© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | Ophio5|8063 |
| Gene name | |
| Location | scaffold_85:37343..40944 |
| Strand | - |
| Gene length (bp) | 3601 |
| Transcript length (bp) | 3549 |
| Coding sequence length (bp) | 3546 |
| Protein length (aa) | 1182 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00368 | HMG-CoA_red | Hydroxymethylglutaryl-coenzyme A reductase | 2.4E-138 | 756 | 1139 |
| PF13323 | HPIH | N-terminal domain with HPIH motif | 2.0E-48 | 30 | 177 |
| PF12349 | Sterol-sensing | Sterol-sensing domain of SREBP cleavage-activation | 2.2E-11 | 268 | 428 |
| PF02460 | Patched | Patched family | 7.4E-06 | 237 | 440 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P0CT44|HMDH_GIBFU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi GN=HMGR PE=3 SV=1 | 222 | 1182 | 0.0E+00 |
| sp|Q0C8L9|HMDH_ASPTN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=ATEG_09965 PE=3 SV=1 | 19 | 1146 | 0.0E+00 |
| sp|Q9Y7D2|HMDH_ASPTE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus PE=3 SV=2 | 19 | 1146 | 0.0E+00 |
| sp|Q12649|HMDH_PHYB8 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Phycomyces blakesleeanus (strain ATCC 8743b / FGSC 10004 / NBRC 33097 / NRRL 1555) GN=hmgA PE=3 SV=2 | 203 | 1155 | 0.0E+00 |
| sp|Q10283|HMDH_SCHPO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hmg1 PE=1 SV=2 | 218 | 1167 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P0CT44|HMDH_GIBFU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi GN=HMGR PE=3 SV=1 | 222 | 1182 | 0.0E+00 |
| sp|Q0C8L9|HMDH_ASPTN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=ATEG_09965 PE=3 SV=1 | 19 | 1146 | 0.0E+00 |
| sp|Q9Y7D2|HMDH_ASPTE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aspergillus terreus PE=3 SV=2 | 19 | 1146 | 0.0E+00 |
| sp|Q12649|HMDH_PHYB8 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Phycomyces blakesleeanus (strain ATCC 8743b / FGSC 10004 / NBRC 33097 / NRRL 1555) GN=hmgA PE=3 SV=2 | 203 | 1155 | 0.0E+00 |
| sp|Q10283|HMDH_SCHPO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=hmg1 PE=1 SV=2 | 218 | 1167 | 0.0E+00 |
| sp|O74164|HMDH_CYBJA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Cyberlindnera jadinii GN=HMG PE=2 SV=1 | 227 | 1142 | 0.0E+00 |
| sp|P12684|HMDH2_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG2 PE=1 SV=1 | 600 | 1164 | 0.0E+00 |
| sp|S0DQM8|HMDH_GIBF5 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Gibberella fujikuroi (strain CBS 195.34 / IMI 58289 / NRRL A-6831) GN=HMGR PE=3 SV=1 | 6 | 1182 | 0.0E+00 |
| sp|P12683|HMDH1_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG1 PE=1 SV=1 | 607 | 1159 | 0.0E+00 |
| sp|A7Z064|HMDH_BOVIN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Bos taurus GN=HMGCR PE=2 SV=2 | 695 | 1140 | 2.0E-156 |
| sp|Q01237|HMDH_MOUSE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Mus musculus GN=Hmgcr PE=1 SV=3 | 686 | 1140 | 2.0E-156 |
| sp|P00347|HMDH_CRIGR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Cricetulus griseus GN=HMGCR PE=1 SV=1 | 681 | 1140 | 5.0E-156 |
| sp|Q5R6N3|HMDH_PONAB | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pongo abelii GN=HMGCR PE=2 SV=1 | 678 | 1140 | 8.0E-156 |
| sp|P04035|HMDH_HUMAN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Homo sapiens GN=HMGCR PE=1 SV=1 | 678 | 1140 | 1.0E-155 |
| sp|P51639|HMDH_RAT | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Rattus norvegicus GN=Hmgcr PE=1 SV=2 | 707 | 1140 | 1.0E-154 |
