Structure of PDB 5xwl Chain A Binding Site BS02
Receptor Information
>5xwl Chain A (length=223) Species:
9823
(Sus scrofa) [
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IVGGYTCAANSIPYQVSLNSGSHFCGGSLINSQWVVSAAHCYKSRIQVRL
GEHNIDVLEGNEQFINAAKIITHPNFNGNTLDNDIMLIKLSSPATLNSRV
ATVSLPRSCAAAGTECLISGWGNTKSSGSSYPSLLQCLKAPVLSDSSCKS
SYPGQITGNMICVGFLEGGKDSCQGDSGGPVVCNGQLQGIVSWGYGCAQK
NKPGVYTKVCNYVNWIQQTIAAN
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
5xwl Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5xwl
Tripeptides derived from reactive centre loop of potato type II protease inhibitors preferentially inhibit midgut proteases of Helicoverpa armigera.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
E60 V65 L66 E70
Binding residue
(residue number reindexed from 1)
E52 V57 L58 E62
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H48 D92 Q182 G183 D184 S185 G186
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:5xwl
,
PDBe:5xwl
,
PDBj:5xwl
PDBsum
5xwl
PubMed
29486250
UniProt
P00761
|TRYP_PIG Trypsin
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