Structure of PDB 2bza Chain A Binding Site BS02
Receptor Information
>2bza Chain A (length=223) Species:
9913
(Bos taurus) [
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IVGGYTCGANTVPYQVSLNSGYHFCGGSLINSQWVVSAAHCYKSGIQVRL
GEDNINVVEGNEQFISASKSIVHPSYNSNTLNNDIMLIKLKSAASLNSRV
ASISLPTSCASAGTQCLISGWGNTKSSGTSYPDVLKCLKAPILSDSSCKS
AYPGQITSNMFCAGYLEGGKDSCQGDSGGPVVCSGKLQGIVSWGSGCAQK
NKPGVYTKVCNYVSWIKQTIASN
Ligand information
Ligand ID
ABN
InChI
InChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2
InChIKey
WGQKYBSKWIADBV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1ccc(cc1)CN
ACDLabs 10.04
CACTVS 3.341
NCc1ccccc1
Formula
C7 H9 N
Name
BENZYLAMINE
ChEMBL
CHEMBL522
DrugBank
DB02464
ZINC
ZINC000006096244
PDB chain
2bza Chain A Residue 703 [
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Receptor-Ligand Complex Structure
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PDB
2bza
Non-Boltzmann thermodynamic integration (NBTI) for macromolecular systems: relative free energy of binding of trypsin to benzamidine and benzylamine.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
D189 S190 C191 Q192 W215 G219
Binding residue
(residue number reindexed from 1)
D171 S172 C173 Q174 W193 G196
Annotation score
1
Binding affinity
MOAD
: Ki=1.58mM
PDBbind-CN
: -logKd/Ki=2.80,Ki=1.58mM
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: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:2bza
,
PDBe:2bza
,
PDBj:2bza
PDBsum
2bza
PubMed
10651279
UniProt
P00760
|TRY1_BOVIN Serine protease 1 (Gene Name=PRSS1)
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