Structure of PDB 3ea2 Chain A Binding Site BS04
Receptor Information
>3ea2 Chain A (length=296) Species:
1428
(Bacillus thuringiensis) [
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ASSVNELENWSKWMQPIPDNIPLARISIPGTHDSGTFKLQNPIKQVWGMT
QEYDFRYQMDHGARIFDIRGRLTDDNTIVLHHGPLYLYVTLHEFINEAKQ
FLKDNPSETIIMSLKKEYEDMKGAEGSFSSTFEKNYFVDPIFLKTEGNIK
LGDARGKIVLLKRYSGSNESGGYNNFYWPDNETFTTTVNQNVNVTVQDKY
KVNYDEKVKSIKDTMDETMNNSEDLNHLYINFTSLSSGGTAWNSPYSYAS
SINPEIANDIKQKNPTRVGWVIQDYINEKWSPLLYQEVIRANKSLI
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
3ea2 Chain A Residue 905 [
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Receptor-Ligand Complex Structure
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PDB
3ea2
Modulation of bacillus thuringiensis phosphatidylinositol-specific phospholipase C activity by mutations in the putative dimerization interface.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
D74 D75
Binding residue
(residue number reindexed from 1)
D74 D75
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H32 D33 R69 H82 D274
Catalytic site (residue number reindexed from 1)
H32 D33 R69 H82 D274
Enzyme Commision number
4.6.1.13
: phosphatidylinositol diacylglycerol-lyase.
Gene Ontology
Molecular Function
GO:0004436
phosphatidylinositol diacylglycerol-lyase activity
GO:0008081
phosphoric diester hydrolase activity
GO:0016829
lyase activity
Biological Process
GO:0006629
lipid metabolic process
GO:0016042
lipid catabolic process
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3ea2
,
PDBe:3ea2
,
PDBj:3ea2
PDBsum
3ea2
PubMed
19369255
UniProt
P08954
|PLC_BACTU 1-phosphatidylinositol phosphodiesterase
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