Structure of PDB 1l1g Chain A Binding Site BS03
Receptor Information
>1l1g Chain A (length=240) Species:
9823
(Sus scrofa) [
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VVGGTEAQRNSWPSQISLQYRSGSSWAHTCGGTLIRQNWVMTAAHCVDRE
LTFRVVVGEHNLNQNDGTEQYVGVQKIVVHPYWNTDDVAAGYDIALLRLA
QSVTLNSYVQLGVLPRAGTILANNSPCYITGWGLTRTNGQLAQTLQQAYL
PTVDYAICSSSSYWGSTVKNSMVCAGGDGVRSGCQGDSGGPLHCLVNGQY
AVHGVTSFVSRLGCNVTRKPTVFTRVSAYISWINNVIASN
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
1l1g Chain A Residue 250 [
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Receptor-Ligand Complex Structure
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PDB
1l1g
Xenon derivatization of halide-soaked protein crystals.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
F208 V209 R211
Binding residue
(residue number reindexed from 1)
F208 V209 R211
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H45 D93 Q185 G186 D187 S188 G189
Catalytic site (residue number reindexed from 1)
H45 D93 Q185 G186 D187 S188 G189
Enzyme Commision number
3.4.21.36
: pancreatic elastase.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1l1g
,
PDBe:1l1g
,
PDBj:1l1g
PDBsum
1l1g
PubMed
12198297
UniProt
P00772
|CELA1_PIG Chymotrypsin-like elastase family member 1 (Gene Name=CELA1)
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