Structure of PDB 2z5g Chain B Binding Site BS01
Receptor Information
>2z5g Chain B (length=387) Species:
213419
(Geobacillus zalihae) [
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SLRANDAPIVLLHGLTGWGREEMFGFKYWGGVRGDIEQWLNDNGYRTYTL
AVGPLSSNWDRACEAYAQLVGGTVDYGAAHAAKHGHARFGRTYPGLLPEL
KRGGRIHIIAHSQGGQTARMLVSLLENGSQEEREYAKAHNVSLSPLFEGG
HHFVLSVTTIATPHDGTTLVNMVDFTDRFFDLQKAVLEAAAVASNVPYTS
QVYDFKLDQWGLRRQPGESFDHYFERLKRSPVWTSTDTARYDLSVSGAEK
LNQWVQASPNTYYLSFSTERTYRGALTGNHYPELGMNAFSAVVCAPFLGS
YRNPTLGIDDRWLENDGIVNTVSMNGPKRGSSDRIVPYDGTLKKGVWNDM
GTYNVDHLEIIGVDPNPSFDIRAFYLRLAEQLASLQP
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
2z5g Chain B Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
2z5g
Novel cation-pi interaction revealed by crystal structure of thermoalkalophilic lipase
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D61 H81 H87 D238
Binding residue
(residue number reindexed from 1)
D60 H80 H86 D237
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.1.3
: triacylglycerol lipase.
Gene Ontology
Molecular Function
GO:0004806
triacylglycerol lipase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Biological 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:2z5g
,
PDBe:2z5g
,
PDBj:2z5g
PDBsum
2z5g
PubMed
17932933
UniProt
Q842J9
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