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MolNFT v1 · #142387 · protein

Crystal structure of wild type plasmodium falciparum DHFR-ts complexed with BT3, NADPH, and dump

6A2O · Bifunctional dihydrofolate reductase-thymidylate synthase: “Crystal structure of wild type plasmodium falciparum DHFR-ts complexed with BT3, NADPH, and dump”. X-ray diffraction, 3 ligands (9RR, NAP, UMP), 16 pockets (best…

PDB
6A2O
Type
protein
Length
1,089 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional dihydrofolate reductase-thymidylate synthase
UniProt
A7UD81
Ligands
9RR, NAP, UMP
Pockets
16 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional dihydrofolate reductase-thymidylate synthaseprotein54733% helix, 24% strandA7UD81
BBifunctional dihydrofolate reductase-thymidylate synthaseprotein54231% helix, 25% strandA7UD81

Ligands and binding sites

  • 9RR · 5,5'-[propane-1,3-diylbis(oxy-4,1-phenylene)]bis(6-ethylpyrimidine-2,4-diamine) · ligand · 2 copies · chains A, B
  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • UMP · 2'-deoxyuridine 5'-monophosphate · ligand · 2 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

16 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15430.740.82509RR, NAP
25290.730.81509RR, NAP
35520.710.8051UMP
46750.710.7866UMP
52630.500.7438empty

Interfaces

1 interface between chains.

  • A–B · 4226 Ų buried · 58 hydrogen bonds · protein-protein

Compared structures

  • 6A2O · Crystal structure of wild type Plasmodium falciparum DHFR-TS complexed with BT3, NADPH… · the same entry in another collection · chain A against A, TM-score 1.00

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