Protein ID | Ophio5|2371 |
Gene name | |
Location | scaffold_2:103761..105286 |
Strand | + |
Gene length (bp) | 1525 |
Transcript length (bp) | 1218 |
Coding sequence length (bp) | 1215 |
Protein length (aa) | 405 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF04406 | TP6A_N | Type IIB DNA topoisomerase | 4.2E-20 | 86 | 147 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9Y5K1|SPO11_HUMAN | Meiotic recombination protein SPO11 OS=Homo sapiens GN=SPO11 PE=2 SV=1 | 23 | 292 | 5.0E-38 |
sp|P40384|REC12_SCHPO | Meiotic recombination protein rec12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rec12 PE=1 SV=2 | 31 | 394 | 1.0E-37 |
sp|Q0DSV9|TOP6A_ORYSJ | Topoisomerase 6 subunit A3 OS=Oryza sativa subsp. japonica GN=SPO11-3 PE=2 SV=2 | 72 | 384 | 1.0E-35 |
sp|A2XFC1|TOP6A_ORYSI | DNA topoisomerase 6 subunit A3 OS=Oryza sativa subsp. indica GN=TOP6A3 PE=1 SV=2 | 72 | 384 | 1.0E-35 |
sp|Q7Y021|SPO11_ORYSJ | Meiotic recombination protein SPO11-1 OS=Oryza sativa subsp. japonica GN=SPO11-1 PE=2 SV=1 | 109 | 395 | 3.0E-34 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q9Y5K1|SPO11_HUMAN | Meiotic recombination protein SPO11 OS=Homo sapiens GN=SPO11 PE=2 SV=1 | 23 | 292 | 5.0E-38 |
sp|P40384|REC12_SCHPO | Meiotic recombination protein rec12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rec12 PE=1 SV=2 | 31 | 394 | 1.0E-37 |
sp|Q0DSV9|TOP6A_ORYSJ | Topoisomerase 6 subunit A3 OS=Oryza sativa subsp. japonica GN=SPO11-3 PE=2 SV=2 | 72 | 384 | 1.0E-35 |
sp|A2XFC1|TOP6A_ORYSI | DNA topoisomerase 6 subunit A3 OS=Oryza sativa subsp. indica GN=TOP6A3 PE=1 SV=2 | 72 | 384 | 1.0E-35 |
sp|Q7Y021|SPO11_ORYSJ | Meiotic recombination protein SPO11-1 OS=Oryza sativa subsp. japonica GN=SPO11-1 PE=2 SV=1 | 109 | 395 | 3.0E-34 |
sp|Q5ZPV8|SPO11_ORYSI | Meiotic recombination protein SPO11-1 OS=Oryza sativa subsp. indica GN=SPO11-1 PE=2 SV=1 | 109 | 395 | 3.0E-34 |
sp|Q9WTK8|SPO11_MOUSE | Meiotic recombination protein SPO11 OS=Mus musculus GN=Spo11 PE=2 SV=2 | 23 | 298 | 4.0E-34 |
sp|Q9LZ03|TOP6A_ARATH | DNA topoisomerase 6 subunit A OS=Arabidopsis thaliana GN=TOP6A PE=1 SV=1 | 31 | 384 | 7.0E-31 |
sp|Q9M4A2|SPO11_ARATH | Meiotic recombination protein SPO11-1 OS=Arabidopsis thaliana GN=SPO11-1 PE=1 SV=1 | 29 | 405 | 3.0E-29 |
sp|Q6ZD95|SPO12_ORYSJ | Meiotic recombination protein SPO11-2 OS=Oryza sativa subsp. japonica GN=SPO11-2 PE=2 SV=1 | 84 | 298 | 2.0E-28 |
