Structure of PDB 5c3q Chain C Binding Site BS02
Receptor Information
>5c3q Chain C (length=311) Species:
5141
(Neurospora crassa) [
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MEKAAVNEDGLVIPLIDFSKFLEGDETLKLETAKAILHGFQTAGFIYLKN
IPIQPDFREHVFNTSAKFFKLPKEKKLEVGWTTPEANRGYSAPPDIKESY
EIGREDEPGHPNPWPAEQDDLVGFKSTMNNFFDQCKALHIEVMRAIAVGM
GIDANYFDSFVDVGDNILRLLHYPAVKSEVFKINPGQVRAGEHTDYGSIT
LLFQDSRGGLQVKSPNGQFIDATPIENTVVVNAGDLLARWSNDTIKSTVH
RVVEPPKQEDVHPPRYSIAYFCNPNHKSYIEAIPGTYAAESERKYEGINS
GKYLVQRLAAT
Ligand information
Ligand ID
TDR
InChI
InChI=1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9)
InChIKey
RWQNBRDOKXIBIV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
OpenEye OEToolkits 1.5.0
CC1=CNC(=O)NC1=O
ACDLabs 10.04
O=C1C(=CNC(=O)N1)C
Formula
C5 H6 N2 O2
Name
THYMINE
ChEMBL
CHEMBL993
DrugBank
DB03462
ZINC
ZINC000000157062
PDB chain
5c3q Chain C Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
5c3q
Molecular basis for the substrate specificity and catalytic mechanism of thymine-7-hydroxylase in fungi
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
R190 D216 Y217 F292
Binding residue
(residue number reindexed from 1)
R169 D195 Y196 F271
Annotation score
4
Binding affinity
MOAD
: Kd=32uM
Enzymatic activity
Catalytic site (original residue number in PDB)
R190 A211 H214 D216 H271
Catalytic site (residue number reindexed from 1)
R169 A190 H193 D195 H250
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0044283
small molecule biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5c3q
,
PDBe:5c3q
,
PDBj:5c3q
PDBsum
5c3q
PubMed
26429971
UniProt
Q7RYZ9
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