blastp_kegg |
lcl|pxb:103953471
|
245 |
451 |
+ |
207 |
Gaps:7 |
52.61 |
403 |
81.60 |
1e-89 |
26S proteasome non-ATPase regulatory subunit 4 homolog
|
blastp_kegg |
lcl|gmx:100791370
|
245 |
455 |
+ |
211 |
Gaps:12 |
52.51 |
398 |
76.56 |
6e-89 |
26S proteasome non-ATPase regulatory subunit 4-like
|
blastp_kegg |
lcl|tcc:TCM_000185
|
245 |
450 |
+ |
206 |
Gaps:5 |
51.72 |
408 |
84.36 |
2e-86 |
26S proteasome non-ATPase regulatory subunit 4 isoform 1
|
blastp_kegg |
lcl|pop:POPTR_0007s09740g
|
245 |
451 |
+ |
207 |
Gaps:5 |
50.24 |
422 |
77.83 |
2e-86 |
hypothetical protein
|
blastp_kegg |
lcl|cam:101506262
|
245 |
451 |
+ |
207 |
Gaps:9 |
53.20 |
406 |
81.48 |
4e-86 |
26S proteasome non-ATPase regulatory subunit 4-like
|
blastp_kegg |
lcl|gmx:100780583
|
245 |
450 |
+ |
206 |
Gaps:5 |
52.10 |
405 |
81.04 |
1e-84 |
26S proteasome non-ATPase regulatory subunit 4 homolog
|
blastp_kegg |
lcl|gmx:100814594
|
245 |
511 |
+ |
267 |
Gaps:9 |
66.67 |
405 |
68.15 |
1e-84 |
26S proteasome non-ATPase regulatory subunit 4-like
|
blastp_kegg |
lcl|gmx:100803975
|
245 |
511 |
+ |
267 |
Gaps:9 |
66.67 |
405 |
67.04 |
2e-83 |
26S proteasome non-ATPase regulatory subunit 4-like
|
blastp_kegg |
lcl|pvu:PHAVU_003G264300g
|
245 |
450 |
+ |
206 |
Gaps:8 |
51.74 |
402 |
80.77 |
2e-83 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103967795
|
245 |
451 |
+ |
207 |
Gaps:7 |
52.74 |
402 |
82.55 |
3e-83 |
26S proteasome non-ATPase regulatory subunit 4 homolog
|
blastp_pdb |
2x5n_A
|
245 |
353 |
+ |
109 |
Gaps:7 |
58.33 |
192 |
37.50 |
5e-17 |
mol:protein length:192 26S PROTEASOME REGULATORY SUBUNIT RPN10
|
blastp_uniprot_sprot |
sp|P55034|PSMD4_ARATH
|
245 |
429 |
+ |
185 |
Gaps:8 |
48.96 |
386 |
67.72 |
1e-62 |
26S proteasome non-ATPase regulatory subunit 4 homolog OS Arabidopsis thaliana GN RPN10 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O94444|RPN10_SCHPO
|
245 |
421 |
+ |
177 |
Gaps:22 |
67.90 |
243 |
45.45 |
1e-33 |
26S proteasome regulatory subunit rpn10 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN rpn10 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q58DA0|PSMD4_BOVIN
|
249 |
396 |
+ |
148 |
Gaps:19 |
37.43 |
382 |
48.95 |
6e-29 |
26S proteasome non-ATPase regulatory subunit 4 OS Bos taurus GN PSMD4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P55036|PSMD4_HUMAN
|
249 |
396 |
+ |
148 |
Gaps:19 |
37.93 |
377 |
48.95 |
6e-29 |
26S proteasome non-ATPase regulatory subunit 4 OS Homo sapiens GN PSMD4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O35226|PSMD4_MOUSE
|
249 |
396 |
+ |
148 |
Gaps:19 |
38.03 |
376 |
48.95 |
8e-29 |
26S proteasome non-ATPase regulatory subunit 4 OS Mus musculus GN Psmd4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P38886|RPN10_YEAST
|
246 |
396 |
+ |
151 |
Gaps:8 |
58.58 |
268 |
42.68 |
4e-27 |
26S proteasome regulatory subunit RPN10 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN RPN10 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q553E0|PSMD4_DICDI
|
245 |
396 |
+ |
152 |
Gaps:25 |
39.83 |
349 |
43.17 |
1e-26 |
26S proteasome non-ATPase regulatory subunit 4 OS Dictyostelium discoideum GN psmD4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P55035|PSMD4_DROME
|
249 |
410 |
+ |
162 |
Gaps:18 |
39.90 |
396 |
47.47 |
3e-26 |
26S proteasome non-ATPase regulatory subunit 4 OS Drosophila melanogaster GN Rpn10 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|A2A3N6|PIPSL_HUMAN
|
249 |
396 |
+ |
148 |
Gaps:19 |
16.59 |
862 |
48.95 |
8e-25 |
Putative PIP5K1A and PSMD4-like protein OS Homo sapiens GN PIPSL PE 5 SV 1
|
blastp_uniprot_sprot |
sp|O17453|PSMD4_SCHMA
|
249 |
445 |
+ |
197 |
Gaps:19 |
45.71 |
420 |
35.94 |
2e-23 |
26S proteasome non-ATPase regulatory subunit 4 OS Schistosoma mansoni PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|34749
|
243 |
421 |
+ |
179 |
Gaps:22 |
68.72 |
243 |
43.11 |
1e-33 |
COG5148 RPN10 26S proteasome regulatory complex subunit RPN10/PSMD4 [Posttranslational modification protein turnover chaperones].
|
rpsblast_cdd |
gnl|CDD|29225
|
245 |
349 |
+ |
105 |
Gaps:6 |
58.29 |
187 |
50.46 |
1e-30 |
cd01452 VWA_26S_proteasome_subunit 26S proteasome plays a major role in eukaryotic protein breakdown especially for ubiquitin-tagged proteins. It is an ATP-dependent protease responsible for the bulk of non-lysosomal proteolysis in eukaryotes often using covalent modification of proteins by ubiquitylation. It consists of a 20S proteolytic core particle (CP) and a 19S regulatory particle (RP). The CP is an ATP independent peptidase consisting of hydrolyzing activities. One or both ends of CP carry the RP that confers both ubiquitin and ATP dependence to the 26S proteosome. The RP's proposed functions include recognition of substrates and translocation of these to CP for proteolysis. The RP can dissociate into a stable lid and base subcomplexes. The base is composed of three non-ATPase subunits (Rpn 1 2 and 10). A single residue in the vWA domain of Rpn10 has been implicated to be responsible for stabilizing the lid-base association..
|
rpsblast_cdd |
gnl|CDD|182059
|
40 |
103 |
+ |
64 |
Gaps:4 |
4.80 |
1250 |
45.00 |
3e-07 |
PRK09752 PRK09752 adhesin Provisional.
|
rpsblast_kog |
gnl|CDD|38095
|
243 |
430 |
+ |
188 |
Gaps:17 |
70.66 |
259 |
50.27 |
1e-47 |
KOG2884 KOG2884 KOG2884 26S proteasome regulatory complex subunit RPN10/PSMD4 [Posttranslational modification protein turnover chaperones].
|
rpsblast_kog |
gnl|CDD|36570
|
446 |
584 |
+ |
139 |
Gaps:7 |
14.85 |
889 |
34.09 |
2e-19 |
KOG1356 KOG1356 KOG1356 Putative transcription factor 5qNCA contains JmjC domain [Transcription].
|