sp|Q5ZPI9|SPO12_ORYSI | Meiotic recombination protein SPO11-2 OS=Oryza sativa subsp. indica GN=SPO11-2 PE=1 SV=1 | 84 | 298 | 4.0E-28 |
sp|Q9M4A1|SPO12_ARATH | Meiotic recombination protein SPO11-2 OS=Arabidopsis thaliana GN=SPO11-2 PE=1 SV=1 | 13 | 293 | 6.0E-28 |
sp|Q22236|SPO11_CAEEL | Meiotic recombination protein spo-11 OS=Caenorhabditis elegans GN=spo-11 PE=3 SV=1 | 87 | 292 | 4.0E-25 |
sp|Q9YE67|TOP6A_AERPE | Type 2 DNA topoisomerase 6 subunit A OS=Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) GN=top6A PE=3 SV=2 | 81 | 293 | 7.0E-25 |
sp|O05208|TOP6A_SULSH | Type 2 DNA topoisomerase 6 subunit A OS=Sulfolobus shibatae GN=top6A PE=1 SV=1 | 82 | 292 | 1.0E-22 |
sp|Q971T1|TOP6A_SULTO | Type 2 DNA topoisomerase 6 subunit A OS=Sulfolobus tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) GN=top6A PE=3 SV=1 | 82 | 292 | 4.0E-22 |
sp|A2BLE8|TOP6A_HYPBU | Type 2 DNA topoisomerase 6 subunit A OS=Hyperthermus butylicus (strain DSM 5456 / JCM 9403 / PLM1-5) GN=top6A PE=3 SV=1 | 82 | 292 | 7.0E-22 |
sp|Q2QM00|SPO14_ORYSJ | Meiotic recombination protein SPO11-4 OS=Oryza sativa subsp. japonica GN=SPO11-4 PE=1 SV=2 | 89 | 294 | 4.0E-19 |
sp|Q57815|TOP6A_METJA | Type 2 DNA topoisomerase 6 subunit A OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=top6A PE=1 SV=1 | 44 | 299 | 2.0E-15 |
sp|P23179|SPO11_YEAST | Meiosis-specific protein SPO11 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SPO11 PE=1 SV=1 | 2 | 381 | 3.0E-15 |
sp|Q8SVS9|SPO11_ENCCU | Probable meiosis-specific protein SPO11 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=SPO11 PE=3 SV=1 | 109 | 273 | 2.0E-13 |
sp|Q9V134|TOP6A_PYRAB | Type 2 DNA topoisomerase 6 subunit A OS=Pyrococcus abyssi (strain GE5 / Orsay) GN=top6A PE=3 SV=1 | 26 | 278 | 4.0E-12 |
sp|Q8U0K9|TOP6A_PYRFU | Type 2 DNA topoisomerase 6 subunit A OS=Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) GN=top6A PE=3 SV=1 | 26 | 278 | 5.0E-12 |
sp|Q5JH82|TOP6A_THEKO | Type 2 DNA topoisomerase 6 subunit A OS=Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) GN=top6A PE=3 SV=1 | 81 | 278 | 2.0E-11 |
sp|O59209|TOP6A_PYRHO | Type 2 DNA topoisomerase 6 subunit A OS=Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) GN=top6A PE=3 SV=2 | 26 | 278 | 2.0E-10 |
