Human SIRT3 bound to p53-AMC peptide and Honokiol. Determined by X-ray diffraction at 1.48 Å resolution. Released 6 Nov 2024.
Explore 8V5U in 3D Show helices and sheets RCSB PDB PDBe
8V5U contains 22 α-helices and 15 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 |
|---|---|---|---|
| α-helix | 122-124 | 3 | |
| α-helix | 125-133 | 9 | |
| β-strand | 140-144 | 5 | 1 |
| α-helix | 146-148 | 3 | |
| α-helix | 150-152 | 3 | |
| α-helix | 164-167 | 4 | |
| α-helix | 176-180 | 5 | |
| β-strand | 181 | 1 | 2 |
| α-helix | 182-187 | 6 | |
| α-helix | 190-199 | 10 | |
| α-helix | 208-218 | 11 | |
| β-strand | 222-227 | 6 | 1 |
| α-helix | 233-236 | 4 | |
| α-helix | 241-243 | 3 | |
| β-strand | 244-246 | 3 | 1 |
| β-strand | 249-256 | 8 | 3 |
| β-strand | 262-264 | 3 | 3 |
| α-helix | 265-268 | 4 | |
| α-helix | 269-273 | 5 | |
| α-helix | 276-278 | 3 | |
| β-strand | 279 | 1 | 4 |
| β-strand | 286 | 1 | 4 |
| β-strand | 287-291 | 5 | 3 |
| α-helix | 292-293 | 2 | |
| β-strand | 294 | 1 | 2 |
| β-strand | 297 | 1 | 5 |
| α-helix | 298-299 | 2 | |
| α-helix | 300-304 | 5 | |
| α-helix | 305-311 | 7 | |
| β-strand | 314-318 | 5 | 1 |
| α-helix | 327-333 | 7 | |
| β-strand | 340-344 | 5 | 1 |
| α-helix | 349-353 | 5 | |
| β-strand | 359-363 | 5 | 1 |
| α-helix | 366-377 | 12 | |
| α-helix | 380-391 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3 | 1 | 5 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| NAD-dependent protein deacetylase sirtuin-3, mitochondrial | A | protein | 282 | Homo sapiens | Q9NTG7 (AlphaFold model) |
| p53-AMC peptide | B | protein | 5 | Homo sapiens |
>8V5U_1 NAD-dependent protein deacetylase sirtuin-3, mitochondrial (chains A) SDKGKLSLQDVAELIRARACQRVVVMVGAGISTPSGIPDFRSPGSGLYSNLQQYDLPYPE AIFELPFFFHNPKPFFTLAKELYPGNYKPNVTHYFLRLLHDKGLLLRLYTQNIDGLERVS GIPASKLVEAHGTFASATCTVCQRPFPGEDIRADVMADRVPRCPVCTGVVKPDIVFFGEP LPQRFLLHVVDFPMADLLLILGTSLEVEPFASLTEAVRSSVPRLLINRDLVGPLAWHPRS RDVAQLGDVVHGVESLVELLGWTEEMRDLVQRETGKLDGPDK
>8V5U_2 p53-AMC peptide (chains B) QPKKX
Computationally Driven Discovery and Characterization of SIRT3-Activating Compounds that Fully Recover Catalytic Activity under ${\mathrm{NAD}}^{+}$ Depletion. Guan, X., Dumpati, R.K., Munshi, S. et al. Phys Rev X (2024) 14. DOI 10.1103/PhysRevX.14.041019
Other PDB entries of the same protein (UniProt Q9NTG7 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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