Structure of PDB 4bnr Chain A Binding Site BS02
Receptor Information
>4bnr Chain A (length=237) Species:
6717
(Astacus leptodactylus) [
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IVGGTDATLGEFPYQLSFQETFIGFSFHFCGASIYNENYAITAGHCVYGD
DYENPSGLQIVAGELDMSVNEGSEQIITVSKIILHENFDYNLLDNDISLL
KLSGSLTFNDNVAPIALPEQGHTATGDVIVTGWGTTSEGGNTPDVLQKVT
VPLVSDEDCRADYGADEILDSMICAGVPEGGKDSCQGDSGGPLAASDTGS
TYLAGIVSWGYGCARPGYPGVYTEVSYHVDWIKANAV
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
4bnr Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
4bnr
Comparison of Complexes Formed by a Crustacean and a Vertebrate Trypsin with Bovine Pancreatic Trypsin Inhibitor - the Key to Achieving Extreme Stability?
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D165 D178 M180 E231
Binding residue
(residue number reindexed from 1)
D156 D170 M172 E224
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 Q192 G193 D194 S195 G196
Catalytic site (residue number reindexed from 1)
H45 D96 Q186 G187 D188 S189 G190
Enzyme Commision number
3.4.21.4
: trypsin.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:4bnr
,
PDBe:4bnr
,
PDBj:4bnr
PDBsum
4bnr
PubMed
24034223
UniProt
Q52V24
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