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1TM4

crystal structure of the complex of subtilsin BPN'with chymotrypsin inhibitor 2 M59G mutant

Functional Information from GO Data
ChainGOidnamespacecontents
E0004252molecular_functionserine-type endopeptidase activity
E0006508biological_processproteolysis
E0008236molecular_functionserine-type peptidase activity
I0004867molecular_functionserine-type endopeptidase inhibitor activity
I0009611biological_processresponse to wounding
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA E 450
ChainResidue
EGLN2
EASP41
ELEU75
EASN77
EILE79
EVAL81

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NA E 451
ChainResidue
EHOH488
EHOH592
EGLY169
ETYR171
EVAL174

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE CIT E 452
ChainResidue
EALA1
ETYR21
ELYS237
EHIS238
EHIS238
EASN240
ETRP241
EHIS276
EHIS276
ECIT453
EHOH484
EHOH539
EHOH573
EHOH778
EHOH800

site_idAC4
Number of Residues13
DetailsBINDING SITE FOR RESIDUE CIT E 453
ChainResidue
ETRP241
EGLN245
EHIS276
EHIS276
ECIT452
EHOH516
EHOH539
EHOH674
EHOH682
EHOH760
EHOH778
EHOH800
EHOH801

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE 1PE E 454
ChainResidue
EHIS17
ETHR22
EASN76
EASN76
EHOH530
EHOH773

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE 1PE E 455
ChainResidue
EILE115
EASN118
EMET119
ESER145
EHOH617
EHOH802

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE 1PE E 456
ChainResidue
ESER37
EVAL44
EALA45
EPHE58
EHOH779

Functional Information from PROSITE/UniProt
site_idPS00136
Number of Residues12
DetailsSUBTILASE_ASP Serine proteases, subtilase family, aspartic acid active site. VAVIDSGIdssH
ChainResidueDetails
EVAL28-HIS39

site_idPS00137
Number of Residues11
DetailsSUBTILASE_HIS Serine proteases, subtilase family, histidine active site. HGThVAGtVAA
ChainResidueDetails
EHIS64-ALA74

site_idPS00138
Number of Residues11
DetailsSUBTILASE_SER Serine proteases, subtilase family, serine active site. GTSmAsPhVAG
ChainResidueDetails
EGLY219-GLY229

site_idPS00285
Number of Residues12
DetailsPOTATO_INHIBITOR Potato inhibitor I family signature. WPELVGksVeeA
ChainResidueDetails
ITRP24-ALA35

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues3
DetailsACT_SITE: Charge relay system => ECO:0000255|PROSITE-ProRule:PRU01240, ECO:0000269|PubMed:5249818
ChainResidueDetails
EASP32
EHIS64
ESER221

site_idSWS_FT_FI2
Number of Residues9
DetailsBINDING:
ChainResidueDetails
EGLN2
EASP41
ELEU75
EASN77
EILE79
EVAL81
EGLY169
ETYR171
EVAL174

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1sca
ChainResidueDetails
ESER221
EHIS64
EASP32

site_idMCSA1
Number of Residues4
DetailsM-CSA 723
ChainResidueDetails
EASP32electrostatic interaction, electrostatic stabiliser
EHIS64proton acceptor, proton donor
EASN155electrostatic interaction, electrostatic stabiliser
ESER221nucleofuge, nucleophile, proton acceptor, proton donor

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PDB entries from 2024-07-17

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