Structure of PDB 2e5a Chain A Binding Site BS02
Receptor Information
>2e5a Chain A (length=329) Species:
9913
(Bos taurus) [
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GLILQSISNDVYHNLAVEDWIHDHMNLEGKPVLFLWRNSPTVVIGRHQNP
WQECNLNLMREEGVKLARRRSGGGTVYHDMGNINLTFFTTKKKYDRMENL
KLVVRALKAVHPHLDVQATKRFDLLLDGQFKISGTASKIGRNAAYHHCTL
LCGTDGTFLSSLLKSPYQGIRSNATASTPALVKNLMEKDPTLTCEVVINA
VATEYATSHQIDNHIHLINPTDETVFPGINSKAIELQTWEWIYGKTPKFS
VDTSFTVLHSHVEIKVFIDVKNGRIEVCNIEAPDHWLPLEICDQLNSSLI
GSKFSPIETTVDELHSKWNILCEKIKGIM
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
2e5a Chain A Residue 4002 [
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Receptor-Ligand Complex Structure
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PDB
2e5a
Crystal structure of bovine Lipoyltransferase in complex with lipoyl-AMP
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
K112 H117
Binding residue
(residue number reindexed from 1)
K108 H113
Annotation score
1
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
PDBsum
2e5a
PubMed
17570395
UniProt
O46419
|LIPT_BOVIN Lipoyl amidotransferase LIPT1, mitochondrial (Gene Name=LIPT1)
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