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Literature summary extracted from

  • Ran, Y.; Ladd, G.Z.; Ceballos-Diaz, C.; Jung, J.I.; Greenbaum, D.; Felsenstein, K.M.; Golde, T.E.
    Differential inhibition of signal peptide peptidase family members by established gamma-secretase inhibitors (2015), PLoS ONE, 10, e0128619 .
    View publication on PubMedView publication on EuropePMC

Application

EC Number Application Comment Organism
3.4.23.B24 medicine the signal peptide peptidase hSPP is a biomedically important protease implicated as therapeutic target for hepatitis C Homo sapiens
3.4.23.B24 medicine the signal peptide peptidase pSPP is a biomedically important protease implicated as therapeutic target for treatement of Plasmodia and malaria Plasmodium sp.
3.4.23.B24 medicine the signal peptide peptidase SPPL2a is a biomedically important protease implicated as therapeutic target for B-cell immunomodulation and neoplasia Mus musculus

Cloned(Commentary)

EC Number Cloned (Comment) Organism
3.4.23.B24 recombinant expression of FLAG-tagged enzyme in HEK-293T cells, coexpression with FLAG-tagged substrate FBA Mus musculus
3.4.23.B24 recombinant expression of FLAG-tagged enzyme in HEK-293T cells, coexpression with FLAG-tagged substrate FBA Homo sapiens
3.4.23.B24 recombinant expression of FLAG-tagged enzyme in HEK-293T cells, coexpression with FLAG-tagged substrate FBA Plasmodium sp.

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.23.B24 (S,S)-2-[2-(3,5-difluorophenyl)-acetylamino]-N-(1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-propionamide i.e. Compound E Homo sapiens
3.4.23.B24 (S,S)-2-[2-(3,5-difluorophenyl)-acetylamino]-N-(1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-propionamide i.e. Compound E, below 50% inhibition Mus musculus
3.4.23.B24 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide] i.e. (Z-LL)2 ketone, causes over 75% inhibition of FBA cleavage at 0.01 mM Homo sapiens
3.4.23.B24 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide] i.e. (Z-LL)2 ketone, causes over 75% inhibition of FBA cleavage at 0.01 mM Mus musculus
3.4.23.B24 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide] i.e. (Z-LL)2 ketone, causes over 75% inhibition of FBA cleavage at 0.01 mM Plasmodium sp.
3.4.23.B24 GSI II a gamma-secretase inhibitor Homo sapiens
3.4.23.B24 GSI II a gamma-secretase inhibitor Mus musculus
3.4.23.B24 GSI II a gamma-secretase inhibitor Plasmodium sp.
3.4.23.B24 L685,458
-
Homo sapiens
3.4.23.B24 L685,458
-
Mus musculus
3.4.23.B24 L685,458
-
Plasmodium sp.
3.4.23.B24 LY-411,575
-
Homo sapiens
3.4.23.B24 LY-411,575
-
Mus musculus
3.4.23.B24 LY-411,575
-
Plasmodium sp.
3.4.23.B24 additional information no inhibition by N-[(1S)-2-[[(7S)-6,7-Dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluorobenzeneacetamide (DBZ); no inhibition by (S,S)-2-[2-(3,5-difluorophenyl)-acetylamino]-N-(1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-propionamide (Compound E) and N-[(1S)-2-[[(7S)-6,7-Dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluorobenzeneacetamide (DBZ) Mus musculus
3.4.23.B24 additional information no inhibition by (S,S)-2-[2-(3,5-difluorophenyl)-acetylamino]-N-(1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-propionamide (Compound E) and N-[(1S)-2-[[(7S)-6,7-Dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluorobenzeneacetamide (DBZ) Plasmodium sp.
3.4.23.B24 N-[(1S)-2-[[(7S)-6,7-dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluorobenzeneacetamide i.e. DBZ Homo sapiens

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.4.23.B24 CD74 + H2O Mus musculus although SPPL2b can cleave CD74 when overexpressed, it does not appear contribute to CD74 NH2-terminal fragment turnover ?
-
?
3.4.23.B24 CD74 + H2O Mus musculus SPPL2a cleaves CD74 and contributes to CD74 NH2-terminal fragment turnover ?
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.4.23.B24 Homo sapiens
-
-
-
3.4.23.B24 Mus musculus
-
-
-
3.4.23.B24 Plasmodium sp.
-
-
-

