blastp_kegg |
lcl|pop:POPTR_0518s00220g
|
1 |
597 |
+ |
597 |
Gaps:7 |
78.18 |
779 |
60.92 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_001389
|
1 |
597 |
+ |
597 |
Gaps:5 |
77.86 |
777 |
60.83 |
0.0 |
Receptor-like protein kinase 1
|
blastp_kegg |
lcl|pop:POPTR_0005s05830g
|
1 |
597 |
+ |
597 |
Gaps:4 |
78.09 |
776 |
60.56 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_0576180
|
1 |
597 |
+ |
597 |
Gaps:6 |
77.27 |
783 |
60.83 |
0.0 |
ATP binding protein putative (EC:2.7.11.25)
|
blastp_kegg |
lcl|tcc:TCM_001388
|
1 |
597 |
+ |
597 |
Gaps:5 |
76.96 |
777 |
60.87 |
0.0 |
Receptor-like protein kinase 1
|
blastp_kegg |
lcl|rcu:RCOM_0576160
|
1 |
597 |
+ |
597 |
Gaps:6 |
73.81 |
817 |
61.36 |
0.0 |
ATP binding protein putative (EC:2.7.11.25)
|
blastp_kegg |
lcl|vvi:100265971
|
17 |
597 |
+ |
581 |
Gaps:5 |
75.71 |
774 |
61.77 |
0.0 |
G-type lectin S-receptor-like serine/threonine-protein kinase RLK1-like
|
blastp_kegg |
lcl|cic:CICLE_v10027040mg
|
1 |
597 |
+ |
597 |
Gaps:15 |
77.21 |
781 |
59.20 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102627774
|
1 |
597 |
+ |
597 |
Gaps:15 |
77.21 |
781 |
59.20 |
0.0 |
G-type lectin S-receptor-like serine/threonine-protein kinase RLK1-like
|
blastp_kegg |
lcl|vvi:100267699
|
17 |
597 |
+ |
581 |
Gaps:9 |
75.52 |
768 |
63.62 |
0.0 |
G-type lectin S-receptor-like serine/threonine-protein kinase RLK1-like
|
blastp_uniprot_sprot |
sp|Q9FLV4|Y5248_ARATH
|
1 |
597 |
+ |
597 |
Gaps:80 |
72.02 |
872 |
31.85 |
2e-42 |
G-type lectin S-receptor-like serine/threonine-protein kinase At5g24080 OS Arabidopsis thaliana GN At5g24080 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q39202|RLK1_ARATH
|
36 |
591 |
+ |
556 |
Gaps:60 |
72.72 |
832 |
29.92 |
1e-40 |
G-type lectin S-receptor-like serine/threonine-protein kinase RLK1 OS Arabidopsis thaliana GN RLK1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P17801|KPRO_MAIZE
|
4 |
519 |
+ |
516 |
Gaps:91 |
67.44 |
817 |
29.04 |
3e-40 |
Putative receptor protein kinase ZmPK1 OS Zea mays GN PK1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9ZT07|RKS1_ARATH
|
39 |
520 |
+ |
482 |
Gaps:79 |
61.58 |
833 |
28.85 |
3e-31 |
G-type lectin S-receptor-like serine/threonine-protein kinase RKS1 OS Arabidopsis thaliana GN RKS1 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|Q39086|SD17_ARATH
|
30 |
520 |
+ |
491 |
Gaps:107 |
61.21 |
843 |
28.88 |
2e-30 |
Receptor-like serine/threonine-protein kinase SD1-7 OS Arabidopsis thaliana GN SD17 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9XID3|Y1343_ARATH
|
22 |
593 |
+ |
572 |
Gaps:56 |
68.03 |
829 |
29.96 |
4e-29 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g34300 OS Arabidopsis thaliana GN At1g34300 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64782|SD129_ARATH
|
1 |
567 |
+ |
567 |
Gaps:79 |
69.32 |
805 |
29.93 |
7e-29 |
G-type lectin S-receptor-like serine/threonine-protein kinase SD1-29 OS Arabidopsis thaliana GN SD129 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64477|Y2913_ARATH
|
5 |
519 |
+ |
515 |
Gaps:58 |
62.20 |
828 |
27.57 |
9e-29 |
G-type lectin S-receptor-like serine/threonine-protein kinase At2g19130 OS Arabidopsis thaliana GN At2g19130 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O81905|SD18_ARATH
|
30 |
524 |
+ |
495 |
Gaps:84 |
61.76 |
850 |
27.43 |
1e-28 |
Receptor-like serine/threonine-protein kinase SD1-8 OS Arabidopsis thaliana GN SD18 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O64778|Y1142_ARATH
|
40 |
567 |
+ |
528 |
Gaps:83 |
65.06 |
807 |
28.38 |
4e-28 |
G-type lectin S-receptor-like serine/threonine-protein kinase At1g61420 OS Arabidopsis thaliana GN At1g61420 PE 3 SV 2
|
rpsblast_cdd |
gnl|CDD|201803
|
67 |
168 |
+ |
102 |
Gaps:9 |
100.00 |
109 |
37.61 |
1e-22 |
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
|
33 |
141 |
+ |
109 |
Gaps:7 |
96.49 |
114 |
33.64 |
2e-15 |
smart00108 B_lectin Bulb-type mannose-specific lectin.
|
rpsblast_cdd |
gnl|CDD|28910
|
33 |
142 |
+ |
110 |
Gaps:8 |
96.55 |
116 |
32.14 |
9e-14 |
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_kog |
gnl|CDD|36401
|
473 |
539 |
+ |
67 |
Gaps:3 |
18.84 |
361 |
42.65 |
3e-09 |
KOG1187 KOG1187 KOG1187 Serine/threonine protein kinase [Signal transduction mechanisms].
|