© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|4077 |
| Gene name | |
| Location | scaffold_32:15932..17302 |
| Strand | + |
| Gene length (bp) | 1370 |
| Transcript length (bp) | 1314 |
| Coding sequence length (bp) | 1311 |
| Protein length (aa) | 437 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00141 | peroxidase | Peroxidase | 5.8E-29 | 106 | 315 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P11543|LIG5_PHACH | Ligninase LG5 OS=Phanerochaete chrysosporium GN=GLG5 PE=2 SV=1 | 93 | 353 | 2.0E-32 |
| sp|P20013|LIGC_TRAVE | Ligninase C OS=Trametes versicolor PE=1 SV=2 | 93 | 353 | 3.0E-32 |
| sp|Q9UR19|VPL1_PLEER | Versatile peroxidase VPL1 OS=Pleurotus eryngii GN=vpl1 PE=1 SV=1 | 93 | 353 | 5.0E-32 |
| sp|O94753|VPL2_PLEER | Versatile peroxidase VPL2 OS=Pleurotus eryngii GN=vpl2 PE=1 SV=1 | 93 | 353 | 9.0E-32 |
| sp|P78733|PEM3_PHACH | Manganese peroxidase H3 OS=Phanerochaete chrysosporium PE=1 SV=2 | 86 | 353 | 1.0E-30 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P11543|LIG5_PHACH | Ligninase LG5 OS=Phanerochaete chrysosporium GN=GLG5 PE=2 SV=1 | 93 | 353 | 2.0E-32 |
| sp|P20013|LIGC_TRAVE | Ligninase C OS=Trametes versicolor PE=1 SV=2 | 93 | 353 | 3.0E-32 |
| sp|Q9UR19|VPL1_PLEER | Versatile peroxidase VPL1 OS=Pleurotus eryngii GN=vpl1 PE=1 SV=1 | 93 | 353 | 5.0E-32 |
| sp|O94753|VPL2_PLEER | Versatile peroxidase VPL2 OS=Pleurotus eryngii GN=vpl2 PE=1 SV=1 | 93 | 353 | 9.0E-32 |
| sp|P78733|PEM3_PHACH | Manganese peroxidase H3 OS=Phanerochaete chrysosporium PE=1 SV=2 | 86 | 353 | 1.0E-30 |
| sp|P49012|LIG2_PHACH | Ligninase LG2 OS=Phanerochaete chrysosporium GN=GLG2 PE=1 SV=1 | 93 | 353 | 1.0E-28 |
| sp|P19136|PEM4_PHACH | Manganese peroxidase H4 OS=Phanerochaete chrysosporium PE=1 SV=1 | 93 | 392 | 2.0E-28 |
| sp|Q02567|PEM1_PHACH | Manganese peroxidase 1 OS=Phanerochaete chrysosporium GN=MNP1 PE=1 SV=1 | 93 | 353 | 3.0E-28 |
| sp|P06181|LIG8_PHACH | Ligninase H8 OS=Phanerochaete chrysosporium GN=LPOA PE=1 SV=1 | 93 | 353 | 5.0E-28 |
| sp|Q70LM3|PEM2_PHLRA | Manganese peroxidase 2 OS=Phlebia radiata GN=mnp2 PE=1 SV=1 | 92 | 353 | 2.0E-27 |
| sp|Q96TS6|PEM3_PHLRA | Manganese peroxidase 3 OS=Phlebia radiata GN=mnp3 PE=2 SV=1 | 84 | 356 | 6.0E-27 |
