Evidence map›Paper›PMID 26573747›Full record

ArticleProteins2016

A composite approach towards a complete model of the myosin rod.

E Nihal Korkmaz, Keenan C Taylor, Michael P Andreas, Guatam Ajay, Nathan T Heinze, Qiang Cui, Ivan Rayment

Open access · greenAbstract read
In one paragraph

Article in Proteins, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Structure, regulation, and mechanisms of nonmuscle myosin-2.Cellular and molecular life sciences : CMLS · 2024
    Review
  2. Article
  3. Article
  4. Review
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  7. The myosin II coiled-coil domain atomic structure in its native environment.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Article
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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

7 authors at 1 institution in 1 country.

E Nihal Korkmaz *Department of Chemistry and Theoretical Chemistry Institute, University of Wisconsin, Madison, WI 53706, USA.
Keenan C Taylor *Department of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.
Michael P AndreasDepartment of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.
Guatam AjayDepartment of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.
Nathan T HeinzeDepartment of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.
Qiang CuiDepartment of Chemistry and Theoretical Chemistry Institute, University of Wisconsin, Madison, WI 53706, USA.
Ivan RaymentDepartment of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.
University of Wisconsin–Madison · US

Funding

Structural Framework for Understanding Myosin Thick-Filament CardiomyopathiesR21HL111237 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI RAYMENT, IVAN · 2013 to 2014
$389k
NHLBI NIH HHS R21 HL111237
6 · The paper itself

Abstract

Sarcomeric myosins have the remarkable ability to form regular bipolar thick filaments that, together with actin thin filaments, constitute the fundamental contractile unit of skeletal and cardiac muscle. This has been established for over 50 years and yet a molecular model for the thick filament has not been attained. In part this is due to the lack of a detailed molecular model for the coiled-coil that constitutes the myosin rod. The ability to self-assemble resides in the C-terminal section of myosin known as light meromyosin (LMM) which exhibits strong salt-dependent aggregation that has inhibited structural studies. Here we evaluate the feasibility of generating a complete model for the myosin rod by combining overlapping structures of five sections of coiled-coil covering 164 amino acid residues which constitute 20% of LMM. Each section contains ∼ 7-9 heptads of myosin. The problem of aggregation was overcome by incorporating the globular folding domains, Gp7 and Xrcc4 which enhance crystallization. The effect of these domains on the stability and conformation of the myosin rod was examined through biophysical studies and overlapping structures. In addition, a computational approach was developed to combine the sections into a contiguous model. The structures were aligned, trimmed to form a contiguous model, and simulated for >700 ns to remove the discontinuities and achieve an equilibrated conformation that represents the native state. This experimental and computational strategy lays the foundation for building a model for the entire myosin rod.

Indexed as

Amino Acid SequenceCardiomyopathiesCrystallography, X-RayHumansMolecular Dynamics SimulationMolecular Sequence DataMutationMyosin SubfragmentsProtein ConformationProtein StabilityProtein Structure, SecondaryRecombinant Fusion ProteinsTemperatureMyosin SubfragmentsRecombinant Fusion Proteinscardiac muscle: coiled-coilmolecular dynamicsprotein structureX-ray crystallization

Identifiers

PMID26573747
PMCPMC4715562
OpenAlexW2175393649

What OpenQuestion holds

Textmetadata
LicenceTDM
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.