Cardiomyopathic troponin mutations predominantly occur at its interface with actin and tropomyosin
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Title
Cardiomyopathic troponin mutations predominantly occur at its interface with actin and tropomyosin
Authors
Keywords
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Journal
JOURNAL OF GENERAL PHYSIOLOGY
Volume 153, Issue 3, Pages -
Publisher
Rockefeller University Press
Online
2021-01-26
DOI
10.1085/jgp.202012815
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Note: Only part of the references are listed.- Cryo-EM structures of cardiac thin filaments reveal the 3D architecture of troponin
- (2020) Toshiyuki Oda et al. JOURNAL OF STRUCTURAL BIOLOGY
- Cardiac muscle thin filament structures reveal calcium regulatory mechanism
- (2020) Yurika Yamada et al. Nature Communications
- Protein-protein docking reveals dynamic interactions of tropomyosin on actin filaments
- (2020) Elumalai Pavadai et al. BIOPHYSICAL JOURNAL
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- Cryo-EM and Molecular Docking Shows Myosin Loop 4 Contacts Actin and Tropomyosin on Thin Filaments
- (2020) Matthew H. Doran et al. BIOPHYSICAL JOURNAL
- TNNT2mutations in the tropomyosin binding region of TNT1 disrupt its role in contractile inhibition and stimulate cardiac dysfunction
- (2020) Aditi Madan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Troponin Revealed: Uncovering the Structure of the Thin Filament On-Off Switch in Striated Muscle
- (2020) Larry S. Tobacman BIOPHYSICAL JOURNAL
- Docking Troponin T onto the Tropomyosin Overlapping Domain of Thin Filaments
- (2019) Elumalai Pavadai et al. BIOPHYSICAL JOURNAL
- Desensitizing mouse cardiac troponin C to calcium converts slow muscle towards a fast muscle phenotype
- (2018) Svetlana Tikunova et al. JOURNAL OF PHYSIOLOGY-LONDON
- Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy
- (2018) Carolyn Y. Ho et al. CIRCULATION
- The myosin mesa and the basis of hypercontractility caused by hypertrophic cardiomyopathy mutations
- (2017) Suman Nag et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Molecular mechanisms and structural features of cardiomyopathy-causing troponin T mutants in the tropomyosin overlap region
- (2017) Binnu Gangadharan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The myosin mesa and the basis of hypercontractility caused by hypertrophic cardiomyopathy mutations
- (2017) Suman Nag et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypes
- (2017) Lorenzo Alamo et al. eLife
- Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
- (2016) Roddy Walsh et al. GENETICS IN MEDICINE
- Restrictive Cardiomyopathy Troponin I R145W Mutation Does Not Perturb Myofilament Length-dependent Activation in Human Cardiac Sarcomeres
- (2016) Alexey V. Dvornikov et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Investigating the effects of tropomyosin mutations on its flexibility and interactions with filamentous actin using molecular dynamics simulation
- (2016) Wenjun Zheng et al. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
- Myofilament Calcium Sensitivity: Consequences of the Effective Concentration of Troponin I
- (2016) Jalal K. Siddiqui et al. Frontiers in Physiology
- The functional effect of dilated cardiomyopathy mutation (R144W) in mouse cardiac troponin T is differently affected by α- and β-myosin heavy chain isoforms
- (2015) Sampath K. Gollapudi et al. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
- Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity
- (2015) Ahmed A. Alfares et al. GENETICS IN MEDICINE
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Troponin I Mutations R146G and R21C Alter Cardiac Troponin Function, Contractile Properties, and Modulation by Protein Kinase A (PKA)-mediated Phosphorylation
- (2015) Yuanhua Cheng et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Molecular Effects of Familial Hypertrophic Cardiomyopathy-Related Mutations in the TNT1 Domain of cTnT
- (2012) Edward P. Manning et al. JOURNAL OF MOLECULAR BIOLOGY
- Thin Filament Mutations
- (2011) Jil C. Tardiff CIRCULATION RESEARCH
- Inherited Cardiomyopathies
- (2011) Hugh Watkins et al. NEW ENGLAND JOURNAL OF MEDICINE
- Localization of the two tropomyosin-binding sites of troponin T
- (2010) J.-P. Jin et al. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
- Structural basis for tropomyosin overlap in thin (actin) filaments and the generation of a molecular swivel by troponin-T
- (2008) K. Murakami et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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