| sp|P09610|HMDH_MESAU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Mesocricetus auratus GN=HMGCR PE=1 SV=1 | 685 | 1140 | 4.0E-154 |
| sp|Q1W675|HMDH_PIG | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Sus scrofa GN=HMGCR PE=2 SV=1 | 687 | 1140 | 3.0E-153 |
| sp|P20715|HMDH_XENLA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Xenopus laevis GN=hmgcr PE=2 SV=1 | 720 | 1140 | 1.0E-152 |
| sp|P16393|HMDH_STRPU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Strongylocentrotus purpuratus GN=HMGCR PE=2 SV=2 | 697 | 1151 | 3.0E-152 |
| sp|P54960|HMDH_BLAGE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Blattella germanica PE=2 SV=1 | 679 | 1152 | 8.0E-152 |
| sp|Q01559|HMDH_NICSY | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Nicotiana sylvestris GN=HMGR PE=2 SV=1 | 683 | 1148 | 9.0E-152 |
| sp|Q29512|HMDH_RABIT | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Oryctolagus cuniculus GN=HMGCR PE=3 SV=1 | 687 | 1140 | 1.0E-151 |
| sp|P34136|HMDH2_DICDI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Dictyostelium discoideum GN=hmgB PE=2 SV=2 | 724 | 1155 | 5.0E-151 |
| sp|P48022|HMDH2_SOLLC | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Solanum lycopersicum GN=HMG2 PE=3 SV=1 | 670 | 1148 | 8.0E-151 |
| sp|O24594|HMDH_MAIZE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Zea mays GN=HMGR PE=3 SV=1 | 688 | 1141 | 2.0E-150 |
| sp|Q9XEL8|HMDH2_CAPAN | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Capsicum annuum GN=HMGR2 PE=2 SV=1 | 728 | 1148 | 4.0E-150 |
| sp|Q9XHL5|HMDH3_ORYSJ | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Oryza sativa subsp. japonica GN=HMG3 PE=2 SV=2 | 728 | 1146 | 1.0E-149 |
| sp|P29057|HMDH1_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Hevea brasiliensis GN=HMGR1 PE=2 SV=1 | 694 | 1147 | 2.0E-149 |
| sp|O64967|HMDH2_GOSHI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Gossypium hirsutum GN=HMG2 PE=3 SV=1 | 719 | 1141 | 5.0E-148 |
| sp|Q03163|HMDH_CATRO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Catharanthus roseus GN=HMGR PE=2 SV=1 | 728 | 1141 | 5.0E-148 |
| sp|O64966|HMDH1_GOSHI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Gossypium hirsutum GN=HMG1 PE=3 SV=1 | 653 | 1139 | 6.0E-148 |
| sp|P34135|HMDH1_DICDI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Dictyostelium discoideum GN=hmgA PE=2 SV=1 | 724 | 1140 | 5.0E-147 |
| sp|P48020|HMDH1_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Solanum tuberosum GN=HMG1 PE=2 SV=1 | 670 | 1140 | 8.0E-147 |
| sp|Q41437|HMDH2_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Solanum tuberosum GN=HMG2 PE=2 SV=1 | 670 | 1144 | 1.0E-146 |
| sp|P14891|HMDH1_ARATH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Arabidopsis thaliana GN=HMG1 PE=1 SV=1 | 679 | 1141 | 3.0E-146 |
| sp|Q41438|HMDH3_SOLTU | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Solanum tuberosum GN=HMG3 PE=2 SV=1 | 704 | 1141 | 1.0E-145 |
| sp|P48021|HMDH_CAMAC | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Camptotheca acuminata PE=3 SV=1 | 728 | 1148 | 8.0E-145 |
| sp|Q00583|HMDH3_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 3 OS=Hevea brasiliensis GN=HMGR3 PE=2 SV=1 | 729 | 1148 | 2.0E-144 |
| sp|P43256|HMDH2_ARATH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Arabidopsis thaliana GN=HMG2 PE=2 SV=1 | 720 | 1141 | 5.0E-141 |
