Structure of PDB 4l5c Chain E Binding Site BS01
Receptor Information
>4l5c Chain E (length=289) Species:
6183
(Schistosoma mansoni) [
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KVKVGIIGGSGFDDPNLFKKVGVRQVTTPFGKPSDTLVEGFVGDVACVVL
PRHGKGHLIPPSEVNYRANVWALKDLGCTHILATACGSLQEDLVPGDFVV
LNQFMDKTWGRENTFYGSKPDSLKGVLHMPMAEPFCERTRQILIQAARNK
SINVYDKKTMDKSACIHPCVHAEGSAVTINGPRFSTRCESFIHKAMGLDI
VNMTLVPEVSLAREAGLSYASIAIVTDFDCWKSEEEHVCVDMVLEQFRKS
VVHVREILLEAVALIGAEDWTKTIEANKALVMSSRQDLL
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
4l5c Chain E Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
4l5c
Crystal Structure of Schistosoma mansoni Adenosine Phosphorylase/5'-Methylthioadenosine Phosphorylase and Its Importance on Adenosine Salvage Pathway.
Resolution
2.075 Å
Binding residue
(original residue number in PDB)
A88 C89 G90 F187 N205 M206 T229 D230
Binding residue
(residue number reindexed from 1)
A85 C86 G87 F184 N202 M203 T226 D227
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K34 H59 D230 D232
Catalytic site (residue number reindexed from 1)
K32 H57 D227 D229
Enzyme Commision number
2.4.2.28
: S-methyl-5'-thioadenosine phosphorylase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
GO:0017061
S-methyl-5-thioadenosine phosphorylase activity
Biological Process
GO:0006166
purine ribonucleoside salvage
GO:0009116
nucleoside metabolic process
GO:0019509
L-methionine salvage from methylthioadenosine
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4l5c
,
PDBe:4l5c
,
PDBj:4l5c
PDBsum
4l5c
PubMed
27935959
UniProt
I0B503
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