Evidence map›Paper›PMID 17433365›Full record

ArticleJournal of molecular biology2007

Diversity of structural behavior in vertebrate conventional myosins complexed with actin.

Hiroyuki Iwamoto, Kazuhiro Oiwa, Mihály Kovács, James R Sellers, Takuya Suzuki, Jun'ichi Wakayama, Takumi Tamura, Naoto Yagi, Tetsuro Fujisawa

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Unconventional processive mechanics of non-muscle myosin IIB.The Journal of biological chemistry · 2010
    Article
  5. Article
  6. Article
  7. Load-dependent mechanism of nonmuscle myosin 2.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
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

9 authors at 5 institutions in 3 countries.

Hiroyuki IwamotoResearch and Utilization Division, SPring-8, Japan Synchrotron Radiation Research Institute, Hyogo 679-6198, Japan. iwamoto@spring8.or.jp
Kazuhiro Oiwa
Mihály Kovács
James R Sellers
Takuya Suzuki
Jun'ichi Wakayama
Takumi Tamura
Naoto Yagi
Tetsuro Fujisawa
Japan Synchrotron Radiation Research Institute · JPRIKEN · JPSPring-8 · JPNational Institute of Information and Communications Technology · JPNational Institutes of Health · US

Funding

ROLE OF PHOSPHORYLATION AS A REGULATORY MECHANISM IN MUSCLE CONTRACTIONZ01HL001786 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI SELLERS, JAMES R. · 1985 to 2008
$601k
Widow inheritance and HIV infection in KenyaR01TW006230 · FIC · UNIVERSITY OF NAIROBI · PI AGOT, KAWANGO · 2002 to 2006
$313k
Emerging New Types of MotilityR01TW007241 · FIC · EOTVOS LORAND UNIVERSITY · PI KOVACS, MIHALY · 2005 to 2009
$260k
FIC NIH HHS 1 R01 TW007241-01FIC NIH HHS D43 TW006230FIC NIH HHS R01 TW006230FIC NIH HHS R01 TW007241
6 · The paper itself

Abstract

Low-resolution three-dimensional structures of acto-myosin subfragment-1 (S1) complexes were retrieved from X-ray fiber diffraction patterns, recorded either in the presence or absence of ADP. The S1 was obtained from various myosin-II isoforms from vertebrates, including rabbit fast-skeletal and cardiac, chicken smooth and human non-muscle IIA and IIB species, and was diffused into an array of overstretched, skinned skeletal muscle fibers. The S1 attached to the exposed actin filaments according to their helical symmetry. Upon addition of ADP, the diffraction patterns from acto-S1 showed an increasing magnitude of response in the order as listed above, with features of a lateral compression of the whole diffraction pattern (indicative of increased radius of the acto-S1 complex) and an enhancement of the fifth layer-line reflection. The structure retrieval indicates that these changes are mainly due to the swing of the light chain (LC) domain in the direction consistent with the cryo-electron microscopic results. In the non-muscle isoforms, the swing is large enough to affect the manner of quasi-crystal packing of the S1-decorated actin filaments and their lattice dimension, with a small change in the twist of actin filaments. Variations also exist in the behavior of the 50K-cleft, which apparently opens upon addition of ADP to the non-muscle isoforms but not to other isoforms. The fast-skeletal S1 remains as the only isoform that does not clearly exhibit either of the structural changes. The results indicate that the "conventional" myosin-II isoforms exhibit a wide variety of structural behavior, possibly depending on their functions and/or the history of molecular evolution.

Indexed as

ActinsActomyosinAdenosine DiphosphateAnimalsChickensCrystallography, X-RayKineticsModels, MolecularMuscle Fibers, SkeletalMyosinsRabbitsStructure-Activity RelationshipVertebratesActinsActomyosinAdenosine DiphosphateMyosins

Identifiers

PMID17433365
PMCPMC1997293
OpenAlexW2078623120

What OpenQuestion holds

Textmetadata
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.