blastp_kegg |
lcl|vvi:100256990
|
1 |
201 |
+ |
201 |
Gaps:29 |
25.70 |
677 |
83.33 |
1e-77 |
probable protein phosphatase 2C 23-like
|
blastp_kegg |
lcl|tcc:TCM_041847
|
1 |
206 |
+ |
206 |
Gaps:36 |
26.19 |
733 |
71.88 |
9e-73 |
Pol-like 5 isoform 1
|
blastp_kegg |
lcl|pvu:PHAVU_011G064200g
|
1 |
198 |
+ |
198 |
Gaps:22 |
24.72 |
712 |
76.14 |
7e-72 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0001s24620g
|
1 |
200 |
+ |
200 |
Gaps:31 |
23.70 |
730 |
80.35 |
9e-72 |
POPTRDRAFT_797687 hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_0229510
|
1 |
206 |
+ |
206 |
Gaps:31 |
26.92 |
702 |
74.60 |
9e-72 |
protein phosphatase 2c putative (EC:3.1.3.16)
|
blastp_kegg |
lcl|fve:101293175
|
1 |
207 |
+ |
207 |
Gaps:34 |
26.25 |
720 |
70.90 |
1e-71 |
probable protein phosphatase 2C 4-like isoform 1
|
blastp_kegg |
lcl|cam:101499809
|
1 |
198 |
+ |
198 |
Gaps:25 |
24.45 |
724 |
78.53 |
2e-71 |
probable protein phosphatase 2C 4-like
|
blastp_kegg |
lcl|pop:POPTR_0009s03590g
|
1 |
201 |
+ |
201 |
Gaps:33 |
26.27 |
670 |
78.98 |
3e-70 |
POPTRDRAFT_723282 hypothetical protein
|
blastp_kegg |
lcl|gmx:100812903
|
1 |
197 |
+ |
197 |
Gaps:21 |
24.72 |
720 |
75.28 |
4e-70 |
probable protein phosphatase 2C 4-like
|
blastp_kegg |
lcl|gmx:100810214
|
1 |
214 |
+ |
214 |
Gaps:26 |
27.22 |
720 |
71.94 |
7e-70 |
probable protein phosphatase 2C 4-like
|
blastp_uniprot_sprot |
sp|Q9LQN6|P2C04_ARATH
|
1 |
197 |
+ |
197 |
Gaps:34 |
26.44 |
662 |
72.57 |
2e-66 |
Probable protein phosphatase 2C 4 OS Arabidopsis thaliana GN PLL5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9ZV25|P2C23_ARATH
|
1 |
205 |
+ |
205 |
Gaps:24 |
28.90 |
654 |
67.20 |
1e-64 |
Probable protein phosphatase 2C 23 OS Arabidopsis thaliana GN PLL4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LZ86|P2C66_ARATH
|
4 |
197 |
+ |
194 |
Gaps:33 |
29.23 |
674 |
44.67 |
3e-31 |
Probable protein phosphatase 2C 66 OS Arabidopsis thaliana GN PLL2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q84T94|P2C35_ORYSJ
|
1 |
196 |
+ |
196 |
Gaps:66 |
23.16 |
639 |
54.73 |
7e-29 |
Protein phosphatase 2C 35 OS Oryza sativa subsp. japonica GN XB15 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8RWN7|P2C32_ARATH
|
2 |
196 |
+ |
195 |
Gaps:35 |
19.63 |
856 |
51.19 |
1e-28 |
Protein phosphatase 2C 32 OS Arabidopsis thaliana GN POL PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q10NB9|P2C31_ORYSJ
|
123 |
197 |
+ |
75 |
Gaps:3 |
11.41 |
631 |
75.00 |
3e-28 |
Probable protein phosphatase 2C 31 OS Oryza sativa subsp. japonica GN Os03g0275100 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SR24|P2C36_ARATH
|
130 |
201 |
+ |
72 |
none |
11.08 |
650 |
69.44 |
8e-28 |
Probable protein phosphatase 2C 36 OS Arabidopsis thaliana GN PLL3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A3AZ89|P2C46_ORYSJ
|
136 |
194 |
+ |
59 |
none |
9.95 |
593 |
76.27 |
8e-24 |
Putative protein phosphatase 2C 46 OS Oryza sativa subsp. japonica GN Os05g0111800 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q6ZGY0|P2C26_ORYSJ
|
138 |
198 |
+ |
61 |
none |
10.23 |
596 |
63.93 |
2e-22 |
Probable protein phosphatase 2C 26 OS Oryza sativa subsp. japonica GN Os02g0690500 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O82302|P2C29_ARATH
|
137 |
196 |
+ |
60 |
none |
7.66 |
783 |
66.67 |
7e-22 |
Protein phosphatase 2C 29 OS Arabidopsis thaliana GN PLL1 PE 1 SV 2
|
rpsblast_kog |
gnl|CDD|35919
|
61 |
197 |
+ |
137 |
Gaps:4 |
34.62 |
390 |
37.78 |
6e-26 |
KOG0700 KOG0700 KOG0700 Protein phosphatase 2C/pyruvate dehydrogenase (lipoamide) phosphatase [Signal transduction mechanisms].
|