Structure of PDB 1obr Chain A Binding Site BS02
Receptor Information
>1obr Chain A (length=323) Species:
2026
(Thermoactinomyces vulgaris) [
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DFPSYDSGYHNYNEMVNKINTVASNYPNIVKKFSIGKSYEGRELWAVKIS
DNVGTDENEPEVLYTALHHAREHLTVEMALYTLDLFTQNYNLDSRITNLV
NNREIYIVFNINPDGGEYDISSGSYKSWRKNRQPNSGSSYVGTDLNRNYG
YKWGCCGGSSGSPSSETYRGRSAFSAPETAAMRDFINSRVVGGKQQIKTL
ITFHTYSELILYPYGYTYTDVPSDMTQDDFNVFKTMANTMAQTNGYTPQQ
ASDLYITDGDMTDWAYGQHKIFAFTFEMYPTSYNPGFYPPDEVIGRETSR
NKEAVLYVAEKADCPYSVIGKSC
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
1obr Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
1obr
Crystal structure of carboxypeptidase T from Thermoactinomyces vulgaris.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
D56 E57 E61 E104
Binding residue
(residue number reindexed from 1)
D56 E57 E61 E104
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H69 E72 R129 H204 E277
Catalytic site (residue number reindexed from 1)
H69 E72 R129 H204 E277
Enzyme Commision number
3.4.17.18
: carboxypeptidase T.
Gene Ontology
Molecular Function
GO:0004181
metallocarboxypeptidase activity
GO:0008270
zinc ion binding
Biological Process
GO:0006508
proteolysis
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1obr
,
PDBe:1obr
,
PDBj:1obr
PDBsum
1obr
PubMed
1521526
UniProt
P29068
|CBPT_THEVU Carboxypeptidase T (Gene Name=cpt)
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