Structure of PDB 3uav Chain A Binding Site BS01
Receptor Information
>3uav Chain A (length=227) Species:
1396
(Bacillus cereus) [
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SVHIEAKQGEIAESILLPGDPLRAKYIAETFLEDVTCYNNVRGMLGFTGT
YKGKRVSVQGTGMGVPSISIYVNELIQSYGVKNLIRVGTCGAIQKDVKVR
DVIIAMTACTDSNMNRLTFPGFDFAPAANFDLLKKAYDAGTEKGLHVRVG
NVLTADVFYRESMDMVKKLGDYGVLAVEMETTALYTLAAKYGVNALSVLT
VSDHIFSEERQTTFNEMIEIALDAAIQ
Ligand information
Ligand ID
SO4
InChI
InChI=1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4)/p-2
InChIKey
QAOWNCQODCNURD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
[O-]S(=O)(=O)[O-]
CACTVS 3.341
[O-][S]([O-])(=O)=O
ACDLabs 10.04
[O-]S([O-])(=O)=O
Formula
O4 S
Name
SULFATE ION
ChEMBL
DrugBank
DB14546
ZINC
PDB chain
3uav Chain A Residue 236 [
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Receptor-Ligand Complex Structure
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PDB
3uav
Structural basis of the substrate specificity of Bacillus cereus adenosine phosphorylase.
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
G20 R87 T90
Binding residue
(residue number reindexed from 1)
G19 R86 T89
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H4 G20 R24 R43 E75 R87 T90 S203 D204 I206 R217
Catalytic site (residue number reindexed from 1)
H3 G19 R23 R42 E74 R86 T89 S202 D203 I205 R210
Enzyme Commision number
2.4.2.1
: purine-nucleoside phosphorylase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004731
purine-nucleoside phosphorylase activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006152
purine nucleoside catabolic process
GO:0009116
nucleoside metabolic process
GO:0009164
nucleoside catabolic process
GO:0042278
purine nucleoside metabolic process
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3uav
,
PDBe:3uav
,
PDBj:3uav
PDBsum
3uav
PubMed
22349225
UniProt
Q5EEL8
|DEOD_BACCE Purine nucleoside phosphorylase DeoD-type (Gene Name=deoD)
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