ID:ACD11_HUMAN DESCRIPTION: RecName: Full=Acyl-CoA dehydrogenase family member 11; Short=ACAD-11; EC=1.3.99.-; FUNCTION: Acyl-CoA dehydrogenase, that exhibits maximal activity towards saturated C22-CoA. CATALYTIC ACTIVITY: Acyl-CoA + acceptor = 2,3-dehydroacyl-CoA + reduced acceptor. COFACTOR: FAD. SUBUNIT: Homodimer. SUBCELLULAR LOCATION: Peroxisome (By similarity). Mitochondrion. Note=Has been detected associated with mitochondrial membrane, but no matrix, in kidney and cerebellum, as well as in a neuroblastoma cell line, but not in skin fibroblasts, where it is observed in cytoplasmic vesicles (PubMed:21237683). No mitochondrial targeting signals could be predicted for any known isoform, including a putative isoform starting at Met-316. TISSUE SPECIFICITY: Widely expressed with highest levels in brain followed by liver, heart and kidney. SIMILARITY: Belongs to the acyl-CoA dehydrogenase family. SEQUENCE CAUTION: Sequence=BAB14158.1; Type=Erroneous initiation; Note=Translation N-terminally extended;
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 Q709F0
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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.