Source Tissue

EC Number Source Tissue Comment Organism Textmining
3.4.23.B24 B-lymphocyte
-
Mus musculus
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.4.23.B24 CD74 + H2O
-
Mus musculus ?
-
?
3.4.23.B24 CD74 + H2O although SPPL2b can cleave CD74 when overexpressed, it does not appear contribute to CD74 NH2-terminal fragment turnover Mus musculus ?
-
?
3.4.23.B24 CD74 + H2O SPPL2a cleaves CD74 and contributes to CD74 NH2-terminal fragment turnover Mus musculus ?
-
?
3.4.23.B24 Fba + H2O a recombinant substrate consisting of the amino-terminus of BRI2 fused to amyloid beta 1-25, with a K16A mutation incorporated to prevent potential alpha-secretase cleavage that would preclude ELISA based detection of the released COOH-terminal fragment. The enzyme shows different cleavage site specificity compared to other signal peptide peptidases, the cleavage may be processive Mus musculus ?
-
?
3.4.23.B24 Fba + H2O a recombinant substrate consisting of the amino-terminus of BRI2 fused to amyloid beta 1-25, with a K16A mutation incorporated to prevent potential alpha-secretase cleavage that would preclude ELISA based detection of the released COOH-terminal fragment. The enzyme shows different cleavage site specificity compared to other signal peptide peptidases, the cleavage may be processive. hSPP processes of FBA resulting in a gap between the carboxyl end of the ICD and the NH2-terminus of the CTF Homo sapiens ?
-
?
3.4.23.B24 Fba + H2O a recombinant substrate consisting of the amino-terminus of BRI2 fused to amyloid beta 1-25, with a K16A mutation incorporated to prevent potential alpha-secretase cleavage that would preclude ELISA based detection of the released COOH-terminal fragment. The enzyme shows different cleavage site specificity compared to other signal peptide peptidases, the cleavage may be processive. hSPP processes of FBA resulting in a gap between the carboxyl end of the ICD and the NH2-terminus of the CTF. Enzyme pSPP may have more than one cleavage site Plasmodium sp. ?
-
?
3.4.23.B24 Fba + H2O a recombinant substrate consisting of the amino-terminus of BRI2 fused to amyloid beta 1-25, with a K16A mutation incorporated to prevent potential alpha-secretase cleavage that would preclude ELISA based detection of the released COOH-terminal fragment. The enzyme shows different cleavage site specificity compared to other signal peptide peptidases, the cleavage may be processive. hSPP processes of FBA resulting in a gap between the carboxyl end of the ICD and the NH2-terminus of the CTF. SPPL2b reduced levels of the intact FBA substrate by over 90%, which is higher than the activity of other SPPs Mus musculus ?
-
?
3.4.23.B24 additional information cleavage occurs following ectodomain shedding by signal peptidase (SP) for hSPP Mus musculus ?
-
-
3.4.23.B24 additional information cleavage occurs following ectodomain shedding by signal peptidase (SP) for hSPP Mus musculus ?
-
?
3.4.23.B24 additional information cleavage occurs following ectodomain shedding by signal peptidase (SP) for hSPP Homo sapiens ?
-
-
3.4.23.B24 additional information cleavage occurs following ectodomain shedding by signal peptidase (SP) for hSPP Homo sapiens ?
-
?
3.4.23.B24 TfR 1 + H2O intramembrane cleavage sites Mus musculus ?
-
?
3.4.23.B24 TNF-alpha + H2O intramembrane cleavage sites Mus musculus ?
-
?

