Crystal structure of Rab1b covalently modified with AMP at Y77. Determined by X-ray diffraction at 1.7 Å resolution. Released 4 Aug 2010.
Explore 3NKV in 3D Show helices and sheets RCSB PDB PDBe
3NKV contains 14 α-helices and 12 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 | 7-15 | 9 | 1 |
| α-helix | 21-30 | 10 | |
| β-strand | 43-52 | 10 | 1 |
| β-strand | 55-64 | 10 | 1 |
| α-helix | 68-70 | 3 | |
| α-helix | 71-75 | 5 | |
| β-strand | 83-89 | 7 | 1 |
| α-helix | 93-97 | 5 | |
| α-helix | 99-109 | 11 | |
| β-strand | 115-121 | 7 | 1 |
| α-helix | 133-143 | 11 | |
| β-strand | 147-149 | 3 | 1 |
| α-helix | 158-171 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7-15 | 9 | 2 |
| α-helix | 21-30 | 10 | |
| β-strand | 43-52 | 10 | 2 |
| β-strand | 55-64 | 10 | 2 |
| α-helix | 68-70 | 3 | |
| α-helix | 71-75 | 5 | |
| β-strand | 83-89 | 7 | 2 |
| α-helix | 93-97 | 5 | |
| α-helix | 99-109 | 11 | |
| β-strand | 115-121 | 7 | 2 |
| α-helix | 133-142 | 10 | |
| β-strand | 147-150 | 4 | 2 |
| α-helix | 158-172 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Ras-related protein Rab-1B | A, B | protein | 175 | Homo sapiens | Q9H0U4 (AlphaFold model) |
>3NKV_1 Ras-related protein Rab-1B (chains A, B) GHMPEYDYLFKLLLIGDSGVGKSCLLLRFADDTYTESYISTIGVDFKIRTIELDGKTIKL QIWDTAGQERFRTITSSYYRGAHGIIVVYDVTDQESYANVKQWLQEIDRYASENVNKLLV GNKSDLTTKKVVDNTTAKEFADSLGIPFLETSAKNATNVEQAFMTMAAEIKKRMG
| ID | Name | Formula | Copies |
|---|---|---|---|
| AMP | Adenosine monophosphate | C10 H14 N5 O7 P | 2 |
| BA | Barium ion | Ba | 2 |
| MG | Magnesium ion | Mg | 2 |
| GNP | Phosphoaminophosphonic acid-guanylate ester | C10 H17 N6 O13 P3 | 2 |
The Legionella effector protein DrrA AMPylates the membrane traffic regulator Rab1b. Muller, M.P., Peters, H., Blumer, J. et al. Science (2010) 329:946-949. DOI 10.1126/science.1192276 · PubMed
Other PDB entries of the same protein (UniProt Q9H0U4 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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