ID:LC7L3_HUMAN DESCRIPTION: RecName: Full=Luc7-like protein 3; AltName: Full=Cisplatin resistance-associated-overexpressed protein; AltName: Full=Luc7A; AltName: Full=Okadaic acid-inducible phosphoprotein OA48-18; AltName: Full=cAMP regulatory element-associated protein 1; Short=CRE-associated protein 1; Short=CREAP-1; FUNCTION: Binds cAMP regulatory element DNA sequence. May play a role in RNA splicing. SUBUNIT: May interact with SFRS1 and form homodimers. Interacts with JMJD6 and RBM25. Interacts with RSRC1 (via Arg/Ser-rich domain). INTERACTION: Q15287:RNPS1; NbExp=1; IntAct=EBI-395671, EBI-395959; SUBCELLULAR LOCATION: Nucleus speckle. Note=The subnuclear localization is affected by cisplatin. TISSUE SPECIFICITY: Widely expressed. Highest levels in heart, brain, pancreas, thymus, ovary, small intestine and peripheral blood leukocytes, as well as cerebellum, putamen and pituitary gland. Lowest levels in lung, liver and kidney. Also expressed in fetal tissues, including brain, heart, kidney, thymus and lung. PTM: Phosphorylated in vitro by SRPK1, SRPK2 and CLK1. Phosphorylated upon DNA damage, probably by ATM or ATR. SIMILARITY: Belongs to the Luc7 family. SEQUENCE CAUTION: Sequence=AAC79807.1; Type=Erroneous translation; Note=Erroneous CDS prediction;
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 O95232
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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.