Crystal structure of sigm54 activator (AAA+ ATPase) in the inactive state. Determined by X-ray diffraction at 2.4 Å resolution. Released 11 Nov 2003.
Explore 1NY5 in 3D Show helices and sheets RCSB PDB PDBe
1NY5 contains 35 α-helices and 40 β-strands across 2 chains. 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 | 2-6 | 5 | 1 |
| α-helix | 10-23 | 14 | |
| β-strand | 26-30 | 5 | 1 |
| α-helix | 33-42 | 10 | |
| β-strand | 47-51 | 5 | 1 |
| β-strand | 53 | 1 | 2 |
| β-strand | 58 | 1 | 2 |
| α-helix | 59-69 | 11 | |
| β-strand | 74-80 | 7 | 1 |
| α-helix | 84-91 | 8 | |
| β-strand | 97-101 | 5 | 1 |
| α-helix | 105-133 | 29 | |
| α-helix | 144-156 | 13 | |
| β-strand | 163-166 | 4 | 3 |
| α-helix | 173-183 | 11 | |
| β-strand | 191-195 | 5 | 3 |
| α-helix | 201-209 | 9 | |
| β-strand | 211 | 1 | 4 |
| β-strand | 223 | 1 | 4 |
| α-helix | 226-229 | 4 | |
| β-strand | 234-238 | 5 | 3 |
| α-helix | 240-242 | 3 | |
| α-helix | 245-257 | 13 | |
| β-strand | 259-260 | 2 | 5 |
| β-strand | 263 | 1 | 4 |
| β-strand | 268 | 1 | 6 |
| β-strand | 269-270 | 2 | 5 |
| β-strand | 274-279 | 6 | 3 |
| α-helix | 283-288 | 6 | |
| α-helix | 294-300 | 7 | |
| β-strand | 303-306 | 4 | 3 |
| α-helix | 310-312 | 3 | |
| α-helix | 314-331 | 18 | |
| β-strand | 338-339 | 2 | 7 |
| α-helix | 341-349 | 9 | |
| α-helix | 355-369 | 15 | |
| β-strand | 374-375 | 2 | 7 |
| α-helix | 377-383 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-6 | 5 | 8 |
| α-helix | 10-23 | 14 | |
| β-strand | 26-30 | 5 | 8 |
| α-helix | 33-42 | 10 | |
| β-strand | 43 | 1 | 6 |
| β-strand | 47-51 | 5 | 8 |
| β-strand | 53 | 1 | 9 |
| β-strand | 58 | 1 | 9 |
| α-helix | 59-69 | 11 | |
| β-strand | 74-79 | 6 | 8 |
| α-helix | 84-92 | 9 | |
| β-strand | 97-100 | 4 | 8 |
| α-helix | 105-134 | 30 | |
| α-helix | 144-156 | 13 | |
| β-strand | 163-166 | 4 | 10 |
| α-helix | 173-182 | 10 | |
| β-strand | 191-195 | 5 | 10 |
| α-helix | 201-209 | 9 | |
| β-strand | 211 | 1 | 11 |
| β-strand | 223 | 1 | 11 |
| α-helix | 226-229 | 4 | |
| β-strand | 234-238 | 5 | 10 |
| α-helix | 240-242 | 3 | |
| α-helix | 245-257 | 13 | |
| β-strand | 259-260 | 2 | 12 |
| β-strand | 263 | 1 | 11 |
| β-strand | 269-270 | 2 | 12 |
| β-strand | 274-279 | 6 | 10 |
| α-helix | 283-288 | 6 | |
| α-helix | 294-300 | 7 | |
| β-strand | 303-306 | 4 | 10 |
| α-helix | 307-309 | 3 | |
| α-helix | 314-331 | 18 | |
| β-strand | 338-339 | 2 | 13 |
| α-helix | 341-349 | 9 | |
| α-helix | 355-368 | 14 | |
| β-strand | 374-375 | 2 | 13 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| transcriptional regulator (NtrC family) | A, B | protein | 387 | Aquifex aeolicus | O67198 (AlphaFold model) |
>1NY5_1 transcriptional regulator (NtrC family) (chains A, B) MNVLVIEDDKVFRGLLEEYLSMKGIKVESAERGKEAYKLLSEKHFNVVLLDLLLPDVNGL EILKWIKERSPETEVIVITGHGTIKTAVEAMKMGAYDFLTKPCMLEEIELTINKAIEHRK LRKENELLRREKDLKEEEYVFESPKMKEILEKIKKISCAECPVLITGESGVGKEVVARLI HKLSDRSKEPFVALNVASIPRDIFEAELFGYEKGAFTGAVSSKEGFFELADGGTLFLDEI GELSLEAQAKLLRVIESGKFYRLGGRKEIEVNVRILAATNRNIKELVKEGKFREDLYYRL GVIEIEIPPLRERKEDIIPLANHFLKKFSRKYAKEVEGFTKSAQELLLSYPWYGNVRELK NVIERAVLFSEGKFIDRGELSCLVNSK
| ID | Name | Formula | Copies |
|---|---|---|---|
| ADP | Adenosine-5'-diphosphate | C10 H15 N5 O10 P2 | 2 |
| PO4 | Phosphate ion | O4 P | 4 |
| MG | Magnesium ion | Mg | 1 |
Water and common crystallization additives (GOL) are not listed.
Regulation of the transcriptional activator NtrC1: structural studies of the regulatory and AAA+ ATPase domains. Lee, S.Y., de la Torre, A., Yan, D. et al. Genes Dev (2003) 17:2552-2563. DOI 10.1101/gad.1125603 · PubMed
Other PDB entries of the same protein (UniProt O67198 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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