blastp_kegg |
lcl|mdm:103413472
|
2 |
1005 |
+ |
1004 |
Gaps:148 |
85.06 |
1272 |
45.56 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pxb:103935009
|
2 |
1005 |
+ |
1004 |
Gaps:149 |
87.41 |
1239 |
44.97 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|cic:CICLE_v10023938mg
|
2 |
1055 |
+ |
1054 |
Gaps:175 |
90.35 |
1254 |
43.42 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa022091mg
|
2 |
1019 |
+ |
1018 |
Gaps:182 |
91.58 |
1105 |
46.34 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cic:CICLE_v10024735mg
|
2 |
1055 |
+ |
1054 |
Gaps:180 |
94.87 |
1189 |
40.87 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103939877
|
2 |
806 |
+ |
805 |
Gaps:118 |
68.65 |
1292 |
46.67 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pxb:103939875
|
2 |
806 |
+ |
805 |
Gaps:118 |
53.34 |
1663 |
46.67 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|pxb:103956565
|
2 |
806 |
+ |
805 |
Gaps:118 |
53.31 |
1664 |
47.13 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|vvi:100256761
|
2 |
1073 |
+ |
1072 |
Gaps:197 |
93.20 |
1250 |
41.72 |
0.0 |
TMV resistance protein N-like
|
blastp_kegg |
lcl|cit:102620345
|
2 |
1006 |
+ |
1005 |
Gaps:148 |
94.84 |
1144 |
41.47 |
0.0 |
TMV resistance protein N-like
|
blastp_pdb |
3ozi_B
|
2 |
77 |
+ |
76 |
Gaps:1 |
37.75 |
204 |
49.35 |
9e-16 |
mol:protein length:204 L6tr
|
blastp_pdb |
3ozi_A
|
2 |
77 |
+ |
76 |
Gaps:1 |
37.75 |
204 |
49.35 |
9e-16 |
mol:protein length:204 L6tr
|
blastp_pdb |
3jrn_A
|
2 |
75 |
+ |
74 |
none |
42.05 |
176 |
45.95 |
3e-14 |
mol:protein length:176 AT1G72930 protein
|
blastp_uniprot_sprot |
sp|Q40392|TMVRN_NICGU
|
3 |
890 |
+ |
888 |
Gaps:150 |
83.57 |
1144 |
35.77 |
1e-141 |
TMV resistance protein N OS Nicotiana glutinosa GN N PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O82500|Y4117_ARATH
|
3 |
893 |
+ |
891 |
Gaps:173 |
77.90 |
1095 |
35.99 |
4e-102 |
Putative disease resistance protein At4g11170 OS Arabidopsis thaliana GN At4g11170 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O23530|SNC1_ARATH
|
2 |
818 |
+ |
817 |
Gaps:263 |
74.10 |
1301 |
38.69 |
7e-91 |
Protein SUPPRESSOR OF npr1-1 CONSTITUTIVE 1 OS Arabidopsis thaliana GN SNC1 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9SZ67|WRK19_ARATH
|
5 |
742 |
+ |
738 |
Gaps:121 |
39.21 |
1895 |
32.44 |
5e-78 |
Probable WRKY transcription factor 19 OS Arabidopsis thaliana GN WRKY19 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FL92|WRK16_ARATH
|
8 |
830 |
+ |
823 |
Gaps:168 |
57.22 |
1372 |
32.23 |
1e-69 |
Probable WRKY transcription factor 16 OS Arabidopsis thaliana GN WRKY16 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FH83|WRK52_ARATH
|
8 |
830 |
+ |
823 |
Gaps:179 |
71.97 |
1288 |
32.36 |
2e-66 |
Probable WRKY transcription factor 52 OS Arabidopsis thaliana GN WRKY52 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q9FKN7|DAR4_ARATH
|
11 |
839 |
+ |
829 |
Gaps:158 |
49.66 |
1613 |
30.96 |
2e-60 |
Protein DA1-related 4 OS Arabidopsis thaliana GN DAR4 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|P0CB16|DRL25_ARATH
|
458 |
805 |
+ |
348 |
Gaps:118 |
27.56 |
1201 |
46.83 |
1e-14 |
Putative disease resistance protein At4g19050 OS Arabidopsis thaliana GN At4g19050 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9SSN3|TIR_ARATH
|
2 |
75 |
+ |
74 |
none |
42.05 |
176 |
45.95 |
1e-13 |
Toll/interleukin-1 receptor-like protein OS Arabidopsis thaliana GN TIR PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FHE9|P2A08_ARATH
|
4 |
79 |
+ |
76 |
none |
21.47 |
354 |
44.74 |
3e-12 |
Protein PHLOEM PROTEIN 2-LIKE A8 OS Arabidopsis thaliana GN PP2A8 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|178749
|
2 |
876 |
+ |
875 |
Gaps:161 |
79.97 |
1153 |
34.38 |
1e-110 |
PLN03210 PLN03210 Resistant to P. syringae 6 Provisional.
|
rpsblast_cdd |
gnl|CDD|201512
|
125 |
332 |
+ |
208 |
Gaps:53 |
88.77 |
285 |
29.64 |
2e-23 |
pfam00931 NB-ARC NB-ARC domain.
|
rpsblast_cdd |
gnl|CDD|201870
|
4 |
78 |
+ |
75 |
Gaps:2 |
57.04 |
135 |
57.14 |
6e-20 |
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
|
4 |
75 |
+ |
72 |
Gaps:1 |
52.14 |
140 |
47.95 |
7e-19 |
smart00255 TIR Toll - interleukin 1 - resistance.
|
rpsblast_cdd |
gnl|CDD|34495
|
512 |
798 |
+ |
287 |
Gaps:17 |
74.11 |
394 |
23.97 |
7e-08 |
COG4886 COG4886 Leucine-rich repeat (LRR) protein [Function unknown].
|
rpsblast_kog |
gnl|CDD|39857
|
98 |
799 |
+ |
702 |
Gaps:170 |
78.74 |
889 |
26.29 |
4e-31 |
KOG4658 KOG4658 KOG4658 Apoptotic ATPase [Signal transduction mechanisms].
|
rpsblast_kog |
gnl|CDD|35838
|
505 |
799 |
+ |
295 |
Gaps:81 |
42.83 |
1081 |
34.13 |
2e-10 |
KOG0618 KOG0618 KOG0618 Serine/threonine phosphatase 2C containing leucine-rich repeats similar to SCN circadian oscillatory protein (SCOP) [Signal transduction mechanisms].
|