EMD-15631

Single-particle
7.7 Å
EMD-15631 Deposition: 22/08/2022
Map released: 28/09/2022
Last modified: 24/07/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-15631

Cryo-EM reconstruction of the augmin TIII subcomplex

EMD-15631

Single-particle
7.7 Å
EMD-15631 Deposition: 22/08/2022
Map released: 28/09/2022
Last modified: 24/07/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Xenopus laevis
Sample: Augmin TIII subcomplex
Fitted models: 8at2 (Avg. Q-score: 0.124)

Deposition Authors: Zupa E , Pfeffer S
The augmin complex architecture reveals structural insights into microtubule branching.
Zupa E , Wurtz M , Neuner A, Hoffmann T , Rettel M , Bohler A, Vermeulen BJA , Eustermann S , Schiebel E , Pfeffer S
(2022) Nat Commun , 13 , 5635 - 5635
PUBMED: 36163468
DOI: doi:10.1038/s41467-022-33228-6
ISSN: 2041-1723
Abstract:
In mitosis, the augmin complex binds to spindle microtubules to recruit the γ-tubulin ring complex (γ-TuRC), the principal microtubule nucleator, for the formation of branched microtubules. Our understanding of augmin-mediated microtubule branching is hampered by the lack of structural information on the augmin complex. Here, we elucidate the molecular architecture and conformational plasticity of the augmin complex using an integrative structural biology approach. The elongated structure of the augmin complex is characterised by extensive coiled-coil segments and comprises two structural elements with distinct but complementary functions in γ-TuRC and microtubule binding, linked by a flexible hinge. The augmin complex is recruited to microtubules via a composite microtubule binding site comprising a positively charged unordered extension and two calponin homology domains. Our study provides the structural basis for augmin function in branched microtubule formation, decisively fostering our understanding of spindle formation in mitosis.