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17883 Ensembl ENSG00000109063 ENSMUSG00000020908 UniProt P11055 P13541 RefSeq (mRNA) NM_002470 NM_001099635 RefSeq (protein) NP_002461 NP_001093105 Location (UCSC) Chr 17: 10.63 – 10.66 Mb Chr 11: 66.97 – 66.99 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Myosin-3 is a protein that in humans is encoded by the MYH3 gene. Function Myosin is a major contractile protein which ...
Myosin VI is an unconventional myosin motor, which is primarily processive as a dimer, but also acts as a nonprocessive monomer. It walks along actin filaments, travelling towards the pointed end (- end) of the filaments. [44] Myosin VI is thought to transport endocytic vesicles into the cell. [45]
4624 17888 Ensembl ENSG00000197616 ENSMUSG00000040752 UniProt P13533 Q02566 RefSeq (mRNA) NM_002471 NM_001164171 NM_010856 RefSeq (protein) NP_002462 NP_001157643 NP_034986 Location (UCSC) Chr 14: 23.38 – 23.41 Mb Chr 14: 55.18 – 55.2 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Myosin heavy chain, α isoform (MHC-α) is a protein that in humans is encoded by the MYH6 gene ...
Myosin VIIA is protein that in humans is encoded by the MYO7A gene. [5] Myosin VIIA is a member of the unconventional myosin superfamily of proteins. [ 6 ] Myosins are actin binding molecular motors that use the enzymatic conversion of ATP - ADP + inorganic phosphate (Pi) to provide the energy for movement.
The thick filament, myosin, has a double-headed structure, with the heads positioned at opposite ends of the molecule. During muscle contraction, the heads of the myosin filaments attach to oppositely oriented thin filaments, actin, and pull them past one another. The action of myosin attachment and actin movement results in sarcomere shortening.
Unconventional myosin-Va is a motor protein in charge of the intracellular transport of vesicles, organelles and protein complexes along the actin filaments. [ 5 ] [ 6 ] [ 7 ] In humans it is coded for by the MYO5A gene .
Supplemental tests: blood tests, exercise stress test, 12-minute Walk Test, non-ischemic forearm test, EMG Glycogen storage disease type V ( GSD5 , GSD-V ), [ 1 ] also known as McArdle's disease , [ 2 ] is a metabolic disorder , one of the metabolic myopathies , more specifically a muscle glycogen storage disease , caused by a deficiency of ...
Because myosin undergoes a conformational change, the muscle will stay contracted even if calcium and activated MLC kinase concentrations are brought to normal levels. The conformational change must be undone to relax the muscle. [4] When myosin phosphatase binds to myosin, it removes the phosphate group. Without the group, the myosin reverts ...