ID:DHRS3_HUMAN DESCRIPTION: RecName: Full=Short-chain dehydrogenase/reductase 3; EC=1.1.1.300; AltName: Full=DD83.1; AltName: Full=Retinal short-chain dehydrogenase/reductase 1; Short=retSDR1; FUNCTION: Catalyzes the reduction of all-trans-retinal to all- trans-retinol in the presence of NADPH. CATALYTIC ACTIVITY: All-trans-retinol + NADP(+) = all-trans- retinal + NADPH. SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein (Potential). TISSUE SPECIFICITY: Widely expressed with highest levels found in heart, placenta, lung, liver, kidney, pancreas, thyroid, testis, stomach, trachea and spinal cord. Lower levels found in skeletal muscle, intestine and lymph node. No expression detected in brain. In the retina, expressed in cone but not rod outer segments. INDUCTION: By retinoic acid. MISCELLANEOUS: Located in a region of chromosome 1 which is often deleted in aggressive neuroblastoma tumors. SIMILARITY: Belongs to the short-chain dehydrogenases/reductases (SDR) family. SEQUENCE CAUTION: Sequence=AAQ88460.1; Type=Frameshift; Positions=15;
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 O75911
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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.