New model in OGS2.0 | DPOGS213698  |
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Genomic Position | scaffold487:+ 45978-46899 |
See gene structure | |
CDS Length | 645 |
Paired RNAseq reads   | 633 |
Single RNAseq reads   | 2117 |
Migratory profiles | Query via corresponding ESTs |
Best Bmobyx hit | BGIBMGA010671 (4e-114) |
Best Drosophila hit   | CG10306 (2e-64) |
Best Human hit | eukaryotic translation initiation factor 3 subunit K (3e-66) |
Best NR hit (blastp)   | eukaryotic translation initiation factor 3 subunit K [Bombyx mori] (2e-115) |
Best NR hit (blastx)   | eukaryotic translation initiation factor 3 subunit K [Bombyx mori] (1e-112) |
GeneOntology terms    | GO:0005515 protein binding GO:0003743 translation initiation factor activity GO:0006413 translational initiation GO:0005852 eukaryotic translation initiation factor 3 complex GO:0005737 cytoplasm GO:0005634 nucleus GO:0005829 cytosol GO:0043022 ribosome binding GO:0006446 regulation of translational initiation |
InterPro families    | IPR016024 Armadillo-type fold IPR019280 COP9 signalosome, subunit CSN8 IPR016020 Translation initiation factor 3, subunit 12, N-terminal, eukaryotic IPR011991 Winged helix-turn-helix transcription repressor DNA-binding IPR009374 Translation initiation factor 3, subunit 12, eukaryotic |
Orthology group | MCL13705 |
Nucleotide sequence:
ATGGCAGAAACCATGAGACAAACTGTGGCTTCAATTTTGAAAAGTATCGAGAGATATAAC
CCAGCCAATCTTCAGACACTCGAACGATACGTTGAGTTACAATCAAGGGAGAATACATAC
GATTTAGAAGCAAATTTAGCGGTTCTGAAACTTTATCAGTTCAATCCAGAAAGGTTCAAC
CCTGACATAACGTGCCAGATACTTTTAAAGGCACTTACAAATTTCCCTCACACCGACTTT
ACATTGTGCAAGTGTCTGCTTTTAGAATCTGTAGTGGAAAACGAGACCATTTCCCAAATA
AAGTATCTGGCTGATATTCTTGAGCAATGCGATTTTGCCCAGTTCTGGAACAGAGTACAC
CAAATGCCGGAACTGTGTAACCGTATCAGCAGCTTCCATGATTCCATTCGCAAGTTTGTT
TGTCATGTTGTCGGCATTACTTTCCAGACTATTGACAAGAATAACCTTGCTAACTTGTTA
GGTGGAATCGATGATGTGACCCTGAAGCACTGGGTTAAAAAATATGGTTGGAAGGATGAG
GGTAACCTTATCTTCATCGCAAATCAAGATGAGAACATCAAGACTAAGAATATTACAGAG
AAAATTGAATTTGATCATCTCGCTCCCTTAATGGCAATTTTGTAA
Protein sequence:
MAETMRQTVASILKSIERYNPANLQTLERYVELQSRENTYDLEANLAVLKLYQFNPERFN
PDITCQILLKALTNFPHTDFTLCKCLLLESVVENETISQIKYLADILEQCDFAQFWNRVH
QMPELCNRISSFHDSIRKFVCHVVGITFQTIDKNNLANLLGGIDDVTLKHWVKKYGWKDE
GNLIFIANQDENIKTKNITEKIEFDHLAPLMAIL