Structure of PDB 1iuq Chain A Binding Site BS05
Receptor Information
>1iuq Chain A (length=357) Species:
3662
(Cucurbita moschata) [
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ASHSRKFLDVRSEEELLSCIKKETEAGKLPPNVAAGMEELYQNYRNAVIE
SGNPKADEIVLSNMTVALDRILLDVEDPFVFSSHHKAIREPFDYYIFGQN
YIRPLIDFGNSFVGNLSLFKDIEEKLQQGHNVVLISNHQTEADPAIISLL
LEKTNPYIAENTIFVAGDRVLADPLCKPFSIGRNLICVYSKKHMFDIPEL
TETKRKANTRSLKEMALLLRGGSQLIWIAPSGGRDRPDPSTGEWYPAPFD
ASSVDNMRRLIQHSDVPGHLFPLALLCHDIMPPPRVIAFNGAGLSVAPEI
SFEEIAATHKNPEEVREAYSKALFDSVAMQYNVLKTAISGKQGLGASTAD
VSLSQPW
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
1iuq Chain A Residue 1006 [
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Receptor-Ligand Complex Structure
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PDB
1iuq
Substrate recognition and selectivity of plant glycerol-3-phosphate acyltransferases (GPATs) from Cucurbita moscata and Spinacea oleracea.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
Y246 A339
Binding residue
(residue number reindexed from 1)
Y245 A328
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
H139 D144
Catalytic site (residue number reindexed from 1)
H138 D143
Enzyme Commision number
2.3.1.15
: glycerol-3-phosphate 1-O-acyltransferase.
2.3.1.n5
: glycerol-3-phosphate acyltransferase (acyl-[acyl-carrier-protein]- transferring).
Gene Ontology
Molecular Function
GO:0004366
glycerol-3-phosphate O-acyltransferase activity
GO:0016746
acyltransferase activity
Biological Process
GO:0006650
glycerophospholipid metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1iuq
,
PDBe:1iuq
,
PDBj:1iuq
PDBsum
1iuq
PubMed
14684887
UniProt
P10349
|GPAT2_CUCMO Glycerol-3-phosphate acyltransferase ATS12, chloroplastic (Gene Name=ATS1;2)
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