Evidence map›Paper›PMID 36129769›Full record

ArticleMolecular biology of the cell2022

Divergent polo boxes in KKT2 bind KKT1 to initiate the kinetochore assembly cascade in

Midori Ishii, Patryk Ludzia, Gabriele Marcianò, William Allen, Olga O Nerusheva, Bungo Akiyoshi

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Midori IshiiDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
Patryk LudziaDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
Gabriele MarcianòDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
William AllenDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
Olga O NerushevaDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
Bungo AkiyoshiDepartment of Biochemistry, University of Oxford, Oxford, OX1 3QU, UK.
University of Oxford · GBUniversity of North Carolina at Chapel Hill · US

Funding

Wellcome TrustWellcome Trust 210622/Z/18/Z
6 · The paper itself

Abstract

Chromosome segregation requires assembly of the macromolecular kinetochore complex onto centromeric DNA. While most eukaryotes have canonical kinetochore proteins that are widely conserved among eukaryotes, evolutionarily divergent kinetoplastids have a unique set of kinetochore proteins. Little is known about the mechanism of kinetochore assembly in kinetoplastids. Here we characterize two homologous kinetoplastid kinetochore proteins, KKT2 and KKT3, that constitutively localize at centromeres. They have three domains that are highly conserved among kinetoplastids: an N-terminal kinase domain of unknown function, the centromere localization domain in the middle, and the C-terminal domain that has weak similarity to polo boxes of Polo-like kinases. We show that the kinase activity of KKT2 is essential for accurate chromosome segregation, while that of KKT3 is dispensable for cell growth in

Indexed as

Trypanosoma brucei bruceiCell Cycle ProteinsCentromereChromosome SegregationKinetochoresProtozoan ProteinsCell Cycle ProteinsProtozoan Proteins

Identifiers

PMID36129769
PMCPMC9727816
OpenAlexW4296552599

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.