Select | Gene | Cds | Cds_length | GC_content | Pep | Pep_length |
---|---|---|---|---|---|---|
Tsu05g00798 | ATGCTTTACCAAACTCCCTATCCTCTTCTCTTTCAATTTCATCCCttaccttcatcttcttcttctttcaccATTCCTCTCTCAACCATATCACAACCCCAACTTCCTCTCACAAAggTTTCAAAAACAGAAATGGAGTGCGTTGAAACAGCGTTGAAAACAAGTTTAAGGAAAGACATAACTCCTCAAACATTTGTTGATGAGCTTACAAGTCTTAATGCACAAAATGGAACAACCTCCGACGATTTTTTCGTCGACGACCTCCTTGATTTCTCTCATGttgaagaacaacaacaacaagacgAAGAACAgcaacaacagcagcaacaacaacaagacTCTGTTTTTGTCTCTGTCAAACAAACCCATGAAATTTCAAACCTCAACAACACCAACAGCAACAGTTTTTCTGTCAAAAATGATTATGCTTCTCTACCCACTAGCGAACTCAACGTCCCGaGTGATGATGTAGCAGATGATTTAGAATGGCTTTCACATTTTGTTGAAGATTCTGATTCTTTCTCGGAATTTTCTGCTGTTATGCCGGTTGTAACTTCAACAACAACAGAGAAAAACCCAAAGGGTGTTGTGGTTTCTGAGAACAAGCCCAAGAATGAAAACCCAAGCCCGGGCCCGGTTGTTACTACTTTCAAAACTCCGGTTCAGACAAAAGCAAGAAGCAAAAGGACAAGAACCGGAACCGGTGTTCGGGTTTGGCCATTCGGGTCAAATACTACTTTAACCGACTCTTCTTCAAGCTCCACAACTTCATCTTCAACTTCTTCGTCTCCAACTAGCCCCTTGTTGATTTACACCAACTTGGTTCAAAAATTTGACTCGGTTCCGGTGAAAAAGCAGAAGAAAACGACAAATTTTAATGGGTCAGGTCATGGCACGGTGGTTGCAGCGGCGGCGCCGCGACGGTGCAGTCATTGCGGTGTAACTAAGACTCCTCAGTGGCGAACTGGTCCTCTTGGTGCAAAAACGCTTTGTAATGCTTGTGGGGTCCGGTATAAATCTGGTCGGTTATTACCGGAATACCGACCCGCTTGTAGTCCTACATTTTCAAGTGAATTGCACTCTAACCATCACAGGAAAGTGATTGAAATGCGGCGGAAGAAGGAGGTTGCTGGTGgtgttgaaattgaaactgGTTTGTCCCCTTCTCCGGTTGTTCCAAGTTTTTGA | 1188 | 0.4007 | MLYQTPYPLLFQFHPLPSSSSSFTIPLSTISQPQLPLTKVSKTEMECVETALKTSLRKDITPQTFVDELTSLNAQNGTTSDDFFVDDLLDFSHVEEQQQQDEEQQQQQQQQQDSVFVSVKQTHEISNLNNTNSNSFSVKNDYASLPTSELNVPSDDVADDLEWLSHFVEDSDSFSEFSAVMPVVTSTTTEKNPKGVVVSENKPKNENPSPGPVVTTFKTPVQTKARSKRTRTGTGVRVWPFGSNTTLTDSSSSSTTSSSTSSSPTSPLLIYTNLVQKFDSVPVKKQKKTTNFNGSGHGTVVAAAAPRRCSHCGVTKTPQWRTGPLGAKTLCNACGVRYKSGRLLPEYRPACSPTFSSELHSNHHRKVIEMRRKKEVAGGVEIETGLSPSPVVPSF | 395 |
Select | Seq ID | Length | Analysis | Description | Start | End | IPR | GO |
---|---|---|---|---|---|---|---|---|
Tsu05g00798 | 395 | MobiDBLite | consensus disorder prediction | 187 | 266 | - | - | |
Tsu05g00798 | 395 | CDD | ZnF_GATA | 308 | 356 | IPR000679 | GO:0006355|GO:0043565 | |
Tsu05g00798 | 395 | PANTHER | GATA TRANSCRIPTION FACTOR | 45 | 378 | - | - | |
Tsu05g00798 | 395 | SUPERFAMILY | Glucocorticoid receptor-like (DNA-binding domain) | 303 | 365 | - | - | |
Tsu05g00798 | 395 | Pfam | GATA zinc finger | 309 | 343 | IPR000679 | GO:0006355|GO:0043565 | |
Tsu05g00798 | 395 | ProSitePatterns | GATA-type zinc finger domain. | 309 | 334 | IPR000679 | GO:0006355|GO:0043565 | |
Tsu05g00798 | 395 | PANTHER | GATA TRANSCRIPTION FACTOR | 45 | 378 | - | - | |
Tsu05g00798 | 395 | Gene3D | - | 302 | 376 | IPR013088 | GO:0006355|GO:0008270 | |
Tsu05g00798 | 395 | MobiDBLite | consensus disorder prediction | 237 | 266 | - | - | |
Tsu05g00798 | 395 | SMART | GATA_3 | 303 | 357 | IPR000679 | GO:0006355|GO:0043565 | |
Tsu05g00798 | 395 | Coils | Coil | 94 | 114 | - | - | |
Tsu05g00798 | 395 | ProSiteProfiles | GATA-type zinc finger domain profile. | 303 | 339 | IPR000679 | GO:0006355|GO:0043565 | |
Tsu05g00798 | 395 | MobiDBLite | consensus disorder prediction | 202 | 229 | - | - |
Select | Gene | Chromosome | Start | End | Duplicated_type |
---|---|---|---|---|---|
Tsu05g00798 | Tsu-Chr5 | 6761649 | 6763292 | Wgd |
Select | Gene | Gene_start | Gene_end | Function | Ath_gene | Identity(%) | E-value | Score |
---|---|---|---|---|---|---|---|---|
Tsu05g00798 | 49 | 395 | C2C2-Gata Transcription Factor Family | AT5G66320 | 47.765 | 7.82e-71 | 224 |
Select | Regulatory Factors | Family | Gene | Hmm_acc | Hmm_name | E_value | Clan |
---|---|---|---|---|---|---|---|
TF | C2C2-GATA | Tsu05g00798 | GATA | 1.4e-16 | CL0167 |
Select | Query | KO | Definition | Second KO | KEGG Genes ID | GHOSTX Score |
---|---|---|---|---|---|---|
Tsu05g00798 | - | - | var:108335072 | 339.347 |
Select | Gene_1 | Chr_1 | Start_1 | End_1 | Gene_2 | Chr_2 | Start_2 | End_2 | Event_name |
---|---|---|---|---|---|---|---|---|---|
Tsu05g00798 | 05 | 6761649 | 6763292 | Tsu04g03477 | 04 | 43919630 | 43921122 | ECH | |
Tsu05g00798 | 05 | 6761649 | 6763292 | Tsu05g00798 | 05 | 6761649 | 6763292 | ECH | |
Tsu05g00798 | 05 | 6761649 | 6763292 | Tsu04g03477 | 04 | 43919630 | 43921122 | PCT |