ID:CAND1_HUMAN DESCRIPTION: RecName: Full=Cullin-associated NEDD8-dissociated protein 1; AltName: Full=Cullin-associated and neddylation-dissociated protein 1; AltName: Full=TBP-interacting protein of 120 kDa A; Short=TBP-interacting protein 120A; AltName: Full=p120 CAND1; FUNCTION: Enhances transcription from various types of promoters (By similarity). Regulatory protein that interferes with the assembly of the SCF (SKP1-CUL1-F-box protein) ubiquitin ligase complex and thereby down-regulates ubiquitination of target proteins. Prevents neddylation of CUL1 by physically blocking access to the neddylation site. Disrupts interactions between CUL1 and SKP1 and between CUL1 and F-box proteins. SUBUNIT: Binds TBP (By similarity). Part of a complex that contains CUL1 and RBX1. Binds unneddylated CUL1, but cannot bind CUL1 once it has been neddylated. Binds CUL2, CUL3, CUL4A, CUL4B and CUL5. INTERACTION: Q13616:CUL1; NbExp=18; IntAct=EBI-456077, EBI-359390; Q13617:CUL2; NbExp=3; IntAct=EBI-456077, EBI-456179; Q13618:CUL3; NbExp=2; IntAct=EBI-456077, EBI-456129; Q13619:CUL4A; NbExp=3; IntAct=EBI-456077, EBI-456106; Q13620:CUL4B; NbExp=3; IntAct=EBI-456077, EBI-456067; SUBCELLULAR LOCATION: Nucleus (By similarity). SIMILARITY: Belongs to the CAND family. SIMILARITY: Contains 27 HEAT repeats. SEQUENCE CAUTION: Sequence=BAA74852.2; Type=Erroneous initiation; Sequence=BAB55090.1; Type=Erroneous initiation;
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 Q86VP6
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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.