< rmsk | When analyzing the data tables of this track, keep in mind that Repbase is not the same < rmsk | as the Repeatmasker sequence database and that the repeat names in the < rmsk | Repeatmasker output are not the same as the sequence names in the Repeatmasker < rmsk | database. Concretely, you can find a name such as "L1PA4" in the Repeatmasker < rmsk | output and this track, but there is not necessarily a single sequence "L1PA4" < rmsk | in the Repeatmasker database. This is because Repeatmasker creates annotations < rmsk | by joining matches to partial pieces of the database together so there is no < rmsk | 1:1 relationship between its sequence database and the annotations. To learn < rmsk | more, you can read the Repeatmasker paper, its source code or reach out to the < rmsk | Repeatmasker authors, your local expert on transposable elements or us. < rmsk |
< rmsk | 1689,1690c1676,1677 < rmsk | < rmsk | https://www.repeatmasker.org/. 1996-2010. --- > rmsk | > rmsk | http://www.repeatmasker.org. 1996-2010. 2710,2715c2697,2700 < uniprot | Features in the "UniProt Modifications" (modified residues) track are drawn in < uniprot | light green. Disulfide bonds are shown in < uniprot | dark grey. Topological domains < uniprot | in maroon and zinc finger regions in < uniprot | olive green. < uniprot | --- > uniprot | In the "UniProt Modifications" track, lipoification sites are highlighted in > uniprot | dark blue, glycosylation sites in > uniprot | dark green, and phosphorylation in > uniprot | light green.