blastp_kegg |
lcl|pper:PRUPE_ppa025229mg
|
20 |
624 |
+ |
605 |
Gaps:24 |
71.63 |
853 |
49.59 |
3e-174 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa000577mg
|
12 |
617 |
+ |
606 |
Gaps:23 |
56.11 |
1089 |
48.77 |
1e-173 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa020421mg
|
14 |
617 |
+ |
604 |
Gaps:15 |
68.52 |
880 |
49.25 |
3e-172 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa022914mg
|
20 |
624 |
+ |
605 |
Gaps:24 |
69.99 |
873 |
49.43 |
9e-172 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103435656
|
20 |
617 |
+ |
598 |
Gaps:16 |
95.22 |
628 |
47.66 |
4e-170 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pmum:103335496
|
20 |
624 |
+ |
605 |
Gaps:20 |
56.03 |
1087 |
49.59 |
1e-169 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pmum:103335518
|
20 |
617 |
+ |
598 |
Gaps:23 |
55.02 |
1096 |
48.59 |
2e-169 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pxb:103928023
|
1 |
625 |
+ |
625 |
Gaps:20 |
61.11 |
1026 |
47.37 |
8e-169 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa021703mg
|
20 |
617 |
+ |
598 |
Gaps:19 |
54.62 |
1104 |
49.59 |
3e-168 |
hypothetical protein
|
blastp_kegg |
lcl|cam:101491438
|
12 |
624 |
+ |
613 |
Gaps:18 |
72.12 |
850 |
49.59 |
3e-168 |
TMV resistance protein N-like
|
blastp_pdb |
3ozi_B
|
10 |
178 |
+ |
169 |
Gaps:4 |
83.82 |
204 |
42.69 |
1e-34 |
mol:protein length:204 L6tr
|
blastp_pdb |
3ozi_A
|
10 |
178 |
+ |
169 |
Gaps:4 |
83.82 |
204 |
42.69 |
1e-34 |
mol:protein length:204 L6tr
|
blastp_pdb |
3jrn_A
|
18 |
188 |
+ |
171 |
Gaps:5 |
96.59 |
176 |
46.47 |
4e-34 |
mol:protein length:176 AT1G72930 protein
|
blastp_uniprot_sprot |
sp|Q40392|TMVRN_NICGU
|
20 |
618 |
+ |
599 |
Gaps:35 |
52.27 |
1144 |
40.64 |
4e-117 |
TMV resistance protein N OS Nicotiana glutinosa GN N PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O82500|Y4117_ARATH
|
12 |
618 |
+ |
607 |
Gaps:38 |
56.53 |
1095 |
36.51 |
1e-104 |
Putative disease resistance protein At4g11170 OS Arabidopsis thaliana GN At4g11170 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O23530|SNC1_ARATH
|
19 |
618 |
+ |
600 |
Gaps:31 |
45.58 |
1301 |
35.58 |
1e-96 |
Protein SUPPRESSOR OF npr1-1 CONSTITUTIVE 1 OS Arabidopsis thaliana GN SNC1 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9FL92|WRK16_ARATH
|
29 |
618 |
+ |
590 |
Gaps:94 |
48.18 |
1372 |
32.38 |
2e-59 |
Probable WRKY transcription factor 16 OS Arabidopsis thaliana GN WRKY16 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SZ67|WRK19_ARATH
|
7 |
618 |
+ |
612 |
Gaps:78 |
30.92 |
1895 |
33.28 |
5e-54 |
Probable WRKY transcription factor 19 OS Arabidopsis thaliana GN WRKY19 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FH83|WRK52_ARATH
|
29 |
618 |
+ |
590 |
Gaps:85 |
44.49 |
1288 |
31.76 |
9e-48 |
Probable WRKY transcription factor 52 OS Arabidopsis thaliana GN WRKY52 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q9FKN7|DAR4_ARATH
|
29 |
617 |
+ |
589 |
Gaps:75 |
35.96 |
1613 |
30.00 |
8e-46 |
Protein DA1-related 4 OS Arabidopsis thaliana GN DAR4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9SSN3|TIR_ARATH
|
18 |
188 |
+ |
171 |
Gaps:5 |
96.59 |
176 |
46.47 |
1e-33 |
Toll/interleukin-1 receptor-like protein OS Arabidopsis thaliana GN TIR PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FHE9|P2A08_ARATH
|
22 |
181 |
+ |
160 |
Gaps:5 |
46.05 |
354 |
37.42 |
1e-23 |
Protein PHLOEM PROTEIN 2-LIKE A8 OS Arabidopsis thaliana GN PP2A8 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SYC9|VAP14_ARATH
|
19 |
158 |
+ |
140 |
Gaps:3 |
24.69 |
571 |
40.43 |
2e-21 |
Vesicle-associated protein 1-4 OS Arabidopsis thaliana GN PVA14 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|178749
|
10 |
618 |
+ |
609 |
Gaps:39 |
53.95 |
1153 |
34.24 |
1e-96 |
PLN03210 PLN03210 Resistant to P. syringae 6 Provisional.
|
rpsblast_cdd |
gnl|CDD|201870
|
22 |
150 |
+ |
129 |
Gaps:5 |
99.26 |
135 |
47.76 |
2e-33 |
pfam01582 TIR TIR domain. The Toll/interleukin-1 receptor (TIR) homology domain is an intracellular signalling domain found in MyD88 interleukin 1 receptor and the Toll receptor. It contains three highly-conserved regions and mediates protein-protein interactions between the Toll-like receptors (TLRs) and signal-transduction components. TIR-like motifs are also found in plant proteins thought to be involved in resistance to disease. When activated TIR domains recruit cytoplasmic adaptor proteins MyD88 and TOLLIP (Toll interacting protein). In turn these associate with various kinases to set off signalling cascades.
|
rpsblast_cdd |
gnl|CDD|197607
|
19 |
150 |
+ |
132 |
Gaps:4 |
95.71 |
140 |
46.27 |
1e-31 |
smart00255 TIR Toll - interleukin 1 - resistance.
|
rpsblast_cdd |
gnl|CDD|201512
|
197 |
459 |
+ |
263 |
Gaps:19 |
92.63 |
285 |
26.52 |
3e-25 |
pfam00931 NB-ARC NB-ARC domain.
|
rpsblast_cdd |
gnl|CDD|178736
|
11 |
158 |
+ |
148 |
Gaps:15 |
72.19 |
187 |
31.85 |
2e-11 |
PLN03194 PLN03194 putative disease resistance protein Provisional.
|
rpsblast_cdd |
gnl|CDD|205852
|
22 |
119 |
+ |
98 |
Gaps:7 |
89.22 |
102 |
27.47 |
2e-10 |
pfam13676 TIR_2 TIR domain. This is a family of bacterial Toll-like receptors.
|
rpsblast_kog |
gnl|CDD|39857
|
171 |
612 |
+ |
442 |
Gaps:97 |
55.46 |
889 |
23.53 |
2e-21 |
KOG4658 KOG4658 KOG4658 Apoptotic ATPase [Signal transduction mechanisms].
|