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3I1U

Carboxypeptidase A Inhibited by a Thiirane Mechanism-Based inactivator

Functional Information from GO Data
ChainGOidnamespacecontents
A0004181molecular_functionmetallocarboxypeptidase activity
A0006508biological_processproteolysis
A0008270molecular_functionzinc ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 401
ChainResidue
AHIS69
AGLU72
AHIS196
ABTW402

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE BTW A 402
ChainResidue
AHIS196
AILE243
ATYR248
AALA250
ATHR268
AGLU270
AGOL311
AZN401
AHIS69
AGLU72
AARG127
AASN144
AARG145

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 310
ChainResidue
AVAL183
ALYS184
AGLY187
AASN188
APHE189
AGLN261
AHOH448

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 311
ChainResidue
AARG127
AGLU163
ATHR164
ATYR248
ABTW402
AHOH593

site_idAC5
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL A 312
ChainResidue
AGLU43
AGOL314

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 313
ChainResidue
ATRP126
ALYS128
ACYS138
AVAL139
APRO160
ACYS161
AGLU163

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 314
ChainResidue
ASER121
AGLN122
AGOL312
AHOH482
AHOH494
AHOH610

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 315
ChainResidue
ATYR12
ATRP73
AARG124
ALEU280
ALEU281
APRO282

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 316
ChainResidue
AARG40
ASER41
ATYR42
AGLY44
AVAL174
AHOH443
AHOH449
AHOH464

Functional Information from PROSITE/UniProt
site_idPS00132
Number of Residues23
DetailsCARBOXYPEPT_ZN_1 Zinc carboxypeptidases, zinc-binding region 1 signature. PaIwIdlGiHSrEwITQatgvwF
ChainResidueDetails
APRO60-PHE82

site_idPS00133
Number of Residues11
DetailsCARBOXYPEPT_ZN_2 Zinc carboxypeptidases, zinc-binding region 2 signature. HSYSQLLlYPY
ChainResidueDetails
AHIS196-TYR206

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton donor/acceptor => ECO:0000255|PROSITE-ProRule:PRU01379
ChainResidueDetails
AGLU270

site_idSWS_FT_FI2
Number of Residues3
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU01379, ECO:0000269|PubMed:12431056, ECO:0007744|PDB:1IY7
ChainResidueDetails
AHIS69
AGLU72
AHIS196

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12431056, ECO:0007744|PDB:1IY7
ChainResidueDetails
AARG127
AASN144
ASER197
ATYR248

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1cbx
ChainResidueDetails
AARG127
AGLU270

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1cbx
ChainResidueDetails
AARG71
AGLU270
AARG127

site_idMCSA1
Number of Residues5
DetailsM-CSA 171
ChainResidueDetails
AHIS69metal ligand
AGLU72metal ligand
AARG127electrostatic stabiliser, hydrogen bond donor
AHIS196metal ligand
AGLU270covalently attached, electrofuge, electrophile, hydrogen bond acceptor, hydrogen bond donor, nucleophile, proton acceptor, proton donor

222624

PDB entries from 2024-07-17

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