Structure of PDB 2wwh Chain C Binding Site BS01
Receptor Information
>2wwh Chain C (length=210) Species:
36329
(Plasmodium falciparum 3D7) [
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MTDDKKKGKFIVFEGLDRSGKSTQSKLLVEYLKNNNVEVKHLYFPNRETG
IGQIISKYLKMENSMSNETIHLLFSANRWEHMNEIKSLLLKGIWVVCDRY
AYSGVAYSSGALNLNKTWCMNPDQGLIKPDVVFYLNVPPNYAQNRSDYGE
EIYEKVETQKKIYETYKHFAHEDYWINIDATRKIEDIHNDIVKEVTKIKV
EPEEFNFLWS
Ligand information
Ligand ID
T5A
InChI
InChI=1S/C20H30N7O23P5/c1-8-3-26(20(32)25-18(8)31)12-2-9(28)10(45-12)4-43-51(33,34)47-53(37,38)49-55(41,42)50-54(39,40)48-52(35,36)44-5-11-14(29)15(30)19(46-11)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)(H,41,42)(H2,21,22,23)(H,25,31,32)/t9-,10+,11+,12+,14+,15+,19+/m0/s1
InChIKey
JCFDSPQTEMXXLO-SLFMBYJQSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC1=CN([CH]2C[CH](O)[CH](CO[P](O)(=O)O[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 1.5.0
CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O
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)O[P@@](=O)(O)O[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)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[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 H30 N7 O23 P5
Name
P1-(5'-ADENOSYL)P5-(5'-THYMIDYL)PENTAPHOSPHATE
ChEMBL
CHEMBL1236157
DrugBank
DB03280
ZINC
ZINC000169331553
PDB chain
2wwh Chain C Residue 211 [
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Receptor-Ligand Complex Structure
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PDB
2wwh
Structural Basis for the Efficient Phosphorylation of Aztmp and Dgmp by Plasmodium Falciparum Type I Thymidylate Kinase.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
D17 R18 G20 K21 S22 T23 F44 P45 R47 L59 F74 R78 R99 G104 Y107 R145 R182 I184
Binding residue
(residue number reindexed from 1)
D17 R18 G20 K21 S22 T23 F44 P45 R47 L59 F74 R78 R99 G104 Y107 R145 R182 I184
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.4.8
: guanylate kinase.
2.7.4.9
: dTMP kinase.
Gene Ontology
Molecular Function
GO:0004385
guanylate kinase activity
GO:0004550
nucleoside diphosphate kinase activity
GO:0004798
thymidylate kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0050316
T2-induced deoxynucleotide kinase activity
Biological Process
GO:0006177
GMP biosynthetic process
GO:0006227
dUDP biosynthetic process
GO:0006233
dTDP biosynthetic process
GO:0006235
dTTP biosynthetic process
GO:0009165
nucleotide biosynthetic process
GO:0016310
phosphorylation
GO:0046710
GDP metabolic process
GO:0046940
nucleoside monophosphate phosphorylation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2wwh
,
PDBe:2wwh
,
PDBj:2wwh
PDBsum
2wwh
PubMed
20353400
UniProt
Q8I4S1
|KTHY_PLAF7 Thymidylate kinase (Gene Name=TMK)
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