Structure of PDB 2tsr Chain A Binding Site BS02
Receptor Information
>2tsr Chain A (length=281) Species:
10116
(Rattus norvegicus) [
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QHGELQYLRQVEHIMRCGFKKEDRTGTGTLSVFGMQARYSLRDEFPLLTT
KRVFWKGVLEELLWFIKGSTNAKELSSKGVRIWDANGSRDFLDSLGFSAR
QEGDLGPVYGFQWRHFGADYKDMDSDYSGQGVDQLQKVIDTIKTNPDDRR
IIMCAWNPKDLPLMALPPCHALCQFYVVNGELSCQLYQRSGDMGLGVPFN
IASYALLTYMIAHITGLQPGDFVHTLGDAHIYLNHIEPLKIQLQREPRPF
PKLRILRKVETIDDFKVEDFQIEGYNPHPTI
Ligand information
Ligand ID
D16
InChI
InChI=1S/C21H22N4O6S/c1-11-22-14-4-3-12(9-13(14)19(28)23-11)10-25(2)17-7-6-16(32-17)20(29)24-15(21(30)31)5-8-18(26)27/h3-4,6-7,9,15H,5,8,10H2,1-2H3,(H,24,29)(H,26,27)(H,30,31)(H,22,23,28)/t15-/m0/s1
InChIKey
IVTVGDXNLFLDRM-HNNXBMFYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(c3sc(N(C)Cc2ccc1NC(=NC(=O)c1c2)C)cc3)NC(C(=O)O)CCC(=O)O
CACTVS 3.370
CN(Cc1ccc2NC(=NC(=O)c2c1)C)c3sc(cc3)C(=O)N[CH](CCC(O)=O)C(O)=O
OpenEye OEToolkits 1.7.6
CC1=NC(=O)c2cc(ccc2N1)CN(C)c3ccc(s3)C(=O)N[C@@H](CCC(=O)O)C(=O)O
CACTVS 3.370
CN(Cc1ccc2NC(=NC(=O)c2c1)C)c3sc(cc3)C(=O)N[C@@H](CCC(O)=O)C(O)=O
OpenEye OEToolkits 1.7.6
CC1=NC(=O)c2cc(ccc2N1)CN(C)c3ccc(s3)C(=O)NC(CCC(=O)O)C(=O)O
Formula
C21 H22 N4 O6 S
Name
TOMUDEX;
ZD1694;
Raltitrexed
ChEMBL
CHEMBL225071
DrugBank
DB00293
ZINC
ZINC000003832372
PDB chain
2tsr Chain A Residue 309 [
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Receptor-Ligand Complex Structure
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PDB
2tsr
Crystal structures of rat thymidylate synthase inhibited by Tomudex, a potent anticancer drug.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
R72 I102 D212 G216 F219 Y252
Binding residue
(residue number reindexed from 1)
R52 I82 D192 G196 F199 Y232
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=7.54,Ki=29nM
Enzymatic activity
Catalytic site (original residue number in PDB)
E81 W103 Y129 C189 R209 D212
Catalytic site (residue number reindexed from 1)
E61 W83 Y109 C169 R189 D192
Enzyme Commision number
2.1.1.45
: thymidylate synthase.
Gene Ontology
Molecular Function
GO:0000900
mRNA regulatory element binding translation repressor activity
GO:0003729
mRNA binding
GO:0004799
thymidylate synthase activity
GO:0005542
folic acid binding
GO:0008168
methyltransferase activity
GO:0016741
transferase activity, transferring one-carbon groups
GO:0042803
protein homodimerization activity
GO:1901363
heterocyclic compound binding
GO:1990825
sequence-specific mRNA binding
Biological Process
GO:0006206
pyrimidine nucleobase metabolic process
GO:0006231
dTMP biosynthetic process
GO:0006235
dTTP biosynthetic process
GO:0006417
regulation of translation
GO:0007623
circadian rhythm
GO:0009165
nucleotide biosynthetic process
GO:0009410
response to xenobiotic stimulus
GO:0009636
response to toxic substance
GO:0014070
response to organic cyclic compound
GO:0017148
negative regulation of translation
GO:0019860
uracil metabolic process
GO:0032259
methylation
GO:0032570
response to progesterone
GO:0033189
response to vitamin A
GO:0034097
response to cytokine
GO:0035999
tetrahydrofolate interconversion
GO:0045471
response to ethanol
GO:0046653
tetrahydrofolate metabolic process
GO:0046683
response to organophosphorus
GO:0048589
developmental growth
GO:0051216
cartilage development
GO:0051384
response to glucocorticoid
GO:0051593
response to folic acid
GO:0060574
intestinal epithelial cell maturation
GO:0097421
liver regeneration
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005759
mitochondrial matrix
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2tsr
,
PDBe:2tsr
,
PDBj:2tsr
PDBsum
2tsr
PubMed
9894005
UniProt
P45352
|TYSY_RAT Thymidylate synthase (Gene Name=Tyms)
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