ID:TWF2_HUMAN DESCRIPTION: RecName: Full=Twinfilin-2; AltName: Full=A6-related protein; Short=hA6RP; AltName: Full=Protein tyrosine kinase 9-like; AltName: Full=Twinfilin-1-like protein; FUNCTION: Actin-binding protein involved in motile and morphological processes. Inhibits actin polymerization, likely by sequestering G-actin. By capping the barbed ends of filaments, it also regulates motility. Seems to play an important role in clathrin-mediated endocytosis and distribution of endocytic organelles. May play a role in regulating the mature length of the middle and short rows of stereocilia (By similarity). SUBUNIT: Interacts with G-actin; ADP-actin form and capping protein (CP). May also be able to interact with TWF1 and phosphoinositides, PI(4,5)P2. When bound to PI(4,5)P2, it is down- regulated. Interacts with MYO7A (By similarity). SUBCELLULAR LOCATION: Cytoplasm, cytoskeleton. Cytoplasm, perinuclear region. Cell projection, stereocilium (By similarity). Note=Perinuclear and G-actin-rich cortical actin structure sublocalization. TISSUE SPECIFICITY: Ubiquitously expressed (at protein level). PTM: In vitro, phosphorylated by PRKCZ, CK2 and SRC. SIMILARITY: Belongs to the actin-binding proteins ADF family. Twinfilin subfamily. SIMILARITY: Contains 2 ADF-H domains. WEB RESOURCE: Name=Protein Spotlight; Note=Molecular embrace - Issue 73 of August 2006; URL="http://web.expasy.org/spotlight/back_issues/sptlt073.shtml";
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on Q6IBS0
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.