6-conformation model of Escherichia coli dihydrofolate reductase at 100K. Determined by X-ray diffraction at 0.85 Å resolution. Released 30 Sept 2026.
Explore 45PC in 3D Show helices and sheets RCSB PDB PDBe
45PC contains 6 α-helices and 12 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-8 | 7 | 1 |
| α-helix | 10-12 | 3 | |
| β-strand | 13-15 | 3 | 2 |
| β-strand | 16 | 1 | 3 |
| β-strand | 19 | 1 | 3 |
| α-helix | 25-35 | 11 | |
| β-strand | 40-43 | 4 | 1 |
| α-helix | 44-50 | 7 | |
| β-strand | 59-62 | 4 | 1 |
| β-strand | 73-75 | 3 | 1 |
| α-helix | 78-85 | 8 | |
| β-strand | 91-93 | 3 | 1 |
| α-helix | 97-103 | 7 | |
| β-strand | 109-115 | 7 | 1 |
| β-strand | 123-124 | 2 | 2 |
| α-helix | 130-132 | 3 | |
| β-strand | 133-141 | 9 | 1 |
| β-strand | 151-158 | 8 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Dihydrofolate reductase | A | protein | 159 | Escherichia coli str. K-12 substr. MC4100 | P0ABQ4 (AlphaFold model) |
>45PC_1 Dihydrofolate reductase (chains A) MISLIAALAVDRVIGMENAMPWNLPADLAWFKRNTLNKPVIMGRHTWESIGRPLPGRKNI ILSSQPGTDDRVTWVKSVDEAIAACGDVPEIMVIGGGRVYEQFLPKAQKLYLTHIDAEVE GDTHFPDYEPDDWESVFSEFHDADAQNSHSYCFEILERR
| ID | Name | Formula | Copies |
|---|---|---|---|
| FOL | Folic acid | C19 H19 N7 O6 | 1 |
| NAP | NADP nicotinamide-adenine-dinucleotide phosphate | C21 H28 N7 O17 P3 | 1 |
| MN | Manganese (II) ion | Mn | 2 |
Water and common crystallization additives (CL) are not listed.
Optimizing the connectivity of protein conformations to untangle ensemble refinement. Passmore, S.K., Holton, J.M., Zatsepin, N.A. et al. bioRxiv (2026). DOI 10.64898/2026.09.17.752399
Other PDB entries of the same protein (UniProt P0ABQ4 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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