Structure of PDB 1tec Chain E Binding Site BS02

Receptor Information
>1tec Chain E (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
WNKGSVVVAAAGNAGNTAPNYPAYYSNAIAVASTDQNDNKSSFSTYGSVV
DVAAPGSWIYSTYPTSTYASLSGTSMATPHVAGVAGLLASQGRSASNIRA
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 chain1tec Chain E Residue 344 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1tec Crystallographic refinement by incorporation of molecular dynamics: thermostable serine protease thermitase complexed with eglin c.
Resolution2.2 Å
Binding residue
(original residue number in PDB)
D57 D60 D62 T64 Q66
Binding residue
(residue number reindexed from 1)
D57 D60 D62 T64 Q66
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) S225
Catalytic site (residue number reindexed from 1) 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:1tec, PDBe:1tec, PDBj:1tec
PDBsum1tec
PubMed2688688
UniProtP04072|THET_THEVU Thermitase

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