Structure of PDB 1hoz Chain A Binding Site BS01
Receptor Information
>1hoz Chain A (length=316) Species:
5699
(Trypanosoma vivax) [
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GSAKNVVLDHDGNLDDFVAMVLLASNTEKVRLIGALCTDADCFVENGFNV
TGKIMCLMHNNMNLPLFPIGKSAATAVNPFPKEWRCLAKNMDDMPILNIP
ENVELWDKIKAENEKYEGQQLLADLVMNSEEKVTICVTGPLSNVAWCIDK
YGEKFTSKVEECVIMGGAVDVRGNVFLPSTDGTAEWNIYWDPASAKTVFG
CPGLRRIMFSLDSTNTVPVRSPYVQRFGEQTNFLLSILVGTMWAMYYAWD
ALTAAYVVDQKVANVDPVPIDVVVDKQPNEGATVRTDAENYPLTFVARNP
EAEFFLDMLLRSARAC
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
1hoz Chain A Residue 328 [
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Receptor-Ligand Complex Structure
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PDB
1hoz
Structure and function of a novel purine specific nucleoside hydrolase from Trypanosoma vivax.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
D10 D15 T137 D261
Binding residue
(residue number reindexed from 1)
D11 D16 T138 D250
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D10 D15 D40 W83 T137 W185 N186 W260 D261
Catalytic site (residue number reindexed from 1)
D11 D16 D41 W84 T138 W186 N187 W249 D250
Enzyme Commision number
3.2.2.1
: purine nucleosidase.
Gene Ontology
Molecular Function
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0016799
hydrolase activity, hydrolyzing N-glycosyl compounds
GO:0046872
metal ion binding
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1hoz
,
PDBe:1hoz
,
PDBj:1hoz
PDBsum
1hoz
PubMed
11292348
UniProt
Q9GPQ4
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