| sp|P31838|LIGB_PHACH | Ligninase B OS=Phanerochaete chrysosporium GN=LIPB PE=3 SV=1 | 93 | 353 | 8.0E-27 |
| sp|P50622|LIG6_PHACH | Ligninase LG6 OS=Phanerochaete chrysosporium GN=GLG6 PE=2 SV=1 | 94 | 353 | 1.0E-26 |
| sp|P31837|LIGA_PHACH | Ligninase A OS=Phanerochaete chrysosporium GN=LIPA PE=3 SV=1 | 93 | 353 | 3.0E-26 |
| sp|Q9UVP6|VPS1_PLEER | Versatile peroxidase VPS1 OS=Pleurotus eryngii GN=vps1 PE=1 SV=1 | 84 | 353 | 2.0E-25 |
| sp|P21764|LIG3_PHACH | Ligninase LG3 OS=Phanerochaete chrysosporium GN=GLG3 PE=2 SV=1 | 94 | 353 | 8.0E-25 |
| sp|P20010|LIG_PHLRA | Ligninase-3 OS=Phlebia radiata PE=3 SV=1 | 93 | 353 | 1.0E-24 |
| sp|P11542|LIG4_PHACH | Ligninase H2 OS=Phanerochaete chrysosporium GN=GLG4 PE=1 SV=2 | 93 | 353 | 3.0E-24 |
| sp|P28314|PER_COPCI | Peroxidase OS=Coprinopsis cinerea GN=CIP1 PE=1 SV=2 | 61 | 380 | 7.0E-24 |
| sp|A8NK72|PER_COPC7 | Peroxidase OS=Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) GN=CIP1 PE=3 SV=1 | 61 | 380 | 2.0E-23 |
| sp|P28313|PER_ARTRA | Peroxidase OS=Arthromyces ramosus PE=1 SV=3 | 93 | 380 | 3.0E-23 |
| sp|Q8GY91|APX6_ARATH | Putative L-ascorbate peroxidase 6 OS=Arabidopsis thaliana GN=APX6 PE=2 SV=1 | 100 | 334 | 1.0E-19 |
| sp|Q7XZP5|APX5_ARATH | L-ascorbate peroxidase 5, peroxisomal OS=Arabidopsis thaliana GN=APX5 PE=1 SV=2 | 110 | 340 | 2.0E-19 |
| sp|Q05431|APX1_ARATH | L-ascorbate peroxidase 1, cytosolic OS=Arabidopsis thaliana GN=APX1 PE=1 SV=2 | 96 | 341 | 6.0E-18 |
| sp|Q0JEQ2|APX3_ORYSJ | Probable L-ascorbate peroxidase 3 OS=Oryza sativa subsp. japonica GN=APX3 PE=3 SV=1 | 115 | 339 | 2.0E-17 |
| sp|P48534|APX1_PEA | L-ascorbate peroxidase, cytosolic OS=Pisum sativum GN=APX1 PE=1 SV=2 | 110 | 339 | 2.0E-17 |
| sp|Q01MI9|APX3_ORYSI | Probable L-ascorbate peroxidase 3 OS=Oryza sativa subsp. indica GN=APX3 PE=2 SV=1 | 115 | 339 | 3.0E-17 |
| sp|Q42564|APX3_ARATH | L-ascorbate peroxidase 3, peroxisomal OS=Arabidopsis thaliana GN=APX3 PE=1 SV=1 | 98 | 339 | 4.0E-17 |
| sp|Q9FE01|APX2_ORYSJ | L-ascorbate peroxidase 2, cytosolic OS=Oryza sativa subsp. japonica GN=APX2 PE=1 SV=1 | 110 | 339 | 6.0E-17 |
| sp|Q6ZJJ1|APX4_ORYSJ | Probable L-ascorbate peroxidase 4 OS=Oryza sativa subsp. japonica GN=APX4 PE=2 SV=1 | 122 | 339 | 1.0E-16 |
