Structure of PDB 6cxm Chain A Binding Site BS02
Receptor Information
>6cxm Chain A (length=155) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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SMRLIWAQSTSGIIGRDNSIPWRLPEDLARFKEMTMGHPVVMGRLTWESL
PASVRPLPGRRNIVVTRDADYRAEGAEVVTDLPDEPDAWVIGGAQIYAMA
LARADRCEVTEVDIALTPLDGDARAPVLDDSWVATTGEWQTSTSGLRFRF
CSYRR
Ligand information
Ligand ID
MMV
InChI
InChI=1S/C18H24N4O4/c1-2-13-16(17(19)22-18(20)21-13)26-11-5-10-25-14-7-4-3-6-12(14)8-9-15(23)24/h3-4,6-7H,2,5,8-11H2,1H3,(H,23,24)(H4,19,20,21,22)
InChIKey
VDGXZSSDCDPCRF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)CCc2ccccc2OCCCOc1c(nc(nc1CC)N)N
CACTVS 3.370
CCc1nc(N)nc(N)c1OCCCOc2ccccc2CCC(O)=O
OpenEye OEToolkits 1.7.6
CCc1c(c(nc(n1)N)N)OCCCOc2ccccc2CCC(=O)O
Formula
C18 H24 N4 O4
Name
3-(2-{3-[(2,4-diamino-6-ethylpyrimidin-5-yl)oxy]propoxy}phenyl)propanoic acid
ChEMBL
CHEMBL3040038
DrugBank
ZINC
ZINC000095921197
PDB chain
6cxm Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
6cxm
Crystal structure of a dihydrofolate reductase from Mycobacterium smegmatis in complex with NADP and P218
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
I6 W7 D28 L29 F32 P52 V55 L58 R61 I92
Binding residue
(residue number reindexed from 1)
I5 W6 D27 L28 F31 P51 V54 L57 R60 I91
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
I6 I21 W23 D28 L29 F32 L58 A89 T111
Catalytic site (residue number reindexed from 1)
I5 I20 W22 D27 L28 F31 L57 A88 T110
Enzyme Commision number
1.5.1.3
: dihydrofolate reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004146
dihydrofolate reductase activity
GO:0016491
oxidoreductase activity
GO:0050661
NADP binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0046452
dihydrofolate metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046655
folic acid metabolic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6cxm
,
PDBe:6cxm
,
PDBj:6cxm
PDBsum
6cxm
PubMed
UniProt
I7FC10
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