Solution Structure of MCL-1 Complexed with NoxaA. Determined by solution NMR. Released 8 Jul 2008.
Explore 2ROD in 3D Show helices and sheets RCSB PDB PDBe
2ROD contains 11 α-helices and 0 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 | 153-171 | 19 | |
| α-helix | 178-180 | 3 | |
| α-helix | 185-204 | 20 | |
| α-helix | 206-215 | 10 | |
| α-helix | 221-223 | 3 | |
| α-helix | 224-233 | 10 | |
| α-helix | 242-261 | 20 | |
| α-helix | 265-281 | 17 | |
| α-helix | 284-289 | 6 | |
| α-helix | 293-299 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 22-39 | 18 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Induced myeloid leukemia cell differentiation protein Mcl-1 homolog | A | protein | 162 | Mus musculus | P97287 (AlphaFold model) |
| Noxa | B | protein | 27 | Mus musculus | Q9JM54 (AlphaFold model) |
>2ROD_1 Induced myeloid leukemia cell differentiation protein Mcl-1 homolog (chains A) GPLGSEDDLYRQSLEIISRYLREQATGSKDSKPLGEAGAAGRRALETLRRVGDGVQRNHE TAFQGMLRKLDIKNEGDVKSFSRVMVHVFKDGVTNWGRIVTLISFGAFVAKHLKSVNQES FIEPLAETITDVLVRTKRDWLVKQRGWDGFVEFFHVQDLEGG
>2ROD_2 Noxa (chains B) AELPPEFAAQLRKIGDKVYCTWSAPDM
Structure of the BH3 Domains from the p53-Inducible BH3-Only Proteins Noxa and Puma in Complex with Mcl-1. Day, C.L., Smits, C., Fan, F.C. et al. J Mol Biol (2008) 380:958-971. DOI 10.1016/j.jmb.2008.05.071 · PubMed
Other PDB entries of the same protein (UniProt P97287 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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