Structure of PDB 2art Chain A Binding Site BS01

Receptor Information
>2art Chain A (length=247) Species: 2303 (Thermoplasma acidophilum) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MEGRLLLLETPGNTRMSLAYDEAIYRSFQYGDKPILRFYRHDRSVIIGYF
QVAEEEVDLDYMKKNGIMLARRYTGGGAVYHDLGDLNFSVVRSSDDMDIT
SMFRTMNEAVVNSLRILGLDARPGELNDVSIPVNKKTDIMAGEKKIMGAA
GAMRKGAKLWHAAMLVHTDLDMLSAVLKVPSTRERVANVTDFVDVSIDEV
RNALIRGFSETLHIDFREDTITEKEESLARELFDKKYSTEEWNMGLL
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 chain2art Chain A Residue 1301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2art Crystal structure of lipoate-protein ligase A bound with the activated intermediate: insights into interaction with lipoyl domains
Resolution2.4 Å
Binding residue
(original residue number in PDB)
T137 D138 G148 A149
Binding residue
(residue number reindexed from 1)
T137 D138 G148 A149
Annotation score1
Enzymatic activity
Enzyme Commision number 6.3.1.20: lipoate--protein ligase.
Gene Ontology
Molecular Function
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016874 ligase activity
GO:0016979 lipoate-protein ligase activity
GO:0017118 lipoyltransferase activity
GO:0031405 lipoic acid binding
GO:0046872 metal ion binding
Biological Process
GO:0009249 protein lipoylation
GO:0036211 protein modification process
Cellular Component
GO:0005737 cytoplasm
GO:0032991 protein-containing complex

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Biological Process

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Cellular Component
External links
PDB RCSB:2art, PDBe:2art, PDBj:2art
PDBsum2art
PubMed16141198
UniProtQ9HKT1|LPLAN_THEAC Lipoate-protein ligase A subunit 1 (Gene Name=lplA)

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