blastp_kegg |
lcl|pper:PRUPE_ppa001576mg
|
9 |
536 |
+ |
528 |
Gaps:35 |
76.22 |
799 |
53.37 |
5e-174 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103320451
|
9 |
536 |
+ |
528 |
Gaps:26 |
70.98 |
772 |
55.66 |
2e-171 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|pxb:103950605
|
1 |
536 |
+ |
536 |
Gaps:23 |
69.26 |
797 |
53.99 |
2e-169 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|vvi:100260797
|
1 |
530 |
+ |
530 |
Gaps:26 |
68.69 |
792 |
55.88 |
5e-169 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|vvi:100257449
|
1 |
535 |
+ |
535 |
Gaps:22 |
68.88 |
800 |
54.26 |
1e-168 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|vvi:100247193
|
1 |
535 |
+ |
535 |
Gaps:22 |
68.79 |
801 |
54.26 |
3e-168 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|tcc:TCM_034779
|
1 |
536 |
+ |
536 |
Gaps:25 |
69.69 |
805 |
53.30 |
2e-166 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|fve:101312026
|
1 |
536 |
+ |
536 |
Gaps:28 |
68.91 |
801 |
53.44 |
5e-166 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|mdm:103424672
|
1 |
530 |
+ |
530 |
Gaps:30 |
75.56 |
798 |
50.41 |
2e-165 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|mdm:103455936
|
1 |
530 |
+ |
530 |
Gaps:30 |
75.56 |
798 |
50.25 |
7e-165 |
putative receptor protein kinase ZmPK1
|
blastp_uniprot_sprot |
sp|P17801|KPRO_MAIZE
|
4 |
452 |
+ |
449 |
Gaps:48 |
59.36 |
817 |
36.29 |
2e-81 |
Putative receptor protein kinase ZmPK1 OS Zea mays GN PK1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P0DH87|PSRK_ARATH
|
1 |
349 |
+ |
349 |
Gaps:34 |
67.58 |
546 |
29.81 |
9e-35 |
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|P0DH86|SRK_ARATH
|
1 |
349 |
+ |
349 |
Gaps:34 |
43.26 |
853 |
29.81 |
6e-34 |
G-type lectin S-receptor-like serine/threonine-protein kinase SRK OS Arabidopsis thaliana GN SRK PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O81906|B120_ARATH
|
15 |
496 |
+ |
482 |
Gaps:82 |
54.65 |
849 |
28.88 |
2e-33 |
G-type lectin S-receptor-like serine/threonine-protein kinase B120 OS Arabidopsis thaliana GN B120 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FLV4|Y5248_ARATH
|
4 |
362 |
+ |
359 |
Gaps:55 |
46.56 |
872 |
30.30 |
2e-31 |
G-type lectin S-receptor-like serine/threonine-protein kinase At5g24080 OS Arabidopsis thaliana GN At5g24080 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64477|Y2913_ARATH
|
15 |
372 |
+ |
358 |
Gaps:42 |
46.38 |
828 |
29.95 |
2e-31 |
G-type lectin S-receptor-like serine/threonine-protein kinase At2g19130 OS Arabidopsis thaliana GN At2g19130 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P17840|SLSG3_BRAOL
|
1 |
338 |
+ |
338 |
Gaps:37 |
82.53 |
435 |
30.36 |
2e-29 |
S-locus-specific glycoprotein S13 OS Brassica oleracea GN SLSG PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9SXB5|Y1135_ARATH
|
13 |
348 |
+ |
336 |
Gaps:51 |
44.27 |
820 |
29.48 |
3e-29 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11305 OS Arabidopsis thaliana GN At1g11305 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O81905|SD18_ARATH
|
1 |
345 |
+ |
345 |
Gaps:34 |
43.18 |
850 |
28.61 |
8e-29 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64781|Y1639_ARATH
|
15 |
340 |
+ |
326 |
Gaps:50 |
42.36 |
831 |
31.82 |
1e-27 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61390 OS Arabidopsis thaliana GN At1g61390 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|201803
|
43 |
145 |
+ |
103 |
Gaps:6 |
100.00 |
109 |
42.20 |
2e-23 |
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
|
15 |
119 |
+ |
105 |
Gaps:4 |
92.24 |
116 |
39.25 |
6e-16 |
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
|
15 |
116 |
+ |
102 |
Gaps:3 |
90.35 |
114 |
40.78 |
7e-16 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|29032
|
290 |
373 |
+ |
84 |
Gaps:4 |
100.00 |
84 |
28.57 |
1e-08 |
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|201524
|
193 |
278 |
+ |
86 |
Gaps:3 |
77.27 |
110 |
25.88 |
1e-07 |
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_kog |
gnl|CDD|36401
|
455 |
537 |
+ |
83 |
Gaps:7 |
22.16 |
361 |
33.75 |
1e-10 |
KOG1187 KOG1187 KOG1187 Serine/threonine protein kinase [Signal transduction mechanisms].
|