blastp_kegg |
lcl|gmx:100775459
|
1 |
189 |
+ |
189 |
Gaps:38 |
96.28 |
215 |
73.91 |
2e-89 |
vacuolar protein sorting-associated protein 20 homolog 2-like
|
blastp_kegg |
lcl|sly:101250100
|
1 |
183 |
+ |
183 |
Gaps:31 |
91.63 |
227 |
71.15 |
2e-89 |
vacuolar protein sorting-associated protein 20 homolog 2-like
|
blastp_kegg |
lcl|gmx:100820408
|
1 |
189 |
+ |
189 |
Gaps:38 |
96.28 |
215 |
73.43 |
5e-89 |
vacuolar protein sorting-associated protein 20 homolog 2-like
|
blastp_kegg |
lcl|sot:102602334
|
1 |
186 |
+ |
186 |
Gaps:32 |
93.39 |
227 |
70.28 |
3e-88 |
vacuolar protein sorting-associated protein 20 homolog 2-like
|
blastp_kegg |
lcl|pvu:PHAVU_009G154500g
|
1 |
189 |
+ |
189 |
Gaps:38 |
96.28 |
215 |
71.50 |
2e-87 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0007s04580g
|
1 |
186 |
+ |
186 |
Gaps:36 |
92.79 |
222 |
72.33 |
1e-86 |
POPTRDRAFT_802672 HISTIDINOL DEHYDROGENASE family protein
|
blastp_kegg |
lcl|cam:101495680
|
1 |
189 |
+ |
189 |
Gaps:38 |
96.28 |
215 |
71.01 |
2e-86 |
vacuolar protein sorting-associated protein 20 homolog 2-like
|
blastp_kegg |
lcl|ath:AT5G09260
|
1 |
191 |
+ |
191 |
Gaps:31 |
97.22 |
216 |
70.48 |
1e-85 |
VPS20.2 vacuolar protein sorting-associated protein 20-2
|
blastp_kegg |
lcl|pop:POPTR_0005s06870g
|
1 |
191 |
+ |
191 |
Gaps:27 |
97.30 |
222 |
68.98 |
2e-85 |
POPTRDRAFT_558455 HISTIDINOL DEHYDROGENASE family protein
|
blastp_kegg |
lcl|mtr:MTR_3g096680
|
1 |
191 |
+ |
191 |
Gaps:30 |
97.24 |
217 |
68.25 |
2e-85 |
Vacuolar protein sorting-associated protein-like protein
|
blastp_uniprot_sprot |
sp|Q9FY89|VP202_ARATH
|
1 |
191 |
+ |
191 |
Gaps:31 |
97.22 |
216 |
70.48 |
5e-87 |
Vacuolar protein sorting-associated protein 20 homolog 2 OS Arabidopsis thaliana GN VPS20.2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8GXN6|VP201_ARATH
|
1 |
191 |
+ |
191 |
Gaps:28 |
97.26 |
219 |
64.32 |
1e-79 |
Vacuolar protein sorting-associated protein 20 homolog 1 OS Arabidopsis thaliana GN VPS20.1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q54KZ4|CHMP6_DICDI
|
1 |
136 |
+ |
136 |
Gaps:12 |
63.30 |
218 |
47.10 |
2e-26 |
Charged multivesicular body protein 6 OS Dictyostelium discoideum GN chmp6 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q5ZL55|CHMP6_CHICK
|
1 |
135 |
+ |
135 |
Gaps:2 |
68.50 |
200 |
37.96 |
1e-24 |
Charged multivesicular body protein 6 OS Gallus gallus GN CHMP6 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|P0C0A3|CHMP6_MOUSE
|
1 |
156 |
+ |
156 |
Gaps:28 |
92.00 |
200 |
33.70 |
1e-23 |
Charged multivesicular body protein 6 OS Mus musculus GN Chmp6 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q96FZ7|CHMP6_HUMAN
|
1 |
135 |
+ |
135 |
Gaps:2 |
68.16 |
201 |
38.69 |
2e-23 |
Charged multivesicular body protein 6 OS Homo sapiens GN CHMP6 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q5R861|CHMP6_PONAB
|
1 |
135 |
+ |
135 |
Gaps:2 |
68.16 |
201 |
38.69 |
2e-23 |
Charged multivesicular body protein 6 OS Pongo abelii GN CHMP6 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q503V0|CHMP6_DANRE
|
1 |
135 |
+ |
135 |
Gaps:2 |
66.50 |
206 |
43.07 |
6e-21 |
Charged multivesicular body protein 6 OS Danio rerio GN chmp6 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q6GMA4|CHM6A_XENLA
|
1 |
135 |
+ |
135 |
Gaps:2 |
68.50 |
200 |
40.15 |
1e-20 |
Charged multivesicular body protein 6-A OS Xenopus laevis GN chmp6-a PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q6NU11|CHM6B_XENLA
|
1 |
135 |
+ |
135 |
Gaps:2 |
68.50 |
200 |
40.15 |
1e-19 |
Charged multivesicular body protein 6-B OS Xenopus laevis GN chmp6-b PE 2 SV 3
|
rpsblast_cdd |
gnl|CDD|146145
|
16 |
138 |
+ |
123 |
none |
72.78 |
169 |
33.33 |
4e-23 |
pfam03357 Snf7 Snf7. This family of proteins are involved in protein sorting and transport from the endosome to the vacuole/lysosome in eukaryotic cells. Vacuoles/lysosomes play an important role in the degradation of both lipids and cellular proteins. In order to perform this degradative function vacuoles/lysosomes contain numerous hydrolases which have been transported in the form of inactive precursors via the biosynthetic pathway and are proteolytically activated upon delivery to the vacuole/lysosome. The delivery of transmembrane proteins such as activated cell surface receptors to the lumen of the vacuole/lysosome either for degradation/downregulation or in the case of hydrolases for proper localisation requires the formation of multivesicular bodies (MVBs). These late endosomal structures are formed by invaginating and budding of the limiting membrane into the lumen of the compartment. During this process a subset of the endosomal membrane proteins is sorted into the forming vesicles. Mature MVBs fuse with the vacuole/lysosome thereby releasing cargo containing vesicles into its hydrolytic lumen for degradation. Endosomal proteins that are not sorted into the intralumenal MVB vesicles are either recycled back to the plasma membrane or Golgi complex or remain in the limiting membrane of the MVB and are thereby transported to the limiting membrane of the vacuole/lysosome as a consequence of fusion. Therefore the MVB sorting pathway plays a critical role in the decision between recycling and degradation of membrane proteins. A few archaeal sequences are also present within this family.
|
rpsblast_kog |
gnl|CDD|38121
|
1 |
136 |
+ |
136 |
none |
65.07 |
209 |
59.56 |
4e-39 |
KOG2910 KOG2910 KOG2910 Uncharacterized conserved protein predicted to be involved in protein sorting [General function prediction only].
|
rpsblast_kog |
gnl|CDD|38122
|
10 |
163 |
+ |
154 |
Gaps:2 |
35.08 |
439 |
29.22 |
1e-10 |
KOG2911 KOG2911 KOG2911 Uncharacterized conserved protein [Function unknown].
|
rpsblast_kog |
gnl|CDD|36869
|
7 |
133 |
+ |
127 |
none |
57.47 |
221 |
30.71 |
4e-10 |
KOG1656 KOG1656 KOG1656 Protein involved in glucose derepression and pre-vacuolar endosome protein sorting [Intracellular trafficking secretion and vesicular transport].
|