Structure of PDB 2e5a Chain A Binding Site BS01

Receptor Information
>2e5a Chain A (length=329) Species: 9913 (Bos taurus) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GLILQSISNDVYHNLAVEDWIHDHMNLEGKPVLFLWRNSPTVVIGRHQNP
WQECNLNLMREEGVKLARRRSGGGTVYHDMGNINLTFFTTKKKYDRMENL
KLVVRALKAVHPHLDVQATKRFDLLLDGQFKISGTASKIGRNAAYHHCTL
LCGTDGTFLSSLLKSPYQGIRSNATASTPALVKNLMEKDPTLTCEVVINA
VATEYATSHQIDNHIHLINPTDETVFPGINSKAIELQTWEWIYGKTPKFS
VDTSFTVLHSHVEIKVFIDVKNGRIEVCNIEAPDHWLPLEICDQLNSSLI
GSKFSPIETTVDELHSKWNILCEKIKGIM
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 chain2e5a Chain A Residue 3001 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2e5a Crystal structure of bovine Lipoyltransferase in complex with lipoyl-AMP
Resolution2.1 Å
Binding residue
(original residue number in PDB)
F126 D127 G138 T139
Binding residue
(residue number reindexed from 1)
F122 D123 G134 T135
Annotation score1
Enzymatic activity
Enzyme Commision number 2.3.1.-
2.3.1.200: lipoyl amidotransferase.
Gene Ontology
Molecular Function
GO:0016746 acyltransferase activity
GO:0017118 lipoyltransferase activity
Biological Process
GO:0009249 protein lipoylation
GO:0036211 protein modification process
Cellular Component
GO:0005737 cytoplasm
GO:0005739 mitochondrion

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:2e5a, PDBe:2e5a, PDBj:2e5a
PDBsum2e5a
PubMed17570395
UniProtO46419|LIPT_BOVIN Lipoyl amidotransferase LIPT1, mitochondrial (Gene Name=LIPT1)

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