV TKQEDLMREV NTFVKNL
Download this sequence
in fasta format
Download all sequences for 2.7.1.113
in fasta format
in csv (Excel, OpenOffice) format
Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
409591
Johansson M.,Karlsson A.
Cloning and expression of human deoxyguanosine kinase cDNA.
Proc. Natl. Acad. Sci. U.S.A.
93
7258-7262
1996
409592
Hillier L.W.,Graves T.A.,Fulton R.S.,Fulton L.A.,Pepin K.H.,Minx P.,Wagner-McPherson C.,Layman D.,Wylie K.,Sekhon M.,Becker M.C.,Fewell G.A.,Delehaunty K.D.,Miner T.L.,Nash W.E.,Kremitzki C.,Oddy L.,Du H.,Sun H.,Bradshaw-Cordum H.,Ali J.,Carter J.,Cordes M.,Harris A.,Isak A.,van Brunt A.,Nguyen C.,Du F.,Courtney L.,Kalicki J.,Ozersky P.,Abbott S.,Armstrong J.,Belter E.A.,Caruso L.,Cedroni M.,Cotton M.,Davidson T.,Desai A.,Elliott G.,Erb T.,Fronick C.,Gaige T.,Haakenson W.,Haglund K.,Holmes A.,Harkins R.,Kim K.,Kruchowski S.S.,Strong C.M.,Grewal N.,Goyea E.,Hou S.,Levy A.,Martinka S.,Mead K.,McLellan M.D.,Meyer R.,Randall-Maher J.,Tomlinson C.,Dauphin-Kohlberg S.,Kozlowicz-Reilly A.,Shah N.,Swearengen-Shahid S.,Snider J.,Strong J.T.,Thompson J.,Yoakum M.,Leonard S.,Pearman C.,Trani L.,Radionenko M.,Waligorski J.E.,Wang C.,Rock S.M.,Tin-Wollam A.-M.,Maupin R.,Latreille P.,Wendl M.C.,Yang S.-P.,Pohl C.,Wallis J.W.,Spieth J.,Bieri T.A.,Berkowicz N.,Nelson J.O.,Osborne J.,Ding L.,Meyer R.,Sabo A.,Shotland Y.,Sinha P.,Wohldmann P.E.,Cook L.L.,Hickenbotham M.T.,Eldred J.,Williams D.,Jones T.A.,She X.,Ciccarelli F.D.,Izaurralde E.,Taylor J.,Schmutz J.,Myers R.M.,Cox D.R.,Huang X.,McPherson J.D.,Mardis E.R.,Clifton S.W.,Warren W.C.,Chinwalla A.T.,Eddy S.R.,Marra M.A.,Ovcharenko I.,Furey T.S.,Miller W.,Eichler E.E.,Bork P.,Suyama M.,Torrents D.,Waterston R.H.,Wilson R.K.
Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
Nature
434
724-731
2005
409594
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
409595
Wang L.,Hellman U.,Eriksson S.
Cloning and expression of human mitochondrial deoxyguanosine kinase cDNA.
FEBS Lett.
390
39-43
1996
409597
Saada A.,Shaag A.,Mandel H.,Nevo Y.,Eriksson S.,Elpeleg O.
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.
Nat. Genet.
29
342-344
2001
409598
Mousson de Camaret B.,Taanman J.W.,Padet S.,Chassagne M.,Mayencon M.,Clerc-Renaud P.,Mandon G.,Zabot M.T.,Lachaux A.,Bozon D.
Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion.
Biochem. J.
402
377-385
2007
409599
Choudhary C.,Kumar C.,Gnad F.,Nielsen M.L.,Rehman M.,Walther T.C.,Olsen J.V.,Mann M.
Lysine acetylation targets protein complexes and co-regulates major cellular functions.
Science
325
834-840
2009
409600
Johansson K.,Ramaswamy S.,Ljungcrantz C.,Knecht W.,Piskur J.,Munch-Petersen B.,Eriksson S.,Eklund H.
Structural basis for substrate specificities of cellular deoxyribonucleoside kinases.
Nat. Struct. Biol.
8
616-620
2001
409601
Salviati L.,Sacconi S.,Mancuso M.,Otaegui D.,Camano P.,Marina A.,Rabinowitz S.,Shiffman R.,Thompson K.,Wilson C.M.,Feigenbaum A.,Naini A.B.,Hirano M.,Bonilla E.,DiMauro S.,Vu T.H.
Mitochondrial DNA depletion and dGK gene mutations.
Ann. Neurol.
52
311-317
2002
409602
Wang L.,Limongelli A.,Vila M.R.,Carrara F.,Zeviani M.,Eriksson S.
Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes.
Mol. Genet. Metab.
84
75-82
2005
409603
Ronchi D.,Garone C.,Bordoni A.,Gutierrez Rios P.,Calvo S.E.,Ripolone M.,Ranieri M.,Rizzuti M.,Villa L.,Magri F.,Corti S.,Bresolin N.,Mootha V.K.,Moggio M.,DiMauro S.,Comi G.P.,Sciacco M.
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions.
Brain
135
3404-3415
2012
409604
Vilarinho S.,Sari S.,Yilmaz G.,Stiegler A.L.,Boggon T.J.,Jain D.,Akyol G.,Dalgic B.,Guenel M.,Lifton R.P.
Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.
Hepatology
63
1977-1986
2016