Structure of PDB 3ugv Chain G Binding Site BS02

Receptor Information
>3ugv Chain G (length=363) Species: 331869 (alpha proteobacterium BAL199) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TLTFRKLTARPVLLKLQRPVTARIATIPDWPLILIDIETEEGVPGRAYLE
PYVPKAMKYLVPALHDMSDMLAGQPLAPAEIYDKTRKSLHFVGYAGLSMI
AASGVDMAVWDALARAANMPLCTLLGGTPGSVKAYNSNGLWLKSPAEVAA
EAVELKAEGQGTGFKGLKLRMGRDDPAVDIETAEAVWDAVGRDTALMVDF
NQGLDMAEAMHRTRQIDDLGLEWIEEPVVYDNFDGYAQLRHDLKTPLMIG
ENFYGPREMHQALQAGACDLVMPDFMRIGGVSGWMRAAGVAGAWGIPMST
HLYPEVGAHVMRVTETAHWLEWQSWADPILQEPYALSDGDLIVPDKPGLG
LDWDEDVVAANLV
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 chain3ugv Chain G Residue 501 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB3ugv Crystal structure of an enolase from alpha pretobacterium bal199 (EFI TARGET EFI-501650) with bound MG
Resolution2.3 Å
Binding residue
(original residue number in PDB)
R243 L246
Binding residue
(residue number reindexed from 1)
R240 L243
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:3ugv, PDBe:3ugv, PDBj:3ugv
PDBsum3ugv
PubMed
UniProtA8TYI5

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