ID:RBM19_HUMAN DESCRIPTION: RecName: Full=Probable RNA-binding protein 19; AltName: Full=RNA-binding motif protein 19; FUNCTION: Plays a role in embryo pre-implantation development (By similarity). SUBCELLULAR LOCATION: Nucleus, nucleolus. Nucleus, nucleoplasm (By similarity). Cytoplasm (By similarity). Chromosome (By similarity). Note=In discrete foci distributed throughout the cytoplasm and nucleoplasm during the 4 to 8 cell stages and the morula stage, but not in the periphery of the nucleolar precursor body (NPB). During blastocyst development, becomes increasingly localized to the nucleolus and less to the cytoplasm. At the late blastocyst stage, localized predominantly in the nucleolus. Localized in the nucleolus during interphase and to the perichromosomal sheath during mitosis. Does not colocalize in the cytoplasm with GW182 in P-bodies. May translocate to the nucleolus upon early embryonic development (By similarity). Colocalizes with NPM1 during interphase. By late prophase, metaphase, anaphase and telophase, associates with the chromosome periphery. By telophase localizes to NPB. TISSUE SPECIFICITY: Expressed in the crypts of Lieberkuhn of the intestine and in intestinal neoplasia (at protein level). SIMILARITY: Belongs to the RRM MRD1 family. SIMILARITY: Contains 6 RRM (RNA recognition motif) domains. SEQUENCE CAUTION: Sequence=BAA31657.2; Type=Erroneous initiation; Note=Translation N-terminally shortened;
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 Q9Y4C8
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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.