Structure of PDB 1t1g Chain A Binding Site BS01
Receptor Information
>1t1g Chain A (length=357) Species:
198803
(Bacillus sp. MN-32) [
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AAPTAYTPLDVAQAYQFPEGLDGQGQCIAIIALGGGYDETSLAQYFASLG
VSAPQVVSVSVDGATNQPTGDPNGPDGEVELDIEVAGALAPGAKIAVYFA
PNTDAGFLNAITTAVHDPTHKPSIVSISWGGPEDSWAPASIAAMNRAFLD
AAALGVTVLAAAGDSGSTDGEQDGLYHVDFPAASPYVLACGGTRLVASAG
RIERETVWNDGPDGGSTGGGVSRIFPLPSWQERANVPPSANPGAGSGRGV
PDVAGNADPATGYEVVIDGETTVIGGTSAVAPLFAALVARINQKLGKPVG
YLNPTLYQLPPEVFHDITEGNNDIANRARIYQAGPGWDPCTGLGSPIGIR
LLQALLP
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
1t1g Chain A Residue 365 [
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Receptor-Ligand Complex Structure
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PDB
1t1g
1.2 a crystal structure of the serine carboxyl proteinase pro-kumamolisin: structure of an intact pro-subtilase
Resolution
1.18 Å
Binding residue
(original residue number in PDB)
D316 I317 G334 G336 D338
Binding residue
(residue number reindexed from 1)
D316 I317 G334 G336 D338
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
E78 D82 D164 S278
Catalytic site (residue number reindexed from 1)
E78 D82 D164 S278
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0008236
serine-type peptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:1t1g
,
PDBe:1t1g
,
PDBj:1t1g
PDBsum
1t1g
PubMed
15242607
UniProt
Q8RR56
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