Structure of PDB 2g5v Chain A Binding Site BS01
Receptor Information
>2g5v Chain A (length=223) Species:
9913
(Bos taurus) [
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IVGGYTCGANTVPYQVSLNSGYHFCGGSLINSQWVVSAAHCYKSGIQVRL
GEDNINVVEGNEQFISASKSIVHPSYNSNTLNNDIMLIKLKSAASLNSRV
ASISLPTSCASAGTQCLISGWGNTKSSGTSYPDVLKCLKAPILSDSSCKS
AYPGQITSNMFCAGYLEGGKDSCQGDSGGPVVCSGKLQGIVSWGSGCAQK
NKPGVYTKVCNYVSWIKQTIASN
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
2g5v Chain A Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
2g5v
Ligand Epitoping By Proton NMR Chemical Shift Differences
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
E58 N60 V63 E68
Binding residue
(residue number reindexed from 1)
E52 N54 V57 E62
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H46 D90 Q180 G181 D182 S183 G184
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:0004175
endopeptidase activity
GO:0004252
serine-type endopeptidase activity
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
GO:0097655
serpin family protein binding
Biological Process
GO:0006508
proteolysis
GO:0007586
digestion
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0097180
serine protease inhibitor complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2g5v
,
PDBe:2g5v
,
PDBj:2g5v
PDBsum
2g5v
PubMed
UniProt
P00760
|TRY1_BOVIN Serine protease 1 (Gene Name=PRSS1)
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