Structure of PDB 4lhm Chain A Binding Site BS02
Receptor Information
>4lhm Chain A (length=440) Species:
83333
(Escherichia coli K-12) [
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LFLAQEIIRKKRDGHALSDEEIRFFINGIRDNTISEGQIAALAMTIFFHD
MTMPERVSLTMAMRDSGTVLDWKSLHLNGPIVDKHSTGGVGDVTSLMLGP
MVAACGGYIPMISGRGLGHTGGTLDKLESIPGFDIFPDDNRFREIIKDVG
VAIIGQTSSLAPADKRFYATRDITATVDSIPLITASILAKKLAEGLDALV
MDVKVGSGAFMPTYELSEALAEAIVGVANGAGVRTTALLTDMNQVLASSA
GNAVEVREAVQFLTGEYRNPRLFDVTMALCVEMLISGKLAKDDAEARAKL
QAVLDNGKAAEVFGRMVAAQKGPTDFVENYAKYLPTAMLTKAVYADTEGF
VSEMDTRALGMAVVAMGGGRRQASDTIDYSVGFTDMARLGDQVDGQRPLA
VIHAKDENNWQEAAKAVKAAIKLADKAPESTPTVYRRISE
Ligand information
Ligand ID
SO4
InChI
InChI=1S/H2O4S/c1-5(2,3)4/h(H2,1,2,3,4)/p-2
InChIKey
QAOWNCQODCNURD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
[O-]S(=O)(=O)[O-]
CACTVS 3.341
[O-][S]([O-])(=O)=O
ACDLabs 10.04
[O-]S([O-])(=O)=O
Formula
O4 S
Name
SULFATE ION
ChEMBL
DrugBank
DB14546
ZINC
PDB chain
4lhm Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
4lhm
3'-Azidothymidine in the active site of Escherichia coli thymidine phosphorylase: the peculiarity of the binding on the basis of X-ray study.
Resolution
1.52 Å
Binding residue
(original residue number in PDB)
A175 V177 D178
Binding residue
(residue number reindexed from 1)
A175 V177 D178
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D83 K84 H85 S86 T123 D164 R171 S186 K190 K191
Catalytic site (residue number reindexed from 1)
D83 K84 H85 S86 T123 D164 R171 S186 K190 K191
Enzyme Commision number
2.4.2.4
: thymidine phosphorylase.
Gene Ontology
Molecular Function
GO:0004645
1,4-alpha-oligoglucan phosphorylase activity
GO:0009032
thymidine phosphorylase activity
GO:0016154
pyrimidine-nucleoside phosphorylase activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
Biological Process
GO:0006206
pyrimidine nucleobase metabolic process
GO:0006213
pyrimidine nucleoside metabolic process
GO:0006974
DNA damage response
GO:0046104
thymidine metabolic process
Cellular Component
GO:0005829
cytosol
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4lhm
,
PDBe:4lhm
,
PDBj:4lhm
PDBsum
4lhm
PubMed
24699659
UniProt
P07650
|TYPH_ECOLI Thymidine phosphorylase (Gene Name=deoA)
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