blastp_kegg |
lcl|tcc:TCM_030045
|
28 |
420 |
+ |
393 |
Gaps:21 |
47.97 |
838 |
59.45 |
1e-161 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|pper:PRUPE_ppa001615mg
|
9 |
423 |
+ |
415 |
Gaps:23 |
53.03 |
792 |
56.90 |
3e-160 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101292782
|
2 |
423 |
+ |
422 |
Gaps:19 |
53.62 |
800 |
54.31 |
4e-158 |
G-type lectin S-receptor-like serine/threonine-protein kinase RKS1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa023906mg
|
16 |
423 |
+ |
408 |
Gaps:19 |
52.52 |
794 |
55.64 |
7e-157 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103446602
|
12 |
423 |
+ |
412 |
Gaps:21 |
49.64 |
844 |
55.37 |
5e-156 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pmum:103334241
|
10 |
423 |
+ |
414 |
Gaps:31 |
50.41 |
851 |
55.94 |
3e-155 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pxb:103944217
|
10 |
422 |
+ |
413 |
Gaps:23 |
50.06 |
847 |
56.13 |
3e-153 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pmum:103324693
|
9 |
423 |
+ |
415 |
Gaps:41 |
45.80 |
1832 |
57.21 |
6e-153 |
uncharacterized LOC103324693
|
blastp_kegg |
lcl|pmum:103334238
|
10 |
423 |
+ |
414 |
Gaps:29 |
50.41 |
851 |
55.01 |
2e-152 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|mdm:103408821
|
9 |
422 |
+ |
414 |
Gaps:23 |
50.29 |
849 |
54.57 |
5e-150 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_uniprot_sprot |
sp|Q9ZT07|RKS1_ARATH
|
24 |
423 |
+ |
400 |
Gaps:20 |
49.22 |
833 |
50.49 |
2e-131 |
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
|
24 |
423 |
+ |
400 |
Gaps:22 |
48.52 |
845 |
48.29 |
2e-128 |
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
|
26 |
444 |
+ |
419 |
Gaps:31 |
50.12 |
850 |
40.61 |
5e-97 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O81832|Y4729_ARATH
|
11 |
435 |
+ |
425 |
Gaps:25 |
55.17 |
783 |
38.43 |
1e-90 |
G-type lectin S-receptor-like serine/threonine-protein kinase At4g27290 OS Arabidopsis thaliana GN At4g27290 PE 3 SV 4
|
blastp_uniprot_sprot |
sp|P17840|SLSG3_BRAOL
|
11 |
423 |
+ |
413 |
Gaps:29 |
96.09 |
435 |
39.00 |
3e-90 |
S-locus-specific glycoprotein S13 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P22553|SLSG2_BRAOA
|
8 |
418 |
+ |
411 |
Gaps:31 |
96.09 |
435 |
38.28 |
8e-86 |
S-locus-specific glycoprotein BS29-2 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9S972|SD16_ARATH
|
29 |
444 |
+ |
416 |
Gaps:25 |
49.70 |
847 |
37.53 |
8e-86 |
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 |
423 |
+ |
413 |
Gaps:36 |
96.10 |
436 |
39.14 |
4e-85 |
S-locus-specific glycoprotein S6 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q39086|SD17_ARATH
|
26 |
425 |
+ |
400 |
Gaps:25 |
47.81 |
843 |
38.46 |
1e-84 |
Receptor-like serine/threonine-protein kinase SD1-7 OS Arabidopsis thaliana GN SD17 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P22552|SLSG1_BRAOA
|
4 |
423 |
+ |
420 |
Gaps:36 |
98.20 |
444 |
36.93 |
1e-80 |
S-locus-specific glycoprotein BS29-1 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|201803
|
73 |
187 |
+ |
115 |
Gaps:6 |
100.00 |
109 |
51.38 |
1e-27 |
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
|
33 |
155 |
+ |
123 |
Gaps:7 |
100.00 |
116 |
46.55 |
1e-24 |
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
|
33 |
154 |
+ |
122 |
Gaps:8 |
100.00 |
114 |
45.61 |
8e-24 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|203897
|
337 |
403 |
+ |
67 |
Gaps:1 |
100.00 |
66 |
59.09 |
5e-22 |
pfam08276 PAN_2 PAN-like domain.
|
rpsblast_cdd |
gnl|CDD|201524
|
213 |
323 |
+ |
111 |
Gaps:9 |
100.00 |
110 |
34.55 |
1e-18 |
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
|
338 |
418 |
+ |
81 |
Gaps:6 |
89.29 |
84 |
45.33 |
6e-15 |
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|197747
|
338 |
418 |
+ |
81 |
Gaps:7 |
100.00 |
78 |
38.46 |
7e-08 |
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.
|