| TCID | Name | Domain | Kingdom/Phylum | Protein(s) |
|---|---|---|---|---|
|
9.B.392.1.1 | Golgin of 731 aas and 1 C-terminal TMS. | Eukaryota |
Metazoa, Chordata | Golgin of Homo sapiens |
|
9.B.392.1.2 | Golgin-84 of 516 aas and one C-terminal TMS | Eukaryota |
Metazoa, Arthropoda | Golgin-84 of Drosophila melanogaster (fruit fly)
|
|
9.B.392.1.3 | Uncharacterized protein of 554 aas and one C-terminal TMS. | Eukaryota |
Discosea | UP of Acanthamoeba castellanii |
|
9.B.392.1.4 | Uncharacterized protein of 757 aas and one C-terminal TMS. | Eukaryota |
UP of Thecamonas trahens | |
|
9.B.392.1.5 | Uncharacterized protein of 542 aas and 1 C-terminal TMS | Eukaryota |
Oomycota | UP of Saprolegnia parasitica |
|
9.B.392.2.1 | Golgin-84 of 853 aas and one C-terminal TMS. | Eukaryota |
Rhodophyta | Golgin-84 of Porphyridium purpureum |
|
9.B.392.2.2 | Golgin of 707 aas and one C-terminal TMS. It is a golgi matrix protein, playing a role in tethering of vesicles to Golgi membranes and in maintaining the overall structure of the Golgi apparatus. | Eukaryota |
Viridiplantae, Streptophyta | Golgin of Arabidopsis thaliana (Mouse-ear cress) |
|
9.B.392.2.3 | Uncharacterized protein of 603 aas | Eukaryota |
Fungi, Ascomycota | UP of Exophiala dermatitidis |
|
9.B.392.3.1 | CASP C terminal putative protein of 687 aas and one C-terminal TMS. | Eukaryota |
Viridiplantae, Streptophyta | Putative protein of Oryza sativa |
|
9.B.392.3.2 | Coy1p of 679 aas and one C-terminal TMS. | Eukaryota |
Fungi, Ascomycota | Coy1p of Saccharomyces cerevisiae |
|
9.B.392.3.3 | Putative golgi membrane protein of 765 aas and 2 C-terminal TMSs. | Eukaryota |
Fungi, Ascomycota | Membrane protein of Eutypa lata |
|
9.B.392.4.1 | Uncharacterized protein of 542 aas and one C-terminal TMS. | Eukaryota |
Viridiplantae, Chlorophyta | UP of Ostreococcus tauri |
|
9.B.392.4.2 | Uncharacterized protein of 878 aas with one C-terminal TMS. | Eukaryota |
Viridiplantae, Chlorophyta | UP of Micromonas pusilla |
|
9.B.392.4.3 | Uncharacterized protein of 1104 aas and one C-terminal TMS | Eukaryota |
Viridiplantae, Chlorophyta | UP of Trebouxia sp. A1-2 |
|
9.B.392.4.4 | E3 ubiquitin-protein ligase (HUB2 of 844 aas) monoubiquitinates H2B to form H2BK143ub1 which gives a specific tag for epigenetic transcriptional activation and is a prerequisite for H3 Lys-4 methylation (H3K4me). It thereby plays a central role in histone code and gene regulation (Cao et al. 2015, Du et al. 2016). Overexpression of this C3HC4-type E3-ubiquitin ligase contributes to salinity tolerance by modulating Na+ homeostasis in rice (Kim et al. 2023). | Eukaryota |
Viridiplantae, Streptophyta | E3 ubiquitinase of Oryza sativa subsp. japonica (Rice)
|
|
9.B.392.4.5 | Vimentin (VIM) poptosis-inducing factor of 466 aas and 1 TMS near the N-terminus. It interacts with African swine fever virus pE301R as does another protein, AIFM1 (UP acc # O95831) of 613 aas with one N-terminal TMS (Shi et al. 2024). | None |
Metazoa, Chordata | Vimentin of Homo sapiens |
|
9.B.392.4.6 | Pre-lamin-A/C of 664 aas and 1 TMS. Lamins are intermediate filament proteins that assemble into a filamentous meshwork, and which constitute the major components of the nuclear lamina, a fibrous layer on the nucleoplasmic side of the inner nuclear membrane (Kovacs et al. 2023). | None |
Metazoa, Chordata | Pre-lamin-A/C of Homo sapiens |