Structure of PDB 2tbs Chain A Binding Site BS01
Receptor Information
>2tbs Chain A (length=222) Species:
8030
(Salmo salar) [
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IVGGYECKAYSQAHQVSLNSGYHFCGGSLVNENWVVSAAHCYKSRVEVRL
GEHNIKVTEGSEQFISSSRVIRHPNYSSYNIDNDIMLIKLSKPATLNTYV
QPVALPTSCAPAGTMCTVSGWGNTMSSTADSDKLQCLNIPILSYSDCNDS
YPGMITNAMFCAGYLEGGKDSCQGDSGGPVVCNGELQGVVSWGYGCAEPG
NPGVYAKVCIFSDWLTSTMASY
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
2tbs Chain A Residue 247 [
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Receptor-Ligand Complex Structure
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PDB
2tbs
Cold adaption of enzymes: structural comparison between salmon and bovine trypsins.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
E70 N72 V75 E77 E80
Binding residue
(residue number reindexed from 1)
E52 N54 V57 E59 E62
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)
H40 D84 Q173 G174 D175 S176 G177
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:2tbs
,
PDBe:2tbs
,
PDBj:2tbs
PDBsum
2tbs
PubMed
7846025
UniProt
P35031
|TRY1_SALSA Trypsin-1
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