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Actin Proteine (ACTA1)

Bezeichnung:
Actin, alpha 1, Skeletal Muscle Proteine (ACTA1)
Auf www.antikoerper-online.de finden Sie aktuell 26 Actin, alpha 1, Skeletal Muscle (ACTA1) Proteine von 4 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Actin Antikörper (184) und Actin Kits (38) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 256 Actin Produkte verfügbar.
Synonyme:
AA959943, ACTA, Acta-2, Acts, Actsk-1, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3
alle Proteine anzeigen Gen GeneID UniProt
ACTA1 58 P68133
ACTA1 11459 P68134
ACTA1 29437 P68136

Weitere Synonyme anzeigen

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Weitere Proteine zu Actin Interaktionspartnern

Human Actin, alpha 1, Skeletal Muscle (ACTA1) Interaktionspartner

  1. Shorter than normal thin filament length contributes to the impaired force generation in patients with thin filament myopathy, but only in those who harbor specific mutations in NEB or ACTA1.

  2. Over-expression of TNC (zeige TNC Proteine), SMA (zeige SMN1 Proteine), and vimentin (zeige VIM Proteine) were significantly correlated with the lower overall survival in prostate cancer patients.

  3. ANA (zeige BTG3 Proteine) and ASMA evaluation in patients with liver transplantation and no history of autoimmune disease has no clinical relevance, since it varies in time and is not related to any risk factors or liver injury. Routine autoimmunity evaluation should be avoided.

  4. Upon actin engagement, the N-terminal "strap" and helix 1 are displaced from the vinculin tail helical bundle to mediate actin bundling.

  5. This study reported the new information on the frequency and phenotypes of congenital myopathy caused by ACTA1 mutations in subjects >/=5 years of age.

  6. The authors propose that Lpd delivers Ena/VASP proteins to growing barbed ends and increases their actin polymerase activity by tethering them to actin filaments.

  7. Mutations in ACTA1 can cause pathologic features consistent with myofibrillar myopathy.

  8. TIMP-1 (zeige TIMP1 Proteine) significantly increased levels of alpha-SMA (zeige SMN1 Proteine).

  9. Myopathy associated with zebra bodies is part of the spectrum of myopathies associated with the ACTA1 gene.

  10. New scapuloperoneal phenotype associated with an ACTA1 mutation.

Pig (Porcine) Actin, alpha 1, Skeletal Muscle (ACTA1) Interaktionspartner

  1. Titin-actin interaction: PEVK-actin-based viscosity in a large animal.

Mouse (Murine) Actin, alpha 1, Skeletal Muscle (ACTA1) Interaktionspartner

  1. alpha smooth muscle actin (zeige ACTG2 Proteine) (alphaSMA (zeige ACTA2 Proteine)) was identified as a marker of osteoprogenitor cells in bone and periodontium.

  2. WIP is a link between membrane lipid composition and actin cytoskeleton at dendritic spines.

  3. ACTA1(Asp286Gly) mouse model of nemaline myopathy provide evidence of impaired in vivo muscle function, altered muscle structure and disturbed energy metabolism.

  4. Combined MRI (zeige C7ORF49 Proteine) and (3)(1)P-MRS investigations of the ACTA1(H40Y) mouse model of nemaline myopathy show impaired muscle function and altered energy metabolism.

  5. Data indicate roles for linkers of nucleus to cytoskeleton (LINC) molecules nesprin2giant and nesprin3, which anchor actin cap fibers to the nucleus.

  6. Asp286Gly acts as a "poison-protein" and according to the computational analysis it modifies the actin-actin interface. This phenomenon is likely to prevent proper myosin cross-bridge binding.

  7. Data show that upon actin binding, the two domains of utrophin become dramatically separated and ordered, indicating a transition to a single open and extended conformation.

  8. Data indicated that CacyBP/SIP (zeige CACYBP Proteine) could simultaneously interact with tubulin (zeige TUBB Proteine) and actin, suggesting that CacyBP/SIP (zeige CACYBP Proteine) might link actin and tubulin (zeige TUBB Proteine) cytoskeletons.

  9. Results provide the genetic proof that platelet production from megakaryocytes strictly requires dynamic changes in the actin cytoskeleton.

  10. Data show that while increases in cardiac and vascular smooth-muscle actin can partially compensate for the lack of skeletal actin in null mice, this is not sufficient to support adequate skeletal muscle growth and/or function.

Actin (ACTA1) Protein Überblick

Protein Überblick

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.

Alternative names and synonyms associated with Actin (ACTA1)

  • actin, alpha 1, skeletal muscle (ACTA1)
  • actin, alpha 1, skeletal muscle (Acta1)
  • actin, muscle (LOC100533357)
  • AA959943 Protein
  • ACTA Protein
  • Acta-2 Protein
  • Acts Protein
  • Actsk-1 Protein
  • ASMA Protein
  • CFTD Protein
  • CFTD1 Protein
  • CFTDM Protein
  • MPFD Protein
  • NEM1 Protein
  • NEM2 Protein
  • NEM3 Protein

Bezeichner auf Proteinebene für ACTA1

actin, alpha 1, skeletal muscle , actin, alpha skeletal muscle , nemaline myopathy type 3 , alpha actin 1 , alpha-actin-1 , skeletal alpha actin , actin alpha 1 , a-actin

GENE ID SPEZIES
100609865 Pan troglodytes
58 Homo sapiens
100154254 Sus scrofa
281592 Bos taurus
11459 Mus musculus
29437 Rattus norvegicus
100716933 Cavia porcellus
421534 Gallus gallus
100533357 Aplysia californica
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