Structure of PDB 1p73 Chain C Binding Site BS01
Receptor Information
>1p73 Chain C (length=317) Species:
10331
(Equid alphaherpesvirus 4) [
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MVTIVRIYLDGVYGIGKSTTGRVMASSPTLYFPEPMAYWRTLFETDVISG
IYDTQNRVDDAALITAHYQSRFTTPYLILHDHTCTLFGGNSLQRGTQPDL
TLVFDRHPVASTVCFPAARYLLGDMSMCALMAMVATLPREPQGGNIVVTT
LNVEEHIRRLRTRAREQIDITLIATLRNVYFMLVNTCHFLRSGRVWRDGW
GELPTSCGAYKHRATQMDAFQERVSPELGDTLFALFKTQELLDDRGVILE
VHAWALDALMLKLRNLNVFSADLSGTPRQCAAVVESLLPLMSSTLSDFDS
ASALERAARTFNAEMGV
Ligand information
Ligand ID
4TA
InChI
InChI=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
InChIKey
WLGHSSFVEUABFP-SLFMBYJQSA-J
SMILES
Software
SMILES
CACTVS 3.385
CC1=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 1.7.5
CC1=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 1.7.5
CC1=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 3.385
CC1=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
Formula
C20 H25 N7 O20 P4
Name
P1-(5'-ADENOSYL)P4-(5'-(2'-DEOXY-THYMIDYL))TETRAPHOSPHATE
ChEMBL
DrugBank
ZINC
PDB chain
1p73 Chain C Residue 803 [
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Receptor-Ligand Complex Structure
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PDB
1p73
Structural basis for the dual thymidine and thymidylate kinase activity of herpes thymidine kinases.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
Y34 G35 G37 K38 S39 T40 E60 Y78 Q102 F105 R139 S144 F148 R192 P312
Binding residue
(residue number reindexed from 1)
Y13 G14 G16 K17 S18 T19 E34 Y52 Q69 F72 R106 S111 F115 R159 P277
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
K38 E60 D138 R139 R196 R198 E201
Catalytic site (residue number reindexed from 1)
K17 E34 D105 R106 R163 R165 E166
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
PDBsum
1p73
PubMed
14527394
UniProt
P24425
|KITH_EHV4 Thymidine kinase (Gene Name=TK)
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