Structured Summary
Abstract
A subclass of myosins found generally associated with actin-rich membrane structures such as filopodia. Members of the myosin type I family are ubiquitously expressed in eukaryotes. The heavy chains of myosin type I lack coiled-coil forming sequences in their tails and therefore do not dimerize.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
3 entry terms
- Myosin I
- Myosin IA
- Myosin IB
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2002; for MYOSIN IA & MYOSIN IB use MYOSINS 1988-2001
MeSH Record
Previous Indexing
- Myosins (1987-2001)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Myosin Type I. Medical Subject Headings (MeSH). 2026. Unique ID D024461. http://id.nlm.nih.gov/mesh/2026/D024461
- Myosin Type I. In: Wikidata. https://www.wikidata.org/wiki/Q77301697