Structure of PDB 1tec Chain E Binding Site BS02
Receptor Information
>1tec Chain E (length=279) Species:
2026
(Thermoactinomyces vulgaris) [
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YTPNDPYFSSRQYGPQKIQAPQAWDIAEGSGAKIAIVDTGVQSNHPDLAG
KVVGGWDFVDNDSTPQNGNGHGTHCAGIAAAVTNNSTGIAGTAPKASILA
VRVLDNSGSGTWTAVANGITYAADQGAKVISLSLGGTVGNSGLQQAVNYA
WNKGSVVVAAAGNAGNTAPNYPAYYSNAIAVASTDQNDNKSSFSTYGSVV
DVAAPGSWIYSTYPTSTYASLSGTSMATPHVAGVAGLLASQGRSASNIRA
AIENTADKISGTGTYWAKGRVNAYKAVQY
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
1tec Chain E Residue 344 [
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Receptor-Ligand Complex Structure
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PDB
1tec
Crystallographic refinement by incorporation of molecular dynamics: thermostable serine protease thermitase complexed with eglin c.
Resolution
2.2 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 score
4
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
PDBsum
1tec
PubMed
2688688
UniProt
P04072
|THET_THEVU Thermitase
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