7CNA: Spindlin1/C11orf84 complex

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.

Method
X-ray diffraction
Resolution
1.6 Å
Organisms
Homo sapiens, synthetic construct
Chains
6
Atoms
4,254
Mol. weight
58.78 kDa
Ligands
BEN
Released
13 Jan 2021

Explore 7CNA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 8 helices, 18 β-strands

ElementResiduesLengthSheet
β-strand57-6371
β-strand69-79111
β-strand87-9151
β-strand9612
β-strand97-10041
β-strand108-11361
α-helix117-1193
α-helix126-1327
β-strand136-14272
β-strand148-158112
α-helix1591
β-strand166-17052
β-strand173-17422
β-strand17513
β-strand176-17942
α-helix181-1866
β-strand190-19232
α-helix193-1942
α-helix206-2094
α-helix211-2122
α-helix2161
β-strand217-22153
β-strand227-23593
β-strand242-24763
β-strand25211
β-strand254-26073
Chain B: 1 helix, 3 β-strands
ElementResiduesLengthSheet
β-strand261-26223
β-strand264-26523
α-helix270-2712
β-strand274-27853
Chains C and F: 1 helix, 1 β-strand
ElementResiduesLengthSheet
β-strand212
α-helix4-63
Chain D: 8 helices, 18 β-strands
ElementResiduesLengthSheet
β-strand57-6374
β-strand69-79114
β-strand87-9154
β-strand9615
β-strand97-10044
β-strand108-11364
α-helix117-1193
α-helix126-1327
β-strand136-14275
β-strand148-158115
α-helix1591
β-strand166-17055
β-strand173-17425
β-strand17516
β-strand176-17945
α-helix181-1866
β-strand190-19235
α-helix193-1953
α-helix206-2094
α-helix211-2122
α-helix2161
β-strand217-22156
β-strand227-23596
β-strand242-24766
β-strand25214
β-strand254-26076
Chain E: 1 helix, 3 β-strands
ElementResiduesLengthSheet
β-strand261-26226
β-strand26516
α-helix270-2712
β-strand274-27856

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Spindlin-1A, Dprotein212Homo sapiensQ9Y657 (AlphaFold model)
Spindlin interactor and repressor of chromatin-binding proteinB, Eprotein30Homo sapiensQ9BUA3 (AlphaFold model)
Ala-arg-thr-M3L-gln-thr-ala-arg-M3L-ser-thrCprotein12synthetic construct
Ala-arg-thr-M3L-gln-thr-ala-arg-M3L-ser-glyFprotein12synthetic construct
Sequence of entity 1 (A, D), FASTA
>7CNA_1 Spindlin-1 (chains A, D)
RNIVGCRIQHGWKEGNGPVTQWKGTVLDQVPVNPSLYLIKYDGFDCVYGLELNKDERVSA
LEVLPDRVATSRISDAHLADTMIGKAVEHMFETEDGSKDEWRGMVLARAPVMNTWFYITY
EKDPVLYMYQLLDDYKEGDLRIMPDSNDSPPAEREPGEVVDSLVGKQVEYAKEDGSKRTG
MVIHQVEAKPSVYFIKFDDDFHIYVYDLVKTS
Sequence of entity 2 (B, E), FASTA
>7CNA_2 Spindlin interactor and repressor of chromatin-binding protein (chains B, E)
ETFAAPAEVRHFTDGSFPAGFVLQLFSHTQ
Sequence of entity 3 (C), FASTA
>7CNA_3 ALA-ARG-THR-M3L-GLN-THR-ALA-ARG-M3L-SER-THR (chains C)
ARTKQTARKSTG
Sequence of entity 4 (F), FASTA
>7CNA_4 ALA-ARG-THR-M3L-GLN-THR-ALA-ARG-M3L-SER-GLY (chains F)
ARTKQTARKSGG

Ligands and cofactors

IDNameFormulaCopies
BENBenzamidineC7 H8 N26

Water and common crystallization additives (GOL, CL) are not listed.

Primary citation

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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