blastp_kegg |
lcl|rcu:RCOM_0904150
|
4 |
367 |
+ |
364 |
Gaps:14 |
80.18 |
439 |
75.28 |
0.0 |
Vacuolar protein sorting protein putative
|
blastp_kegg |
lcl|csv:101213934
|
1 |
367 |
+ |
367 |
Gaps:21 |
80.64 |
439 |
74.01 |
0.0 |
vacuolar protein sorting-associated protein 36-like
|
blastp_kegg |
lcl|pmum:103331070
|
1 |
367 |
+ |
367 |
Gaps:28 |
81.22 |
442 |
74.93 |
7e-180 |
vacuolar protein sorting-associated protein 36
|
blastp_kegg |
lcl|mdm:103418492
|
1 |
361 |
+ |
361 |
Gaps:28 |
83.33 |
426 |
75.49 |
9e-180 |
vacuolar protein sorting-associated protein 36-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa005815mg
|
1 |
360 |
+ |
360 |
Gaps:28 |
79.64 |
442 |
75.85 |
1e-179 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103946125
|
1 |
368 |
+ |
368 |
Gaps:26 |
81.61 |
446 |
74.18 |
3e-179 |
vacuolar protein sorting-associated protein 36
|
blastp_kegg |
lcl|cmo:103488431
|
1 |
367 |
+ |
367 |
Gaps:19 |
80.64 |
439 |
71.75 |
2e-177 |
vacuolar protein sorting-associated protein 36
|
blastp_kegg |
lcl|fve:101313204
|
1 |
361 |
+ |
361 |
Gaps:28 |
79.95 |
444 |
73.80 |
1e-176 |
vacuolar protein sorting-associated protein 36-like
|
blastp_kegg |
lcl|pvu:PHAVU_011G187600g
|
1 |
361 |
+ |
361 |
Gaps:20 |
80.22 |
450 |
72.02 |
1e-175 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103428437
|
1 |
360 |
+ |
360 |
Gaps:32 |
96.42 |
363 |
75.43 |
7e-174 |
vacuolar protein sorting-associated protein 36-like
|
blastp_pdb |
2zme_B
|
180 |
367 |
+ |
188 |
Gaps:9 |
76.89 |
238 |
46.99 |
1e-50 |
mol:protein length:238 Vacuolar protein-sorting-associated protein 3
|
blastp_pdb |
3cuq_B
|
201 |
367 |
+ |
167 |
Gaps:9 |
74.31 |
218 |
48.15 |
1e-44 |
mol:protein length:218 Vacuolar protein-sorting-associated protein 3
|
blastp_uniprot_sprot |
sp|Q9FF81|VPS36_ARATH
|
9 |
361 |
+ |
353 |
Gaps:21 |
75.91 |
440 |
70.36 |
2e-160 |
Vacuolar protein sorting-associated protein 36 OS Arabidopsis thaliana GN VPS36 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q7ZVK4|VPS36_DANRE
|
45 |
364 |
+ |
320 |
Gaps:44 |
76.96 |
382 |
40.82 |
2e-56 |
Vacuolar protein-sorting-associated protein 36 OS Danio rerio GN vps36 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q91XD6|VPS36_MOUSE
|
47 |
367 |
+ |
321 |
Gaps:44 |
76.42 |
386 |
40.00 |
4e-55 |
Vacuolar protein-sorting-associated protein 36 OS Mus musculus GN Vps36 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q86VN1|VPS36_HUMAN
|
47 |
367 |
+ |
321 |
Gaps:44 |
76.42 |
386 |
40.00 |
1e-54 |
Vacuolar protein-sorting-associated protein 36 OS Homo sapiens GN VPS36 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P0C0A2|VPS36_RAT
|
47 |
367 |
+ |
321 |
Gaps:44 |
76.42 |
386 |
39.66 |
2e-54 |
Vacuolar protein-sorting-associated protein 36 OS Rattus norvegicus GN Vps36 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A5PK00|VPS36_BOVIN
|
48 |
367 |
+ |
320 |
Gaps:44 |
76.17 |
386 |
40.14 |
3e-54 |
Vacuolar protein-sorting-associated protein 36 OS Bos taurus GN VPS36 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6DDF4|VPS36_XENLA
|
47 |
367 |
+ |
321 |
Gaps:48 |
76.55 |
388 |
39.73 |
2e-53 |
Vacuolar protein-sorting-associated protein 36 OS Xenopus laevis GN vps36 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q54T18|VPS36_DICDI
|
180 |
367 |
+ |
188 |
Gaps:13 |
30.93 |
611 |
46.56 |
8e-41 |
Vacuolar protein-sorting-associated protein 36 OS Dictyostelium discoideum GN vps36 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9VU87|VPS36_DROME
|
45 |
356 |
+ |
312 |
Gaps:43 |
74.94 |
399 |
33.44 |
5e-36 |
Vacuolar protein-sorting-associated protein 36 OS Drosophila melanogaster GN Vps36 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O43038|VPS36_SCHPO
|
179 |
353 |
+ |
175 |
Gaps:6 |
37.04 |
467 |
24.86 |
3e-10 |
Vacuolar protein-sorting-associated protein 36 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN vps36 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|190890
|
185 |
370 |
+ |
186 |
Gaps:14 |
84.02 |
219 |
35.33 |
4e-44 |
pfam04157 EAP30 EAP30/Vps36 family. This family includes EAP30 as well as the Vps36 protein. Vps36 is involved in Golgi to endosome trafficking. EAP30 is a subunit of the ELL complex. The ELL is an 80-kDa RNA polymerase II transcription factor. ELL interacts with three other proteins to form the complex known as ELL complex. The ELL complex is capable of increasing that catalytic rate of transcription elongation but is unable to repress initiation of transcription by RNA polymerase II as is the case of ELL. EAP30 is thought to lead to the derepression of ELL's transcriptional inhibitory activity.
|
rpsblast_cdd |
gnl|CDD|204687
|
11 |
109 |
+ |
99 |
Gaps:16 |
95.70 |
93 |
37.08 |
1e-08 |
pfam11605 Vps36_ESCRT-II Vacuolar protein sorting protein 36 Vps36. Vps36 is a subunit of ESCRT-II a protein involved in driving protein sorting from endosomes to lysosomes. The GLUE domain of Vps36 allows for a tight interaction to occur between the protein and Vps28 a subunit of ESCRT-I. This interaction is critical for ubiquitinated cargo progression from early to late endosomes.
|
rpsblast_kog |
gnl|CDD|37971
|
8 |
361 |
+ |
354 |
Gaps:37 |
79.86 |
432 |
39.42 |
4e-80 |
KOG2760 KOG2760 KOG2760 Vacuolar sorting protein VPS36 [Intracellular trafficking secretion and vesicular transport].
|