Structure of PDB 3erp Chain B Binding Site BS01

Receptor Information
>3erp Chain B (length=306) Species: 99287 (Salmonella enterica subsp. enterica serovar Typhimurium str. LT2) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
IYQPDENRYHTMEYRRCGRSGVKLPAISLGLWHNFGDTTRVENSRALLQR
AFDLGITHFDLANNYGPPPGSAECNFGRILQEDFLPWRDELIISTKAGYT
MWDGPYGDWGSRKYLIASLDQSLKRMGLEYVDIFYHHRPDPETPLKETMK
ALDHLVRHGKALYVGISNYPADLARQAIDILEDLGTPCLIHQPKYSLFER
WVEDGLLALLQEKGVGSIAFSPLAGGQLTDRYDKLEKVRRLNELAARRGQ
KLSQMALAWVLRNDNVTSVLIGASKPSQIEDAVGMLANRRFSAAECAEID
AILEGR
Ligand information
Ligand IDCAC
InChIInChI=1S/C2H7AsO2/c1-3(2,4)5/h1-2H3,(H,4,5)/p-1
InChIKeyOGGXGZAMXPVRFZ-UHFFFAOYSA-M
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.0C[As](=O)(C)[O-]
CACTVS 3.370C[As](C)([O-])=O
ACDLabs 12.01[O-][As](=O)(C)C
FormulaC2 H6 As O2
NameCACODYLATE ION;
dimethylarsinate
ChEMBL
DrugBank
ZINC
PDB chain3erp Chain B Residue 338 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3erp Structural and biochemical studies of novel aldo-keto reductases for the biocatalytic conversion of 3-hydroxybutanal to 1,3-butanediol.
Resolution1.55 Å
Binding residue
(original residue number in PDB)
W33 Y66 H138 F221
Binding residue
(residue number reindexed from 1)
W32 Y65 H137 F220
Annotation score3
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0000166 nucleotide binding
GO:0016491 oxidoreductase activity
GO:0046872 metal ion binding
Biological Process
GO:0051596 methylglyoxal catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:3erp, PDBe:3erp, PDBj:3erp
PDBsum3erp
PubMed28130301
UniProtQ8ZNA1

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