Structure of PDB 5cta Chain A Binding Site BS01
Receptor Information
>5cta Chain A (length=179) Species:
1423
(Bacillus subtilis) [
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HNPVVMVHGIGGASFNFAGIKSYLVSQGWSRDKLYAVDFWDETGTNENNG
PVLSEFVQKVLDETGAKKVDIVAHSMGGANTLYYIKNLDGGNKVANVVTL
GGANRLTTGKALPGTDPNQKILYTSIYSSADMIVMNYLSRLDGARNVQIH
GVGHIELLYSSQVNSLIKEGLNGGGQNTN
Ligand information
Ligand ID
BM0
InChI
InChI=1S/C8H15N2/c1-3-4-5-10-7-6-9(2)8-10/h6-8H,3-5H2,1-2H3/q+1
InChIKey
IQQRAVYLUAZUGX-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
C(C)CCn1cc[n+](c1)C
CACTVS 3.385
CCCCn1cc[n+](C)c1
OpenEye OEToolkits 1.9.2
CCCCn1cc[n+](c1)C
Formula
C8 H15 N2
Name
1-butyl-3-methyl-1H-imidazol-3-ium;
1-butyl-3-methylimidazolium
ChEMBL
CHEMBL1198608
DrugBank
ZINC
ZINC000015783059
PDB chain
5cta Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
5cta
Crystallographic Investigation of Imidazolium Ionic Liquid Effects on Enzyme Structure.
Resolution
1.24 Å
Binding residue
(original residue number in PDB)
D34 L36 Y37 K61
Binding residue
(residue number reindexed from 1)
D32 L34 Y35 K59
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
I12 S77 M78 D133 H156
Catalytic site (residue number reindexed from 1)
I10 S75 M76 D131 H154
Enzyme Commision number
3.1.1.3
: triacylglycerol lipase.
Gene Ontology
Molecular Function
GO:0004806
triacylglycerol lipase activity
GO:0016298
lipase activity
GO:0016787
hydrolase activity
Biological Process
GO:0016042
lipid catabolic process
Cellular Component
GO:0005576
extracellular region
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Molecular Function
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Cellular Component
External links
PDB
RCSB:5cta
,
PDBe:5cta
,
PDBj:5cta
PDBsum
5cta
PubMed
26388426
UniProt
P37957
|ESTA_BACSU Lipase EstA (Gene Name=estA)
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