| sp|A2XFC7|APX1_ORYSI | L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. indica GN=APX1 PE=2 SV=1 | 115 | 341 | 8.0E-16 |
| sp|Q10N21|APX1_ORYSJ | L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. japonica GN=APX1 PE=1 SV=1 | 110 | 341 | 8.0E-16 |
| sp|Q1PER6|APX2_ARATH | L-ascorbate peroxidase 2, cytosolic OS=Arabidopsis thaliana GN=APX2 PE=2 SV=3 | 110 | 341 | 9.0E-16 |
| sp|Q69SV0|APX8_ORYSJ | Probable L-ascorbate peroxidase 8, chloroplastic OS=Oryza sativa subsp. japonica GN=APX8 PE=2 SV=2 | 122 | 340 | 1.0E-13 |
| sp|Q7XJ02|APX7_ORYSJ | Probable L-ascorbate peroxidase 7, chloroplastic OS=Oryza sativa subsp. japonica GN=APX7 PE=2 SV=1 | 122 | 340 | 1.0E-13 |
| sp|P0C0L1|APX6_ORYSJ | Probable L-ascorbate peroxidase 6, chloroplastic OS=Oryza sativa subsp. japonica GN=APX6 PE=2 SV=1 | 122 | 340 | 6.0E-13 |
| sp|Q42593|APXT_ARATH | L-ascorbate peroxidase T, chloroplastic OS=Arabidopsis thaliana GN=APXT PE=2 SV=2 | 122 | 340 | 1.0E-12 |
| sp|C0IW58|LNP_TAICA | Low-redox potential peroxidase OS=Taiwanofungus camphoratus GN=LnP PE=1 SV=1 | 157 | 353 | 1.0E-12 |
| sp|Q42592|APXS_ARATH | L-ascorbate peroxidase S, chloroplastic/mitochondrial OS=Arabidopsis thaliana GN=APXS PE=1 SV=2 | 122 | 340 | 7.0E-12 |
| sp|P0CP54|CCPR_CRYNJ | Cytochrome c peroxidase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=CCP1 PE=3 SV=1 | 54 | 339 | 2.0E-11 |
| sp|P0CP55|CCPR_CRYNB | Cytochrome c peroxidase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=CCP1 PE=3 SV=1 | 54 | 339 | 2.0E-11 |
| sp|Q4PBY6|CCPR_USTMA | Cytochrome c peroxidase, mitochondrial OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP1 PE=3 SV=1 | 85 | 339 | 3.0E-11 |
| sp|P0C0V3|CCPR_EMENI | Cytochrome c peroxidase, mitochondrial OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=ccp1 PE=3 SV=1 | 81 | 339 | 1.0E-10 |
| sp|Q6URB0|CCPR_CRYNH | Cytochrome c peroxidase, mitochondrial OS=Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) GN=CCP1 PE=3 SV=1 | 43 | 339 | 2.0E-10 |
| sp|Q96511|PER69_ARATH | Peroxidase 69 OS=Arabidopsis thaliana GN=PER69 PE=1 SV=1 | 122 | 344 | 2.0E-10 |
| sp|P0C0L0|APX5_ORYSJ | Probable L-ascorbate peroxidase 5, chloroplastic OS=Oryza sativa subsp. japonica GN=APX5 PE=2 SV=1 | 122 | 340 | 3.0E-10 |
