blastp_kegg |
lcl|vvi:100256990
|
1 |
133 |
+ |
133 |
Gaps:19 |
16.84 |
677 |
72.81 |
2e-40 |
probable protein phosphatase 2C 23-like
|
blastp_kegg |
lcl|pop:POPTR_0009s03590g
|
7 |
106 |
+ |
100 |
none |
14.93 |
670 |
72.00 |
2e-40 |
POPTRDRAFT_723282 hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_041847
|
7 |
91 |
+ |
85 |
none |
11.60 |
733 |
81.18 |
4e-40 |
Pol-like 5 isoform 1
|
blastp_kegg |
lcl|pop:POPTR_0001s24620g
|
1 |
125 |
+ |
125 |
Gaps:2 |
17.12 |
730 |
61.60 |
1e-39 |
POPTRDRAFT_797687 hypothetical protein
|
blastp_kegg |
lcl|cmo:103502087
|
1 |
130 |
+ |
130 |
Gaps:22 |
15.94 |
715 |
70.18 |
3e-39 |
probable protein phosphatase 2C 4
|
blastp_kegg |
lcl|csv:101223863
|
1 |
130 |
+ |
130 |
Gaps:16 |
15.94 |
715 |
65.79 |
8e-39 |
probable protein phosphatase 2C 4-like
|
blastp_kegg |
lcl|csv:101222644
|
1 |
130 |
+ |
130 |
Gaps:16 |
15.94 |
715 |
65.79 |
8e-39 |
probable protein phosphatase 2C 4-like
|
blastp_kegg |
lcl|gmx:100810214
|
3 |
135 |
+ |
133 |
Gaps:3 |
18.61 |
720 |
56.72 |
4e-38 |
probable protein phosphatase 2C 4-like
|
blastp_kegg |
lcl|pvu:PHAVU_011G064200g
|
3 |
84 |
+ |
82 |
Gaps:1 |
11.38 |
712 |
83.95 |
5e-38 |
hypothetical protein
|
blastp_kegg |
lcl|cic:CICLE_v10027924mg
|
2 |
102 |
+ |
101 |
Gaps:2 |
14.63 |
704 |
69.90 |
6e-38 |
hypothetical protein
|
blastp_uniprot_sprot |
sp|Q9ZV25|P2C23_ARATH
|
1 |
83 |
+ |
83 |
none |
12.69 |
654 |
75.90 |
2e-36 |
Probable protein phosphatase 2C 23 OS Arabidopsis thaliana GN PLL4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LQN6|P2C04_ARATH
|
1 |
83 |
+ |
83 |
Gaps:1 |
12.39 |
662 |
78.05 |
3e-36 |
Probable protein phosphatase 2C 4 OS Arabidopsis thaliana GN PLL5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q10NB9|P2C31_ORYSJ
|
9 |
83 |
+ |
75 |
Gaps:3 |
11.41 |
631 |
65.28 |
6e-25 |
Probable protein phosphatase 2C 31 OS Oryza sativa subsp. japonica GN Os03g0275100 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LZ86|P2C66_ARATH
|
13 |
83 |
+ |
71 |
Gaps:4 |
11.13 |
674 |
62.67 |
1e-24 |
Probable protein phosphatase 2C 66 OS Arabidopsis thaliana GN PLL2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SR24|P2C36_ARATH
|
16 |
87 |
+ |
72 |
none |
11.08 |
650 |
61.11 |
4e-24 |
Probable protein phosphatase 2C 36 OS Arabidopsis thaliana GN PLL3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q84T94|P2C35_ORYSJ
|
24 |
82 |
+ |
59 |
none |
9.23 |
639 |
72.88 |
4e-24 |
Protein phosphatase 2C 35 OS Oryza sativa subsp. japonica GN XB15 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8RWN7|P2C32_ARATH
|
7 |
82 |
+ |
76 |
Gaps:4 |
9.35 |
856 |
61.25 |
1e-23 |
Protein phosphatase 2C 32 OS Arabidopsis thaliana GN POL PE 1 SV 2
|
blastp_uniprot_sprot |
sp|A3AZ89|P2C46_ORYSJ
|
22 |
80 |
+ |
59 |
none |
9.95 |
593 |
66.10 |
1e-20 |
Putative protein phosphatase 2C 46 OS Oryza sativa subsp. japonica GN Os05g0111800 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q6ZGY0|P2C26_ORYSJ
|
24 |
84 |
+ |
61 |
none |
10.23 |
596 |
57.38 |
3e-19 |
Probable protein phosphatase 2C 26 OS Oryza sativa subsp. japonica GN Os02g0690500 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O82302|P2C29_ARATH
|
23 |
82 |
+ |
60 |
none |
7.66 |
783 |
60.00 |
7e-19 |
Protein phosphatase 2C 29 OS Arabidopsis thaliana GN PLL1 PE 1 SV 2
|
rpsblast_kog |
gnl|CDD|35919
|
2 |
115 |
+ |
114 |
Gaps:3 |
30.00 |
390 |
35.90 |
2e-19 |
KOG0700 KOG0700 KOG0700 Protein phosphatase 2C/pyruvate dehydrogenase (lipoamide) phosphatase [Signal transduction mechanisms].
|