Structure of PDB 1ubn Chain A Binding Site BS02

Receptor Information
>1ubn Chain A (length=275) Species: 1390 (Bacillus amyloliquefaciens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
AQSVPYGVSQIKAPALHSQGYTGSNVKVAVIDSGIDSSHPDLKVAGGASM
VPSETNPFQDNNSHGTHVAGTVAALNNSIGVLGVAPSASLYAVKVLGADG
SGQYSWIINGIEWAIANNMDVINMSLGGPSGSAALKAAVDKAVASGVVVV
AAAGNEGTSGSSSTVGYPGKYPSVIAVGAVDSSNQRASFSSVGPELDVMA
PGVSIQSTLPGNKYGAYNGTCMASPHVAGAAALILSKHPNWTNTQVRSSL
ENTTTKLGDSFYYGKGLINVQAAAQ
Ligand information
Ligand IDCA
InChIInChI=1S/Ca/q+2
InChIKeyBHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
FormulaCa
NameCALCIUM ION
ChEMBL
DrugBankDB14577
ZINC
PDB chain1ubn Chain A Residue 277 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1ubn Electric fields in active sites: substrate switching from null to strong fields in thiol- and selenol-subtilisins.
Resolution2.4 Å
Binding residue
(original residue number in PDB)
G169 Y171 P172 V174
Binding residue
(residue number reindexed from 1)
G169 Y171 P172 V174
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) D32 H64 N155 C221
Catalytic site (residue number reindexed from 1) D32 H64 N155 C221
Enzyme Commision number 3.4.21.62: subtilisin.
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:1ubn, PDBe:1ubn, PDBj:1ubn
PDBsum1ubn
PubMed10350485
UniProtP00782|SUBT_BACAM Subtilisin BPN' (Gene Name=apr)

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