Structure of PDB 4qg7 Chain A Binding Site BS01
Receptor Information
>4qg7 Chain A (length=197) Species:
282458
(Staphylococcus aureus subsp. aureus MRSA252) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SAFITFEGPEGSGKTTVINEVYHRLVKDYDVIMTREPGGVPTGEEIRKIV
LEGNDMDIRTEAMLFAASRREHLVLKVIPALKEGKVVLCDRYIDSSLAYQ
GYARGIGVEEVRALNEFAINGLYPDLTIYLNVSAEVGRERIIKNDQEDLK
FHEKVIEGYQEIIHNESQRFKSVNADQPLENVVEDTYQTIIKYLEKI
Ligand information
Ligand ID
32K
InChI
InChI=1S/C25H26ClN3O6/c1-15-12-29(25(33)27-23(15)30)18-6-4-10-28(14-18)13-16-8-9-20(24(31)32)22(21(16)34-2)35-19-7-3-5-17(26)11-19/h3,5,7-9,11-12,18H,4,6,10,13-14H2,1-2H3,(H,31,32)(H,27,30,33)/t18-/m0/s1
InChIKey
ZKCQEFJHWRKVMG-SFHVURJKSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CC1=CN(C(=O)NC1=O)C2CCCN(C2)Cc3ccc(c(c3OC)Oc4cccc(c4)Cl)C(=O)O
OpenEye OEToolkits 1.7.6
CC1=CN(C(=O)NC1=O)[C@H]2CCCN(C2)Cc3ccc(c(c3OC)Oc4cccc(c4)Cl)C(=O)O
CACTVS 3.385
COc1c(CN2CCC[C@@H](C2)N3C=C(C)C(=O)NC3=O)ccc(C(O)=O)c1Oc4cccc(Cl)c4
ACDLabs 12.01
O=C(O)c2ccc(c(OC)c2Oc1cccc(Cl)c1)CN4CCCC(N3C=C(C(=O)NC3=O)C)C4
CACTVS 3.385
COc1c(CN2CCC[CH](C2)N3C=C(C)C(=O)NC3=O)ccc(C(O)=O)c1Oc4cccc(Cl)c4
Formula
C25 H26 Cl N3 O6
Name
2-(3-chlorophenoxy)-3-methoxy-4-{[(3S)-3-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)piperidin-1-yl]methyl}benzoic acid
ChEMBL
CHEMBL3297776
DrugBank
ZINC
ZINC000098208386
PDB chain
4qg7 Chain A Residue 301 [
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
4qg7
Antibacterial inhibitors of gram-positive thymidylate kinase: structure-activity relationships and chiral preference of a new hydrophobic binding region.
Resolution
1.67 Å
Binding residue
(original residue number in PDB)
E37 R48 L52 F66 R70 R92 S96 S97 Y100 Q101
Binding residue
(residue number reindexed from 1)
E36 R47 L51 F65 R69 R91 S95 S96 Y99 Q100
Annotation score
1
Binding affinity
MOAD
: ic50=10nM
PDBbind-CN
: -logKd/Ki=8.00,IC50=10nM
Enzymatic activity
Enzyme Commision number
2.7.4.9
: dTMP kinase.
Gene Ontology
Molecular Function
GO:0004798
thymidylate kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
Biological 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:0046940
nucleoside monophosphate phosphorylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4qg7
,
PDBe:4qg7
,
PDBj:4qg7
PDBsum
4qg7
PubMed
24828090
UniProt
Q6GJI9
|KTHY_STAAR Thymidylate kinase (Gene Name=tmk)
[
Back to BioLiP
]