ID:CCND3_HUMAN DESCRIPTION: RecName: Full=G1/S-specific cyclin-D3; FUNCTION: Regulatory component of the cyclin D3-CDK4 (DC) complex that phosphorylates and inhibits members of the retinoblastoma (RB) protein family including RB1 and regulates the cell-cycle during G(1)/S transition. Phosphorylation of RB1 allows dissociation of the transcription factor E2F from the RB/E2F complex and the subsequent transcription of E2F target genes which are responsible for the progression through the G(1) phase. Hypophosphorylates RB1 in early G(1) phase. Cyclin D-CDK4 complexes are major integrators of various mitogenenic and antimitogenic signals. Also substrate for SMAD3, phosphorylating SMAD3 in a cell-cycle-dependent manner and repressing its transcriptional activity. Component of the ternary complex, cyclin D3/CDK4/CDKN1B, required for nuclear translocation and activity of the cyclin D-CDK4 complex. SUBUNIT: Interacts with the CDK4 and CDK6 protein kinases to form a serine/threonine kinase holoenzyme complex. The cyclin subunit imparts substrate specificity to the complex. Interacts with ATF5. Interacts with EIF3K. Component of the ternary complex cyclin D/CDK4/CDKN1B required for nuclear translocation and modulation of CDK4-mediated kinase activity. Can form similar complexes with either CDKN1A or CDKN2A. INTERACTION: O94921:CDK14; NbExp=5; IntAct=EBI-375013, EBI-1043945; P11802:CDK4; NbExp=6; IntAct=EBI-375013, EBI-295644; Q00534:CDK6; NbExp=2; IntAct=EBI-375013, EBI-295663; P38936:CDKN1A; NbExp=3; IntAct=EBI-375013, EBI-375077; SUBCELLULAR LOCATION: Nucleus. Cytoplasm. Membrane. Note=Cyclin D- CDK4 complexes accumulate at the nuclear membrane and are then translocated to the nucleus through interaction with KIP/CIP family members (By similarity). PTM: Polyubiquitinated by the SCF(FBXL2) complex, leading to proteasomal degradation. SIMILARITY: Belongs to the cyclin family. Cyclin D subfamily. SIMILARITY: Contains 1 cyclin N-terminal domain. WEB RESOURCE: Name=NIEHS-SNPs; URL="http://egp.gs.washington.edu/data/ccnd3/";
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 P30281
Front
Top
Side
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.
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.
Gene Ontology (GO) Annotations with Structured Vocabulary
Molecular Function: GO:0004693 cyclin-dependent protein serine/threonine kinase activity GO:0005515 protein binding GO:0019901 protein kinase binding
Biological Process: GO:0000122 negative regulation of transcription from RNA polymerase II promoter GO:0001934 positive regulation of protein phosphorylation GO:0007049 cell cycle GO:0007165 signal transduction GO:0042098 T cell proliferation GO:0042127 regulation of cell proliferation GO:0045737 positive regulation of cyclin-dependent protein serine/threonine kinase activity GO:0046626 regulation of insulin receptor signaling pathway GO:0051301 cell division GO:0051726 regulation of cell cycle