Structure of PDB 1bra Chain A Binding Site BS02
Receptor Information
>1bra Chain A (length=223) Species:
10117
(Rattus rattus) [
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IVGGYTCQENSVPYQVSLNSGYHFCGGSLINDQWVVSAAHCYKSRIQVRL
GEHNINVLEGNEQFVNAAKIIKHPNFDRKTLNNDIMLIKLSSPVKLNARV
ATVALPSSCAPAGTQCLISGWGNTLSSGVNEPDLLQCLDAPLLPQADCEA
SYPGKITDNMVCVGFLEGGKGSCQGDSGGPVVCNGELQGIVSWGYGCALP
DNPDVYTKVCNYVDWIQDTIAAN
Ligand information
Ligand ID
BEN
InChI
InChI=1S/C7H8N2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H3,8,9)
InChIKey
PXXJHWLDUBFPOL-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
[H]/N=C(\c1ccccc1)/N
CACTVS 3.341
NC(=N)c1ccccc1
ACDLabs 10.04
[N@H]=C(N)c1ccccc1
OpenEye OEToolkits 1.5.0
[H]N=C(c1ccccc1)N
Formula
C7 H8 N2
Name
BENZAMIDINE
ChEMBL
CHEMBL20936
DrugBank
ZINC
ZINC000000036634
PDB chain
1bra Chain A Residue 246 [
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Receptor-Ligand Complex Structure
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PDB
1bra
Relocating a negative charge in the binding pocket of trypsin.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
S190 Q192 S195 V213 G216 G219
Binding residue
(residue number reindexed from 1)
S172 Q174 S177 V191 G194 G196
Annotation score
1
Binding affinity
MOAD
: Ki=15000uM
PDBbind-CN
: -logKd/Ki=1.82,Ki=15000uM
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:0005509
calcium ion binding
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
GO:0007584
response to nutrient
GO:0007586
digestion
GO:0030574
collagen catabolic process
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1bra
,
PDBe:1bra
,
PDBj:1bra
PDBsum
1bra
PubMed
8478942
UniProt
P00763
|TRY2_RAT Anionic trypsin-2 (Gene Name=Prss2)
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