Structure of PDB 3op2 Chain B Binding Site BS01

Receptor Information
>3op2 Chain B (length=368) Species: 518 (Bordetella bronchiseptica) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
SLKITEVKAHALSTPIPERMRVKLNRQMILVEVRTDEGVTGVGSPSGPYD
LAVLKRAIEDVIGPQLIGEDPANINYLWHKVFHGEVSRSVGIAAMSGVDI
ALWDLKGRAMNQPIYQLLGGKFHTRGVRAYASSIYWDLTPDQAADELAGW
VEQGFTAAKLKVGRAPRKDAANLRAMRQRVGADVEILVDANQSLGRHDAL
AMLRILDEAGCYWFEEPLSIDDIEGHRILRAQGTPVRIATGENLYTRNAF
NDYIRNDAIDVLQADASRAGGITEALAISASAASAHLAWNPHTFNDIITV
AANLHLVAASPHPAMFEWDITHNDLMTRLASYDLKLENGLVQPPQGPGLG
FEIDWDFVAAHAWKGEPA
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain3op2 Chain B Residue 500 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3op2 Crystal structure of putative mandelate racemase from Bordetella bronchiseptica RB50 complexed with 2-oxoglutarate/phosphate
Resolution2.0 Å
Binding residue
(original residue number in PDB)
D201 E227 E254
Binding residue
(residue number reindexed from 1)
D189 E215 E242
Annotation score4
Enzymatic activity
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0016836 hydro-lyase activity
GO:0046872 metal ion binding
Biological Process
GO:0009063 amino acid catabolic process
GO:0016052 carbohydrate catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:3op2, PDBe:3op2, PDBj:3op2
PDBsum3op2
PubMed
UniProtA0A0H3LT39

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