Structure of PDB 1w4r Chain E Binding Site BS01
Receptor Information
>1w4r Chain E (length=160) Species:
9606
(Homo sapiens) [
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RGQIQVILGPMFSGKSTELMRRVRRFQIAQYKCLVIKYAKDTRALPACLL
RDVAQEALGVAVIGIDEGQFFPDIVEFCEAMANAGKTVIVAALDGTFQRK
PFGAILNLVPLAESVVKLTAVCMECFREAAYTKRLGTEKEVEVIGGADKY
HSVCRLCYFK
Ligand information
Ligand ID
TTP
InChI
InChI=1S/C10H17N2O14P3/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(24-8)4-23-28(19,20)26-29(21,22)25-27(16,17)18/h3,6-8,13H,2,4H2,1H3,(H,19,20)(H,21,22)(H,11,14,15)(H2,16,17,18)/t6-,7+,8+/m0/s1
InChIKey
NHVNXKFIZYSCEB-XLPZGREQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)CO[P@](=O)(O)O[P@@](=O)(O)OP(=O)(O)O)O
CACTVS 3.341
CC1=CN([CH]2C[CH](O)[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)O2)C(=O)NC1=O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)NC(=O)C(=C1)C)CC2O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O
CACTVS 3.341
CC1=CN([C@H]2C[C@H](O)[C@@H](CO[P@@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)O2)C(=O)NC1=O
Formula
C10 H17 N2 O14 P3
Name
THYMIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL363559
DrugBank
DB02452
ZINC
ZINC000008215959
PDB chain
1w4r Chain E Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
1w4r
Structure of a Type II Thymidine Kinase with Bound Dttp
Resolution
1.83 Å
Binding residue
(original residue number in PDB)
M28 G31 K32 S33 D58 D97 E98 Q100 F101 L124 T127 F128 F133 T163 V172 E173 V174 G176 Y181
Binding residue
(residue number reindexed from 1)
M11 G14 K15 S16 D41 D66 E67 Q69 F70 L93 T96 F97 F102 T132 V141 E142 V143 G145 Y150
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.1.21
: thymidine kinase.
Gene Ontology
Molecular Function
GO:0004797
thymidine kinase activity
GO:0005524
ATP binding
View graph for
Molecular Function
External links
PDB
RCSB:1w4r
,
PDBe:1w4r
,
PDBj:1w4r
PDBsum
1w4r
PubMed
15733844
UniProt
P04183
|KITH_HUMAN Thymidine kinase, cytosolic (Gene Name=TK1)
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