sp|C4VB43|SPO11_NOSCE | Probable meiosis-specific protein SPO11 homolog OS=Nosema ceranae (strain BRL01) GN=SPO11 PE=3 SV=1 | 99 | 302 | 2.0E-08 |
sp|O27089|TOP6A_METTH | Type 2 DNA topoisomerase 6 subunit A OS=Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) GN=top6A PE=3 SV=1 | 81 | 292 | 3.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0005694 | chromosome | Yes |
GO:0003824 | catalytic activity | Yes |
GO:0005524 | ATP binding | Yes |
GO:0006259 | DNA metabolic process | Yes |
GO:0003677 | DNA binding | Yes |
GO:0090304 | nucleic acid metabolic process | No |
GO:0044260 | cellular macromolecule metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0044237 | cellular metabolic process | No |
GO:0008152 | metabolic process | No |
GO:0043167 | ion binding | No |
GO:0006139 | nucleobase-containing compound metabolic process | No |
GO:0043226 | organelle | No |
GO:0046483 | heterocycle metabolic process | No |
GO:0003676 | nucleic acid binding | No |
GO:0032555 | purine ribonucleotide binding | No |
GO:0044238 | primary metabolic process | No |
GO:0043228 | non-membrane-bounded organelle | No |
GO:0043232 | intracellular non-membrane-bounded organelle | No |
GO:0043168 | anion binding | No |
GO:0006725 | cellular aromatic compound metabolic process | No |
GO:0008150 | biological_process | No |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0005575 | cellular_component | No |
GO:0035639 | purine ribonucleoside triphosphate binding | No |
GO:0034641 | cellular nitrogen compound metabolic process | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0032559 | adenyl ribonucleotide binding | No |
GO:0036094 | small molecule binding | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0097367 | carbohydrate derivative binding | No |
GO:0000166 | nucleotide binding | No |
GO:0032553 | ribonucleotide binding | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:0043229 | intracellular organelle | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0017076 | purine nucleotide binding | No |
GO:0030554 | adenyl nucleotide binding | No |
GO:0009987 | cellular process | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0005488 | binding | No |
GO:0110165 | cellular anatomical entity | No |
GO:0071704 | organic substance metabolic process | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Cytoplasm|Nucleus | Nuclear localization signal|Nuclear export signal | 0.6651 | 0.8059 | 0.0315 | 0.0474 | 0.3148 | 0.0012 | 0.1004 | 0.168 | 0.0689 | 0.03 |
