HDAC6 ist ein Gen, das durch das Symbol HDAC6 kodiert wird. Im Allgemeinen auch bezeichnet als: Histone deacetylase 6; HD6; Tubulin-lysine deacetylase KIAA0901. HDAC6 hat eine Masse von 131.42kDa, eine Aminosäurelänge von 1215, und ist an Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia beteiligt.
Wir bieten 25 antikörper gegen HDAC6, aufgewachsen in Kaninchen, Maus und Ziege, welche geeignet sind für WB, IHC, ELISA, ICC/IF, FC and IP mit Proben abgeleitet von Human, Maus und Ratte.
Gen- und Proteininformationen
UniProt Zusammenfassung
Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) (PubMed:10220385). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events (PubMed:10220385). Histone deacetylases act via the formation of large multiprotein complexes (PubMed:10220385). In addition to histones, deacetylates other proteins: plays a central role in microtubule-dependent cell motility by mediating deacetylation of tubulin (PubMed:12024216, PubMed:20308065). Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer (PubMed:24413532). In addition to its protein deacetylase activity, plays a key role in the degradation of misfolded proteins: when misfolded proteins are too abundant to be degraded by the chaperone refolding system and the ubiquitin-proteasome, mediates the transport of misfolded proteins to a cytoplasmic juxtanuclear structure called aggresome (PubMed:17846173). Probably acts as an adapter that recognizes polyubiquitinated misfolded proteins and target them to the aggresome, facilitating their clearance by autophagy (PubMed:17846173).
Entrez Zusammenfassung
Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It contains an internal duplication of two catalytic domains which appear to function independently of each other. This protein possesses histone deacetylase activity and represses transcription.
Rolle bei Krankheiten
Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia: A disease characterized by chondrodysplasia, severe platyspondyly, hydrocephaly, and facial features with microphthalmia. Bone abnormalities include a distinctive metaphyseal cupping of the metacarpals, metatarsals, and phalanges. Affected females show a milder phenotype with small stature, sometimes associated with body asymmetry and mild mental retardation.
Sequenzähnlichkeiten
Belongs to the histone deacetylase family. HD type 2 subfamily.
Posttranslationale Modifikation
Phosphorylated by AURKA.
Zellort
Cytoplasm. Cytoplasm > Cytoskeleton. Nucleus. Perikaryon. Cell projection > Dendrite. Cell projection > Axon.
It is mainly cytoplasmic, where it is associated with microtubules.
