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This orthogroup contains 408 genes from 145 species. The functional annotation below is the consensus of the family's member genes — each term is reported with the number of member genes that carry it.
Support counts the member genes carrying the term. % of genes is that count over all 408 members — the strict reading of “the whole family agrees”. % annotated is the same count over only those members for which this database has a prediction of that type, which shows how uniform the evidence is where evidence exists.
| Source | Term | Name / description | Support | % of genes | % annotated | Consistency |
|---|---|---|---|---|---|---|
| PANTHER | PTHR11482 | ARGININE/DIAMINOPIMELATE/ORNITHINE DECARBOXYLASE | 338 / 408 | 82.8% | 98.8% of 342 | ≥80% support |
| GO | GO:0003824 Molecular Function | catalytic activity | 344 / 408 | 84.3% | 100.0% of 344 | ≥80% support |
| GO | GO:0006596 Biological Process | polyamine biosynthetic process | 340 / 408 | 83.3% | 98.8% of 344 | ≥80% support |
| GO | GO:0004586 Molecular Function | ornithine decarboxylase activity | 338 / 408 | 82.8% | 98.3% of 344 | ≥80% support |
| GO | GO:0005737 Cellular Component | cytoplasm | 338 / 408 | 82.8% | 98.3% of 344 | ≥80% support |
| GO | GO:0033387 Biological Process | putrescine biosynthetic process from ornithine | 338 / 408 | 82.8% | 98.3% of 344 | ≥80% support |
| Pfam | PF02784 | Orn_Arg_deC_N — Pyridoxal-dependent decarboxylase, pyridoxal binding domain | 320 / 408 | 78.4% | 94.1% of 340 | ≥50% support |
| Pfam | PF00278 | Orn_DAP_Arg_deC — Pyridoxal-dependent decarboxylase, C-terminal sheet domain | 303 / 408 | 74.3% | 89.1% of 340 | ≥50% support |
| KEGG | K01581 | E4.1.1.17, ODC1, speC, speF — Efferocytosis | 251 / 408 | 61.5% | 96.5% of 260 | ≥50% support |
Column guide: Top NCBI-NR hit and Top UniProt hit are the closest characterised sequences found by homology search — they are not identifiers of the CnidoSite gene itself. Where a species has no Swiss-Prot hit above threshold the UniProt column is shown as –. Click a gene ID for its full annotation page.
