Structure of PDB 1slv Chain B Binding Site BS01
Receptor Information
>1slv Chain B (length=215) Species:
10116
(Rattus norvegicus) [
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IVGGYTCQENSVPYQVSLNSGYHFCGGSLINDQWVVSAAHCYKSRIQVRL
GEHNINVLEGNEQFVNAAKIIKHPNFDRKTLNNDIMLIKLSSPVKVATVA
LPSSCAPAGTQCLISGWGHTLNHPDLLQCLDAPLLPQADCEASYPGKITD
NMVCVGFLEGGKDSCQGDSGGPVVCNGELQGIVSWGYGCALPDNPGVYTK
VCNYVDWIQDTIAAN
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
1slv Chain B Residue 246 [
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Receptor-Ligand Complex Structure
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PDB
1slv
X-ray structures of a designed binding site in trypsin show metal-dependent geometry.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
E70 N72 V75 L76 E77
Binding residue
(residue number reindexed from 1)
E52 N54 V57 L58 E59
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 Q166 G167 D168 S169 G170
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1slv
,
PDBe:1slv
,
PDBj:1slv
PDBsum
1slv
PubMed
8634241
UniProt
P00763
|TRY2_RAT Anionic trypsin-2 (Gene Name=Prss2)
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