Structure of PDB 1thm Chain A Binding Site BS02

Receptor Information
>1thm Chain A (length=279) Species: 2026 (Thermoactinomyces vulgaris) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
YTPNDPYFSSRQYGPQKIQAPQAWDIAEGSGAKIAIVDTGVQSNHPDLAG
KVVGGWDFVDNDSTPQNGNGHGTHCAGIAAAVTNNSTGIAGTAPKASILA
VRVLDNSGSGTWTAVANGITYAADQGAKVISLSLGGTVGNSGLQQAVNYA
WNKGSVVVAAAGNAGNTAPNYPAYYSNAIAVASTDQNDNKSSFSTYGSWV
DVAAPGSSIYSTYPTSTYASLSGTSMATPHVAGVAGLLASQGRSASNIRA
AIENTADKISGTGTYWAKGRVNAYKAVQY
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 chain1thm Chain A Residue 302 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1thm Crystal structure of thermitase at 1.4 A resolution.
Resolution1.37 Å
Binding residue
(original residue number in PDB)
D57 D62 T64 Q66
Binding residue
(residue number reindexed from 1)
D57 D62 T64 Q66
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) D38 H71 N163 S225
Catalytic site (residue number reindexed from 1) D38 H71 N163 S225
Enzyme Commision number 3.4.21.66: thermitase.
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
Cellular Component
GO:0005576 extracellular region

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:1thm, PDBe:1thm, PDBj:1thm
PDBsum1thm
PubMed2196375
UniProtP04072|THET_THEVU Thermitase

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