Human SIRT2 in complex with myristoylated peptide (TNF-alphaK20myr). Determined by X-ray diffraction at 1.6 Å resolution. Released 6 Jan 2016.
Explore 4Y6O in 3D Show helices and sheets RCSB PDB PDBe
4Y6O contains 33 α-helices and 34 β-strands across 4 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 | 64-72 | 9 | |
| β-strand | 79-83 | 5 | 1 |
| α-helix | 85-87 | 3 | |
| α-helix | 89-91 | 3 | |
| α-helix | 108-110 | 3 | |
| α-helix | 115-119 | 5 | |
| β-strand | 120 | 1 | 2 |
| α-helix | 121-126 | 6 | |
| α-helix | 129-138 | 10 | |
| α-helix | 147-157 | 11 | |
| β-strand | 161-166 | 6 | 1 |
| α-helix | 172-175 | 4 | |
| α-helix | 180-182 | 3 | |
| β-strand | 183-185 | 3 | 1 |
| β-strand | 188-195 | 8 | 3 |
| β-strand | 203-205 | 3 | 3 |
| α-helix | 206-215 | 10 | |
| β-strand | 220 | 1 | 4 |
| β-strand | 227 | 1 | 4 |
| β-strand | 228-232 | 5 | 3 |
| β-strand | 235 | 1 | 2 |
| β-strand | 238 | 1 | 5 |
| α-helix | 239-240 | 2 | |
| α-helix | 241-250 | 10 | |
| β-strand | 256-260 | 5 | 1 |
| β-strand | 267 | 1 | 6 |
| α-helix | 269-275 | 7 | |
| β-strand | 282-286 | 5 | 1 |
| β-strand | 317-321 | 5 | 1 |
| α-helix | 324-335 | 12 | |
| α-helix | 338-353 | 16 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 64-72 | 9 | |
| β-strand | 79-83 | 5 | 7 |
| α-helix | 85-87 | 3 | |
| α-helix | 89-91 | 3 | |
| α-helix | 115-119 | 5 | |
| β-strand | 120 | 1 | 8 |
| α-helix | 121-126 | 6 | |
| α-helix | 129-138 | 10 | |
| α-helix | 147-157 | 11 | |
| β-strand | 161-166 | 6 | 7 |
| α-helix | 172-175 | 4 | |
| α-helix | 180-182 | 3 | |
| β-strand | 183-185 | 3 | 7 |
| β-strand | 188-195 | 8 | 9 |
| β-strand | 203-205 | 3 | 9 |
| α-helix | 206-214 | 9 | |
| β-strand | 220 | 1 | 10 |
| β-strand | 227 | 1 | 10 |
| β-strand | 228-232 | 5 | 9 |
| β-strand | 235 | 1 | 8 |
| β-strand | 238 | 1 | 11 |
| α-helix | 239-240 | 2 | |
| α-helix | 241-250 | 10 | |
| β-strand | 256-260 | 5 | 7 |
| β-strand | 266-267 | 2 | 12 |
| α-helix | 269-275 | 7 | |
| β-strand | 282-286 | 5 | 7 |
| β-strand | 317-321 | 5 | 7 |
| α-helix | 324-334 | 11 | |
| α-helix | 338-353 | 16 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 8 | 1 | |
| β-strand | 9 | 1 | 5 |
| α-helix | 10 | 1 | |
| β-strand | 11 | 1 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5 | 1 | 11 |
| β-strand | 7-8 | 2 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| NAD-dependent protein deacetylase sirtuin-2 | A, B | protein | 293 | Homo sapiens | Q8IXJ6 (AlphaFold model) |
| peptide LEU-PRO-LYS-MYK-THR-GLY-GLY | C, D | protein | 7 | Homo sapiens | P01375 (AlphaFold model) |
>4Y6O_1 NAD-dependent protein deacetylase sirtuin-2 (chains A, B) GSQKERLLDELTLEGVARYMQSERCRRVICLVGAGISTSAGIPDFRSPSTGLYDNLEKYH LPYPEAIFEISYFKKHPEPFFALAKELYPGQFKPTICHYFMRLLKDKGLLLRCYTQNIDT LERIAGLEQEDLVEAHGTFYTSHCVSASCRHEYPLSWMKEKIFSEVTPKCEDCQSLVKPD IVFFGESLPARFFSCMQSDFLKVDLLLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAG GGGMDFDSKKAYRDVAWLGECDQGCLALAELLGWKKELEDLVRREHASIDAQS
>4Y6O_2 peptide LEU-PRO-LYS-MYK-THR-GLY-GLY (chains C, D) LPKXTGG
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 2 |
Kinetic and Structural Basis for Acyl-Group Selectivity and NAD(+) Dependence in Sirtuin-Catalyzed Deacylation. Feldman, J.L., Dittenhafer-Reed, K.E., Kudo, N. et al. Biochemistry (2015) 54:3037-3050. DOI 10.1021/acs.biochem.5b00150 · PubMed
Other PDB entries of the same protein (UniProt Q8IXJ6 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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