Structure of PDB 1p73 Chain D Binding Site BS01

Receptor Information
>1p73 Chain D (length=326) Species: 10331 (Equid alphaherpesvirus 4) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
HMVTIVRIYLDGVYGIGKSTTGRVMASAASGGSPTLYFPEPMAYWRTLFE
TDVISGIYDTQNRAVDDAALITAHYQSRFTTPYLILHDHTCTLFGGNSLQ
RGTQPDLTLVFDRHPVASTVCFPAARYLLGDMSMCALMAMVATLPREPQG
GNIVVTTLNVEEHIRRLRTRARIGEQIDITLIATLRNVYFMLVNTCHFLR
SGRVWRDGWGELPTSCGAYKHRATQMDAFQERVSPELGDTLFALFKTQEL
LDDRGVILEVHAWALDALMLKLRNLNVFSADLSGTPRQCAAVVESLLPLM
SSTLSDFDSASALERAARTFNAEMGV
Ligand information
Ligand ID4TA
InChIInChI=1S/C20H29N7O20P4/c1-8-3-26(20(32)25-18(8)31)12-2-9(28)10(43-12)4-41-48(33,34)45-50(37,38)47-51(39,40)46-49(35,36)42-5-11-14(29)15(30)19(44-11)27-7-24-13-16(21)22-6-23-17(13)27/h3,6-7,9-12,14-15,19,28-30H,2,4-5H2,1H3,(H,33,34)(H,35,36)(H,37,38)(H,39,40)(H2,21,22,23)(H,25,31,32)/p-4/t9-,10+,11+,12+,14+,15+,19+/m0/s1
InChIKeyWLGHSSFVEUABFP-SLFMBYJQSA-J
SMILES
SoftwareSMILES
CACTVS 3.385CC1=CN([CH]2C[CH](O)[CH](CO[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)O2)C(=O)NC1=O
OpenEye OEToolkits 1.7.5CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O
OpenEye OEToolkits 1.7.5CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O
CACTVS 3.385CC1=CN([C@H]2C[C@H](O)[C@@H](CO[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)O2)C(=O)NC1=O
FormulaC20 H25 N7 O20 P4
NameP1-(5'-ADENOSYL)P4-(5'-(2'-DEOXY-THYMIDYL))TETRAPHOSPHATE
ChEMBL
DrugBank
ZINC
PDB chain1p73 Chain D Residue 804 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB1p73 Structural basis for the dual thymidine and thymidylate kinase activity of herpes thymidine kinases.
Resolution2.7 Å
Binding residue
(original residue number in PDB)		Y34 G35 G37 K38 S39 T40 E60 Q102 F105 R139 S144 F148 R192 P312
Binding residue
(residue number reindexed from 1)		Y14 G15 G17 K18 S19 T20 E40 Q76 F79 R113 S118 F122 R166 P286
Annotation score3
Enzymatic activity
Catalytic site (original residue number in PDB) K38 E60 D138 R139 R196 R198 E201
Catalytic site (residue number reindexed from 1) K18 E40 D112 R113 R170 R172 E175
Enzyme Commision number 2.7.1.21: thymidine kinase.
Gene Ontology
Molecular Function
GO:0004797 thymidine kinase activity
GO:0005524 ATP binding
GO:0016301 kinase activity
Biological Process
GO:0006230 TMP biosynthetic process
GO:0009157 deoxyribonucleoside monophosphate biosynthetic process
GO:0016310 phosphorylation
GO:0071897 DNA biosynthetic process

View graph for
Molecular Function
View graph for
Biological Process
External links
PDB RCSB:1p73, PDBe:1p73, PDBj:1p73
PDBsum1p73
PubMed14527394
UniProtP24425|KITH_EHV4 Thymidine kinase (Gene Name=TK)

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