Select | Gene | Cds | Cds_length | GC_content | Pep | Pep_length |
---|---|---|---|---|---|---|
Aev08g2199 | ATGGAAACAGATCCATCCATGTCTTCTCCGCCACCTCCCGCTGCCACCGATCCCTCTTCTCGTCACCACACCTACAACCGCAAGCAAAAATCCCTCGGCCTCTTGTGCACCAAGTTCTTGAGTTTGTATGATCGGGAGGATGTCCACTTGATCGGACTCGATGATGCCGCCGCTCGATTAGGGGTGGAGAGGCGGCGGATCTATGATATAGTCAATGTTTTGGAGAGTATCGGGATGCTTGCGAGAAAAGCCAAGAATCAGTACACTTGGAAAGGGTTTGGTGCAATTCCTGGGACTTTACAAGAGCTCAAGGACGAGGGTTTGAAGGAGAATCCATATGGTTTTGATGGTGCCACTGACAGTGCAAAGGTTTCTGATGATGAGGATGACGAAGAAACATTGTCCAATCCTAGTACTGGAAGTCAGAATGACAGATCCAATACTAGTTCCTCAGTTGTCAAGTCAAAGACTGAAAACAGAAGGGAAAAATCTCTGGCACTGCTTACTCAGAATTTTGTCAAGCTCTTTATCTGCTCTAATATGGAAATGATTTCCCTCGACGAAGCTGCAAAATTGTTGCTTGGAAATGCCCATAATTCATCAATAATGAGAACAAAAGTCAGACGCCTGTATGATATTGCAAATGTATTGTCTTCCATGAACCTGATTGAGAAGACCCATACAAGAAACACAAGAAAACCAGCATTCAAGTGGTTGGGTTTGAAAGGGAAAACATGTACTGAGTCAGTTGACTCAGCTCATAACTCAACTCTCAACAATGAGTCGAGCAAAAGGATGTTCGGAGATGACATCACAAACATCAGTTTCAAGAGGACCAAGGTGGATTTATTCATGGATGGACACAATAGCAAGAACTCCGGAATGCAAGAAAATGATAGTCGACATGCTCTTTCAGATAAAAGCAATCAAAAGCAAAATGCAAAACAGGCTTCAAGGAACTATCAGTTTGGTCCATTTGCTCCAGCTTTTGTGTCCAAAGTTGGAGGTGCCTCTGAGAGTAGTAGCACTGCAAAGCAAGTGCATGATTGGGAGAGCCTCTCTACGAAACATCGTCCTCAGTATCAAAACCAAGCTATGAAGGACCTGTTCTTTCACTACATGGAAGCATGGAAATCTTGGTACTCTGAAGCTGCAGCGAAGAGGCCGCAGCGACGAGGCCAGTAA | 1185 | 0.4464 | METDPSMSSPPPPAATDPSSRHHTYNRKQKSLGLLCTKFLSLYDREDVHLIGLDDAAARLGVERRRIYDIVNVLESIGMLARKAKNQYTWKGFGAIPGTLQELKDEGLKENPYGFDGATDSAKVSDDEDDEETLSNPSTGSQNDRSNTSSSVVKSKTENRREKSLALLTQNFVKLFICSNMEMISLDEAAKLLLGNAHNSSIMRTKVRRLYDIANVLSSMNLIEKTHTRNTRKPAFKWLGLKGKTCTESVDSAHNSTLNNESSKRMFGDDITNISFKRTKVDLFMDGHNSKNSGMQENDSRHALSDKSNQKQNAKQASRNYQFGPFAPAFVSKVGGASESSSTAKQVHDWESLSTKHRPQYQNQAMKDLFFHYMEAWKSWYSEAAAKRPQRRGQ* | 395 |
Select | Seq ID | Length | Analysis | Description | Start | End | IPR | GO |
---|---|---|---|---|---|---|---|---|
Aev08g2199 | 394 | MobiDBLite | consensus disorder prediction | 135 | 154 | - | - | |
Aev08g2199 | 394 | PANTHER | E2F TRANSCRIPTION FACTOR-LIKE E2FF | 19 | 384 | - | - | |
Aev08g2199 | 394 | SUPERFAMILY | "Winged helix" DNA-binding domain | 162 | 241 | IPR036390 | - | |
Aev08g2199 | 394 | Gene3D | - | 22 | 95 | IPR036388 | - | |
Aev08g2199 | 394 | Gene3D | - | 154 | 242 | IPR036388 | - | |
Aev08g2199 | 394 | MobiDBLite | consensus disorder prediction | 1 | 26 | - | - | |
Aev08g2199 | 394 | SMART | E2F_TDP_2 | 160 | 240 | IPR003316 | GO:0005667|GO:0006355 | |
Aev08g2199 | 394 | SMART | E2F_TDP_2 | 27 | 92 | IPR003316 | GO:0005667|GO:0006355 | |
Aev08g2199 | 394 | SUPERFAMILY | "Winged helix" DNA-binding domain | 26 | 90 | IPR036390 | - | |
Aev08g2199 | 394 | MobiDBLite | consensus disorder prediction | 287 | 317 | - | - | |
Aev08g2199 | 394 | MobiDBLite | consensus disorder prediction | 108 | 160 | - | - | |
Aev08g2199 | 394 | MobiDBLite | consensus disorder prediction | 1 | 17 | - | - | |
Aev08g2199 | 394 | Pfam | E2F/DP family winged-helix DNA-binding domain | 28 | 92 | IPR003316 | GO:0005667|GO:0006355 | |
Aev08g2199 | 394 | Pfam | E2F/DP family winged-helix DNA-binding domain | 162 | 240 | IPR003316 | GO:0005667|GO:0006355 | |
Aev08g2199 | 394 | PANTHER | TRANSCRIPTION FACTOR E2F | 19 | 384 | IPR015633 | GO:0000978|GO:0006357 |
Select | Gene | Chromosome | Start | End | Duplicated_type |
---|---|---|---|---|---|
Aev08g2199 | Aev-Chr8 | 21184368 | 21196977 | Dispersed/Wgd |
Select | Gene | Gene_start | Gene_end | Function | Ath_gene | Identity(%) | E-value | Score |
---|---|---|---|---|---|---|---|---|
Aev08g2199 | 13 | 97 | E2F-DP Transcription Factor Family | AT3G48160 | 34.653 | 3.32e-08 | 53.1 |
Select | Regulatory Factors | Family | Gene | Hmm_acc | Hmm_name | E_value | Clan |
---|---|---|---|---|---|---|---|
TF | E2F-DP | Aev08g2199 | E2F_TDP | 1.2e-20 | CL0123 |
Select | Query | KO | Definition | Second KO | KEGG Genes ID | GHOSTX Score |
---|---|---|---|---|---|---|
Aev08g2199 | K09391 | - | qsu:112020170 | 499.204 |
Select | Gene_1 | Chr_1 | Start_1 | End_1 | Gene_2 | Chr_2 | Start_2 | End_2 | Event_name |
---|---|---|---|---|---|---|---|---|---|
Aev01g2055 | 01 | 25151472 | 25153937 | Aev08g2199 | 08 | 21184368 | 21196977 | PCT |