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8FH5

Crystal Structure Of Aldose Reductase (AKR1B1) Complexed With NADP+ And AT-001

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 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_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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