Structure of PDB 1s6f Chain A Binding Site BS04
Receptor Information
>1s6f Chain A (length=223) Species:
9823
(Sus scrofa) [
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IVGGYTCAANSIPYQVSLNSGSHFCGGSLINSQWVVSAAHCYKSRIQVRL
GEHNIDVLEGNEQFINAAKIITHPNFNGNTLDNDIMLIKLSSPATLNSRV
ATVSLPRSCAAAGTECLISGWGNTKSSGSSYPSLLQCLKAPVLSDSSCKS
SYPGQITGNMICVGFLEGGKDSCQGDSGGPVVCNGQLQGIVSWGYGCAQK
NKPGVYTKVCNYVNWIQQTIAAN
Ligand information
Ligand ID
EDO
InChI
InChI=1S/C2H6O2/c3-1-2-4/h3-4H,1-2H2
InChIKey
LYCAIKOWRPUZTN-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OCCO
OpenEye OEToolkits 1.5.0
C(CO)O
Formula
C2 H6 O2
Name
1,2-ETHANEDIOL;
ETHYLENE GLYCOL
ChEMBL
CHEMBL457299
DrugBank
ZINC
ZINC000005224354
PDB chain
1s6f Chain A Residue 8 [
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Receptor-Ligand Complex Structure
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PDB
1s6f
X-ray and NMR characterization of covalent complexes of trypsin, borate, and alcohols.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
S164 S166
Binding residue
(residue number reindexed from 1)
S144 S146
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 Q192 G193 D194 S195 G196
Catalytic site (residue number reindexed from 1)
H40 D84 Q174 G175 D176 S177 G178
Enzyme Commision number
3.4.21.4
: trypsin.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
GO:0007586
digestion
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1s6f
,
PDBe:1s6f
,
PDBj:1s6f
PDBsum
1s6f
PubMed
15005618
UniProt
P00761
|TRYP_PIG Trypsin
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