Structure of PDB 2eb6 Chain D Binding Site BS01

Receptor Information
>2eb6 Chain D (length=266) Species: 562 (Escherichia coli) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MFDKHTHTLIAQRLDQAEKQREQIRAISLDYPEITIEDAYAVQREWVRLK
IAEGRTLKGHKIGLTSKAMQASSQISEPDYGALLDDMFFHDGSDIPTDRF
IVPRIEVELAFVLAKPLRGPNCTLFDVYNATDYVIPALELIDARCHNIDP
TQRPRKVFDTISDNAANAGVILGGRPIKPDELDLRWISALMYRNGVIEET
GVAAGVLNHPANGVAWLANKLAPYDVQLEAGQIILGGSFTRPVPARKGDT
FHVDYGNMGSISCRFV
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 chain2eb6 Chain D Residue 1004 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2eb6 Structure and Mechanism of HpcG, a Hydratase in the Homoprotocatechuate Degradation Pathway of Escherichia coli
Resolution1.69 Å
Binding residue
(original residue number in PDB)
E106 E108 E139
Binding residue
(residue number reindexed from 1)
E106 E108 E139
Annotation score1
Enzymatic activity
Enzyme Commision number 4.1.1.77: 2-oxo-3-hexenedioate decarboxylase.
4.2.1.80: 2-oxopent-4-enoate hydratase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0008684 2-oxopent-4-enoate hydratase activity
GO:0016829 lyase activity
GO:0018817 2-oxo-hept-3-ene-1,7-dioate hydratase activity
GO:0034856 2-hydroxyhexa-2,4-dienoate hydratase activity
GO:0046872 metal ion binding
GO:0047437 4-oxalocrotonate decarboxylase activity
Biological Process
GO:0009056 catabolic process
Cellular Component
GO:0005737 cytoplasm

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:2eb6, PDBe:2eb6, PDBj:2eb6
PDBsum2eb6
PubMed17559873
UniProtQ46982

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