D95A oxidized flavodoxin mutant from D. Vulgaris. Determined by X-ray diffraction at 1.9 Å resolution. Released 2 Dec 1998.
Explore 1AKQ in 3D Show helices and sheets RCSB PDB PDBe
1AKQ contains 8 α-helices and 8 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 | 3-9 | 7 | 1 |
| α-helix | 14-28 | 15 | |
| β-strand | 32-37 | 6 | 1 |
| α-helix | 38-40 | 3 | |
| β-strand | 52-57 | 6 | 1 |
| β-strand | 59-60 | 2 | 2 |
| β-strand | 66-67 | 2 | 2 |
| α-helix | 72-76 | 5 | |
| α-helix | 78-80 | 3 | |
| β-strand | 87-94 | 8 | 1 |
| α-helix | 103-114 | 12 | |
| β-strand | 118-119 | 2 | 1 |
| α-helix | 122-123 | 2 | |
| β-strand | 124-127 | 4 | 1 |
| α-helix | 130-133 | 4 | |
| α-helix | 134-145 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Flavodoxin | A | protein | 147 | Desulfovibrio vulgaris subsp. vulgaris str. Hildenborough | P00323 (AlphaFold model) |
>1AKQ_1 FLAVODOXIN (chains A) PKALIVYGSTTGNTEYTAETIARELADAGYEVDSRDAASVEAGGLFEGFDLVLLGCSTWG DDSIELQDDFIPLFDSLEETGAQGRKVACFGCGASSYEYFCGAVDAIEEKLKNLGAEIVQ DGLRIDGDPRAARDDIVGWAHDVRGAI
| ID | Name | Formula | Copies |
|---|---|---|---|
| FMN | Flavin mononucleotide | C17 H21 N4 O9 P | 1 |
Crystallographic investigation of the role of aspartate 95 in the modulation of the redox potentials of Desulfovibrio vulgaris flavodoxin. McCarthy, A.A., Walsh, M.A., Verma, C.S. et al. Biochemistry (2002) 41:10950-10962. DOI 10.1021/bi020225h · PubMed
Other PDB entries of the same protein (UniProt P00323 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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