blastp_kegg |
lcl|pper:PRUPE_ppa001576mg
|
37 |
568 |
+ |
532 |
Gaps:32 |
68.09 |
799 |
53.12 |
5e-151 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_034779
|
28 |
568 |
+ |
541 |
Gaps:31 |
69.32 |
805 |
50.90 |
4e-150 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|pxb:103950605
|
8 |
571 |
+ |
564 |
Gaps:29 |
70.39 |
797 |
51.34 |
2e-149 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|pmum:103320451
|
37 |
568 |
+ |
532 |
Gaps:32 |
70.47 |
772 |
52.39 |
4e-149 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|pop:POPTR_0013s08990g
|
25 |
573 |
+ |
549 |
Gaps:36 |
69.76 |
787 |
53.19 |
6e-148 |
POPTRDRAFT_571616 hypothetical protein
|
blastp_kegg |
lcl|vvi:100257449
|
29 |
571 |
+ |
543 |
Gaps:32 |
69.25 |
800 |
51.26 |
2e-147 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|pop:POPTR_0090s00200g
|
25 |
573 |
+ |
549 |
Gaps:35 |
69.72 |
786 |
52.37 |
2e-146 |
hypothetical protein
|
blastp_kegg |
lcl|mdm:103455936
|
32 |
571 |
+ |
540 |
Gaps:28 |
66.67 |
798 |
52.07 |
2e-143 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|mdm:103424672
|
1 |
571 |
+ |
571 |
Gaps:31 |
70.18 |
798 |
51.25 |
3e-143 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|fve:101312026
|
6 |
568 |
+ |
563 |
Gaps:34 |
70.54 |
801 |
49.91 |
4e-143 |
putative receptor protein kinase ZmPK1-like
|
blastp_uniprot_sprot |
sp|P17801|KPRO_MAIZE
|
8 |
415 |
+ |
408 |
Gaps:35 |
51.04 |
817 |
37.17 |
7e-72 |
Putative receptor protein kinase ZmPK1 OS Zea mays GN PK1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9FLV4|Y5248_ARATH
|
5 |
397 |
+ |
393 |
Gaps:65 |
49.31 |
872 |
31.16 |
2e-34 |
G-type lectin S-receptor-like serine/threonine-protein kinase At5g24080 OS Arabidopsis thaliana GN At5g24080 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P0DH87|PSRK_ARATH
|
24 |
384 |
+ |
361 |
Gaps:45 |
68.50 |
546 |
29.41 |
1e-30 |
Putative inactive G-type lectin S-receptor-like serine/threonine-protein kinase SRK OS Arabidopsis thaliana GN PSEUDOSRKA PE 5 SV 1
|
blastp_uniprot_sprot |
sp|P93756|SD31_ARATH
|
24 |
406 |
+ |
383 |
Gaps:44 |
51.18 |
764 |
32.23 |
3e-30 |
G-type lectin S-receptor-like serine/threonine-protein kinase SD3-1 OS Arabidopsis thaliana GN SD31 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O64477|Y2913_ARATH
|
43 |
384 |
+ |
342 |
Gaps:51 |
43.12 |
828 |
28.85 |
5e-30 |
G-type lectin S-receptor-like serine/threonine-protein kinase At2g19130 OS Arabidopsis thaliana GN At2g19130 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P0DH86|SRK_ARATH
|
24 |
384 |
+ |
361 |
Gaps:45 |
43.85 |
853 |
29.14 |
6e-30 |
G-type lectin S-receptor-like serine/threonine-protein kinase SRK OS Arabidopsis thaliana GN SRK PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LPZ3|Y1141_ARATH
|
41 |
410 |
+ |
370 |
Gaps:28 |
46.39 |
845 |
26.53 |
8e-30 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11410 OS Arabidopsis thaliana GN At1g11410 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|P17840|SLSG3_BRAOL
|
7 |
407 |
+ |
401 |
Gaps:65 |
95.17 |
435 |
30.68 |
1e-29 |
S-locus-specific glycoprotein S13 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O81906|B120_ARATH
|
38 |
371 |
+ |
334 |
Gaps:40 |
41.70 |
849 |
29.66 |
5e-28 |
G-type lectin S-receptor-like serine/threonine-protein kinase B120 OS Arabidopsis thaliana GN B120 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q39203|SD22_ARATH
|
30 |
371 |
+ |
342 |
Gaps:35 |
44.29 |
797 |
28.33 |
2e-27 |
G-type lectin S-receptor-like serine/threonine-protein kinase SD2-2 OS Arabidopsis thaliana GN SD22 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|201803
|
71 |
175 |
+ |
105 |
Gaps:8 |
100.00 |
109 |
45.87 |
6e-24 |
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
|
43 |
148 |
+ |
106 |
Gaps:5 |
92.11 |
114 |
44.76 |
1e-19 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|28910
|
43 |
149 |
+ |
107 |
Gaps:6 |
92.24 |
116 |
42.99 |
4e-18 |
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|29032
|
320 |
408 |
+ |
89 |
Gaps:11 |
100.00 |
84 |
33.33 |
9e-09 |
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_kog |
gnl|CDD|36401
|
488 |
573 |
+ |
86 |
Gaps:7 |
22.99 |
361 |
34.94 |
1e-11 |
KOG1187 KOG1187 KOG1187 Serine/threonine protein kinase [Signal transduction mechanisms].
|