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Wild-type E.COLI dihydrofolate reductase complexed with 5,10- dideazatetrahydrofolate and oxidized nicotinamide adenine dinucleotide phosphate

Analyse Wild-type E.COLI dihydrofolate reductase complexed with 5,10… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5CCC
Type
protein
Length
159 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Dihydrofolate reductase
EC
1.5.1.3
UniProt
P0ABQ5
Ligands
DDF, NAP
Pockets
1 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 26% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADihydrofolate reductase (EC 1.5.1.3)protein15926% helix, 30% strandP0ABQ5

Ligands and binding sites

  • DDF · 5,10-dideazatetrahydrofolic acid · ligand · chains A
  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13920.670.8042DDF, NAP

Compared structures

  • 5CCC · wild-type E.coli dihydrofolate reductase complexed with 5,10-dideazatetrahydrofolate and… · the same entry in another collection · chain A against A, TM-score 1.00
  • P0ABQ5 · AlphaFold monomer V2.0 prediction for dihydrofolate reductase (P0ABQ5) · a predicted model of the same protein · chain A against A, TM-score 0.97

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