Structure of PDB 7lj9 Chain C Binding Site BS01
Receptor Information
>7lj9 Chain C (length=279) Species:
9606
(Homo sapiens) [
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VPMDYSWARELGLIRKPASFMTSICDERGQELIYAGMPITEVFKEEMGIG
GVLGLLWFQKRLPKYSCQFIEMCLMVTADHGPAVSGAHNTIICARAGKDL
VSSLTSGLLTIGDRFGGALDAAAKMFSKAFDSGIIPMEFVNKMKKEGKLI
MGIGHRVKSINNPDMRVQILKDYVRQHFPATPLLDYALEVEKITTSKKPN
LILNVDGLIGVAFVDMLRNCGSFTREEADEYIDIGALNGIFVLGRSMGFI
GHYLDQKRLKQGLYRHPWDDISYVLPEHM
Ligand information
Ligand ID
OAA
InChI
InChI=1S/C4H4O5/c5-2(4(8)9)1-3(6)7/h1H2,(H,6,7)(H,8,9)/p-1
InChIKey
KHPXUQMNIQBQEV-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
[O-]C(=O)CC(=O)C(=O)O
OpenEye OEToolkits 1.5.0
C(C(=O)C(=O)O)C(=O)[O-]
CACTVS 3.341
OC(=O)C(=O)CC([O-])=O
Formula
C4 H3 O5
Name
OXALOACETATE ION
ChEMBL
DrugBank
DB02637
ZINC
PDB chain
7lj9 Chain C Residue 1201 [
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Receptor-Ligand Complex Structure
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PDB
7lj9
Reply to: Acetyl-CoA is produced by the citrate synthase homology module of ATP-citrate lyase.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
H900 D1026
Binding residue
(residue number reindexed from 1)
H80 D206
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.3.3.8
: ATP citrate synthase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003878
ATP citrate synthase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016740
transferase activity
GO:0046872
metal ion binding
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
Biological Process
GO:0006085
acetyl-CoA biosynthetic process
GO:0006101
citrate metabolic process
GO:0006107
oxaloacetate metabolic process
GO:0006629
lipid metabolic process
GO:0006633
fatty acid biosynthetic process
GO:0006695
cholesterol biosynthetic process
GO:0008610
lipid biosynthetic process
GO:0015936
coenzyme A metabolic process
Cellular Component
GO:0005576
extracellular region
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
GO:0035578
azurophil granule lumen
GO:0070062
extracellular exosome
GO:1904813
ficolin-1-rich granule lumen
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7lj9
,
PDBe:7lj9
,
PDBj:7lj9
PDBsum
7lj9
PubMed
34294921
UniProt
P53396
|ACLY_HUMAN ATP-citrate synthase (Gene Name=ACLY)
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