Structure of PDB 2lip Chain A Binding Site BS01
Receptor Information
>2lip Chain A (length=320) Species:
292
(Burkholderia cepacia) [
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ADNYAATRYPIILVHGLTGTDKYAGVLEYWYGIQEDLQQRGATVYVANLS
GFQSDDGPNGRGEQLLAYVKTVLAATGATKVNLVGHSQGGLTSRYVAAVA
PDLVASVTTIGTPHRGSEFADFVQGVLAYDPTGLSSTVIAAFVNVFGILT
SSSNNTNQDALAALKTLTTAQAATYNQNYPSAGLGAPGSCQTGAPTETVG
GNTHLLYSWAGTAIQPTISVFGVTGATDTSTIPLVDPANALDPSTLALFG
TGTVMVNRGSGQNDGVVSKCSALYGQVLSTSYKWNHLDEINQLLGVRGAN
AEDPVAVIRTHANRLKLAGV
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
2lip Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
2lip
The open conformation of a Pseudomonas lipase.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D242 D288 Q292 V296
Binding residue
(residue number reindexed from 1)
D242 D288 Q292 V296
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L17 S87 Q88 D242 D264 H286 D288 Q292 V296
Catalytic site (residue number reindexed from 1)
L17 S87 Q88 D242 D264 H286 D288 Q292 V296
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:2lip
,
PDBe:2lip
,
PDBj:2lip
PDBsum
2lip
PubMed
9032074
UniProt
P22088
|LIP_BURCE Triacylglycerol lipase (Gene Name=lip)
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