Aocu019529.1


Basic Information
Transcription Factor Domain
Sequence Information
Similer Transcription Factors

Basic Information

Insect
Amphipoea oculea
Gene Symbol
Abl
Assembly
GCA_945859585.1
Location
CAMAOF010000203.1:36202-42977[-]

Transcription Factor Domain

TF Family
POU
Domain
Homeobox|Pou
PFAM
PF00157
TF Group
Helix-turn-helix
Description
The POU domain is a bipartite domain composed of two subunits separated by a non-conserved region of 15-55 aa. The N-terminal subunit is known as the POU-specific (POUs) domain (this entry), while the C-terminal subunit is a homeobox domain (IPR001356). Both subdomains contain the structural motif 'helix-turn-helix', which directly associates with the two components of bipartite DNA binding sites, and both are required for high affinity sequence-specific DNA-binding. 3D structures of complexes including both POU subdomains bound to DNA are available. The domain may also be involved in protein-protein interactions [6]. The subdomains are connected by a flexible linker [7, 5, 8]. Despite of the lack of sequence homology, the tridimensional structure of POUs is similar to 3D structure of bacteriophage lambda repressor and other members of HTH_3 family [7, 5]. POU proteins are eukaryotic transcription factors containing a bipartite DNA binding domain referred to as the POU domain. The acronym POU (pronounced 'pow') is derived from the names of three mammalian transcription factors, the pituitary-specific Pit-1, the octamer-binding proteins Oct-1 and Oct-2, and the neural Unc-86 from Caenorhabditis elegans. POU domain genes have been identified in diverse organisms including nematodes, flies, amphibians, fish and mammals but have not been yet identified in plants and fungi. The various members of the POU family have a wide variety of functions, all of which are related to the function of the neuroendocrine system [4] and the development of an organism [1]. Some other genes are also regulated, including those for immunoglobulin light and heavy chains (Oct-2) [3, 2], and trophic hormone genes, such as those for prolactin and growth hormone (Pit-1).
Hmmscan Out
# of c-Evalue i-Evalue score bias hmm coord from hmm coord to ali coord from ali coord to env coord from env coord to acc
1 54 1.9 8.9e+03 -2.9 0.0 13 37 40 64 36 70 0.78
2 54 1.3 5.8e+03 -2.3 0.0 11 36 82 107 72 112 0.71
3 54 0.2 9.3e+02 0.2 0.0 11 38 126 153 116 171 0.80
4 54 0.18 8.2e+02 0.4 0.0 8 38 167 197 159 216 0.78
5 54 0.49 2.2e+03 -1.0 0.0 11 37 236 262 225 276 0.84
6 54 0.64 3e+03 -1.4 0.0 12 44 259 292 252 303 0.73
7 54 0.072 3.3e+02 1.6 0.0 8 38 295 325 287 334 0.86
8 54 0.16 7.3e+02 0.5 0.0 11 38 342 369 331 388 0.77
9 54 0.19 8.5e+02 0.3 0.0 8 38 383 413 375 431 0.79
10 54 0.53 2.5e+03 -1.2 0.0 11 37 452 478 441 483 0.82
11 54 0.82 3.8e+03 -1.8 0.0 11 37 496 522 485 527 0.75
12 54 0.069 3.2e+02 1.7 0.0 8 38 537 567 529 573 0.85
13 54 0.18 8.2e+02 0.4 0.0 8 38 581 611 573 629 0.79
14 54 0.067 3.1e+02 1.7 0.0 8 38 625 655 617 663 0.85
15 54 0.16 7.6e+02 0.5 0.0 11 38 672 699 661 717 0.79
16 54 0.19 8.5e+02 0.3 0.0 8 38 713 743 705 761 0.79
17 54 0.51 2.4e+03 -1.1 0.0 11 37 782 808 771 815 0.82
18 54 0.42 1.9e+03 -0.8 0.0 12 38 827 853 815 871 0.72
19 54 0.43 2e+03 -0.9 0.0 10 37 847 874 837 881 0.76
20 54 0.03 1.4e+02 2.9 0.0 10 37 891 918 881 924 0.85
21 54 1.1 5e+03 -2.2 0.0 11 37 936 962 925 969 0.73
22 54 0.45 2.1e+03 -0.9 0.0 12 38 959 985 949 1003 0.72
23 54 0.06 2.8e+02 1.9 0.0 8 38 999 1029 991 1046 0.85
24 54 0.19 8.5e+02 0.3 0.0 8 38 1043 1073 1035 1091 0.79
25 54 0.26 1.2e+03 -0.1 0.0 8 38 1087 1117 1080 1125 0.84
26 54 0.19 8.6e+02 0.3 0.0 9 38 1110 1139 1101 1144 0.81
27 54 0.0053 24 5.3 0.0 8 38 1153 1183 1145 1187 0.88
28 54 0.45 2e+03 -0.9 0.0 12 38 1201 1227 1190 1245 0.75
29 54 0.26 1.2e+03 -0.1 0.0 11 38 1266 1293 1255 1299 0.83
30 54 0.32 1.5e+03 -0.5 0.0 11 38 1288 1315 1277 1328 0.79
31 54 0.38 1.8e+03 -0.7 0.0 8 36 1307 1335 1299 1350 0.83
32 54 0.56 2.6e+03 -1.2 0.0 11 37 1332 1358 1322 1363 0.82
33 54 0.58 2.7e+03 -1.3 0.0 11 38 1376 1403 1365 1409 0.76
34 54 0.068 3.1e+02 1.7 0.0 8 38 1417 1447 1409 1454 0.85
35 54 0.18 8.2e+02 0.4 0.0 8 38 1461 1491 1453 1510 0.78
36 54 0.25 1.1e+03 -0.1 0.0 8 38 1505 1535 1497 1542 0.83
37 54 0.17 8e+02 0.4 0.0 9 38 1528 1557 1519 1564 0.81
38 54 0.18 8.2e+02 0.4 0.0 11 38 1552 1579 1543 1597 0.79
39 54 0.51 2.3e+03 -1.1 0.0 11 37 1618 1644 1607 1652 0.83
40 54 1.1 5.1e+03 -2.2 0.0 11 37 1662 1688 1652 1698 0.75
41 54 0.2 9.4e+02 0.2 0.0 11 38 1706 1733 1697 1741 0.83
42 54 0.22 1e+03 0.1 0.0 11 38 1728 1755 1719 1764 0.82
43 54 0.17 7.9e+02 0.4 0.0 11 38 1750 1777 1740 1795 0.79
44 54 0.19 8.5e+02 0.3 0.0 8 38 1791 1821 1783 1839 0.79
45 54 0.5 2.3e+03 -1.1 0.0 11 37 1860 1886 1849 1895 0.83
46 54 0.42 1.9e+03 -0.8 0.0 12 38 1905 1931 1895 1950 0.69
47 54 0.36 1.6e+03 -0.6 0.0 8 36 1945 1973 1937 1983 0.83
48 54 0.53 2.5e+03 -1.2 0.0 11 37 1970 1996 1959 2001 0.82
49 54 0.58 2.7e+03 -1.3 0.0 11 38 2014 2041 2003 2047 0.76
50 54 0.05 2.3e+02 2.1 0.0 8 38 2055 2085 2047 2104 0.81
51 54 0.42 1.9e+03 -0.8 0.0 10 37 2123 2150 2113 2163 0.79
52 54 0.24 1.1e+03 -0.1 0.0 8 38 2143 2173 2135 2181 0.84
53 54 0.18 8.2e+02 0.4 0.0 9 38 2166 2195 2157 2201 0.81
54 54 0.21 9.4e+02 0.2 0.0 8 31 2209 2232 2201 2232 0.86

