Mondal et al., 2016 - Google Patents
Protein structure-function relationship at work: learning from myopathy mutations of the slow skeletal muscle isoform of troponin TMondal et al., 2016
View HTML- Document ID
- 550369510655340099
- Author
- Mondal A
- Jin J
- Publication year
- Publication venue
- Frontiers in Physiology
External Links
Snippet
Troponin T (TnT) is the sarcomeric thin filament anchoring subunit of the troponin complex in striated muscles. A nonsense mutation in exon 11 of the slow skeletal muscle isoform of TnT (ssTnT) gene (TNNT1) was found in the Amish populations in Pennsylvania and Ohio. This …
- 102000004987 Troponin T 0 title abstract description 211
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4702—Regulators; Modulating activity
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/46—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
- G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
Similar Documents
Publication | Publication Date | Title |
---|---|---|
McNamara et al. | MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy | |
Sheng et al. | Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused review | |
Mondal et al. | Protein structure-function relationship at work: learning from myopathy mutations of the slow skeletal muscle isoform of troponin T | |
Lu et al. | Inherited cardiomyopathies caused by troponin mutations | |
Tardiff | Thin filament mutations: developing an integrative approach to a complex disorder | |
Tardiff | Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes | |
Moolman-Smook et al. | Identification of novel interactions between domains of myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations | |
Redwood et al. | Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy | |
Kampourakis et al. | Myosin light chain phosphorylation enhances contraction of heart muscle via structural changes in both thick and thin filaments | |
Eddinger et al. | Myosin II isoforms in smooth muscle: heterogeneity and function | |
Wei et al. | Troponin T isoforms and posttranscriptional modifications: Evolution, regulation and function | |
Pusapati et al. | EFCAB7 and IQCE regulate hedgehog signaling by tethering the EVC-EVC2 complex to the base of primary cilia | |
Carballo et al. | Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy | |
Rajan et al. | Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity | |
Xu et al. | Ephrin-B3 reverse signaling through Grb4 and cytoskeletal regulators mediates axon pruning | |
Galinska et al. | The C terminus of cardiac troponin I stabilizes the Ca2+-activated state of tropomyosin on actin filaments | |
Ohtsuki et al. | Troponin: regulatory function and disorders | |
Rasmussen et al. | Troponin variants as markers of skeletal muscle health and diseases | |
Hitchcock-DeGregori et al. | Functions of tropomyosin's periodic repeats | |
Ceco et al. | Targeting latent TGFβ release in muscular dystrophy | |
Golitsina et al. | Effects of two familial hypertrophic cardiomyopathy-causing mutations on α-tropomyosin structure and function | |
Matyushenko et al. | Structural and functional effects of cardiomyopathy-causing mutations in the troponin T-binding region of cardiac tropomyosin | |
Feng et al. | Restricted N‐terminal truncation of cardiac troponin T: a novel mechanism for functional adaptation to energetic crisis | |
Szczesna-Cordary et al. | Familial hypertrophic cardiomyopathy-linked alterations in Ca2+ binding of human cardiac myosin regulatory light chain affect cardiac muscle contraction | |
Marques et al. | Cardiac troponin and tropomyosin: structural and cellular perspectives to unveil the hypertrophic cardiomyopathy phenotype |