Select | Gene | Cds | Cds_length | GC_content | Pep | Pep_length |
---|---|---|---|---|---|---|
Gma11g00500 | ATGGGTGACATGTACCACTTTGACAAGAACCTCTCCTCACAAGACGAAATCTCACTTTTTCTGCGTCAGATTCTGCTCCGTTCATCTTCACCTTCCCACTCCATGCCTGCTGGATCCTGCACCTCCAACGCTGCTCAACAAAACGTAAATGCACACCACCCTTCTTTCACGGCGTCACAGCTCCAAGATGGGAAGATCTTGGCCGTTGATTCCACCGCTTCTTTTGTCTCCGGTTCTGCTGCTTGCAGTTCCTTCAAGGGCCATGGTGCTTCTGCTGCAAATGTGTCTTCTTCTTCTGCTGGAGTGAGTGAGAACGAGAATGATGACTATGATTGTGAGAGTGAGGAGGGTGTTGAGGCTCCGGCCGAAGAAGTTCCAACAAAGGCTGCTTCTTCTAGGAGTTCATCTAAAAGATCAAGAGCTGCAGAAGTTCATAATTTGTCAGAGAAGCGGAGAAGGGGTAGGATCAACGAGAAAATGAAGGCTTTGCAAAACCTAATTCCAAATTCTAACAAGACAGATAAGGCTTCAATGCTCGATGAAGCTATTGAATACCTTAAACAGCTTCAGCTACAAGTACAGATGCTGTCAATGAGAAATGGGTTGAGTTTGCATCCTATGTGCTTTCCTGAAGGCTTGCAGCCTCTGCAGTTGTCTCAGATGGGTATGGAATTAAGTGAAAGAAACAGGTTTACCTCTTTAAACATGTCAGCTACTCTGCCTCTGCACCAAGACAACAATCCCTTGCACTATGCATCCAATCTACCTAACAAACACAATCTCCCAAATCAGCCATCTGTGCCCTATCCTCCATACATTGACAACCCAGAAACTTCTTTCGGTCTGGAACCCCGAATCCAAACGGATATGAAACCTCTTCAACACAAAGGAGGATCTTCTGAGCCAATACGAGGGGAAGACATTTTGCAGCACCAGCAATCAAGTGGTATCCATTCAGATGCCAATACATTAGGTGGTTCTCAAGTTGTCAAAGAATTCGAATCAGGCACGAGACTATCATTCCCTTTTGACACGCAAGCATGTGAACCCAAAGACAACAGCAACTCTTCGCAACCATGCATTGGCGGAAGAGATCATTCAGGAGTGATCATAAGAAATAGTGAGACCAACATTGTTGGTAGGTAG | 1146 | 0.4555 | MGDMYHFDKNLSSQDEISLFLRQILLRSSSPSHSMPAGSCTSNAAQQNVNAHHPSFTASQLQDGKILAVDSTASFVSGSAACSSFKGHGASAANVSSSSAGVSENENDDYDCESEEGVEAPAEEVPTKAASSRSSSKRSRAAEVHNLSEKRRRGRINEKMKALQNLIPNSNKTDKASMLDEAIEYLKQLQLQVQMLSMRNGLSLHPMCFPEGLQPLQLSQMGMELSERNRFTSLNMSATLPLHQDNNPLHYASNLPNKHNLPNQPSVPYPPYIDNPETSFGLEPRIQTDMKPLQHKGGSSEPIRGEDILQHQQSSGIHSDANTLGGSQVVKEFESGTRLSFPFDTQACEPKDNSNSSQPCIGGRDHSGVIIRNSETNIVGR | 381 |
Select | Seq ID | Length | Analysis | Description | Start | End | IPR | GO |
---|---|---|---|---|---|---|---|---|
Gma11g00500 | 381 | PANTHER | TRANSCRIPTION FACTOR SPATULA | 12 | 320 | - | - | |
Gma11g00500 | 381 | Gene3D | - | 135 | 199 | IPR036638 | GO:0046983 | |
Gma11g00500 | 381 | MobiDBLite | consensus disorder prediction | 138 | 153 | - | - | |
Gma11g00500 | 381 | MobiDBLite | consensus disorder prediction | 344 | 362 | - | - | |
Gma11g00500 | 381 | MobiDBLite | consensus disorder prediction | 344 | 367 | - | - | |
Gma11g00500 | 381 | CDD | bHLH_AtPIF_like | 143 | 202 | - | - | |
Gma11g00500 | 381 | SMART | finulus | 146 | 195 | IPR011598 | GO:0046983 | |
Gma11g00500 | 381 | PANTHER | TRANSCRIPTION FACTOR PIF1-RELATED | 12 | 320 | IPR031066 | - | |
Gma11g00500 | 381 | Coils | Coil | 179 | 199 | - | - | |
Gma11g00500 | 381 | Pfam | Helix-loop-helix DNA-binding domain | 144 | 190 | IPR011598 | GO:0046983 | |
Gma11g00500 | 381 | SUPERFAMILY | HLH, helix-loop-helix DNA-binding domain | 137 | 200 | IPR036638 | GO:0046983 | |
Gma11g00500 | 381 | MobiDBLite | consensus disorder prediction | 106 | 120 | - | - | |
Gma11g00500 | 381 | ProSiteProfiles | Myc-type, basic helix-loop-helix (bHLH) domain profile. | 140 | 189 | IPR011598 | GO:0046983 | |
Gma11g00500 | 381 | MobiDBLite | consensus disorder prediction | 93 | 153 | - | - |
Select | Gene | Chromosome | Start | End | Duplicated_type |
---|---|---|---|---|---|
Gma11g00500 | Gma-Chr11 | 4176148 | 4180266 | Wgd |
Select | Gene | Gene_start | Gene_end | Function | Ath_gene | Identity(%) | E-value | Score |
---|---|---|---|---|---|---|---|---|
Gma11g00500 | 5 | 325 | Basic Helix-Loop-Helix Transcription Factor Gene Family | AT4G36930 | 41.379 | 6.03e-51 | 173 |
Select | Regulatory Factors | Family | Gene | Hmm_acc | Hmm_name | E_value | Clan |
---|---|---|---|---|---|---|---|
TF | bHLH | Gma11g00500 | HLH | 6e-14 | No_clan |
Select | Query | KO | Definition | Second KO | KEGG Genes ID | GHOSTX Score |
---|---|---|---|---|---|---|
Gma11g00500 | - | - | gmx:100793754 | 732.635 |
Select | Gene_1 | Chr_1 | Start_1 | End_1 | Gene_2 | Chr_2 | Start_2 | End_2 | Event_name |
---|---|---|---|---|---|---|---|---|---|
Gma01g01904 | 01 | 54581297 | 54584325 | Gma11g00500 | 11 | 4176148 | 4180266 | GST | |
Gma11g00500 | 11 | 4176148 | 4180266 | Gma17g01596 | 17 | 17771842 | 17774466 | PCT | |
Gma17g01596 | 17 | 17771842 | 17774466 | Gma11g00500 | 11 | 4176148 | 4180266 | PCT |