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1Y3F

Crystal structure of the complex of subtilisin BPN' with chymotrypsin inhibitor 2 F69A 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 1001
ChainResidue
EGLN2
EASP41
ELEU75
EASN77
EILE79
EVAL81

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NA E 1002
ChainResidue
EHOH5036
EHOH5141
EGLY169
ETYR171
EVAL174

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE CIT E 2001
ChainResidue
EALA1
ETYR21
ELYS237
EHIS238
EHIS238
EASN240
ETRP241
EHIS276
EHIS276
ECIT2002
EHOH5032
EHOH5087
EHOH5122
EHOH5324
EHOH5390

site_idAC4
Number of Residues14
DetailsBINDING SITE FOR RESIDUE CIT E 2002
ChainResidue
ETRP241
EGLN245
EHIS276
EHIS276
ECIT2001
EHOH5064
EHOH5087
EHOH5223
EHOH5231
EHOH5306
EHOH5324
EHOH5387
EHOH5390
EHOH5391

site_idAC5
Number of Residues12
DetailsBINDING SITE FOR RESIDUE CIT E 2003
ChainResidue
EPRO172
EGLY211
ELYS213
EARG247
EHOH5039
EHOH5065
EHOH5091
EHOH5125
EHOH5189
EHOH5216
EHOH5279
EHOH5377

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 15P E 5001
ChainResidue
EHIS17
ETHR22
ESER24
EASN76
EASN76
ESER87
EHOH5321

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE 15P E 5002
ChainResidue
EILE115
EASN118
EMET119
ESER145
EHOH5166
EHOH5268

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 15P E 5003
ChainResidue
ESER37
EVAL44
EALA45
EGLY46
EGLY47
EPHE58
EHOH5325

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 2024-10-30

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