blastp_kegg |
lcl|mdm:103411000
|
61 |
260 |
+ |
200 |
Gaps:17 |
76.54 |
260 |
41.21 |
1e-41 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa016982mg
|
61 |
260 |
+ |
200 |
Gaps:13 |
35.01 |
557 |
44.62 |
6e-41 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103319382
|
61 |
260 |
+ |
200 |
Gaps:13 |
28.97 |
673 |
45.13 |
9e-41 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|pxb:103926820
|
61 |
260 |
+ |
200 |
Gaps:17 |
13.69 |
1454 |
40.70 |
2e-39 |
uncharacterized LOC103926820
|
blastp_kegg |
lcl|mdm:103441842
|
61 |
260 |
+ |
200 |
Gaps:17 |
31.19 |
638 |
41.71 |
2e-39 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|pxb:103928207
|
61 |
260 |
+ |
200 |
Gaps:17 |
26.89 |
740 |
41.21 |
5e-38 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa003186mg
|
78 |
260 |
+ |
183 |
Gaps:23 |
31.26 |
595 |
39.25 |
5e-35 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101314615
|
70 |
260 |
+ |
191 |
Gaps:14 |
24.93 |
742 |
41.08 |
5e-35 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|pmum:103333657
|
53 |
260 |
+ |
208 |
Gaps:17 |
28.64 |
667 |
44.50 |
9e-35 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_kegg |
lcl|fve:101308225
|
61 |
260 |
+ |
200 |
Gaps:18 |
29.74 |
659 |
39.29 |
1e-33 |
cyclic nucleotide-gated ion channel 1-like
|
blastp_pdb |
1wgp_A
|
149 |
258 |
+ |
110 |
Gaps:6 |
77.37 |
137 |
42.45 |
2e-17 |
mol:protein length:137 Probable cyclic nucleotide-gated ion channel
|
blastp_uniprot_sprot |
sp|O65717|CNGC1_ARATH
|
53 |
260 |
+ |
208 |
Gaps:19 |
26.68 |
716 |
40.84 |
8e-32 |
Cyclic nucleotide-gated ion channel 1 OS Arabidopsis thaliana GN CNGC1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LNJ0|CNG10_ARATH
|
57 |
260 |
+ |
204 |
Gaps:14 |
27.29 |
711 |
36.60 |
1e-29 |
Probable cyclic nucleotide-gated ion channel 10 OS Arabidopsis thaliana GN CNGC10 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9LD40|CNG13_ARATH
|
57 |
258 |
+ |
202 |
Gaps:12 |
27.59 |
696 |
36.98 |
1e-28 |
Putative cyclic nucleotide-gated ion channel 13 OS Arabidopsis thaliana GN CNGC13 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9M0A4|CNGC9_ARATH
|
59 |
260 |
+ |
202 |
Gaps:21 |
25.24 |
733 |
39.46 |
5e-28 |
Putative cyclic nucleotide-gated ion channel 9 OS Arabidopsis thaliana GN CNGC9 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O82226|CNGC6_ARATH
|
59 |
260 |
+ |
202 |
Gaps:19 |
24.77 |
747 |
38.38 |
1e-27 |
Probable cyclic nucleotide-gated ion channel 6 OS Arabidopsis thaliana GN CNGC6 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9FXH6|CNGC8_ARATH
|
59 |
260 |
+ |
202 |
Gaps:21 |
24.57 |
753 |
37.84 |
2e-26 |
Putative cyclic nucleotide-gated ion channel 8 OS Arabidopsis thaliana GN CNGC8 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9S9N5|CNGC7_ARATH
|
59 |
260 |
+ |
202 |
Gaps:21 |
25.07 |
738 |
37.30 |
6e-26 |
Putative cyclic nucleotide-gated ion channel 7 OS Arabidopsis thaliana GN CNGC7 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8RWS9|CNGC5_ARATH
|
59 |
260 |
+ |
202 |
Gaps:21 |
25.80 |
717 |
37.30 |
2e-25 |
Probable cyclic nucleotide-gated ion channel 5 OS Arabidopsis thaliana GN CNGC5 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SKD7|CNGC3_ARATH
|
57 |
260 |
+ |
204 |
Gaps:14 |
27.20 |
706 |
35.94 |
1e-22 |
Probable cyclic nucleotide-gated ion channel 3 OS Arabidopsis thaliana GN CNGC3 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9SL29|CNG15_ARATH
|
74 |
260 |
+ |
187 |
Gaps:10 |
26.40 |
678 |
31.84 |
2e-22 |
Putative cyclic nucleotide-gated ion channel 15 OS Arabidopsis thaliana GN CNGC15 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|28920
|
149 |
260 |
+ |
112 |
Gaps:14 |
85.22 |
115 |
25.51 |
3e-07 |
cd00038 CAP_ED effector domain of the CAP family of transcription factors members include CAP (or cAMP receptor protein (CRP)) which binds cAMP FNR (fumarate and nitrate reduction) which uses an iron-sulfur cluster to sense oxygen) and CooA a heme containing CO sensor. In all cases binding of the effector leads to conformational changes and the ability to activate transcription. Cyclic nucleotide-binding domain similar to CAP are also present in cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) and vertebrate cyclic nucleotide-gated ion-channels. Cyclic nucleotide-monophosphate binding domain proteins that bind cyclic nucleotides (cAMP or cGMP) share a structural domain of about 120 residues the best studied is the prokaryotic catabolite gene activator CAP where such a domain is known to be composed of three alpha-helices and a distinctive eight-stranded antiparallel beta-barrel structure three conserved glycine residues are thought to be essential for maintenance of the structural integrity of the beta-barrel CooA is a homodimeric transcription factor that belongs to CAP family cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) contain two tandem copies of the cyclic nucleotide-binding domain cAPK's are composed of two different subunits a catalytic chain and a regulatory chain which contains both copies of the domain cGPK's are single chain enzymes that include the two copies of the domain in their N-terminal section also found in vertebrate cyclic nucleotide-gated ion-channels.
|
rpsblast_cdd |
gnl|CDD|197516
|
149 |
217 |
+ |
69 |
none |
57.50 |
120 |
31.88 |
9e-07 |
smart00100 cNMP Cyclic nucleotide-monophosphate binding domain. Catabolite gene activator protein (CAP) is a prokaryotic homologue of eukaryotic cNMP-binding domains present in ion channels and cNMP-dependent kinases.
|
rpsblast_kog |
gnl|CDD|35719
|
64 |
267 |
+ |
204 |
Gaps:26 |
26.96 |
727 |
30.10 |
6e-26 |
KOG0498 KOG0498 KOG0498 K+-channel ERG and related proteins contain PAS/PAC sensor domain [Inorganic ion transport and metabolism Signal transduction mechanisms].
|