blastp_kegg |
lcl|fve:101294818
|
1 |
575 |
+ |
575 |
Gaps:24 |
70.43 |
788 |
55.14 |
5e-163 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|pxb:103950605
|
1 |
576 |
+ |
576 |
Gaps:20 |
70.77 |
797 |
53.55 |
1e-162 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|tcc:TCM_034781
|
1 |
572 |
+ |
572 |
Gaps:20 |
71.52 |
797 |
50.88 |
2e-162 |
S-locus lectin protein kinase family protein putative isoform 1
|
blastp_kegg |
lcl|pvu:PHAVU_009G068300g
|
5 |
576 |
+ |
572 |
Gaps:29 |
70.83 |
809 |
50.26 |
4e-160 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_034779
|
26 |
568 |
+ |
543 |
Gaps:23 |
68.57 |
805 |
53.44 |
4e-160 |
S-locus lectin protein kinase family protein putative
|
blastp_kegg |
lcl|fve:101312026
|
3 |
573 |
+ |
571 |
Gaps:21 |
70.91 |
801 |
51.94 |
2e-159 |
putative receptor protein kinase ZmPK1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa001576mg
|
1 |
573 |
+ |
573 |
Gaps:26 |
72.47 |
799 |
53.20 |
1e-158 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0013s08990g
|
1 |
578 |
+ |
578 |
Gaps:28 |
72.43 |
787 |
53.16 |
6e-158 |
POPTRDRAFT_571616 hypothetical protein
|
blastp_kegg |
lcl|pmum:103320451
|
1 |
573 |
+ |
573 |
Gaps:26 |
75.00 |
772 |
52.50 |
2e-157 |
putative receptor protein kinase ZmPK1
|
blastp_kegg |
lcl|pop:POPTR_0090s00200g
|
1 |
578 |
+ |
578 |
Gaps:27 |
72.39 |
786 |
52.90 |
3e-157 |
hypothetical protein
|
blastp_uniprot_sprot |
sp|P17801|KPRO_MAIZE
|
6 |
413 |
+ |
408 |
Gaps:29 |
49.82 |
817 |
39.80 |
6e-81 |
Putative receptor protein kinase ZmPK1 OS Zea mays GN PK1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O64477|Y2913_ARATH
|
6 |
417 |
+ |
412 |
Gaps:53 |
51.09 |
828 |
31.44 |
1e-36 |
G-type lectin S-receptor-like serine/threonine-protein kinase At2g19130 OS Arabidopsis thaliana GN At2g19130 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FLV4|Y5248_ARATH
|
16 |
411 |
+ |
396 |
Gaps:66 |
48.85 |
872 |
31.22 |
7e-33 |
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
|
17 |
416 |
+ |
400 |
Gaps:34 |
74.36 |
546 |
28.33 |
2e-31 |
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|O81906|B120_ARATH
|
8 |
376 |
+ |
369 |
Gaps:65 |
45.47 |
849 |
30.57 |
5e-31 |
G-type lectin S-receptor-like serine/threonine-protein kinase B120 OS Arabidopsis thaliana GN B120 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P0DH86|SRK_ARATH
|
17 |
416 |
+ |
400 |
Gaps:34 |
47.60 |
853 |
28.33 |
1e-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|O81905|SD18_ARATH
|
17 |
490 |
+ |
474 |
Gaps:60 |
54.35 |
850 |
27.49 |
4e-30 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O81832|Y4729_ARATH
|
5 |
420 |
+ |
416 |
Gaps:47 |
54.28 |
783 |
28.47 |
9e-30 |
G-type lectin S-receptor-like serine/threonine-protein kinase At4g27290 OS Arabidopsis thaliana GN At4g27290 PE 3 SV 4
|
blastp_uniprot_sprot |
sp|Q9SXB3|Y1112_ARATH
|
6 |
378 |
+ |
373 |
Gaps:59 |
46.10 |
820 |
33.33 |
4e-29 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g11280 OS Arabidopsis thaliana GN At1g11280 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O64781|Y1639_ARATH
|
1 |
378 |
+ |
378 |
Gaps:52 |
46.45 |
831 |
31.87 |
6e-29 |
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
|
68 |
170 |
+ |
103 |
Gaps:6 |
100.00 |
109 |
43.12 |
3e-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|128418
|
39 |
143 |
+ |
105 |
Gaps:3 |
92.98 |
114 |
41.51 |
1e-16 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|28910
|
39 |
144 |
+ |
106 |
Gaps:4 |
93.10 |
116 |
40.74 |
3e-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|29032
|
325 |
413 |
+ |
89 |
Gaps:11 |
100.00 |
84 |
34.52 |
3e-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
|
493 |
578 |
+ |
86 |
Gaps:7 |
22.99 |
361 |
36.14 |
6e-12 |
KOG1187 KOG1187 KOG1187 Serine/threonine protein kinase [Signal transduction mechanisms].
|