Structure of PDB 1n3i Chain B Binding Site BS01
Receptor Information
>1n3i Chain B (length=262) Species:
1773
(Mycobacterium tuberculosis) [
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DPDELARRAAQVIADRTGIGEHDVAVVLGSGWLPAVAALGSPTTVLPQAE
LPGFVPPTAAGHAGELLSVPIGAHRVLVLAGRIHAYEGHDLRYVVHPVRA
ARAAGAQIMVLTNAAGGLRADLQVGQPVLISDHLNLTARSPLVGGEFVDL
TDAYSPRLRELARQSDPQLAEGVYAGLPGPHYETPAEIRMLQTLGADLVG
MSTVHETIAARAAGAEVLGVSLVTNLAAGITGEPLSHAEVLAAGAASATR
MGALLADVIARF
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1n3i Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
1n3i
Over-The-Barrier Transition State Analogues Provide New Chemistries for Inhibitor Design: The Case of Purine Nucleoside Phosphorylase
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G35 S36 R88 H90 N119 S208
Binding residue
(residue number reindexed from 1)
G29 S30 R82 H84 N113 S202
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H68 H90 Y92 E93 A120 M207 S208 N231 A233 H243
Catalytic site (residue number reindexed from 1)
H62 H84 Y86 E87 A114 M201 S202 N225 A227 H237
Enzyme Commision number
6.3.2.1
: pantoate--beta-alanine ligase (AMP-forming).
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004731
purine-nucleoside phosphorylase activity
GO:0016763
pentosyltransferase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0009116
nucleoside metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1n3i
,
PDBe:1n3i
,
PDBj:1n3i
PDBsum
1n3i
PubMed
12755607
UniProt
P9WIL5
|PANC_MYCTU Pantothenate synthetase (Gene Name=panC)
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