| sp|Q9SK52|PER18_ARATH | Peroxidase 18 OS=Arabidopsis thaliana GN=PER18 PE=3 SV=1 | 122 | 340 | 4.0E-10 |
| sp|Q02200|PERX_NICSY | Lignin-forming anionic peroxidase OS=Nicotiana sylvestris PE=2 SV=1 | 108 | 334 | 7.0E-10 |
| sp|Q9SD46|PER36_ARATH | Peroxidase 36 OS=Arabidopsis thaliana GN=PER36 PE=2 SV=2 | 117 | 259 | 2.0E-09 |
| sp|Q9SJZ2|PER17_ARATH | Peroxidase 17 OS=Arabidopsis thaliana GN=PER17 PE=2 SV=1 | 98 | 334 | 2.0E-09 |
| sp|Q9M9Q9|PER5_ARATH | Peroxidase 5 OS=Arabidopsis thaliana GN=PER5 PE=3 SV=2 | 105 | 334 | 3.0E-09 |
| sp|Q4ING3|CCPR_GIBZE | Cytochrome c peroxidase, mitochondrial OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=CCP1 PE=3 SV=1 | 89 | 339 | 3.0E-09 |
| sp|Q6BKY9|CCPR_DEBHA | Cytochrome c peroxidase, mitochondrial OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=CCP1 PE=3 SV=1 | 123 | 350 | 7.0E-09 |
| sp|Q9LVL1|PER68_ARATH | Peroxidase 68 OS=Arabidopsis thaliana GN=PER68 PE=2 SV=1 | 77 | 334 | 7.0E-09 |
| sp|P11965|PERX_TOBAC | Lignin-forming anionic peroxidase OS=Nicotiana tabacum PE=2 SV=1 | 122 | 334 | 1.0E-08 |
| sp|O48677|PER6_ARATH | Peroxidase 6 OS=Arabidopsis thaliana GN=PER6 PE=2 SV=1 | 118 | 340 | 1.0E-08 |
| sp|Q4WLG9|CCPR2_ASPFU | Putative heme-binding peroxidase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=AFUA_6G13570 PE=3 SV=1 | 122 | 386 | 5.0E-08 |
| sp|Q9FL16|PER63_ARATH | Peroxidase 63 OS=Arabidopsis thaliana GN=PER63 PE=2 SV=1 | 101 | 339 | 8.0E-08 |
| sp|Q96512|PER9_ARATH | Peroxidase 9 OS=Arabidopsis thaliana GN=PER9 PE=1 SV=1 | 117 | 257 | 8.0E-08 |
| sp|O04795|PERA_IPOBA | Anionic peroxidase OS=Ipomoea batatas PE=1 SV=1 | 78 | 337 | 3.0E-07 |
| sp|Q4PD66|CCPR2_USTMA | Putative heme-binding peroxidase OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP2 PE=3 SV=1 | 122 | 339 | 3.0E-07 |
| sp|Q6CAB5|CCPR2_YARLI | Putative cytochrome c peroxidase, mitochondrial OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=YALI0D04268g PE=3 SV=1 | 116 | 340 | 4.0E-07 |
| sp|Q9SZB9|PER47_ARATH | Peroxidase 47 OS=Arabidopsis thaliana GN=PER47 PE=2 SV=2 | 99 | 340 | 5.0E-07 |
| sp|P00431|CCPR_YEAST | Cytochrome c peroxidase, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CCP1 PE=1 SV=2 | 90 | 339 | 6.0E-07 |
