Human Gene ADAM2 (ENST00000521880.5) from GENCODE V44
Description: Homo sapiens ADAM metallopeptidase domain 2 (ADAM2), transcript variant 3, mRNA. (from RefSeq NM_001278114) RefSeq Summary (NM_001278114): This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded protein is a subunit of an integral sperm membrane glycoprotein called fertilin, which plays an important role in sperm-egg interactions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]. Gencode Transcript: ENST00000521880.5 Gencode Gene: ENSG00000104755.16 Transcript (Including UTRs) Position: hg38 chr8:39,744,031-39,838,227 Size: 94,197 Total Exon Count: 20 Strand: - Coding Region Position: hg38 chr8:39,744,860-39,838,185 Size: 93,326 Coding Exon Count: 19
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.
Pfam Domains: PF08516 - ADAM cysteine-rich PF00200 - Disintegrin PF01562 - Reprolysin family propeptide PF01421 - Reprolysin (M12B) family zinc metalloprotease
ModBase Predicted Comparative 3D Structure on B4DWY7
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.