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4H4I

OYE1-W116V complexed with the dismutation product of (S)-carvone

Functional Information from GO Data
ChainGOidnamespacecontents
A0003959molecular_functionNADPH dehydrogenase activity
A0005829cellular_componentcytosol
A0010181molecular_functionFMN binding
A0016491molecular_functionoxidoreductase activity
A0018548molecular_functionpentaerythritol trinitrate reductase activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 401
ChainResidue
AHOH914
AHOH1052
AHOH1088
AHOH1089
AHOH1123
AHOH1124

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 0WV A 402
ChainResidue
AASN194
ATYR196
ATYR375
AFMN412
ATHR37
ATYR82
AHIS191

site_idAC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE NA A 403
ChainResidue
A1PE409
AHOH916

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE 1PE A 404
ChainResidue
AASP51
ATRP52
AASP358
AGLU389
ANA408
AHOH1126

site_idAC5
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 1PE A 405
ChainResidue
AGLU305
AGLY307
ASER308
AASP310
ATYR313
AARG322
AASP339
ANA417
AHOH974
AHOH1036

site_idAC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE MG A 406
ChainResidue
AHOH1017
AHOH1017
AHOH1043
AHOH1043
AHOH1051
AHOH1051
AHOH1129
AHOH1129

site_idAC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE NA A 407
ChainResidue
AGLN9
AALA10
A1PE410

site_idAC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE NA A 408
ChainResidue
ATRP52
A1PE404

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE 1PE A 409
ChainResidue
APHE123
APHE296
ANA403
AHOH769

site_idBC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE 1PE A 410
ChainResidue
APRO8
AGLN9
AALA10
AHIS43
AASP83
AARG334
ALYS362
AGLY363
ANA407

site_idBC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 411
ChainResidue
AGLU336
AHOH1015
AHOH1036
AHOH1060
AHOH1092

site_idBC3
Number of Residues20
DetailsBINDING SITE FOR RESIDUE FMN A 412
ChainResidue
APRO34
APRO35
ALEU36
ATHR37
AGLY72
AGLN114
AHIS191
AASN194
AARG243
APRO295
AGLY324
AASN325
AGLY347
AARG348
APHE374
A0WV402
AHOH503
AHOH504
AHOH506
AHOH515

site_idBC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 413
ChainResidue
ALYS4
ALYS368

site_idBC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE NA A 414
ChainResidue
A1PE415

site_idBC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE 1PE A 415
ChainResidue
AASP370
AHIS380
AASP384
ANA414
AHOH820

site_idBC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 416
ChainResidue
AASP83
AASN126

site_idBC8
Number of Residues1
DetailsBINDING SITE FOR RESIDUE NA A 417
ChainResidue
A1PE405

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:9830020
ChainResidueDetails
ATYR196

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:11668181, ECO:0000269|PubMed:7881908, ECO:0000269|PubMed:9830019
ChainResidueDetails
ATHR37
AGLN114
AARG243
AARG348

site_idSWS_FT_FI3
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:11668181, ECO:0000269|PubMed:7881908
ChainResidueDetails
AHIS191
AASN194
ATYR375

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 319
ChainResidueDetails
ATHR37electrostatic stabiliser, hydrogen bond donor
AHIS191electrostatic stabiliser, hydrogen bond donor
AASN194electrostatic stabiliser, hydrogen bond donor
ATYR196electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AASN251hydrogen bond donor, increase acidity

222036

PDB entries from 2024-07-03

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