Structure of PDB 4m1e Chain A Binding Site BS01
Receptor Information
>4m1e Chain A (length=272) Species:
521674
(Planctopirus limnophila DSM 3776) [
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ELKSRIDQATAKISQLWQGEPAVGMILGTGLGGLAEQIEQDIAIPYSDIP
HFPTSTVKSHAGRLVCGRLRGIPIVAMEGRFHYYEGYSLEQVTFPVRVMK
AMGVKTLLVTNAAGGINPQLDLSDVLIIEDHINLMPENPLRGPNDEELGP
RFPDMSHPYDCQHMEVARQVALELGIHCPKGVFVAVSGPNLETRAEYRML
KLMGADVVGMSTVPEVLVAVHAGLRVLGFSVVTDLCLPDALEPVELNKIL
EVAARGGAKLARLIPEILPRIA
Ligand information
Ligand ID
ADE
InChI
InChI=1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)
InChIKey
GFFGJBXGBJISGV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Nc1ncnc2[nH]cnc12
OpenEye OEToolkits 1.5.0
c1[nH]c2c(n1)c(ncn2)N
ACDLabs 10.04
n1c(c2ncnc2nc1)N
Formula
C5 H5 N5
Name
ADENINE
ChEMBL
CHEMBL226345
DrugBank
DB00173
ZINC
ZINC000000000882
PDB chain
4m1e Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4m1e
Crystal structure of purine nucleoside phosphorylase I from Planctomyces limnophilus DSM 3776, NYSGRC Target 029364.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
A114 A115 G116 L193 E194 V210 M212 D236
Binding residue
(residue number reindexed from 1)
A112 A113 G114 L191 E192 V208 M210 D234
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T31 H62 H84 Y86 E87 A114 M212 S213 D236 C238 L248
Catalytic site (residue number reindexed from 1)
T29 H60 H82 Y84 E85 A112 M210 S211 D234 C236 L246
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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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4m1e
,
PDBe:4m1e
,
PDBj:4m1e
PDBsum
4m1e
PubMed
UniProt
D5SMY7
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