crystal structure of BCL-2 F104L mutation with venetoclax. Determined by X-ray diffraction at 1.75 Å resolution. Released 22 May 2019.
Explore 6O0M in 3D Show helices and sheets RCSB PDB PDBe
6O0M contains 10 α-helices and 0 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 |
|---|---|---|---|
| α-helix | 11-25 | 15 | |
| α-helix | 31-33 | 3 | |
| α-helix | 91-107 | 17 | |
| α-helix | 109-118 | 10 | |
| α-helix | 126-137 | 12 | |
| α-helix | 144-163 | 20 | |
| α-helix | 168-179 | 12 | |
| α-helix | 180-184 | 5 | |
| α-helix | 186-191 | 6 | |
| α-helix | 194-202 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Apoptosis regulator Bcl-2,Bcl-2-like protein 1,Apoptosis regulator Bcl-2 | A | protein | 166 | Homo sapiens | P10415 (AlphaFold model), Q07817 (AlphaFold model) |
>6O0M_1 Apoptosis regulator Bcl-2,Bcl-2-like protein 1,Apoptosis regulator Bcl-2 (chains A) MAHAGRTGYDNREIVMKYIHYKLSQRGYEWDAGDDVEENRTEAPEGTESEVVHLTLRQAG DDLSRRYRRDFAEMSSQLHLTPFTARGRFATVVEELFRDGVNWGRIVAFFEFGGVMCVES VNREMSPLVDNIALWMTEYLNRHLHTWIQDNGGWDAFVELYGPSMR
| ID | Name | Formula | Copies |
|---|---|---|---|
| LBM | 4-{4-[(4'-chloro-5,5-dimethyl[3,4,5,6-tetrahydro[1,1'-biphenyl]]-2-yl)methyl]pi… | C45 H50 Cl N7 O7 S | 1 |
Water and common crystallization additives (PEG) are not listed.
Structures of BCL-2 in complex with venetoclax reveal the molecular basis of resistance mutations. Birkinshaw, R.W., Gong, J.N., Luo, C.S. et al. Nat Commun (2019) 10:2385-2385. DOI 10.1038/s41467-019-10363-1 · PubMed
Other PDB entries of the same protein (UniProt P10415 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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