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Solution structure of L.CASEI dihydrofolate reductase complexed with NADPH, 32 structures

Analyse Solution structure of L.CASEI dihydrofolate reductase complexed with NADPH, 32… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2HQP
Type
protein
Length
162 residues
Chains
1
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydrofolate reductase
EC
1.5.1.3
UniProt
P00381
Ligands
NDP
Pockets
2 · best druggability 0.82

Structure

solution nmr · 1 distinct chain · 19% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydrofolate reductase (EC 1.5.1.3)protein16219% helix, 33% strandP00381

Ligands and binding sites

  • NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17520.820.8579NDP
2870.420.7813empty

Compared structures

  • 2HQP · Solution structure of L.casei dihydrofolate reductase complexed with NADPH, 32 structures · the same entry in another collection · chain A against A, TM-score 1.00
  • P00381 · AlphaFold monomer V2.0 prediction for dihydrofolate reductase (P00381) · a predicted model of the same protein · chain A against A, TM-score 0.88

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