blastp_kegg |
lcl|pper:PRUPE_ppa001615mg
|
9 |
387 |
+ |
379 |
Gaps:54 |
53.16 |
792 |
49.64 |
1e-136 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101292782
|
10 |
394 |
+ |
385 |
Gaps:55 |
53.50 |
800 |
49.53 |
8e-135 |
G-type lectin S-receptor-like serine/threonine-protein kinase RKS1-like
|
blastp_kegg |
lcl|pmum:103334241
|
10 |
387 |
+ |
378 |
Gaps:68 |
50.53 |
851 |
49.07 |
4e-134 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pper:PRUPE_ppa023906mg
|
12 |
387 |
+ |
376 |
Gaps:55 |
52.77 |
794 |
49.16 |
4e-134 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103446602
|
10 |
387 |
+ |
378 |
Gaps:55 |
49.88 |
844 |
49.88 |
6e-133 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|tcc:TCM_030045
|
27 |
383 |
+ |
357 |
Gaps:55 |
47.97 |
838 |
51.49 |
1e-130 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|pmum:103324693
|
1 |
402 |
+ |
402 |
Gaps:106 |
47.00 |
1832 |
48.32 |
1e-128 |
uncharacterized LOC103324693
|
blastp_kegg |
lcl|pmum:103334242
|
10 |
387 |
+ |
378 |
Gaps:65 |
50.76 |
853 |
48.04 |
4e-128 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pxb:103944217
|
9 |
385 |
+ |
377 |
Gaps:59 |
50.06 |
847 |
49.76 |
7e-128 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pmum:103334238
|
10 |
387 |
+ |
378 |
Gaps:64 |
50.53 |
851 |
47.67 |
7e-127 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_uniprot_sprot |
sp|Q9ZT07|RKS1_ARATH
|
23 |
387 |
+ |
365 |
Gaps:56 |
49.34 |
833 |
44.28 |
2e-114 |
G-type lectin S-receptor-like serine/threonine-protein kinase RKS1 OS Arabidopsis thaliana GN RKS1 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|Q9LPZ3|Y1141_ARATH
|
23 |
387 |
+ |
365 |
Gaps:58 |
48.64 |
845 |
43.31 |
3e-108 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410 OS Arabidopsis thaliana GN At1g11410 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|O81905|SD18_ARATH
|
41 |
386 |
+ |
346 |
Gaps:57 |
45.53 |
850 |
37.98 |
4e-80 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9S972|SD16_ARATH
|
28 |
383 |
+ |
356 |
Gaps:53 |
46.87 |
847 |
35.52 |
2e-77 |
Receptor-like serine/threonine-protein kinase SD1-6 OS Arabidopsis thaliana GN SD16 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|P07761|SLSG6_BRAOL
|
11 |
386 |
+ |
376 |
Gaps:62 |
95.87 |
436 |
34.93 |
1e-75 |
S-locus-specific glycoprotein S6 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P17840|SLSG3_BRAOL
|
11 |
386 |
+ |
376 |
Gaps:60 |
96.09 |
435 |
34.93 |
1e-74 |
S-locus-specific glycoprotein S13 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O81832|Y4729_ARATH
|
11 |
389 |
+ |
379 |
Gaps:62 |
54.02 |
783 |
34.75 |
2e-73 |
G-type lectin S-receptor-like serine/threonine-protein kinase At4g27290 OS Arabidopsis thaliana GN At4g27290 PE 3 SV 4
|
blastp_uniprot_sprot |
sp|Q39086|SD17_ARATH
|
28 |
386 |
+ |
359 |
Gaps:53 |
46.98 |
843 |
33.33 |
1e-72 |
Receptor-like serine/threonine-protein kinase SD1-7 OS Arabidopsis thaliana GN SD17 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P22553|SLSG2_BRAOA
|
11 |
381 |
+ |
371 |
Gaps:61 |
95.17 |
435 |
34.30 |
1e-71 |
S-locus-specific glycoprotein BS29-2 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P22552|SLSG1_BRAOA
|
10 |
386 |
+ |
377 |
Gaps:72 |
96.62 |
444 |
34.03 |
5e-67 |
S-locus-specific glycoprotein BS29-1 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|203897
|
301 |
366 |
+ |
66 |
Gaps:1 |
98.48 |
66 |
56.92 |
4e-21 |
pfam08276 PAN_2 PAN-like domain.
|
rpsblast_cdd |
gnl|CDD|201524
|
174 |
287 |
+ |
114 |
Gaps:8 |
100.00 |
110 |
36.36 |
1e-20 |
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.
|
rpsblast_cdd |
gnl|CDD|29032
|
302 |
381 |
+ |
80 |
Gaps:5 |
89.29 |
84 |
45.33 |
8e-16 |
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|201803
|
72 |
148 |
+ |
77 |
Gaps:34 |
100.00 |
109 |
35.78 |
3e-13 |
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|28910
|
32 |
109 |
+ |
78 |
Gaps:2 |
65.52 |
116 |
36.84 |
8e-13 |
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|128418
|
32 |
109 |
+ |
78 |
Gaps:3 |
65.79 |
114 |
37.33 |
3e-12 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|197747
|
302 |
381 |
+ |
80 |
Gaps:6 |
100.00 |
78 |
38.46 |
7e-09 |
smart00473 PAN_AP divergent subfamily of APPLE domains. Apple-like domains present in Plasminogen C. elegans hypothetical ORFs and the extracellular portion of plant receptor-like protein kinases. Predicted to possess protein- and/or carbohydrate-binding functions.
|