Crystal structure of Spindlin1/C11orf84 complex bound to histone H3K4me3K9me3 peptide. Determined by X-ray diffraction at 1.6 Å resolution. Released 13 Jan 2021.
Explore 7CNA in 3D Show helices and sheets RCSB PDB PDBe
7CNA contains 20 α-helices and 44 β-strands across 6 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 | 57-63 | 7 | 1 |
| β-strand | 69-79 | 11 | 1 |
| β-strand | 87-91 | 5 | 1 |
| β-strand | 96 | 1 | 2 |
| β-strand | 97-100 | 4 | 1 |
| β-strand | 108-113 | 6 | 1 |
| α-helix | 117-119 | 3 | |
| α-helix | 126-132 | 7 | |
| β-strand | 136-142 | 7 | 2 |
| β-strand | 148-158 | 11 | 2 |
| α-helix | 159 | 1 | |
| β-strand | 166-170 | 5 | 2 |
| β-strand | 173-174 | 2 | 2 |
| β-strand | 175 | 1 | 3 |
| β-strand | 176-179 | 4 | 2 |
| α-helix | 181-186 | 6 | |
| β-strand | 190-192 | 3 | 2 |
| α-helix | 193-194 | 2 | |
| α-helix | 206-209 | 4 | |
| α-helix | 211-212 | 2 | |
| α-helix | 216 | 1 | |
| β-strand | 217-221 | 5 | 3 |
| β-strand | 227-235 | 9 | 3 |
| β-strand | 242-247 | 6 | 3 |
| β-strand | 252 | 1 | 1 |
| β-strand | 254-260 | 7 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 261-262 | 2 | 3 |
| β-strand | 264-265 | 2 | 3 |
| α-helix | 270-271 | 2 | |
| β-strand | 274-278 | 5 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2 | 1 | 2 |
| α-helix | 4-6 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 57-63 | 7 | 4 |
| β-strand | 69-79 | 11 | 4 |
| β-strand | 87-91 | 5 | 4 |
| β-strand | 96 | 1 | 5 |
| β-strand | 97-100 | 4 | 4 |
| β-strand | 108-113 | 6 | 4 |
| α-helix | 117-119 | 3 | |
| α-helix | 126-132 | 7 | |
| β-strand | 136-142 | 7 | 5 |
| β-strand | 148-158 | 11 | 5 |
| α-helix | 159 | 1 | |
| β-strand | 166-170 | 5 | 5 |
| β-strand | 173-174 | 2 | 5 |
| β-strand | 175 | 1 | 6 |
| β-strand | 176-179 | 4 | 5 |
| α-helix | 181-186 | 6 | |
| β-strand | 190-192 | 3 | 5 |
| α-helix | 193-195 | 3 | |
| α-helix | 206-209 | 4 | |
| α-helix | 211-212 | 2 | |
| α-helix | 216 | 1 | |
| β-strand | 217-221 | 5 | 6 |
| β-strand | 227-235 | 9 | 6 |
| β-strand | 242-247 | 6 | 6 |
| β-strand | 252 | 1 | 4 |
| β-strand | 254-260 | 7 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 261-262 | 2 | 6 |
| β-strand | 265 | 1 | 6 |
| α-helix | 270-271 | 2 | |
| β-strand | 274-278 | 5 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Spindlin-1 | A, D | protein | 212 | Homo sapiens | Q9Y657 (AlphaFold model) |
| Spindlin interactor and repressor of chromatin-binding protein | B, E | protein | 30 | Homo sapiens | Q9BUA3 (AlphaFold model) |
| Ala-arg-thr-M3L-gln-thr-ala-arg-M3L-ser-thr | C | protein | 12 | synthetic construct | |
| Ala-arg-thr-M3L-gln-thr-ala-arg-M3L-ser-gly | F | protein | 12 | synthetic construct |
>7CNA_1 Spindlin-1 (chains A, D) RNIVGCRIQHGWKEGNGPVTQWKGTVLDQVPVNPSLYLIKYDGFDCVYGLELNKDERVSA LEVLPDRVATSRISDAHLADTMIGKAVEHMFETEDGSKDEWRGMVLARAPVMNTWFYITY EKDPVLYMYQLLDDYKEGDLRIMPDSNDSPPAEREPGEVVDSLVGKQVEYAKEDGSKRTG MVIHQVEAKPSVYFIKFDDDFHIYVYDLVKTS
>7CNA_2 Spindlin interactor and repressor of chromatin-binding protein (chains B, E) ETFAAPAEVRHFTDGSFPAGFVLQLFSHTQ
>7CNA_3 ALA-ARG-THR-M3L-GLN-THR-ALA-ARG-M3L-SER-THR (chains C) ARTKQTARKSTG
>7CNA_4 ALA-ARG-THR-M3L-GLN-THR-ALA-ARG-M3L-SER-GLY (chains F) ARTKQTARKSGG
| ID | Name | Formula | Copies |
|---|---|---|---|
| BEN | Benzamidine | C7 H8 N2 | 6 |
Water and common crystallization additives (GOL, CL) are not listed.
Structural mechanism of bivalent histone H3K4me3K9me3 recognition by the Spindlin1/C11orf84 complex in rRNA transcription activation. Du, Y., Yan, Y., Xie, S. et al. Nat Commun (2021) 12:949-949. DOI 10.1038/s41467-021-21236-x · PubMed
Other PDB entries of the same protein (UniProt Q9Y657 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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