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Crystal structure of bacillus anthracis (Y102F) dihydrofolate reductase complexed with NADPH and trimethoprim

Analyse Crystal structure of bacillus anthracis (Y102F) dihydrofolate reductase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3JW5
Type
protein
Length
330 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydrofolate reductase
EC
1.5.1.3
UniProt
Q81R22
Ligands
NDP, TOP
Pockets
3 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 21% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BDihydrofolate reductase (EC 1.5.1.3)protein16521% helix, 33% strandQ81R22

Ligands and binding sites

  • NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • TOP · Trimethoprim · ligand · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15360.740.8140empty
24210.700.8141NDP, TOP
34110.690.8044NDP, TOP

Interfaces

1 interface between chains.

  • A–B · 487 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 3JW5 · Crystal structure of Bacillus anthracis (Y102F) dihydrofolate reductase complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

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