Sequence Information

Coding Sequence
ATGGAGTGCCCACCAGGCTGCCCCGGCGCCGTGTACGAGTTGATGCGCGGCTGCTGGCAGTGGAACGCGGCCGAGAGGCCCTCGTTCCGCGACATCCACCACGCGCTCGAGCATATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGGGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAAGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAACGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACACCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTTACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGATGGTAACTATCAGCACGAAATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGCGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGAAATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGATGGTAACTATCAGCACGAAATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCAGGATAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACAAGTTCCGGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTCCCAGGACAACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGAGCACATGTTCCGGGACCACTCCATCACCGATGGTAACTATCAGCACGAAATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCGAGCACATGTTCCGGGACCACTCCATCAGCGAGGGTAACTATCAGCACGACATCCACCACGCGTTCGCGCACATGTTCCGGGACCACTCCATCACCGAGGGTAACTATCAGCACGACATCCACCACGCGCTCTAG
Protein Sequence
MECPPGCPGAVYELMRGCWQWNAAERPSFRDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITGHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSINEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHTISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHKFRDNSITEGYYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITDGNYQHEIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFAHMFRDHSITEGNYQHDIHHALEHMFRDHSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHEIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSISEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITDGNYQHEIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFQDNSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHKFRDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMSQDNSITEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFEHMFRDHSITDGNYQHEIHHALEHMFRDHSISEGNYQHDIHHALEHMFRDHSISEGNYQHDIHHAFAHMFRDHSITEGNYQHDIHHAL

Similar Transcription Factors

Sequence clustering based on sequence similarity using MMseqs2

100% Identity
-
90% Identity
-
80% Identity
-