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1EF3

FIDARESTAT BOUND TO HUMAN ALDOSE REDUCTASE

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
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
B0001523biological_processretinoid metabolic process
B0001758molecular_functionretinal dehydrogenase activity
B0002070biological_processepithelial cell maturation
B0003091biological_processrenal water homeostasis
B0004032molecular_functionaldose reductase (NADPH) activity
B0005515molecular_functionprotein binding
B0005615cellular_componentextracellular space
B0005654cellular_componentnucleoplasm
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0005975biological_processcarbohydrate metabolic process
B0006629biological_processlipid metabolic process
B0006693biological_processprostaglandin metabolic process
B0006700biological_processC21-steroid hormone biosynthetic process
B0009055molecular_functionelectron transfer activity
B0016491molecular_functionoxidoreductase activity
B0019853biological_processL-ascorbic acid biosynthetic process
B0035809biological_processregulation of urine volume
B0036130molecular_functionprostaglandin H2 endoperoxidase reductase activity
B0042572biological_processretinol metabolic process
B0043066biological_processnegative regulation of apoptotic process
B0043795molecular_functionglyceraldehyde oxidoreductase activity
B0044597biological_processdaunorubicin metabolic process
B0044598biological_processdoxorubicin metabolic process
B0046370biological_processfructose biosynthetic process
B0047655molecular_functionallyl-alcohol dehydrogenase activity
B0047939molecular_functionL-glucuronate reductase activity
B0047956molecular_functionglycerol dehydrogenase (NADP+) activity
B0052650molecular_functionall-trans-retinol dehydrogenase (NADP+) activity
B0070062cellular_componentextracellular exosome
B0071475biological_processcellular hyperosmotic salinity response
B0072205biological_processmetanephric collecting duct development
Functional Information from PDB Data
site_idAC1
Number of Residues31
DetailsBINDING SITE FOR RESIDUE NAP A 320
ChainResidue
AGLY18
ASER159
AASN160
AGLN183
ATYR209
ASER210
APRO211
ALEU212
AGLY213
ASER214
APRO215
ATHR19
AASP216
AALA245
AILE260
APRO261
ALYS262
ASER263
AVAL264
ATHR265
AARG268
AGLU271
ATRP20
AASN272
AFID340
ALYS21
AGLN26
AASP43
ATYR48
ALYS77
AHIS110

site_idAC2
Number of Residues31
DetailsBINDING SITE FOR RESIDUE NAP B 330
ChainResidue
BGLY18
BTHR19
BTRP20
BLYS21
BGLN26
BASP43
BTYR48
BLYS77
BHIS110
BSER159
BASN160
BGLN183
BTYR209
BSER210
BPRO211
BLEU212
BGLY213
BSER214
BPRO215
BASP216
BALA245
BILE260
BPRO261
BLYS262
BSER263
BVAL264
BTHR265
BARG268
BGLU271
BASN272
BFID350

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE FID A 340
ChainResidue
ATRP20
AVAL47
ATYR48
AHIS110
ATRP111
ATRP219
ACYS298
ALEU300
ANAP320

site_idAC4
Number of Residues12
DetailsBINDING SITE FOR RESIDUE FID B 350
ChainResidue
BTRP20
BVAL47
BTYR48
BTRP79
BHIS110
BTRP111
BPHE122
BTRP219
BCYS298
BALA299
BLEU300
BNAP330

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 Residues2
DetailsACT_SITE: Proton donor => ECO:0000269|PubMed:15272156
ChainResidueDetails
AGLN49
BGLN49

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
AALA10
BALA10

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING:
ChainResidueDetails
ATRP111
BTRP111

site_idSWS_FT_FI4
Number of Residues2
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
APRO211
BPRO211

site_idSWS_FT_FI5
Number of Residues2
DetailsSITE: Lowers pKa of active site Tyr
ChainResidueDetails
ALEU78
BLEU78

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: N-acetylalanine => ECO:0000269|PubMed:8281941, ECO:0007744|PubMed:19413330
ChainResidueDetails
ASER2
BSER2

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:P07943
ChainResidueDetails
AARG3
BARG3

site_idSWS_FT_FI8
Number of Residues6
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ATHR95
APRO222
ASER263
BTHR95
BPRO222
BSER263

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 Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
BTYR48
BASP43
BHIS110
BLYS77

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
ATYR48
ALYS77

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
BTYR48
BLYS77

site_idMCSA1
Number of Residues4
DetailsM-CSA 725
ChainResidueDetails
ACYS44electrostatic stabiliser
AGLN49proton acceptor, proton donor
ALEU78electrostatic stabiliser, modifies pKa
ATRP111electrostatic stabiliser

site_idMCSA2
Number of Residues4
DetailsM-CSA 725
ChainResidueDetails
BCYS44electrostatic stabiliser
BGLN49proton acceptor, proton donor
BLEU78electrostatic stabiliser, modifies pKa
BTRP111electrostatic stabiliser

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PDB entries from 2024-08-07

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