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MAD1: Kinetochore Receptors and Catalytic Mechanisms

Overview of attention for article published in Frontiers in Cell and Developmental Biology, May 2018
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Title
MAD1: Kinetochore Receptors and Catalytic Mechanisms
Published in
Frontiers in Cell and Developmental Biology, May 2018
DOI 10.3389/fcell.2018.00051
Pubmed ID
Authors

Yibo Luo, Ejaz Ahmad, Song-Tao Liu

Abstract

The mitotic checkpoint monitors kinetochore-microtubule attachment, delays anaphase onset and prevents aneuploidy when unattached or tensionless kinetochores are present in cells. Mitotic arrest deficiency 1 (MAD1) is one of the evolutionarily conserved core mitotic checkpoint proteins. MAD1 forms a cell cycle independent complex with MAD2 through its MAD2 interaction motif (MIM) in the middle region. Such a complex is enriched at unattached kinetochores and functions as an unusual catalyst to promote conformational change of additional MAD2 molecules, constituting a crucial signal amplifying mechanism for the mitotic checkpoint. Only MAD2 in its active conformation can be assembled with BUBR1 and CDC20 to form the Mitotic Checkpoint Complex (MCC), which is a potent inhibitor of anaphase onset. Recent research has shed light on how MAD1 is recruited to unattached kinetochores, and how it carries out its catalytic activity. Here we review these advances and discuss their implications for future research.

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The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 38 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 38 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 8 21%
Student > Bachelor 6 16%
Researcher 6 16%
Student > Doctoral Student 4 11%
Professor 2 5%
Other 5 13%
Unknown 7 18%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 21 55%
Agricultural and Biological Sciences 8 21%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Neuroscience 1 3%
Unknown 7 18%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 07 May 2018.
All research outputs
#14,982,922
of 23,047,237 outputs
Outputs from Frontiers in Cell and Developmental Biology
#3,255
of 9,132 outputs
Outputs of similar age
#197,947
of 327,928 outputs
Outputs of similar age from Frontiers in Cell and Developmental Biology
#21
of 34 outputs
Altmetric has tracked 23,047,237 research outputs across all sources so far. This one is in the 32nd percentile – i.e., 32% of other outputs scored the same or lower than it.
So far Altmetric has tracked 9,132 research outputs from this source. They receive a mean Attention Score of 3.4. This one has gotten more attention than average, scoring higher than 56% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 327,928 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 36th percentile – i.e., 36% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 34 others from the same source and published within six weeks on either side of this one. This one is in the 35th percentile – i.e., 35% of its contemporaries scored the same or lower than it.