blastp_kegg |
lcl|tcc:TCM_046868
|
19 |
406 |
+ |
388 |
Gaps:32 |
43.61 |
908 |
46.97 |
6e-103 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|vvi:100256692
|
27 |
405 |
+ |
379 |
Gaps:37 |
46.71 |
865 |
43.56 |
2e-98 |
receptor-like serine/threonine-protein kinase SD1-8-like
|
blastp_kegg |
lcl|vvi:100267572
|
27 |
408 |
+ |
382 |
Gaps:35 |
45.08 |
894 |
41.94 |
5e-92 |
receptor-like serine/threonine-protein kinase SD1-8-like
|
blastp_kegg |
lcl|vvi:100260532
|
27 |
408 |
+ |
382 |
Gaps:35 |
48.55 |
830 |
41.44 |
1e-89 |
receptor-like serine/threonine-protein kinase SD1-8-like
|
blastp_kegg |
lcl|gmx:100811148
|
15 |
406 |
+ |
392 |
Gaps:31 |
47.12 |
834 |
44.02 |
1e-89 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11300-like
|
blastp_kegg |
lcl|vvi:100246936
|
16 |
408 |
+ |
393 |
Gaps:36 |
48.43 |
958 |
42.89 |
4e-88 |
G-type lectin S-receptor-like serine/threonine-protein kinase At4g27290-like
|
blastp_kegg |
lcl|tcc:TCM_031277
|
10 |
405 |
+ |
396 |
Gaps:83 |
49.66 |
1621 |
37.27 |
3e-86 |
Serine/threonine-protein kinase receptor putative
|
blastp_kegg |
lcl|pvu:PHAVU_011G149500g
|
13 |
406 |
+ |
394 |
Gaps:46 |
50.69 |
797 |
43.32 |
7e-86 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100265866
|
21 |
405 |
+ |
385 |
Gaps:157 |
48.64 |
1988 |
35.99 |
2e-84 |
uncharacterized LOC100265866
|
blastp_kegg |
lcl|vvi:100245158
|
27 |
408 |
+ |
382 |
Gaps:116 |
52.35 |
1658 |
40.67 |
1e-83 |
uncharacterized LOC100245158
|
blastp_uniprot_sprot |
sp|O64477|Y2913_ARATH
|
5 |
409 |
+ |
405 |
Gaps:56 |
51.81 |
828 |
36.60 |
1e-69 |
G-type lectin S-receptor-like serine/threonine-protein kinase At2g19130 OS Arabidopsis thaliana GN At2g19130 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64781|Y1639_ARATH
|
8 |
406 |
+ |
399 |
Gaps:51 |
50.54 |
831 |
35.48 |
2e-62 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61390 OS Arabidopsis thaliana GN At1g61390 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SXB4|Y1130_ARATH
|
39 |
411 |
+ |
373 |
Gaps:51 |
48.78 |
820 |
34.00 |
2e-62 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11300 OS Arabidopsis thaliana GN At1g11300 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SXB3|Y1112_ARATH
|
39 |
406 |
+ |
368 |
Gaps:47 |
47.93 |
820 |
34.61 |
4e-59 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11280 OS Arabidopsis thaliana GN At1g11280 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64770|Y1649_ARATH
|
39 |
405 |
+ |
367 |
Gaps:40 |
48.13 |
804 |
33.59 |
2e-58 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61490 OS Arabidopsis thaliana GN At1g61490 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O64771|Y1148_ARATH
|
39 |
405 |
+ |
367 |
Gaps:44 |
47.84 |
809 |
35.14 |
2e-58 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61480 OS Arabidopsis thaliana GN At1g61480 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9SY95|Y1155_ARATH
|
32 |
411 |
+ |
380 |
Gaps:40 |
49.88 |
802 |
34.25 |
3e-58 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61550 OS Arabidopsis thaliana GN At1g61550 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64782|SD129_ARATH
|
8 |
411 |
+ |
404 |
Gaps:53 |
52.55 |
805 |
34.28 |
4e-58 |
G-type lectin S-receptor-like serine/threonine-protein kinase SD1-29 OS Arabidopsis thaliana GN SD129 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LPZ9|SD113_ARATH
|
28 |
411 |
+ |
384 |
Gaps:56 |
49.88 |
830 |
34.78 |
5e-58 |
G-type lectin S-receptor-like serine/threonine-protein kinase SD1-13 OS Arabidopsis thaliana GN SD113 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9SXB5|Y1135_ARATH
|
38 |
411 |
+ |
374 |
Gaps:55 |
48.90 |
820 |
32.92 |
1e-57 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11305 OS Arabidopsis thaliana GN At1g11305 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|28910
|
38 |
151 |
+ |
114 |
Gaps:4 |
98.28 |
116 |
48.25 |
5e-21 |
cd00028 B_lectin Bulb-type mannose-specific lectin. The domain contains a three-fold internal repeat (beta-prism architecture). The consensus sequence motif QXDXNXVXY is involved in alpha-D-mannose recognition. Lectins are carbohydrate-binding proteins which specifically recognize diverse carbohydrates and mediate a wide variety of biological processes such as cell-cell and host-pathogen interactions serum glycoprotein turnover and innate immune responses..
|
rpsblast_cdd |
gnl|CDD|201803
|
76 |
177 |
+ |
102 |
Gaps:7 |
100.00 |
109 |
44.95 |
7e-21 |
pfam01453 B_lectin D-mannose binding lectin. These proteins include mannose-specific lectins from plants as well as bacteriocins from bacteria.
|
rpsblast_cdd |
gnl|CDD|128418
|
39 |
150 |
+ |
112 |
Gaps:7 |
97.37 |
114 |
49.55 |
7e-21 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|29032
|
309 |
401 |
+ |
93 |
Gaps:9 |
100.00 |
84 |
47.62 |
3e-13 |
cd01098 PAN_AP_plant Plant PAN/APPLE-like domain present in plant S-receptor protein kinases and secreted glycoproteins. PAN/APPLE domains fulfill diverse biological functions by mediating protein-protein or protein-carbohydrate interactions. S-receptor protein kinases and S-locus glycoproteins are involved in sporophytic self-incompatibility response in Brassica one of probably many molecular mechanisms by which hermaphrodite flowering plants avoid self-fertilization..
|
rpsblast_cdd |
gnl|CDD|203897
|
321 |
383 |
+ |
63 |
Gaps:4 |
95.45 |
66 |
39.68 |
1e-12 |
pfam08276 PAN_2 PAN-like domain.
|
rpsblast_cdd |
gnl|CDD|201524
|
201 |
292 |
+ |
92 |
Gaps:7 |
82.73 |
110 |
27.47 |
3e-10 |
pfam00954 S_locus_glycop S-locus glycoprotein family. In Brassicaceae self-incompatible plants have a self/non-self recognition system. This is sporophytically controlled by multiple alleles at a single locus (S). S-locus glycoproteins as well as S-receptor kinases are in linkage with the S-alleles.
|