Structure of PDB 8swp Chain E Binding Site BS01
Receptor Information
>8swp Chain E (length=281) Species:
284590
(Kluyveromyces lactis NRRL Y-1140) [
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EQRALIKSAHRYISEKLEDHFSSEFLPKALVICGSGLSGISTKIADEPKP
LILSYSTIPGFKVSTVPGHSGELIFGYMNGAPVVLMNGRLHSYEGHSLAE
TVHPIRALHLLGSINVLIVTNAAGGINASFKAGDLMCVYDHINFPGLCGF
HDAYDLELRKLLFSKKKELNIERKIHEGTYSYVHGPTFESRAESRFLRLA
GTDAVGMSTVPEVVTARHCGWRVLALSLITNECVVDPPASAHDENPVPIQ
EGKATHEEVLENSAKASKDVQELIFSVVAEI
Ligand information
Ligand ID
HPA
InChI
InChI=1S/C5H4N4O/c10-5-3-4(7-1-6-3)8-2-9-5/h1-2H,(H2,6,7,8,9,10)
InChIKey
FDGQSTZJBFJUBT-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C1c2c(N=CN1)ncn2
OpenEye OEToolkits 1.5.0
c1[nH]c2c(n1)N=CNC2=O
CACTVS 3.341
O=C1NC=Nc2nc[nH]c12
Formula
C5 H4 N4 O
Name
HYPOXANTHINE
ChEMBL
CHEMBL1427
DrugBank
DB04076
ZINC
ZINC000018153302
PDB chain
8swp Chain E Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
8swp
Phosphate Binding in PNP Alters Transition-State Analogue Affinity and Subunit Cooperativity.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
A130 G131 F213 E214 M232 N256
Binding residue
(residue number reindexed from 1)
A123 G124 F188 E189 M207 N231
Annotation score
5
Enzymatic activity
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:0009116
nucleoside metabolic process
Cellular Component
GO:0005737
cytoplasm
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Cellular Component
External links
PDB
RCSB:8swp
,
PDBe:8swp
,
PDBj:8swp
PDBsum
8swp
PubMed
37812583
UniProt
Q6CSZ6
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