blastp_kegg |
lcl|rcu:RCOM_1589780
|
9 |
241 |
+ |
233 |
Gaps:8 |
96.76 |
247 |
63.18 |
1e-98 |
hypothetical protein
|
blastp_kegg |
lcl|cic:CICLE_v10003973mg
|
2 |
241 |
+ |
240 |
Gaps:8 |
96.39 |
249 |
62.92 |
2e-98 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_033803
|
10 |
241 |
+ |
232 |
Gaps:8 |
90.23 |
266 |
63.75 |
3e-95 |
Basic helix-loop-helix DNA-binding superfamily protein putative
|
blastp_kegg |
lcl|pop:POPTR_0014s02600g
|
7 |
241 |
+ |
235 |
Gaps:11 |
83.16 |
291 |
63.64 |
5e-91 |
basic helix-loop-helix family protein
|
blastp_kegg |
lcl|pper:PRUPE_ppa018148mg
|
17 |
241 |
+ |
225 |
Gaps:9 |
95.61 |
228 |
64.22 |
2e-88 |
hypothetical protein
|
blastp_kegg |
lcl|vvi:100264010
|
28 |
241 |
+ |
214 |
Gaps:5 |
71.15 |
305 |
58.99 |
4e-84 |
transcription factor bHLH95-like
|
blastp_kegg |
lcl|mdm:103431300
|
3 |
241 |
+ |
239 |
Gaps:9 |
99.14 |
232 |
57.83 |
2e-81 |
transcription factor bHLH95-like
|
blastp_kegg |
lcl|pxb:103955115
|
3 |
241 |
+ |
239 |
Gaps:12 |
82.50 |
280 |
58.44 |
6e-80 |
transcription factor bHLH95-like
|
blastp_kegg |
lcl|mdm:103455955
|
3 |
241 |
+ |
239 |
Gaps:12 |
99.14 |
233 |
57.58 |
8e-80 |
transcription factor bHLH95-like
|
blastp_kegg |
lcl|mus:103997517
|
9 |
241 |
+ |
233 |
Gaps:5 |
99.58 |
237 |
56.36 |
1e-79 |
transcription factor bHLH95
|
blastp_uniprot_sprot |
sp|Q9FXA3|BH095_ARATH
|
10 |
241 |
+ |
232 |
Gaps:41 |
82.79 |
308 |
36.86 |
6e-37 |
Transcription factor bHLH95 OS Arabidopsis thaliana GN BHLH95 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q56YJ8|FAMA_ARATH
|
4 |
237 |
+ |
234 |
Gaps:52 |
55.56 |
414 |
29.13 |
2e-11 |
Transcription factor FAMA OS Arabidopsis thaliana GN FMA PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9T072|BH025_ARATH
|
14 |
186 |
+ |
173 |
Gaps:25 |
45.12 |
328 |
29.05 |
2e-08 |
Transcription factor bHLH25 OS Arabidopsis thaliana GN BHLH25 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9ZPY8|AIB_ARATH
|
8 |
91 |
+ |
84 |
Gaps:4 |
14.13 |
566 |
32.50 |
3e-08 |
Transcription factor ABA-INDUCIBLE bHLH-TYPE OS Arabidopsis thaliana GN AIB PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q39204|MYC2_ARATH
|
5 |
197 |
+ |
193 |
Gaps:30 |
26.16 |
623 |
34.97 |
8e-08 |
Transcription factor MYC2 OS Arabidopsis thaliana GN MYC2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|O49687|MYC4_ARATH
|
11 |
100 |
+ |
90 |
Gaps:9 |
13.75 |
589 |
38.27 |
1e-07 |
Transcription factor MYC4 OS Arabidopsis thaliana GN MYC4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SK91|BH094_ARATH
|
28 |
90 |
+ |
63 |
Gaps:1 |
21.05 |
304 |
42.19 |
2e-07 |
Transcription factor bHLH94 OS Arabidopsis thaliana GN BHLH94 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9LNJ5|BH013_ARATH
|
11 |
90 |
+ |
80 |
Gaps:8 |
12.20 |
590 |
37.50 |
3e-07 |
Transcription factor bHLH13 OS Arabidopsis thaliana GN BHLH13 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q1PF16|BH019_ARATH
|
8 |
100 |
+ |
93 |
Gaps:4 |
30.17 |
295 |
37.08 |
3e-07 |
Transcription factor bHLH19 OS Arabidopsis thaliana GN BHLH19 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q700E4|BH067_ARATH
|
28 |
96 |
+ |
69 |
Gaps:5 |
19.55 |
358 |
41.43 |
4e-07 |
Transcription factor bHLH67 OS Arabidopsis thaliana GN BHLH67 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|200925
|
32 |
80 |
+ |
49 |
Gaps:1 |
96.15 |
52 |
38.00 |
2e-08 |
pfam00010 HLH Helix-loop-helix DNA-binding domain.
|
rpsblast_cdd |
gnl|CDD|28964
|
28 |
84 |
+ |
57 |
Gaps:2 |
98.33 |
60 |
42.37 |
7e-08 |
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..
|