Orthofinder run ID | 4 |
Orthogroup | 4357 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
Protein | >Ophio5|2371 MPSHASVHLPRQDSHTDWSSQPLASPGALISRIENLLASMISALSLGEPMSIDLLSRKSLRSLSCLDGQARRQQI SFPGKTLAEAQKFTRVLLILQLSHDALVSGGVLTKRQIFYQYQDLFDKQKVVDDLVDDIALTLGVHRHDLNIVAS AKGLLSGCLSIRLTDGSTIDTSVGDVGTPIPSLATISAVDCTGLRWILVVEKDATFRSLVSSCFYETSAAGPGLL VTAKGYPDLVTRLFLRRMHQRHAHLPILLLTDLDPDGLNIFRCYRFGTDFVAHDAAAYNPGIRWLGIKTRHVQDA AHQFNQSQRLTPSIVFKTSISSTGCRDPISHLTARDRKLARHMLARITSRCPEEDAEAEQLKLETQTMLMMNVKA EMQWLDDAGDLISWLDEKLVSEVRVRGSLP |
Coding | >Ophio5|2371 ATGCCAAGTCATGCTTCTGTTCATCTTCCACGCCAAGACTCACACACAGATTGGAGCAGCCAACCACTGGCCTCC CCCGGGGCGTTAATCAGTCGCATCGAGAATCTTCTGGCGTCCATGATCAGTGCCCTTTCACTGGGCGAGCCCATG AGTATCGACCTGCTCTCGCGAAAGAGCCTGAGGAGCCTGAGCTGTCTTGACGGCCAGGCCCGTCGTCAGCAGATA AGCTTCCCCGGAAAGACGTTGGCAGAGGCGCAAAAGTTTACTCGCGTTCTCTTGATTCTCCAGCTGTCTCACGAT GCTCTGGTCTCGGGCGGCGTCCTCACCAAACGCCAAATCTTCTACCAGTATCAGGATCTATTCGACAAGCAAAAG GTCGTCGACGATCTCGTGGATGACATCGCGTTAACCCTCGGCGTCCACCGCCACGACTTGAATATTGTCGCATCG GCCAAGGGCCTTCTCTCCGGCTGCTTGTCCATCCGGCTTACAGACGGCTCCACAATCGACACATCGGTGGGAGAC GTGGGCACGCCCATCCCCAGCTTGGCTACCATCTCCGCCGTCGACTGCACCGGGCTGAGATGGATTCTTGTGGTG GAAAAGGACGCCACGTTCCGTTCCTTGGTATCATCATGCTTCTACGAGACATCGGCAGCGGGTCCTGGCTTGCTC GTGACGGCAAAAGGTTACCCGGACCTGGTGACGCGCTTATTTCTGAGACGGATGCACCAGCGCCATGCGCATCTG CCCATCTTACTCCTGACCGACTTGGACCCCGACGGCCTGAACATCTTCCGCTGCTATCGCTTCGGGACCGATTTC GTTGCGCACGACGCAGCGGCTTACAACCCCGGCATACGCTGGCTGGGAATTAAAACACGACACGTTCAAGACGCA GCCCATCAGTTCAACCAAAGCCAGCGTTTGACACCAAGCATCGTCTTCAAGACCTCTATATCATCCACCGGATGC CGAGACCCCATATCCCACCTCACCGCGAGAGACCGCAAGCTGGCAAGACACATGCTAGCCCGAATCACAAGTCGA TGCCCAGAAGAAGACGCCGAGGCAGAACAGCTGAAGCTAGAGACACAGACGATGCTCATGATGAACGTAAAAGCA GAAATGCAGTGGCTAGACGATGCCGGAGACTTAATTAGCTGGCTCGACGAAAAGTTGGTGTCTGAAGTCCGTGTA AGAGGTAGCCTACCC |
Transcript | >Ophio5|2371 ATGCCAAGTCATGCTTCTGTTCATCTTCCACGCCAAGACTCACACACAGATTGGAGCAGCCAACCACTGGCCTCC CCCGGGGCGTTAATCAGTCGCATCGAGAATCTTCTGGCGTCCATGATCAGTGCCCTTTCACTGGGCGAGCCCATG AGTATCGACCTGCTCTCGCGAAAGAGCCTGAGGAGCCTGAGCTGTCTTGACGGCCAGGCCCGTCGTCAGCAGATA AGCTTCCCCGGAAAGACGTTGGCAGAGGCGCAAAAGTTTACTCGCGTTCTCTTGATTCTCCAGCTGTCTCACGAT GCTCTGGTCTCGGGCGGCGTCCTCACCAAACGCCAAATCTTCTACCAGTATCAGGATCTATTCGACAAGCAAAAG GTCGTCGACGATCTCGTGGATGACATCGCGTTAACCCTCGGCGTCCACCGCCACGACTTGAATATTGTCGCATCG