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1IEI

CRYSTAL STRUCTURE OF HUMAN ALDOSE REDUCTASE COMPLEXED WITH THE INHIBITOR ZENARESTAT.

Functional Information from GO Data
ChainGOidnamespacecontents
A0001523biological_processretinoid metabolic process
A0001758molecular_functionretinal dehydrogenase activity
A0002070biological_processepithelial cell maturation
A0003091biological_processrenal water homeostasis
A0004032molecular_functionaldose reductase (NADPH) activity
A0005515molecular_functionprotein binding
A0005615cellular_componentextracellular space
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0005975biological_processcarbohydrate metabolic process
A0006629biological_processlipid metabolic process
A0006693biological_processprostaglandin metabolic process
A0006700biological_processC21-steroid hormone biosynthetic process
A0009055molecular_functionelectron transfer activity
A0016491molecular_functionoxidoreductase activity
A0019853biological_processL-ascorbic acid biosynthetic process
A0035809biological_processregulation of urine volume
A0036130molecular_functionprostaglandin H2 endoperoxidase reductase activity
A0042572biological_processretinol metabolic process
A0043066biological_processnegative regulation of apoptotic process
A0043795molecular_functionglyceraldehyde oxidoreductase activity
A0044597biological_processdaunorubicin metabolic process
A0044598biological_processdoxorubicin metabolic process
A0046370biological_processfructose biosynthetic process
A0047655molecular_functionallyl-alcohol dehydrogenase activity
A0047939molecular_functionL-glucuronate reductase activity
A0047956molecular_functionglycerol dehydrogenase (NADP+) activity
A0052650molecular_functionall-trans-retinol dehydrogenase (NADP+) activity
A0070062cellular_componentextracellular exosome
A0071475biological_processcellular hyperosmotic salinity response
A0072205biological_processmetanephric collecting duct development
Functional Information from PDB Data
site_idAC1
Number of Residues28
DetailsBINDING SITE FOR RESIDUE NAP A 350
ChainResidue
AGLY18
ASER159
AASN160
AGLN183
ATYR209
ASER210
APRO211
ALEU212
ASER214
AASP216
AALA245
ATHR19
AILE260
ALYS262
ASER263
AVAL264
ATHR265
AARG268
AGLU271
AASN272
AZES351
ATRP20
ALYS21
AASP43
ATYR48
ALYS77
AHIS110
ATRP111

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE ZES A 351
ChainResidue
ATRP20
AVAL47
ATYR48
AHIS110
ATRP111
ATHR113
APHE122
ACYS298
AALA299
ALEU300
ATYR309
ANAP350
AHOH477

Functional Information from PROSITE/UniProt
site_idPS00062
Number of Residues18
DetailsALDOKETO_REDUCTASE_2 Aldo/keto reductase family signature 2. MeelvdeglVKAIGISNF
ChainResidueDetails
AMET144-PHE161

site_idPS00063
Number of Residues16
DetailsALDOKETO_REDUCTASE_3 Aldo/keto reductase family putative active site signature. IPKSVTpeRIaENfKV
ChainResidueDetails
AILE260-VAL275

site_idPS00798
Number of Residues18
DetailsALDOKETO_REDUCTASE_1 Aldo/keto reductase family signature 1. GYRHIDCAhvyqnEneVG
ChainResidueDetails
AGLY38-GLY55

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton donor => ECO:0000269|PubMed:15272156
ChainResidueDetails
ATYR48

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
AGLY9

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING:
ChainResidueDetails
AHIS110

site_idSWS_FT_FI4
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:15146478, ECO:0000269|PubMed:15272156, ECO:0000269|PubMed:16337231, ECO:0000269|PubMed:17368668, ECO:0000269|PubMed:17418233, ECO:0000269|PubMed:17505104
ChainResidueDetails
ASER210

site_idSWS_FT_FI5
Number of Residues1
DetailsSITE: Lowers pKa of active site Tyr
ChainResidueDetails
ALYS77

site_idSWS_FT_FI6
Number of Residues1
DetailsMOD_RES: N-acetylalanine => ECO:0000269|PubMed:8281941, ECO:0007744|PubMed:19413330
ChainResidueDetails
AALA1

site_idSWS_FT_FI7
Number of Residues1
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P07943
ChainResidueDetails
ASER2

site_idSWS_FT_FI8
Number of Residues3
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS94
ALYS221
ALYS262

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
ATYR48
AASP43
AHIS110
ALYS77

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
ATYR48
ALYS77

site_idMCSA1
Number of Residues4
DetailsM-CSA 725
ChainResidueDetails
AASP43electrostatic stabiliser
ATYR48proton acceptor, proton donor
ALYS77electrostatic stabiliser, modifies pKa
AHIS110electrostatic stabiliser

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PDB entries from 2024-11-13

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