9OKK image
Deposition Date 2025-05-09
Release Date 2026-07-08
Last Version Date 2026-07-08
Entry Detail
PDB ID:
9OKK
Keywords:
Title:
Bombyx mori bmCENP-LN-HIKM sub-complex structure
Biological Source:
Source Organism(s):
Bombyx mori (Taxon ID: 7091)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
3.23 Å
Aggregation State:
PARTICLE
Reconstruction Method:
SINGLE PARTICLE
Macromolecular Entities
Polymer Type:polypeptide(L)
Molecule:bmCENP-H
Chain IDs:A (auth: H)
Chain Length:239
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:Centromere protein I
Chain IDs:B (auth: I)
Chain Length:661
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:bmCENP-K
Chain IDs:C (auth: K)
Chain Length:219
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:Centromere protein L
Gene (Uniprot):CYP340
Chain IDs:D (auth: L)
Chain Length:302
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:Centromere protein M
Gene (Uniprot):101745870
Chain IDs:E (auth: M)
Chain Length:180
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:bmCENP-N
Chain IDs:F (auth: N)
Chain Length:328
Number of Molecules:1
Biological Source:Bombyx mori
Polymer Type:polypeptide(L)
Molecule:bmCENP-T
Chain IDs:G (auth: T)
Chain Length:1016
Number of Molecules:1
Biological Source:Bombyx mori
Ligand Molecules
Primary Citation
Architecture and function of holocentric CENP-A-independent inner kinetochores.
Sci Adv 12 eaeb5817 eaeb5817 (2026)
PMID: 42319948 DOI: 10.1126/sciadv.aeb5817

Abstact

Kinetochores are essential macromolecular complexes anchoring chromosomes to the mitotic spindle, ensuring faithful cell division. Despite their critical role, the structural organization of kinetochores across diverse species remains poorly understood. We present the inner kinetochore constitutive centromere-associated network (CCAN) structure of the silkmoth Bombyx mori, an insect that lacks the canonical centromere-specifying histone variant CENP-A and exhibits chromosome-wide centromeric activity (holocentric). The B. mori CCAN incorporates four previously uncharacterized centromeric subunit proteins that are structurally related to the Dam1/DASH complex but function in scaffolding the inner kinetochore rather than in microtubule binding. Similar to the yeast and human systems, the B. mori CCAN also entraps DNA within its central closed chamber. However, unlike these systems, the B. mori CCAN can also assemble in vitro into a self-contained head-to-head dimer via atypical histone-fold protein dimerization. On the basis of our findings, we propose that the holocentric organization may emerge from the modular arrangement of discrete kinetochore units.

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Disease

Primary Citation of related structures
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