| sp|Q9LVL2|PER67_ARATH | Peroxidase 67 OS=Arabidopsis thaliana GN=PER67 PE=2 SV=1 | 122 | 334 | 1.0E-06 |
| sp|Q9FLC0|PER52_ARATH | Peroxidase 52 OS=Arabidopsis thaliana GN=PER52 PE=2 SV=1 | 115 | 334 | 1.0E-06 |
| sp|Q5B1Z0|CCPR2_EMENI | Putative heme-binding peroxidase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=AN5440 PE=3 SV=1 | 122 | 340 | 2.0E-06 |
| sp|Q4W1I8|PER1_ZINVI | Basic peroxidase OS=Zinnia violacea GN=POD1 PE=1 SV=1 | 105 | 260 | 2.0E-06 |
| sp|Q4W1I9|PER2_ZINVI | Basic peroxidase OS=Zinnia violacea GN=POD3 PE=1 SV=1 | 105 | 260 | 2.0E-06 |
| sp|P15004|PER2_SOLLC | Suberization-associated anionic peroxidase 2 OS=Solanum lycopersicum GN=TAP2 PE=3 SV=1 | 122 | 359 | 2.0E-06 |
| sp|P00434|PERP7_BRARR | Peroxidase P7 OS=Brassica rapa subsp. rapa PE=1 SV=3 | 122 | 260 | 2.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0006979 | response to oxidative stress | Yes |
| GO:0004601 | peroxidase activity | Yes |
| GO:0020037 | heme binding | Yes |
| GO:0006950 | response to stress | No |
| GO:0005488 | binding | No |
| GO:0097159 | organic cyclic compound binding | No |
| GO:0016491 | oxidoreductase activity | No |
| GO:0050896 | response to stimulus | No |
| GO:0003824 | catalytic activity | No |
| GO:0008150 | biological_process | No |
| GO:0016684 | oxidoreductase activity, acting on peroxide as acceptor | No |
| GO:0003674 | molecular_function | No |
| GO:0046906 | tetrapyrrole binding | No |
| GO:0016209 | antioxidant activity | No |
| GO:1901363 | heterocyclic compound binding | No |
| Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Extracellular | Signal peptide | 0.1416 | 0.058 | 0.9667 | 0.0796 | 0.0795 | 0.0455 | 0.1429 | 0.1207 | 0.2252 | 0.0046 |
| SignalP signal predicted | Location | Score |
|---|---|---|
| Yes | 1 - 19 | 0.999655 |
| CAZyme category | E-value | Start | End |
|---|---|---|---|
| AA2 | 4.7E-60 | 98 | 339 |
| Gene cluster ID | Type of secondary metabolism gene |
|---|---|
| Cluster 14 | (None) |
| Orthofinder run ID | 4 |
| Orthogroup | 72 |
