blastp_kegg |
lcl|fve:101310012
|
17 |
268 |
+ |
252 |
Gaps:9 |
69.15 |
363 |
66.93 |
2e-99 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|pxb:103940198
|
1 |
273 |
+ |
273 |
Gaps:25 |
100.00 |
266 |
65.41 |
2e-97 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|pmum:103324936
|
25 |
268 |
+ |
244 |
Gaps:8 |
92.83 |
265 |
66.26 |
3e-93 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa021837mg
|
48 |
268 |
+ |
221 |
Gaps:7 |
83.77 |
265 |
69.37 |
3e-92 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0004s05490g
|
26 |
267 |
+ |
242 |
Gaps:7 |
92.05 |
264 |
63.79 |
4e-92 |
POPTRDRAFT_555688 POPTRDRAFT_555689 hypothetical protein
|
blastp_kegg |
lcl|gmx:100804756
|
13 |
272 |
+ |
260 |
Gaps:9 |
96.34 |
273 |
60.46 |
3e-91 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|rcu:RCOM_1014730
|
50 |
273 |
+ |
224 |
Gaps:8 |
99.56 |
227 |
68.58 |
9e-91 |
DNA binding protein putative
|
blastp_kegg |
lcl|mdm:103434868
|
13 |
273 |
+ |
261 |
Gaps:16 |
98.87 |
266 |
62.74 |
9e-89 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|mdm:103446328
|
1 |
273 |
+ |
273 |
Gaps:23 |
100.00 |
268 |
62.69 |
1e-88 |
transcription factor bHLH30-like
|
blastp_kegg |
lcl|pxb:103944104
|
31 |
273 |
+ |
243 |
Gaps:13 |
92.54 |
268 |
64.52 |
6e-87 |
transcription factor bHLH30-like
|
blastp_uniprot_sprot |
sp|Q9LET0|BH107_ARATH
|
75 |
245 |
+ |
171 |
Gaps:9 |
73.04 |
230 |
41.67 |
4e-33 |
Putative transcription factor bHLH107 OS Arabidopsis thaliana GN BHLH107 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9S7Y1|BH030_ARATH
|
39 |
268 |
+ |
230 |
Gaps:21 |
64.40 |
368 |
39.66 |
5e-30 |
Transcription factor bHLH30 OS Arabidopsis thaliana GN BHLH30 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O80674|BH106_ARATH
|
75 |
243 |
+ |
169 |
Gaps:6 |
66.01 |
253 |
41.92 |
3e-28 |
Transcription factor bHLH106 OS Arabidopsis thaliana GN BHLH106 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9XEF0|BH051_ARATH
|
74 |
211 |
+ |
138 |
Gaps:5 |
54.72 |
254 |
41.73 |
1e-27 |
Transcription factor bHLH51 OS Arabidopsis thaliana GN BHLH51 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LS08|BH032_ARATH
|
43 |
241 |
+ |
199 |
Gaps:30 |
60.17 |
344 |
38.16 |
4e-26 |
Transcription factor AIG1 OS Arabidopsis thaliana GN BHLH32 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P0CB25|BH131_ARATH
|
73 |
218 |
+ |
146 |
Gaps:10 |
53.12 |
256 |
37.50 |
7e-17 |
Transcription factor bHLH131 OS Arabidopsis thaliana GN BHLH131 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LNJ5|BH013_ARATH
|
69 |
245 |
+ |
177 |
Gaps:21 |
29.49 |
590 |
33.33 |
3e-11 |
Transcription factor bHLH13 OS Arabidopsis thaliana GN BHLH13 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q39204|MYC2_ARATH
|
64 |
154 |
+ |
91 |
Gaps:1 |
14.77 |
623 |
41.30 |
4e-11 |
Transcription factor MYC2 OS Arabidopsis thaliana GN MYC2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9FT81|TT8_ARATH
|
86 |
193 |
+ |
108 |
Gaps:9 |
21.43 |
518 |
36.94 |
1e-09 |
Transcription factor TT8 OS Arabidopsis thaliana GN TT8 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9ZPY8|AIB_ARATH
|
69 |
211 |
+ |
143 |
Gaps:9 |
26.15 |
566 |
33.11 |
5e-09 |
Transcription factor ABA-INDUCIBLE bHLH-TYPE OS Arabidopsis thaliana GN AIB PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|200925
|
85 |
132 |
+ |
48 |
Gaps:2 |
96.15 |
52 |
42.00 |
1e-07 |
pfam00010 HLH Helix-loop-helix DNA-binding domain.
|
rpsblast_cdd |
gnl|CDD|28964
|
85 |
133 |
+ |
49 |
Gaps:3 |
86.67 |
60 |
38.46 |
7e-07 |
cd00083 HLH Helix-loop-helix domain found in specific DNA- binding proteins that act as transcription factors 60-100 amino acids long. A DNA-binding basic region is followed by two alpha-helices separated by a variable loop region HLH forms homo- and heterodimers dimerization creates a parallel left-handed four helix bundle the basic region N-terminal to the first amphipathic helix mediates high-affinity DNA-binding there are several groups of HLH proteins: those (E12/E47) which bind specific hexanucleotide sequences such as E-box (5-CANNTG-3) or StRE 5-ATCACCCCAC-3) those lacking the basic domain (Emc Id) function as negative regulators since they fail to bind DNA those (hairy E(spl) deadpan) which repress transcription although they can bind specific hexanucleotide sequences such as N-box (5-CACGc/aG-3) those which have a COE domain (Collier/Olf-1/EBF) which is involved in both in dimerization and in DNA binding and those which bind pentanucleotides ACGTG or GCGTG and have a PAS domain which allows the dimerization between PAS proteins the binding of small molecules (e.g. dioxin) and interactions with non-PAS proteins..
|