Structure of PDB 1qll Chain B Binding Site BS01
Receptor Information
>1qll Chain B (length=121) Species:
113192
(Bothrops pirajai) [
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SLFELGKMILQETGKNPAKSYGAYGCNCGVLGRGKPKDATDRCCYVHKCC
YKKLTGCNPKKDRYSYSWKDKTIVCGENNPCLKELCECDKAVAICLRENL
GTYNKKYRYHLKPFCKKADKC
Ligand information
Ligand ID
TDA
InChI
InChI=1S/C13H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13(14)15/h2-12H2,1H3,(H,14,15)
InChIKey
SZHOJFHSIKHZHA-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCCCCCCCCCCCC(=O)O
CACTVS 3.341
CCCCCCCCCCCCC(O)=O
ACDLabs 10.04
O=C(O)CCCCCCCCCCCC
Formula
C13 H26 O2
Name
N-TRIDECANOIC ACID
ChEMBL
CHEMBL107874
DrugBank
DB02448
ZINC
ZINC000001628119
PDB chain
1qll Chain B Residue 122 [
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Receptor-Ligand Complex Structure
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PDB
1qll
Structural Basis for Low Catalytic Activity in Lys49 Phospholipases A2-A Hypothesis: The Crystal Structure of Piratoxin II Complexed to Fatty Acid
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
L2 G6 Y21 C28 G29 H47
Binding residue
(residue number reindexed from 1)
L2 G6 Y21 C28 G29 H47
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N27 G29 L31 H47 K48 Y51 Y64 D89
Catalytic site (residue number reindexed from 1)
N27 G29 L31 H47 K48 Y51 Y64 D89
Enzyme Commision number
3.1.1.4
: phospholipase A2.
Gene Ontology
Molecular Function
GO:0004623
phospholipase A2 activity
GO:0005509
calcium ion binding
GO:0005543
phospholipid binding
GO:0047498
calcium-dependent phospholipase A2 activity
GO:0090729
toxin activity
Biological Process
GO:0006644
phospholipid metabolic process
GO:0016042
lipid catabolic process
GO:0035821
modulation of process of another organism
GO:0042130
negative regulation of T cell proliferation
GO:0050482
arachidonate secretion
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:1qll
,
PDBe:1qll
,
PDBj:1qll
PDBsum
1qll
PubMed
11141053
UniProt
P82287
|PA2H2_BOTPI Basic phospholipase A2 homolog piratoxin-2
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