GCCAAGGGCCTTCTCTCCGGCTGCTTGTCCATCCGGCTTACAGACGGCTCCACAATCGACACATCGGTGGGAGAC GTGGGCACGCCCATCCCCAGCTTGGCTACCATCTCCGCCGTCGACTGCACCGGGCTGAGATGGATTCTTGTGGTG GAAAAGGACGCCACGTTCCGTTCCTTGGTATCATCATGCTTCTACGAGACATCGGCAGCGGGTCCTGGCTTGCTC GTGACGGCAAAAGGTTACCCGGACCTGGTGACGCGCTTATTTCTGAGACGGATGCACCAGCGCCATGCGCATCTG CCCATCTTACTCCTGACCGACTTGGACCCCGACGGCCTGAACATCTTCCGCTGCTATCGCTTCGGGACCGATTTC GTTGCGCACGACGCAGCGGCTTACAACCCCGGCATACGCTGGCTGGGAATTAAAACACGACACGTTCAAGACGCA GCCCATCAGTTCAACCAAAGCCAGCGTTTGACACCAAGCATCGTCTTCAAGACCTCTATATCATCCACCGGATGC CGAGACCCCATATCCCACCTCACCGCGAGAGACCGCAAGCTGGCAAGACACATGCTAGCCCGAATCACAAGTCGA TGCCCAGAAGAAGACGCCGAGGCAGAACAGCTGAAGCTAGAGACACAGACGATGCTCATGATGAACGTAAAAGCA GAAATGCAGTGGCTAGACGATGCCGGAGACTTAATTAGCTGGCTCGACGAAAAGTTGGTGTCTGAAGTCCGTGTA AGAGGTAGCCTACCCTAG |
Gene | >Ophio5|2371 ATGCCAAGTCATGCTTCTGTTCATCTTCCACGCCAAGACTCACACACAGATTGGAGCAGCCAACCACTGGCCTCC CCCGGGGCGTTAATCAGTCGCATCGAGAATCTTCTGGCGTCCATGATCAGTGCCCTTTCACTGGGCGAGCCCATG AGTATCGACCTGCTCTCGCGAAAGAGCCTGAGGAGCCTGAGCTGTCTTGACGGCCAGGCCCGTCGTCAGCAGATA AGCTTCCCCGGAAAGACGTTGGCAGAGGCGCAAAAGTTTAGTATGCCTCCGTTCAAGTCAGTTTAGGCATCTGTT TGAAGTCTCACAGTGCAGCTCGCGTTCTCTTGATTCTCCAGCTGTCTCACGATGCTCTGGTCTCGGGCGGCGTCC TCACCAAACGGTTCGTCTCGGAACGTCCCGCCCTTGAATTGCTTTAGACTTGCACTAAGGCAAGTTTTCTTATAG CCAAATCTTCTACCAGTATCAGGATCTATTCGACAAGCAAAAGGTCGTCGACGATCTCGTGGATGACATCGCGTT AACCCTCGGCGTCCACCGCCACGACTTGAATATTGTAGGACAGCAAAGCCTATAGCGCAACGCCGGCTGACTCCT TCAGGTCGCATCGGCCAAGGGCCTTCTCTCCGGCTGCTTGTCCATCCGGCTTACAGACGGCTCCACAATCGACAC ATCGGTGGGAGACGTGGTAGGCATCTCTGCGCTATGCCACGGACTGGTTAGCTGACGAGCCAGGGCACGCCCATC CCCAGCTTGGCTACCATCTCCGCCGTCGACTGCACCGGGCTGAGATGGATTCTTGTGGTGGAAAAGGACGTAGGC AGAGCGTATTAGTCGTCGTGTCTACAAGGCTGACTCGGCGGCAGGCCACGTTCCGTTCCTTGGTATCATCATGCT TCTACGAGACATCGGCAGCGGGTCCTGGCTTGCTCGTGACGGTATGTTCACGTCTACTGCCGCCCTACACAGGCT GACGGGCCTAAAGGCAAAAGGTTACCCGGACCTGGTGACGCGCTTATTTCTGAGACGGATGCACCAGCGCCATGC GCATCTGCCCATCTTACTCCTGACCGACTTGGACCCCGACGGCCTGAACATCTTCCGCTGCTATCGCTTCGGGAC CGATTTCGTTGCGCACGACGCAGCGGCTTACAACCCCGGCATACGCTGGCTGGGAATTAAAACACGACACGTTCA AGACGCAGCCCATCAGTTCAACCAAAGCCAGCGTTTGACACCAAGCATCGTCTTCAAGACCTCTATATCATCCAC CGGATGCCGAGACCCCATATCCCACCTCACCGCGAGAGACCGCAAGCTGGCAAGACACATGCTAGCCCGAATCAC AAGTCGATGCCCAGAAGAAGACGCCGAGGCAGAACAGCTGAAGCTAGAGACACAGACGATGCTCATGATGAACGT AAAAGCAGAAATGCAGTGGCTAGACGATGCCGGAGACTTAATTAGCTGGCTCGACGAAAAGTTGGTGTCTGAAGT CCGTGTAAGAGGTAGCCTACCCTAG |