blastp_kegg |
lcl|vvi:100253657
|
1 |
461 |
+ |
461 |
Gaps:82 |
77.64 |
568 |
64.85 |
1e-159 |
transcription factor bHLH91-like
|
blastp_kegg |
lcl|rcu:RCOM_0275800
|
1 |
465 |
+ |
465 |
Gaps:49 |
99.79 |
469 |
57.69 |
2e-147 |
Transcription factor ICE1 putative
|
blastp_kegg |
lcl|pxb:103962830
|
104 |
468 |
+ |
365 |
Gaps:31 |
73.83 |
512 |
65.87 |
4e-145 |
transcription factor bHLH91-like
|
blastp_kegg |
lcl|pxb:103962812
|
104 |
468 |
+ |
365 |
Gaps:31 |
73.83 |
512 |
65.87 |
4e-145 |
transcription factor bHLH91-like
|
blastp_kegg |
lcl|pxb:103951747
|
34 |
468 |
+ |
435 |
Gaps:46 |
87.13 |
513 |
60.18 |
5e-145 |
transcription factor bHLH91-like
|
blastp_kegg |
lcl|mdm:103410049
|
35 |
467 |
+ |
433 |
Gaps:33 |
87.28 |
511 |
60.09 |
1e-140 |
transcription factor bHLH91-like
|
blastp_kegg |
lcl|mdm:103418457
|
60 |
468 |
+ |
409 |
Gaps:34 |
100.00 |
411 |
60.34 |
1e-140 |
transcription factor bHLH10-like
|
blastp_kegg |
lcl|mdm:103408165
|
60 |
468 |
+ |
409 |
Gaps:34 |
100.00 |
411 |
60.34 |
1e-140 |
transcription factor bHLH10-like
|
blastp_kegg |
lcl|pxb:103962805
|
60 |
468 |
+ |
409 |
Gaps:34 |
100.00 |
415 |
59.28 |
2e-139 |
transcription factor bHLH10-like
|
blastp_kegg |
lcl|pxb:103962780
|
60 |
468 |
+ |
409 |
Gaps:34 |
100.00 |
415 |
59.28 |
2e-139 |
transcription factor bHLH10-like
|
blastp_uniprot_sprot |
sp|Q84TK1|BH010_ARATH
|
104 |
468 |
+ |
365 |
Gaps:59 |
77.29 |
458 |
52.26 |
2e-87 |
Transcription factor bHLH10 OS Arabidopsis thaliana GN BHLH10 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8GX46|BH091_ARATH
|
1 |
468 |
+ |
468 |
Gaps:116 |
100.00 |
428 |
48.13 |
9e-84 |
Transcription factor bHLH91 OS Arabidopsis thaliana GN BHLH91 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LND0|BH089_ARATH
|
1 |
458 |
+ |
458 |
Gaps:80 |
94.76 |
420 |
45.23 |
1e-79 |
Transcription factor bHLH89 OS Arabidopsis thaliana GN BHLH89 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q39204|MYC2_ARATH
|
261 |
448 |
+ |
188 |
Gaps:27 |
28.09 |
623 |
33.71 |
8e-15 |
Transcription factor MYC2 OS Arabidopsis thaliana GN MYC2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9FN69|GL3_ARATH
|
175 |
459 |
+ |
285 |
Gaps:16 |
46.00 |
637 |
25.94 |
7e-12 |
Transcription factor GLABRA 3 OS Arabidopsis thaliana GN GL3 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LSE2|ICE1_ARATH
|
266 |
455 |
+ |
190 |
Gaps:23 |
37.04 |
494 |
32.24 |
1e-11 |
Transcription factor ICE1 OS Arabidopsis thaliana GN SCRM PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9ZPY8|AIB_ARATH
|
261 |
333 |
+ |
73 |
Gaps:4 |
12.19 |
566 |
49.28 |
1e-11 |
Transcription factor ABA-INDUCIBLE bHLH-TYPE OS Arabidopsis thaliana GN AIB PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9FIP9|MYC3_ARATH
|
261 |
427 |
+ |
167 |
Gaps:18 |
25.84 |
592 |
32.68 |
1e-10 |
Transcription factor MYC3 OS Arabidopsis thaliana GN MYC3 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LPW3|SCRM2_ARATH
|
266 |
420 |
+ |
155 |
Gaps:28 |
31.78 |
450 |
35.66 |
1e-10 |
Transcription factor SCREAM2 OS Arabidopsis thaliana GN SCRM2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9ZVX2|AMS_ARATH
|
265 |
454 |
+ |
190 |
Gaps:16 |
33.98 |
571 |
29.38 |
2e-10 |
Transcription factor ABORTED MICROSPORES OS Arabidopsis thaliana GN AMS PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|200925
|
266 |
312 |
+ |
47 |
Gaps:2 |
94.23 |
52 |
40.82 |
7e-09 |
pfam00010 HLH Helix-loop-helix DNA-binding domain.
|
rpsblast_cdd |
gnl|CDD|197674
|
272 |
318 |
+ |
47 |
Gaps:3 |
94.34 |
53 |
38.00 |
2e-08 |
smart00353 HLH helix loop helix domain.
|
rpsblast_cdd |
gnl|CDD|28964
|
266 |
316 |
+ |
51 |
Gaps:3 |
90.00 |
60 |
33.33 |
4e-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..
|