Structure of PDB 1ju6 Chain B Binding Site BS01
Receptor Information
>1ju6 Chain B (length=286) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
HGELQYLGQIQHILRCGVEKDDRTGTGTLSVFGMQARYSLRDEFPLLTTK
RVFWKGVLEELLWFIKGSTNAKELSSKGVKIWDANGSRDFLDSLGFSTRE
EGDLGPVYGFQWRHFGAEYRDMESDYSGQGVDQLQRVIDTIKTNPDDRRI
IMCAWNPRDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLGVPFNI
ASYALLTYMIAHITGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFP
KLRILRKVEKIDDFKAEDFQIEGYNPHPTIKMEMAV
Ligand information
Ligand ID
UMP
InChI
InChI=1S/C9H13N2O8P/c12-5-3-8(11-2-1-7(13)10-9(11)14)19-6(5)4-18-20(15,16)17/h1-2,5-6,8,12H,3-4H2,(H,10,13,14)(H2,15,16,17)/t5-,6+,8+/m0/s1
InChIKey
JSRLJPSBLDHEIO-SHYZEUOFSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=P(O)(O)OCC2OC(N1C(=O)NC(=O)C=C1)CC2O
CACTVS 3.370
O[CH]1C[CH](O[CH]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1[C@@H]([C@H](O[C@H]1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
CACTVS 3.370
O[C@H]1C[C@@H](O[C@@H]1CO[P](O)(O)=O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 1.7.6
C1C(C(OC1N2C=CC(=O)NC2=O)COP(=O)(O)O)O
Formula
C9 H13 N2 O8 P
Name
2'-DEOXYURIDINE 5'-MONOPHOSPHATE;
DUMP
ChEMBL
CHEMBL211312
DrugBank
DB03800
ZINC
ZINC000004228260
PDB chain
1ju6 Chain A Residue 314 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1ju6
Multi-targeted antifolates aimed at avoiding drug resistance form covalent closed inhibitory complexes with human and Escherichia coli thymidylate synthases.
Resolution
2.89 Å
Binding residue
(original residue number in PDB)
R175 R176
Binding residue
(residue number reindexed from 1)
R148 R149
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
E87 W109 Y135 C195 R215 D218
Catalytic site (residue number reindexed from 1)
E60 W82 Y108 C168 R188 D191
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:0071897
DNA biosynthetic process
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
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1ju6
,
PDBe:1ju6
,
PDBj:1ju6
PDBsum
1ju6
PubMed
11697906
UniProt
P04818
|TYSY_HUMAN Thymidylate synthase (Gene Name=TYMS)
[
Back to BioLiP
]