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3.4.22.10: streptopain

This is an abbreviated version!
For detailed information about streptopain, go to the full flat file.

Word Map on EC 3.4.22.10

Reaction

preferential cleavage with hydrophobic residues at P2, P1 and P1' =

Synonyms

EC 3.4.4.18, IdeS, IgG-degrading enzyme of Streptococcus pyogenes, interleukin-1beta convertase, More, proteinase, streptococcal, pyrogenic exotoxin B, SCP, SpcCEP, Spe B, SPE B protease, SPE B/SCP, SpeB, SPP, Steptococcus proteinase, streptococcal cysteine protease, Streptococcal cysteine proteinase, streptococcal erythrogenic toxin B, streptococcal proteinase, streptococcal pyogenic exotoxin B, streptococcal pyrogenic exotoxin B, streptococcal pyrogenic exotoxin B/cysteine protease, Streptococcus peptidase A, Streptococcus protease, streptopain

ECTree

     3 Hydrolases
         3.4 Acting on peptide bonds (peptidases)
             3.4.22 Cysteine endopeptidases
                3.4.22.10 streptopain

Inhibitors

Inhibitors on EC 3.4.22.10 - streptopain

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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(S)-1-azido-2-tosylamino-hexane
-
moderate inhibitor of IdeS
(S)-1-azido-3-methyl-2-tosylamino-butane
-
moderate inhibitor of IdeS
(S)-1-azido-3-phenyl-2-tosylamino-propane
-
moderate inhibitor of IdeS
(S)-3-tosylamino-1-heptanal
-
strong inhibitory activity
(S)-3-tosylamino-heptane-1-nitrile
-
the compound shows some inhibition of IdeS
(S)-4-methyl-3-tosylamino-1-pentanal
-
strong inhibitory activity
(S)-4-phenyl-3-tosylamino-1-butanal
-
strong inhibitory activity
(S)-7-tert-butoxycarbonylamino-3-tosylamino-1-heptanal
-
strong inhibitory activity
1,3-Dibromoacetone
-
rapid and complete loss of activity
2,4-dinitrofluorobenzene
-
-
acetonitrile
-
mixed type
acetyl-Ala-Gln-Ile-(S)-2,6-diaminohexanal
-
-
benzyloxycarbonyl-Ala-Ala-CHN2
-
-
benzyloxycarbonyl-Ala-Ala-Pro-CHN2
-
-
benzyloxycarbonyl-Ala-Phe-Ala-CHN2
-
-
benzyloxycarbonyl-Asn-Val-Gly-CHN2
-
inhibition of protease activity, no influence on the superantigenic properties of the enzyme
Benzyloxycarbonyl-Gly-Phe
-
competitive against benzyloxycarbonyl-Phe-Tyr
benzyloxycarbonyl-Leu-Val-Gly-CHN2
-
inhibits kininogen degradation
Benzyloxycarbonyl-Phe-Ala-CHN2
-
-
benzyloxycarbonyl-Phe-Gly-CHN2
-
-
benzyloxycarbonyl-Phe-Gly-Phe-CHN2
-
-
Cu2+
-
Cu2+ inhibits the proteolytic activity of mature SpeB
dimethyl sulfoxide
-
competitive
E64
-
i.e. trans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane
Gly-Phe-CHN2
-
-
HgCl2
iodoacetamide
-
-
iodoacetate
-
irreversible inhibitor
iodoacetic acid
-
-
L-trans-epoxysuccinyl-leucylamido(4-guanidino)butane
-
-
methyliodine
-
-
N-(N-(L-3-trans-carboxyoxirane-2-carbonyl)-L-leucyl)-agmatine
-
-
N-[N-(L-3-transcarboxyirane-2-carbonyl)-L-leucyl]agmatine
-
Nalpha-benzyloxycarbonyl-Phe-Phe
-
strong inhibition of hydrolysis of Nalpha-benzyloxycarbonyl-Phe-Tyr
Sodium tetrathionate
-
-
Spe B pro-peptide
-
specific inhibition of the mature enzyme, secondary structure and SpeB binding analysis, inhibition modeling and mechanism, overview
-
Spi
-
specific enzyme pro-peptide analogue inhibitor, purification from Streptococcus pyogenes, secondary structure and SpeB binding analysis, inhibition modeling and mechanism, overview
-
sulfite
-
-
tosyl-L-lysine chloromethyl ketone
-
irreversible inhibitor
tosyl-L-phenylalanine chloromethyl ketone
-
irreversible inhibitor
Tosyl-norleucine-Phe
-
competitive against benzyloxycarbonyl-norleucine-Phe
trans-epoxysuccinyl-L-leucylamido(4-guanidino)butane
-
-
trans-epoxysuccinyl-L-leucylamido-(4-guanidino)butane
Z-LVG-CHN2
-
irreversible inhibitor
Zn2+
-
Zinc inhibits the proteolytic activity of mature SpeB
additional information
-