Research workbench
277K Crystal structure of Escherichia Coli dihydrofolate reductase
Analyse 277K Crystal structure of Escherichia Coli dihydrofolate reductase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4RGC
- Type
- protein
- Length
- 159 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 1.05
- Source
- Escherichia coli
- Molecule
- Dihydrofolate reductase
- EC
- 1.5.1.3
- UniProt
- U6N356
- Ligands
- FOL, NAP, MN
- Pockets
- 1 · best druggability 0.69
Structure
x-ray diffraction · resolution 1.05 · 1 distinct chain · 26% helix, 33% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Dihydrofolate reductase (EC 1.5.1.3) | protein | 159 | 26% helix, 33% strand | U6N356 |
Ligands and binding sites
- FOL · Folic acid · ligand · chains A
- NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · chains A
- MN · Manganese (II) ion · metal · 2 copies · 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.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 332 | 0.69 | 0.82 | 42 | FOL, NAP |
Modifications
Observed in the structure: 1 modified (oxidation).
Compared structures
- 4RGC · 277K crystal structure of escherichia COLI dihydrofolate reductase · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt U6N356
- Elsewhere: RCSB PDB 4RGC · PDBe 4RGC · UniProt U6N356
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