Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

6TIS

DROSOPHILA GDP-TUBULIN

Summary for 6TIS
Entry DOI10.2210/pdb6tis/pdb
Related6TIU 6TIY 6TIZ
DescriptorTubulin alpha-1 chain, Tubulin beta-1 chain, Stathmin-4, ... (9 entities in total)
Functional Keywordsmicrotubule, microtubule dynamics, microtule nucleation, cell cycle
Biological sourceDrosophila melanogaster (Fruit fly)
More
Total number of polymer chains5
Total formula weight220440.19
Authors
Gigant, B. (deposition date: 2019-11-22, release date: 2021-01-27, Last modification date: 2024-01-24)
Primary citationAyukawa, R.,Iwata, S.,Imai, H.,Kamimura, S.,Hayashi, M.,Ngo, K.X.,Minoura, I.,Uchimura, S.,Makino, T.,Shirouzu, M.,Shigematsu, H.,Sekimoto, K.,Gigant, B.,Muto, E.
GTP-dependent formation of straight tubulin oligomers leads to microtubule nucleation.
J.Cell Biol., 220:-, 2021
Cited by
PubMed Abstract: Nucleation of microtubules (MTs) is essential for cellular activities, but its mechanism is unknown because of the difficulty involved in capturing rare stochastic events in the early stage of polymerization. Here, combining rapid flush negative stain electron microscopy (EM) and kinetic analysis, we demonstrate that the formation of straight oligomers of critical size is essential for nucleation. Both GDP and GTP tubulin form single-stranded oligomers with a broad range of curvatures, but upon nucleation, the curvature distribution of GTP oligomers is shifted to produce a minor population of straight oligomers. With tubulin having the Y222F mutation in the β subunit, the proportion of straight oligomers increases and nucleation accelerates. Our results support a model in which GTP binding generates a minor population of straight oligomers compatible with lateral association and further growth to MTs. This study suggests that cellular factors involved in nucleation promote it via stabilization of straight oligomers.
PubMed: 33544140
DOI: 10.1083/jcb.202007033
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

236620

PDB entries from 2025-05-28

PDB statisticsPDBj update infoContact PDBjnumon