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1YE6

Crystal structure of the Lys-274 to Arg mutant of Candida tenuis xylose reductase (AKR2B5) bound to NADP+

Functional Information from GO Data
ChainGOidnamespacecontents
A0004032molecular_functionaldose reductase (NADPH) activity
A0005829cellular_componentcytosol
A0016491molecular_functionoxidoreductase activity
A0032866molecular_functionD-xylose reductase (NADPH) activity
A0042732biological_processD-xylose metabolic process
A0042843biological_processD-xylose catabolic process
B0004032molecular_functionaldose reductase (NADPH) activity
B0005829cellular_componentcytosol
B0016491molecular_functionoxidoreductase activity
B0032866molecular_functionD-xylose reductase (NADPH) activity
B0042732biological_processD-xylose metabolic process
B0042843biological_processD-xylose catabolic process
C0004032molecular_functionaldose reductase (NADPH) activity
C0005829cellular_componentcytosol
C0016491molecular_functionoxidoreductase activity
C0032866molecular_functionD-xylose reductase (NADPH) activity
C0042732biological_processD-xylose metabolic process
C0042843biological_processD-xylose catabolic process
D0004032molecular_functionaldose reductase (NADPH) activity
D0005829cellular_componentcytosol
D0016491molecular_functionoxidoreductase activity
D0032866molecular_functionD-xylose reductase (NADPH) activity
D0042732biological_processD-xylose metabolic process
D0042843biological_processD-xylose catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 901
ChainResidue
BLYS25
BLEU26
BALA27
BGLN34
BARG274

site_idAC2
Number of Residues1
DetailsBINDING SITE FOR RESIDUE SO4 D 902
ChainResidue
DARG232

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 C 903
ChainResidue
CHOH1071
CGLY13
CHIS14
CLEU15

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 904
ChainResidue
AHIS14
ALEU15
AHOH1081

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 905
ChainResidue
BHIS14
BLEU15
BHOH1090
BHOH1096

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 D 906
ChainResidue
DLEU26
DALA27
DGLN34
DARG274
DHOH1204

site_idAC7
Number of Residues1
DetailsBINDING SITE FOR RESIDUE SO4 B 907
ChainResidue
BARG232

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 D 908
ChainResidue
DHIS14
DLEU15
DHOH1068

site_idAC9
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NAP A 1000
ChainResidue
AGLY22
ACYS23
ATRP24
AASP47
ATYR52
ALYS81
AHIS114
ASER169
AASN170
AGLN191
ATYR217
APHE220
AGLN223
ASER224
APHE225
AALA257
AILE272
APRO273
AARG274
ASER275
AASN276
AARG280
AASN284
AASN310
AHOH1015
AHOH1077
AHOH1103
AHOH1146
CHOH1122

site_idBC1
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAD B 1001
ChainResidue
BGLY22
BCYS23
BTRP24
BASP47
BTYR52
BLYS81
BHIS114
BSER169
BASN170
BGLN191
BTYR217
BSER218
BSER219
BPHE220
BGLN223
BSER224
BGLU227
BASN229
BPHE240
BALA257
BILE272
BPRO273
BARG274
BASN276
BARG280
BASN284
BASN310
BHOH1038
BHOH1069
BHOH1074
BHOH1088
BHOH1089

site_idBC2
Number of Residues27
DetailsBINDING SITE FOR RESIDUE NAP C 1002
ChainResidue
CGLN223
CSER224
CPHE225
CALA257
CILE272
CPRO273
CARG274
CSER275
CASN276
CARG280
CGLN283
CASN284
CASN310
CHOH1018
CHOH1125
CGLY22
CCYS23
CTRP24
CASP47
CTYR52
CLYS81
CHIS114
CSER169
CASN170
CGLN191
CTYR217
CPHE220

site_idBC3
Number of Residues30
DetailsBINDING SITE FOR RESIDUE NAD D 1003
ChainResidue
DGLY22
DCYS23
DTRP24
DASP47
DTYR52
DLYS81
DSER169
DASN170
DGLN191
DTYR217
DSER218
DSER219
DPHE220
DGLN223
DSER224
DGLU227
DASN229
DPHE240
DILE272
DPRO273
DARG274
DASN276
DARG280
DASN284
DASN310
DHOH1021
DHOH1062
DHOH1105
DHOH1109
DHOH1176

Functional Information from PROSITE/UniProt
site_idPS00062
Number of Residues18
DetailsALDOKETO_REDUCTASE_2 Aldo/keto reductase family signature 2. LeklvaagkIKSIGVSNF
ChainResidueDetails
ALEU154-PHE171

site_idPS00063
Number of Residues16
DetailsALDOKETO_REDUCTASE_3 Aldo/keto reductase family putative active site signature. IPRSNLpeRLvQNrSF
ChainResidueDetails
AILE272-PHE287

site_idPS00798
Number of Residues18
DetailsALDOKETO_REDUCTASE_1 Aldo/keto reductase family signature 1. GYRLFDGAedygnEkeVG
ChainResidueDetails
AGLY42-GLY59

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor
ChainResidueDetails
ATYR52
BTYR52
CTYR52
DTYR52

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000250
ChainResidueDetails
AHIS114
BHIS114
CHIS114
DHIS114

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:12733986, ECO:0000269|PubMed:15320875, ECO:0000269|PubMed:16336198
ChainResidueDetails
ASER169
DSER169
DSER218
DARG274
ASER218
AARG274
BSER169
BSER218
BARG274
CSER169
CSER218
CARG274

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Lowers pKa of active site Tyr => ECO:0000250
ChainResidueDetails
ALYS81
BLYS81
CLYS81
DLYS81

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
ALYS81
AASP47
AHIS114
ATYR52

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
BLYS81
BASP47
BHIS114
BTYR52

site_idCSA3
Number of Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
CLYS81
CASP47
CHIS114
CTYR52

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
DLYS81
DASP47
DHIS114
DTYR52

site_idCSA5
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
ALYS81
ATYR52

site_idCSA6
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
BLYS81
BTYR52

site_idCSA7
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
CLYS81
CTYR52

site_idCSA8
Number of Residues2
DetailsAnnotated By Reference To The Literature 1mrq
ChainResidueDetails
DLYS81
DTYR52

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PDB entries from 2024-09-11

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