blastp_kegg |
lcl|pper:PRUPE_ppa001615mg
|
11 |
429 |
+ |
419 |
Gaps:19 |
53.79 |
792 |
56.10 |
7e-162 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_030045
|
26 |
418 |
+ |
393 |
Gaps:19 |
47.97 |
838 |
58.96 |
4e-159 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|mdm:103446602
|
9 |
422 |
+ |
414 |
Gaps:19 |
49.88 |
844 |
55.82 |
1e-157 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pmum:103334241
|
9 |
422 |
+ |
414 |
Gaps:32 |
50.53 |
851 |
54.65 |
1e-156 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|fve:101292782
|
9 |
429 |
+ |
421 |
Gaps:19 |
53.50 |
800 |
54.21 |
2e-156 |
G-type lectin S-receptor-like serine/threonine-protein kinase RKS1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa023906mg
|
11 |
425 |
+ |
415 |
Gaps:19 |
53.15 |
794 |
54.74 |
2e-156 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103408821
|
7 |
420 |
+ |
414 |
Gaps:25 |
50.29 |
849 |
56.67 |
7e-155 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pmum:103324693
|
11 |
445 |
+ |
435 |
Gaps:35 |
46.89 |
1832 |
55.53 |
1e-152 |
uncharacterized LOC103324693
|
blastp_kegg |
lcl|pmum:103334238
|
9 |
422 |
+ |
414 |
Gaps:30 |
50.53 |
851 |
53.95 |
4e-151 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_kegg |
lcl|pxb:103944217
|
8 |
420 |
+ |
413 |
Gaps:25 |
50.06 |
847 |
55.66 |
1e-150 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410
|
blastp_uniprot_sprot |
sp|Q9ZT07|RKS1_ARATH
|
22 |
422 |
+ |
401 |
Gaps:20 |
49.34 |
833 |
49.39 |
8e-127 |
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
|
22 |
422 |
+ |
401 |
Gaps:20 |
48.64 |
845 |
47.45 |
9e-126 |
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
|
47 |
421 |
+ |
375 |
Gaps:29 |
44.71 |
850 |
43.42 |
9e-96 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P17840|SLSG3_BRAOL
|
10 |
421 |
+ |
412 |
Gaps:28 |
96.09 |
435 |
38.28 |
1e-89 |
S-locus-specific glycoprotein S13 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P07761|SLSG6_BRAOL
|
10 |
421 |
+ |
412 |
Gaps:30 |
95.87 |
436 |
37.32 |
6e-87 |
S-locus-specific glycoprotein S6 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O81832|Y4729_ARATH
|
10 |
425 |
+ |
416 |
Gaps:24 |
54.15 |
783 |
38.44 |
8e-87 |
G-type lectin S-receptor-like serine/threonine-protein kinase At4g27290 OS Arabidopsis thaliana GN At4g27290 PE 3 SV 4
|
blastp_uniprot_sprot |
sp|P22553|SLSG2_BRAOA
|
10 |
421 |
+ |
412 |
Gaps:29 |
96.32 |
435 |
37.47 |
2e-83 |
S-locus-specific glycoprotein BS29-2 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q39086|SD17_ARATH
|
42 |
421 |
+ |
380 |
Gaps:23 |
45.20 |
843 |
39.37 |
4e-82 |
Receptor-like serine/threonine-protein kinase SD1-7 OS Arabidopsis thaliana GN SD17 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9S972|SD16_ARATH
|
42 |
418 |
+ |
377 |
Gaps:25 |
45.10 |
847 |
39.01 |
4e-80 |
Receptor-like serine/threonine-protein kinase SD1-6 OS Arabidopsis thaliana GN SD16 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|P22552|SLSG1_BRAOA
|
9 |
421 |
+ |
413 |
Gaps:36 |
96.62 |
444 |
36.36 |
2e-76 |
S-locus-specific glycoprotein BS29-1 OS Brassica oleracea var. alboglabra GN SLSG PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|201803
|
71 |
185 |
+ |
115 |
Gaps:6 |
100.00 |
109 |
51.38 |
2e-28 |
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
|
31 |
152 |
+ |
122 |
Gaps:8 |
100.00 |
114 |
42.11 |
2e-24 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|28910
|
31 |
153 |
+ |
123 |
Gaps:7 |
100.00 |
116 |
43.97 |
1e-23 |
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|203897
|
336 |
402 |
+ |
67 |
Gaps:1 |
100.00 |
66 |
57.58 |
3e-21 |
pfam08276 PAN_2 PAN-like domain.
|
rpsblast_cdd |
gnl|CDD|201524
|
211 |
322 |
+ |
112 |
Gaps:8 |
100.00 |
110 |
32.73 |
2e-16 |
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
|
337 |
416 |
+ |
80 |
Gaps:5 |
89.29 |
84 |
45.33 |
4e-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|197747
|
337 |
416 |
+ |
80 |
Gaps:6 |
100.00 |
78 |
38.46 |
5e-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.
|
rpsblast_cdd |
gnl|CDD|29031
|
334 |
416 |
+ |
83 |
Gaps:13 |
97.50 |
80 |
23.08 |
4e-07 |
cd00129 PAN_APPLE PAN/APPLE-like domain present in N-terminal (N) domains of plasminogen/ hepatocyte growth factor proteins plasma prekallikrein/coagulation factor XI and microneme antigen proteins plant receptor-like protein kinases and various nematode and leech anti-platelet proteins. Common structural features include two disulfide bonds that link the alpha-helix to the central region of the protein. PAN domains have significant functional versatility fulfilling diverse biological functions by mediating protein-protein or protein-carbohydrate interactions..
|