| 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|4077 MKYTSSFILIAATAGLSSAFSPTQMHEVKVRAARSSSVSPQLLGDLATLSEQQLTSTGRAIKAILLKQDSGLDTG SAPVNGELGSSQCNEDVCCVWKVIADDMAKTMVGSDRQCNSLARAAIRLGFHDAGAWSTESEVGGADGSIVLAGE CESRAENNGLQEICERMRSWFDQYQQYSVSMADLIQMGANVGAVVCPLGPRVRSFVGRKDSNSPAPEGLLPGPEL SADRLITMFASKTISPQGLIALVGSHSVAQQRFVQTNRSGDALDSTPGIWDTNFFRQVLDPKASPRIFKLQSDVS LSRDQRTTDVWSAYAGAQAQQSFIDDYATEYVRLSLLGVQNINDLIECTEALPPYIASFAVSDSNASSRPVDSDR PSCSSGGSTSGILPKGSWPSSSNGLQGLFSGARHANRPPAAGRKPQSSVPRAGNQEEGSNPR |
| Coding | >Ophio5|4077 ATGAAGTATACGAGCTCTTTTATCTTGATAGCCGCCACGGCCGGTCTTTCATCCGCCTTCTCACCGACGCAGATG CACGAGGTCAAGGTCAGGGCAGCAAGGTCGAGCTCAGTCTCGCCCCAGCTGCTCGGCGACCTGGCGACGCTCAGC GAGCAGCAGCTGACGTCGACAGGCAGGGCCATCAAGGCCATACTATTGAAGCAAGACAGCGGACTCGACACTGGC TCGGCCCCGGTGAACGGCGAACTTGGTTCGAGCCAGTGCAACGAGGACGTGTGCTGCGTGTGGAAGGTCATCGCC GACGACATGGCAAAGACCATGGTCGGATCGGACCGTCAATGCAACAGCCTTGCCCGGGCCGCCATTCGGCTCGGC TTCCACGATGCGGGAGCCTGGTCGACGGAGTCGGAGGTTGGAGGCGCCGACGGCTCCATCGTTCTGGCGGGAGAG TGCGAGAGTCGTGCGGAGAATAACGGGTTGCAAGAGATCTGCGAGCGCATGCGATCCTGGTTCGATCAATACCAG CAGTATAGCGTCTCCATGGCCGACTTGATCCAGATGGGCGCCAACGTCGGCGCCGTTGTCTGTCCTCTCGGGCCT CGAGTCCGGTCCTTCGTCGGCCGCAAAGATAGCAATAGTCCTGCCCCTGAGGGTCTGCTCCCGGGTCCTGAATTG AGCGCCGACAGGCTCATCACCATGTTCGCCAGCAAAACTATCAGCCCCCAGGGGCTCATCGCTCTCGTCGGCTCC CATTCGGTCGCACAGCAGCGCTTCGTCCAGACGAACCGAAGCGGCGACGCGCTTGATTCCACCCCTGGCATCTGG GATACCAACTTCTTCCGCCAAGTGCTCGATCCTAAAGCTTCGCCGCGTATCTTTAAGCTGCAAAGCGACGTCAGC CTCAGCAGGGACCAGCGCACCACGGACGTCTGGAGTGCCTATGCCGGAGCCCAAGCACAACAGTCCTTTATAGAT GACTATGCAACCGAATACGTTCGTCTCAGTCTCTTAGGCGTTCAAAACATCAACGACCTGATCGAGTGCACCGAG GCTTTGCCACCTTATATTGCCAGCTTCGCAGTCTCGGACTCGAACGCGTCATCCAGGCCAGTGGACAGCGACAGG CCGAGTTGTTCCTCGGGTGGCTCGACGAGCGGCATCTTGCCAAAGGGATCTTGGCCAAGCAGTAGCAACGGGTTG CAGGGCTTGTTTTCAGGTGCTAGACACGCCAACAGGCCACCTGCTGCTGGTAGGAAGCCACAGAGCTCAGTCCCG CGTGCTGGTAATCAGGAGGAGGGCTCGAATCCGCGT |
| Transcript | >Ophio5|4077 ATGAAGTATACGAGCTCTTTTATCTTGATAGCCGCCACGGCCGGTCTTTCATCCGCCTTCTCACCGACGCAGATG CACGAGGTCAAGGTCAGGGCAGCAAGGTCGAGCTCAGTCTCGCCCCAGCTGCTCGGCGACCTGGCGACGCTCAGC GAGCAGCAGCTGACGTCGACAGGCAGGGCCATCAAGGCCATACTATTGAAGCAAGACAGCGGACTCGACACTGGC TCGGCCCCGGTGAACGGCGAACTTGGTTCGAGCCAGTGCAACGAGGACGTGTGCTGCGTGTGGAAGGTCATCGCC GACGACATGGCAAAGACCATGGTCGGATCGGACCGTCAATGCAACAGCCTTGCCCGGGCCGCCATTCGGCTCGGC TTCCACGATGCGGGAGCCTGGTCGACGGAGTCGGAGGTTGGAGGCGCCGACGGCTCCATCGTTCTGGCGGGAGAG TGCGAGAGTCGTGCGGAGAATAACGGGTTGCAAGAGATCTGCGAGCGCATGCGATCCTGGTTCGATCAATACCAG