Human Gene LTBR (ENST00000228918.9_10) from GENCODE V47lift37
Description: Receptor for the heterotrimeric lymphotoxin containing LTA and LTB, and for TNFS14/LIGHT. Promotes apoptosis via TRAF3 and TRAF5. May play a role in the development of lymphoid organs. (from UniProt P36941) Gencode Transcript: ENST00000228918.9_10 Gencode Gene: ENSG00000111321.11_15 Transcript (Including UTRs) Position: hg19 chr12:6,493,328-6,500,732 Size: 7,405 Total Exon Count: 10 Strand: + Coding Region Position: hg19 chr12:6,493,525-6,500,103 Size: 6,579 Coding Exon Count: 10
ID:TNR3_HUMAN DESCRIPTION: RecName: Full=Tumor necrosis factor receptor superfamily member 3; AltName: Full=Lymphotoxin-beta receptor; AltName: Full=Tumor necrosis factor C receptor; AltName: Full=Tumor necrosis factor receptor 2-related protein; AltName: Full=Tumor necrosis factor receptor type III; Short=TNF-RIII; Short=TNFR-III; Flags: Precursor; FUNCTION: Receptor for the heterotrimeric lymphotoxin containing LTA and LTB, and for TNFS14/LIGHT. Promotes apoptosis via TRAF3 and TRAF5. May play a role in the development of lymphoid organs. SUBUNIT: Self-associates. Associates with TRAF3, TRAF4 and TRAF5. Interacts with HCV core protein. INTERACTION: Self; NbExp=2; IntAct=EBI-3509981, EBI-3509981; Q15326:ZMYND11; NbExp=5; IntAct=EBI-3509981, EBI-2799565; SUBCELLULAR LOCATION: Membrane; Single-pass type I membrane protein. SIMILARITY: Contains 4 TNFR-Cys repeats.
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 P36941
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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.