Structure of PDB 4lip Chain E Binding Site BS02
Receptor Information
>4lip Chain E (length=319) Species:
292
(Burkholderia cepacia) [
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DNYAATRYPIILVHGLTGTDKYAGVLEYWYGIQEDLQQRGATVYVANLSG
FQSDDGPNGRGEQLLAYVKTVLAATGATKVNLVGHSQGGLTSRYVAAVAP
DLVASVTTIGTPHRGSEFADFVQGVLAYDPTGLSSTVIAAFVNVFGILTS
SSNNTNQDALAALKTLTTAQAATYNQNYPSAGLGAPGSCQTGAPTETVGG
NTHLLYSWAGTAIQPTISVFGVTGATDTSTIPLVDPANALDPSTLALFGT
GTVMVNRGSGQNDGVVSKCSALYGQVLSTSYKWNHLDEINQLLGVRGANA
EDPVAVIRTHANRLKLAGV
Ligand information
Ligand ID
CCP
InChI
InChI=1S/C4H11O3P/c1-2-3-4-8(5,6)7/h2-4H2,1H3,(H2,5,6,7)
InChIKey
UOKRBSXOBUKDGE-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)CCCC
OpenEye OEToolkits 1.5.0
CCCCP(=O)(O)O
CACTVS 3.341
CCCC[P](O)(O)=O
Formula
C4 H11 O3 P
Name
BUTYLPHOSPHONATE
ChEMBL
DrugBank
DB03999
ZINC
ZINC000029786428
PDB chain
4lip Chain E Residue 950 [
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Receptor-Ligand Complex Structure
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PDB
4lip
Structural basis of the chiral selectivity of Pseudomonas cepacia lipase
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
G16 L17 S87 Q88 S117 H286
Binding residue
(residue number reindexed from 1)
G15 L16 S86 Q87 S116 H285
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:4lip
,
PDBe:4lip
,
PDBj:4lip
PDBsum
4lip
PubMed
9660188
UniProt
P22088
|LIP_BURCE Triacylglycerol lipase (Gene Name=lip)
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