CAGTATAGCGTCTCCATGGCCGACTTGATCCAGATGGGCGCCAACGTCGGCGCCGTTGTCTGTCCTCTCGGGCCT CGAGTCCGGTCCTTCGTCGGCCGCAAAGATAGCAATAGTCCTGCCCCTGAGGGTCTGCTCCCGGGTCCTGAATTG AGCGCCGACAGGCTCATCACCATGTTCGCCAGCAAAACTATCAGCCCCCAGGGGCTCATCGCTCTCGTCGGCTCC CATTCGGTCGCACAGCAGCGCTTCGTCCAGACGAACCGAAGCGGCGACGCGCTTGATTCCACCCCTGGCATCTGG GATACCAACTTCTTCCGCCAAGTGCTCGATCCTAAAGCTTCGCCGCGTATCTTTAAGCTGCAAAGCGACGTCAGC CTCAGCAGGGACCAGCGCACCACGGACGTCTGGAGTGCCTATGCCGGAGCCCAAGCACAACAGTCCTTTATAGAT GACTATGCAACCGAATACGTTCGTCTCAGTCTCTTAGGCGTTCAAAACATCAACGACCTGATCGAGTGCACCGAG GCTTTGCCACCTTATATTGCCAGCTTCGCAGTCTCGGACTCGAACGCGTCATCCAGGCCAGTGGACAGCGACAGG CCGAGTTGTTCCTCGGGTGGCTCGACGAGCGGCATCTTGCCAAAGGGATCTTGGCCAAGCAGTAGCAACGGGTTG CAGGGCTTGTTTTCAGGTGCTAGACACGCCAACAGGCCACCTGCTGCTGGTAGGAAGCCACAGAGCTCAGTCCCG CGTGCTGGTAATCAGGAGGAGGGCTCGAATCCGCGTTGA |
| Gene | >Ophio5|4077 ATGAAGTATACGAGCTCTTTTATCTTGATAGCCGCCACGGCCGGTCTTTCATCCGCCTTCTCACCGACGCAGATG CACGAGGTCAAGGTCAGGGCAGCAAGGTCGAGCTCAGTCTCGCCCCAGCTGCTCGGCGACCTGGCGACGCTCAGC GAGCAGCAGCTGACGTCGACAGGCAGGGCCATCAAGGCCATACTATTGAAGCAAGACAGCGGACTCGACACTGGC TCGGCCCCGGTGAACGGCGAACTTGGTTCGAGCCAGTGCAACGAGGACGTGTGCTGCGTGTGGAAGGTCATCGCC GACGACATGGCAAAGACCATGGTCGGATCGGACCGTCAATGCAACAGCCTTGCCCGGGCCGCCATTCGGCTCGGC TTCCACGATGCGGGAGCCTGGTCGACGGAGTCGGAGGTTGGAGGCGCCGACGGCTCCATCGTTCTGGCGGGAGAG TGCGAGAGTCGTGCGGAGAATAACGGGTTGCAAGAGATCTGCGAGCGCATGCGATCCTGGTTCGATCAATACCAG CAGTATAGCGTCTCCATGGCCGACTTGATCCAGATGGGCGCCAACGTCGGCGCCGTTGTCTGTCCTCTCGGGCCT CGAGTCCGGTCCTTCGTCGGCCGCAAAGATAGCAATAGTCCTGCCCCTGAGGGTCTGCTCCCGGGTCCTGAATTG AGCGCCGACAGGCTCATCACCATGTTCGCCAGCAAAACTATCAGCCCCCAGGGGCTCATCGCTCTCGTCGGCTCC CATTCGGTCGCACAGCAGCGCTTCGTCCAGACGAACCGAAGCGGCGACGCGCTTGATTCCACCCCTGGCATCTGG GATACCAACTTCTTCCGCCAAGTGCTCGATCCTAAAGCTTCGCCGCGTATCTTTAAGCTGCAAAGCGACGTCAGC CTCAGCAGGGACCAGCGCACCACGGACGTCTGGAGTGCCTATGCCGGAGCCCAAGCACAACAGTCCTTTATAGAT GTGAGCATGTGTGAAGCCGGCGGCTTCGAGTTTCTGACTTGAGCGGTTTTCTATAGGACTATGCAACCGAATACG TTCGTCTCAGTCTCTTAGGCGTTCAAAACATCAACGACCTGATCGAGTGCACCGAGGCTTTGCCACCTTATATTG CCAGCTTCGCAGTCTCGGACTCGAACGCGTCATCCAGGCCAGTGGACAGCGACAGGCCGAGTTGTTCCTCGGGTG GCTCGACGAGCGGCATCTTGCCAAAGGGATCTTGGCCAAGCAGTAGCAACGGGTTGCAGGGCTTGTTTTCAGGTG CTAGACACGCCAACAGGCCACCTGCTGCTGGTAGGAAGCCACAGAGCTCAGTCCCGCGTGCTGGTAATCAGGAGG AGGGCTCGAATCCGCGTTGA |