Structure of PDB 2p4s Chain B Binding Site BS01
Receptor Information
>2p4s Chain B (length=282) Species:
7165
(Anopheles gambiae) [
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YTYDTLQEIATYLLERTELRPKVGIICGSGLGTLAEQLTDVDSFDYETIP
HFPVSTVAGHVGRLVFGYLAGVPVMCMQGRFHHYEGYPLAKCAMPVRVMH
LIGCTHLIATNAAGGANPKYRVGDIMLIKDHINLMGFAGNNPLQGPNDER
FGPRFFGMANTYDPKLNQQAKVIARQIGIENELREGVYTCLGGPNFETVA
EVKMLSMLGVDAIGMSTVHEIITARHCGMTCFAFSLITNMCTMSYEEEEE
HCHDSIVGVGKNREKTLGEFVSRIVKHIHYEA
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
2p4s Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
2p4s
Anopheles gambiae purine nucleoside phosphorylase: catalysis, structure, and inhibition.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G117 S118 R169 H171 N200 S305
Binding residue
(residue number reindexed from 1)
G28 S29 R80 H82 N111 S216
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S118 H149 H171 Y173 E174 A201 M304 S305 N328 C330 H342
Catalytic site (residue number reindexed from 1)
S29 H60 H82 Y84 E85 A112 M215 S216 N239 C241 H253
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
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006166
purine ribonucleoside salvage
GO:0009116
nucleoside metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2p4s
,
PDBe:2p4s
,
PDBj:2p4s
PDBsum
2p4s
PubMed
17918964
UniProt
A4Q998
|PNPH_ANOGA Purine nucleoside phosphorylase (Gene Name=pnp)
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