Evidence map›Paper›PMID 37910016›Full record

ArticleeLife2023

Autoinhibited kinesin-1 adopts a hierarchical folding pattern.

Zhenyu Tan, Yang Yue, Felipe Leprevost, Sarah Haynes, Venkatesha Basrur, Alexey I Nesvizhskii, Kristen J Verhey, Michael A Cianfrocco

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Regulation of kinesin-2 motility by its β-hairpin motif.Nature structural & molecular biology · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Mechanism and regulation of kinesin motors.Nature reviews. Molecular cell biology · 2025
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Zhenyu TanDepartment of Biophysics, University of Michigan, Ann Arbor, United States.ORCID 0000-0001-6491-5806
Yang YueDepartment of Cell & Developmental Biology, University of Michigan, Ann Arbor, United States.
Felipe LeprevostDepartment of Pathology, University of Michigan, Ann Arbor, United States.
Sarah HaynesDepartment of Pathology, University of Michigan, Ann Arbor, United States.
Venkatesha BasrurDepartment of Pathology, University of Michigan, Ann Arbor, United States.
Alexey I NesvizhskiiDepartment of Pathology, University of Michigan, Ann Arbor, United States.
Kristen J VerheyDepartment of Cell & Developmental Biology, University of Michigan, Ann Arbor, United States.ORCID 0000-0001-9329-4981
Michael A CianfroccoLife Sciences Institute, University of Michigan, Ann Arbor, United States.ORCID 0000-0002-2067-4999
University of Michigan · US

Funding

Kinesin Motors and Microtubule-based TraffickingR35GM131744 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kristen J. Verhey · 2019 to 2026
$6.3M
COMPUTATIONAL TOOLS FOR MASS SPECTROMETRY-BASED INTERACTOME DATAR01GM094231 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 2010 to 2026
$5.4M
Mechanisms of kinesin motor protein inhibition: Equipment SupplementR01GM141119 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Michael Cianfrocco · 2022 to 2026
$1.8M
Analysis and Statistical Validation of Proteomic DatasetsR01CA126239 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NESVIZHSKII, ALEXEY I · 2006 to 2009
$1.2M
Compute Cluster for in vitro and in situ Analysis of Molecular MachinesS10OD030275 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OHI, MELANIE DIANE · 2021 to 2021
$600k
Silicon Mechanics Compute ClusterS10OD020011 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SKINIOTIS, GEORGIOS · 2015 to 2015
$490k
NCI NIH HHS R01 CA126239NIGMS NIH HHS R01 GM094231NIGMS NIH HHS R01 GM141119NIGMS NIH HHS R35 GM131744NIH HHS R01GM094231NIH HHS R01GM141119NIH HHS R35GM131744NIH HHS S10 OD020011NIH HHS S10 OD030275
6 · The paper itself

Abstract

Conventional kinesin-1 is the primary anterograde motor in cells for transporting cellular cargo. While there is a consensus that the C-terminal tail of kinesin-1 inhibits motility, the molecular architecture of a full-length autoinhibited kinesin-1 remains unknown. Here, we combine crosslinking mass spectrometry (XL-MS), electron microscopy (EM), and AlphaFold structure prediction to determine the architecture of the full-length autoinhibited kinesin-1 homodimer (kinesin-1 heavy chain [KHC]) and kinesin-1 heterotetramer (KHC bound to kinesin light chain 1 [KLC1]). Our integrative analysis shows that kinesin-1 forms a compact, bent conformation through a break in coiled-coil 3. Moreover, our XL-MS analysis demonstrates that kinesin light chains stabilize the folded inhibited state rather than inducing a new structural state. Using our structural model, we show that disruption of multiple interactions between the motor, stalk, and tail domains is required to activate the full-length kinesin-1. Our work offers a conceptual framework for understanding how cargo adaptors and microtubule-associated proteins relieve autoinhibition to promote activation.

Indexed as

KinesinsMicrotubule-Associated ProteinsBiological TransportConsensusMass SpectrometryKinesinsMicrotubule-Associated ProteinsAlphaFoldcell biologycrosslinking mass spectrometryhumanintegrative modelingkinesinmolecular biophysicsmotor proteinstructural biology

Identifiers

PMID37910016
PMCPMC10619981
OpenAlexW4364365141

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.