blastp_kegg |
lcl|mdm:103410619
|
1 |
94 |
+ |
94 |
none |
37.01 |
254 |
84.04 |
5e-46 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|gmx:100809002
|
1 |
94 |
+ |
94 |
none |
13.51 |
696 |
81.91 |
4e-45 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|pxb:103953811
|
1 |
94 |
+ |
94 |
none |
14.44 |
651 |
86.17 |
4e-45 |
two-component response regulator ARR12
|
blastp_kegg |
lcl|csv:101215220
|
1 |
94 |
+ |
94 |
none |
13.66 |
688 |
82.98 |
5e-45 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|cam:101508241
|
7 |
94 |
+ |
88 |
none |
13.95 |
631 |
87.50 |
1e-44 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|cmo:103493766
|
1 |
94 |
+ |
94 |
none |
13.64 |
689 |
81.91 |
3e-44 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|mdm:103441827
|
1 |
94 |
+ |
94 |
none |
14.44 |
651 |
85.11 |
4e-44 |
two-component response regulator ARR14-like
|
blastp_kegg |
lcl|pxb:103942390
|
1 |
94 |
+ |
94 |
none |
15.04 |
625 |
85.11 |
4e-44 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|pmum:103320756
|
1 |
94 |
+ |
94 |
none |
14.20 |
662 |
82.98 |
8e-44 |
two-component response regulator ARR12-like
|
blastp_kegg |
lcl|mdm:103440743
|
1 |
94 |
+ |
94 |
none |
15.04 |
625 |
84.04 |
1e-43 |
two-component response regulator ARR12
|
blastp_pdb |
2ayx_A
|
3 |
94 |
+ |
92 |
Gaps:12 |
39.37 |
254 |
38.00 |
9e-10 |
mol:protein length:254 Sensor kinase protein rcsC
|
blastp_pdb |
2ayz_A
|
18 |
94 |
+ |
77 |
Gaps:3 |
57.14 |
133 |
42.11 |
4e-08 |
mol:protein length:133 Sensor kinase protein rcsC
|
blastp_pdb |
3f7n_B
|
18 |
108 |
+ |
91 |
Gaps:6 |
72.66 |
128 |
34.41 |
3e-06 |
mol:protein length:128 Chemotaxis protein cheY
|
blastp_pdb |
3f7n_A
|
18 |
108 |
+ |
91 |
Gaps:6 |
72.66 |
128 |
34.41 |
3e-06 |
mol:protein length:128 Chemotaxis protein cheY
|
blastp_uniprot_sprot |
sp|P62598|ARR12_ARATH
|
1 |
94 |
+ |
94 |
Gaps:1 |
15.60 |
596 |
81.72 |
5e-42 |
Two-component response regulator ARR12 OS Arabidopsis thaliana GN ARR12 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O49397|ARR10_ARATH
|
1 |
94 |
+ |
94 |
Gaps:1 |
16.85 |
552 |
80.65 |
1e-40 |
Two-component response regulator ARR10 OS Arabidopsis thaliana GN ARR10 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q940D0|ARR1_ARATH
|
14 |
94 |
+ |
81 |
none |
11.74 |
690 |
71.60 |
4e-30 |
Two-component response regulator ARR1 OS Arabidopsis thaliana GN ARR1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9ZWJ9|ARR2_ARATH
|
12 |
94 |
+ |
83 |
none |
12.50 |
664 |
68.67 |
3e-29 |
Two-component response regulator ARR2 OS Arabidopsis thaliana GN ARR2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FXD6|ARR11_ARATH
|
15 |
94 |
+ |
80 |
none |
15.36 |
521 |
68.75 |
7e-28 |
Two-component response regulator ARR11 OS Arabidopsis thaliana GN ARR11 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9FGT7|ARR18_ARATH
|
1 |
94 |
+ |
94 |
Gaps:1 |
14.65 |
635 |
66.67 |
3e-27 |
Two-component response regulator ARR18 OS Arabidopsis thaliana GN ARR18 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q8L9Y3|ARR14_ARATH
|
12 |
94 |
+ |
83 |
Gaps:1 |
21.99 |
382 |
64.29 |
8e-27 |
Two-component response regulator ARR14 OS Arabidopsis thaliana GN ARR14 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9FJ16|APRR4_ARATH
|
13 |
117 |
+ |
105 |
Gaps:4 |
34.59 |
292 |
39.60 |
7e-16 |
Putative two-component response regulator-like APRR4 OS Arabidopsis thaliana GN APRR4 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q7Y0W5|EHD1_ORYSJ
|
9 |
94 |
+ |
86 |
none |
25.22 |
341 |
38.37 |
5e-11 |
Two-component response regulator EHD1 OS Oryza sativa subsp. japonica GN EHD1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q7Y0W3|EHD1_ORYSI
|
9 |
94 |
+ |
86 |
none |
25.22 |
341 |
38.37 |
5e-11 |
Two-component response regulator EHD1 OS Oryza sativa subsp. indica PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|32386
|
18 |
94 |
+ |
77 |
Gaps:3 |
16.38 |
464 |
47.37 |
2e-12 |
COG2204 AtoC Response regulator containing CheY-like receiver AAA-type ATPase and DNA-binding domains [Signal transduction mechanisms].
|
rpsblast_cdd |
gnl|CDD|162545
|
20 |
94 |
+ |
75 |
Gaps:3 |
15.98 |
463 |
43.24 |
1e-09 |
TIGR01818 ntrC nitrogen regulation protein NR(I). This model represents NtrC a DNA-binding response regulator that is phosphorylated by NtrB and interacts with sigma-54. NtrC usually controls the expression of glutamine synthase GlnA and may be called GlnL GlnG etc.
|
rpsblast_cdd |
gnl|CDD|200976
|
20 |
94 |
+ |
75 |
Gaps:3 |
66.67 |
111 |
40.54 |
2e-09 |
pfam00072 Response_reg Response regulator receiver domain. This domain receives the signal from the sensor partner in bacterial two-component systems. It is usually found N-terminal to a DNA binding effector domain.
|
rpsblast_cdd |
gnl|CDD|185070
|
19 |
94 |
+ |
76 |
Gaps:3 |
16.89 |
444 |
41.33 |
8e-09 |
PRK15115 PRK15115 response regulator GlrR Provisional.
|
rpsblast_cdd |
gnl|CDD|182968
|
18 |
106 |
+ |
89 |
Gaps:11 |
8.49 |
919 |
38.46 |
9e-09 |
PRK11107 PRK11107 hybrid sensory histidine kinase BarA Provisional.
|
rpsblast_cdd |
gnl|CDD|29071
|
21 |
94 |
+ |
74 |
Gaps:3 |
64.60 |
113 |
41.10 |
4e-08 |
cd00156 REC Signal receiver domain originally thought to be unique to bacteria (CheY OmpR NtrC and PhoB) now recently identified in eukaroytes ETR1 Arabidopsis thaliana this domain receives the signal from the sensor partner in a two-component systems contains a phosphoacceptor site that is phosphorylated by histidine kinase homologs usually found N-terminal to a DNA binding effector domain forms homodimers.
|