Subunits

EC Number Subunits Comment Organism
3.4.23.B24 ? x * 48000, about, sequence calculation Homo sapiens
3.4.23.B24 ? x * 63000, about, sequence calculation Mus musculus
3.4.23.B24 ? x * 37000, recombinant FLAG-tagged enzyme, SDS-PAGE, x * 52000, about, sequence calculation Plasmodium sp.
3.4.23.B24 ? x * 69000, about, sequence calculation Mus musculus
3.4.23.B24 More the monomeric form is the dominant species observed for the recombinant enzyme, with lesser amounts of dimer and trimer Mus musculus
3.4.23.B24 More the monomeric form is the dominant species observed for the recombinant enzyme, with lesser amounts of dimer and trimer Homo sapiens
3.4.23.B24 More the monomeric form is the dominant species observed for the recombinant enzyme, with lesser amounts of dimer and trimer. The enzyme has multiple intracellular domains (ICDs) Plasmodium sp.

Synonyms

EC Number Synonyms Comment Organism
3.4.23.B24 hSPP
-
Homo sapiens
3.4.23.B24 hSPP
-
Plasmodium sp.
3.4.23.B24 signal peptide peptidase like 2a
-
Mus musculus
3.4.23.B24 SPP
-
Homo sapiens
3.4.23.B24 SPP
-
Plasmodium sp.
3.4.23.B24 SPPL
-
Mus musculus
3.4.23.B24 SPPL2a
-
Mus musculus
3.4.23.B24 SPPL2b
-
Mus musculus

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.4.23.B24 0.000051
-
pH and temperature not specified in the publication Mus musculus LY-411,575
3.4.23.B24 0.00015
-
pH and temperature not specified in the publication Homo sapiens LY-411,575
3.4.23.B24 0.000161
-
pH and temperature not specified in the publication Plasmodium sp. L685,458
3.4.23.B24 0.000177
-
pH and temperature not specified in the publication Mus musculus 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide]
3.4.23.B24 0.000319
-
pH and temperature not specified in the publication Homo sapiens L685,458
3.4.23.B24 0.000423
-
pH and temperature not specified in the publication Homo sapiens GSI II
3.4.23.B24 0.000427
-
pH and temperature not specified in the publication Plasmodium sp. GSI II
3.4.23.B24 0.000472
-
pH and temperature not specified in the publication Plasmodium sp. 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide]
3.4.23.B24 0.000519
-
pH and temperature not specified in the publication Homo sapiens 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide]
3.4.23.B24 0.00057
-
pH and temperature not specified in the publication Mus musculus L685,458
3.4.23.B24 0.000876
-
pH and temperature not specified in the publication Mus musculus L685,458
3.4.23.B24 0.000948
-
pH and temperature not specified in the publication Homo sapiens N-[(1S)-2-[[(7S)-6,7-dihydro-5-methyl-6-oxo-5H-dibenz[b,d]azepin-7-yl]amino]-1-methyl-2-oxoethyl]-3,5-difluorobenzeneacetamide
3.4.23.B24 0.00146
-
pH and temperature not specified in the publication Homo sapiens (S,S)-2-[2-(3,5-difluorophenyl)-acetylamino]-N-(1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-propionamide
3.4.23.B24 0.00214
-
pH and temperature not specified in the publication Mus musculus 2,2'-(2-oxo-1,3-propanediyl)bis[N-[(phenylmethoxy)carbonyl]-L-leucyl-L-leucinamide]
3.4.23.B24 0.00348
-
pH and temperature not specified in the publication Plasmodium sp. LY-411,575
3.4.23.B24 0.0036
-
pH and temperature not specified in the publication Mus musculus GSI II
3.4.23.B24 0.0055
-
pH and temperature not specified in the publication Mus musculus LY-411,575
3.4.23.B24 0.0088
-
pH and temperature not specified in the publication Mus musculus GSI II

General Information

EC Number General Information Comment Organism
3.4.23.B24 evolution similarities between SPP family member cleavage and cleavage catalyzed by gamma-secretase Mus musculus
3.4.23.B24 evolution similarities between SPP family member cleavage and cleavage catalyzed by gamma-secretase Homo sapiens
3.4.23.B24 evolution similarities between SPP family member cleavage and cleavage catalyzed by gamma-secretase Plasmodium sp.
3.4.23.B24 malfunction depletion of SPPL2a leads to accumulation of an NH2-terminal fragment (NTF) of CD74 which impairs B cell development and survival Mus musculus