| sp|Q0DY59|HMDH1_ORYSJ | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Oryza sativa subsp. japonica GN=HMG1 PE=2 SV=2 | 725 | 1147 | 2.0E-138 |
| sp|A2X8W3|HMDH1_ORYSI | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Oryza sativa subsp. indica GN=HMG1 PE=2 SV=2 | 725 | 1147 | 3.0E-138 |
| sp|P14773|HMDH_DROME | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Drosophila melanogaster GN=Hmgcr PE=2 SV=2 | 726 | 1141 | 3.0E-136 |
| sp|O76819|HMDH_AGRIP | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Agrotis ipsilon GN=HMGR PE=2 SV=1 | 679 | 1140 | 8.0E-133 |
| sp|P16237|HMDH_SCHMA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Schistosoma mansoni PE=2 SV=1 | 691 | 1174 | 2.0E-111 |
| sp|O59469|HMDH_PYRHO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) GN=hmgA PE=3 SV=2 | 729 | 1139 | 1.0E-98 |
| sp|Q9V1R3|HMDH_PYRAB | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Pyrococcus abyssi (strain GE5 / Orsay) GN=hmgA PE=3 SV=2 | 726 | 1139 | 2.0E-97 |
| sp|O26662|HMDH_METTH | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) GN=hmgA PE=3 SV=1 | 731 | 1139 | 3.0E-94 |
| sp|Q59468|HMDH_HALVD | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Haloferax volcanii (strain ATCC 29605 / DSM 3757 / JCM 8879 / NBRC 14742 / NCIMB 2012 / VKM B-1768 / DS2) GN=hmgA PE=1 SV=2 | 797 | 1139 | 6.0E-85 |
| sp|Q58116|HMDH_METJA | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=hmgA PE=3 SV=1 | 729 | 1139 | 1.0E-84 |
| sp|O08424|HMDH_SULSO | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=hmgA PE=1 SV=2 | 726 | 1140 | 4.0E-81 |
| sp|Q9YAS4|HMDH_AERPE | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) GN=hmgA PE=3 SV=1 | 729 | 1134 | 1.0E-80 |
| sp|P29058|HMDH2_HEVBR | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 (Fragment) OS=Hevea brasiliensis GN=HMGR2 PE=2 SV=1 | 943 | 1147 | 1.0E-77 |
| sp|B0R6J9|HMDH_HALS3 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Halobacterium salinarum (strain ATCC 29341 / DSM 671 / R1) GN=hmgA PE=1 SV=1 | 796 | 1139 | 4.0E-73 |
| sp|P12684|HMDH2_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG2 PE=1 SV=1 | 22 | 453 | 4.0E-27 |
| sp|P12683|HMDH1_YEAST | 3-hydroxy-3-methylglutaryl-coenzyme A reductase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=HMG1 PE=1 SV=1 | 7 | 455 | 2.0E-26 |
| sp|O51628|HMDH_BORBU | Probable 3-hydroxy-3-methylglutaryl-coenzyme A reductase OS=Borrelia burgdorferi (strain ATCC 35210 / B31 / CIP 102532 / DSM 4680) GN=BB_0685 PE=3 SV=1 | 751 | 952 | 2.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0015936 | coenzyme A metabolic process | Yes |
| GO:0004420 | hydroxymethylglutaryl-CoA reductase (NADPH) activity | Yes |
| GO:0016021 | integral component of membrane | Yes |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0006793 | phosphorus metabolic process | No |
| GO:0003674 | molecular_function | No |
| GO:0044237 | cellular metabolic process | No |
| GO:0008152 | metabolic process | No |
| GO:0006139 | nucleobase-containing compound metabolic process | No |
| GO:0033875 | ribonucleoside bisphosphate metabolic process | No |
| GO:0044281 | small molecule metabolic process | No |
| GO:0046483 | heterocycle metabolic process | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0016491 | oxidoreductase activity | No |
| GO:0044238 | primary metabolic process | No |
| GO:0006796 | phosphate-containing compound metabolic process | No |
| GO:1901564 | organonitrogen compound metabolic process | No |
| GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | No |
| GO:0006725 | cellular aromatic compound metabolic process | No |
| GO:0008150 | biological_process | No |
| GO:1901360 | organic cyclic compound metabolic process | No |
| GO:1901135 | carbohydrate derivative metabolic process | No |
| GO:0009117 | nucleotide metabolic process | No |
| GO:0006753 | nucleoside phosphate metabolic process | No |
| GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | No |
| GO:0034641 | cellular nitrogen compound metabolic process | No |
| GO:0003824 | catalytic activity | No |
| GO:0006807 | nitrogen compound metabolic process | No |
| GO:0009150 | purine ribonucleotide metabolic process | No |
| GO:0034032 | purine nucleoside bisphosphate metabolic process | No |
| GO:0072521 | purine-containing compound metabolic process | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0006163 | purine nucleotide metabolic process | No |
| GO:0019693 | ribose phosphate metabolic process | No |
| GO:0019637 | organophosphate metabolic process | No |
| GO:0009259 | ribonucleotide metabolic process | No |
| GO:0005575 | cellular_component | No |
| GO:0033865 | nucleoside bisphosphate metabolic process | No |
| GO:0055086 | nucleobase-containing small molecule metabolic process | No |
| GO:0009987 | cellular process | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 49 | 0.5 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 240 | 262 | 22 |
| 2 | 269 | 291 | 22 |
| 3 | 295 | 317 | 22 |
| 4 | 372 | 391 | 19 |
| 5 | 396 | 418 | 22 |
| 6 | 484 | 503 | 19 |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
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|8063 MISNSILPSRFRGESRHDEKAMPSPLAKTISPVLQAMARVACHHPIHTAVIVALLASTSYVSLLQDSLFDVTTGI GKADWSSLVDGSRDLLAGPDTAWRWHSVEHTAAATAADVQHLALLTLVFPDSLTTDSSNTAPQSHAIPTPANLSI TPLPTTENSFTAYSQDTILAYSLPYRQAPEFVSAIQEIPHENAEETMTRHGREKKTWIMKAAKVDTRSTLGQWLY NAWTEFIDLLKNAETLDIFIMILGYISMHLTFVSLFLSMRRMGSNFWLATSTLLASVFAFIFALSVTTKLGVPIS FILLSEGLPFLVVTIGFEKNIVLTRAVLSRAVEYRARRSKPDAAEKAPTQSVIQYAIQAAIKDKGFDILRDYAIE IAILVLGAASGVQGGLQQFCFLAAWILFFDCILLFTFSTAILSIKLEIKRIKRHVDMRMALEADGVSRRVAENVA TAEDEWLLSGGRPSDESSLFGHNVKSSSIPRFKVLMISGFFLVNIINICTIPFRNTASLSSLRSWAGGLGGVASS PPVDPFKVASNGLDAILAASKASGKSVLVTILTPIKYELQYPSVHYGLLSPPCDGNLAACDGAGRLDHYGVGGRM VGGLLKSLEDPVLSKWIVVALALSVGLNGYLFNAARSGIKDPNIPERGIDRKELARAQMFNDSELATLPLGEYVP RTPVQTEPPTPSSSTDDEADVTSKTKPMPTPEHRSATELDQLLAEKRAHEMTDDEIVSSSMRGKIPGYALEKTLN DFTRAVKIRRMIISRTKVTAALTNGLDRSKLPYENYNWERVFGACCENVIGYLPLPVGVAGPLVVDGQSYFIPMA TTEGVLVASTSRGCKAINSGGGAITVLTADGMTRGPCISFETLERAGAAKVWLDSDKGQMLMKEAFDSTSRFARL QTMRTALAGTNLYIRFKTTTGDAMGMNMISKGVEQALNAMAAEGGFEDMMVVSLSGNFCIDKKPAAINWIDGRGK SIVAEAIIPAEVVRSVLKSDVDTLVELNVSKNLIGSAMAGSIGGFNAHAANIVAAVFIATGQDPAQVVESSNCIT TMKNLHGSLQISVSMPSLEVGTLGGGTILEPQSAMLDILGVRGPHPTNPGDNARRLARVIGAAVLAGELSLCSAL AAGHLVRAHMQHNRSAAPSRKATPAPPPATPVSQALTSAHERSTQPLSAAAQQRSRR |
| Coding | >Ophio5|8063 ATGATCTCCAACTCCATTCTCCCATCGCGCTTCCGCGGCGAATCGCGACACGATGAAAAGGCCATGCCCTCACCA CTGGCCAAGACAATCTCGCCCGTCCTTCAGGCCATGGCTAGGGTGGCCTGTCATCACCCCATTCACACCGCCGTC ATCGTCGCCCTCTTGGCAAGCACCTCGTACGTCAGCCTCCTTCAGGACAGCCTATTCGATGTCACTACCGGCATC GGCAAGGCAGACTGGTCGTCTCTGGTCGACGGCAGCAGAGACCTACTCGCCGGACCGGACACGGCATGGAGATGG CATAGCGTCGAGCACACCGCAGCCGCTACCGCCGCCGACGTCCAACACCTCGCTCTCCTGACCCTCGTCTTCCCG GACTCTCTCACCACCGACTCCTCCAACACGGCTCCGCAATCGCACGCCATTCCGACTCCGGCCAACCTCTCCATA ACGCCCCTTCCCACCACCGAAAACTCGTTTACCGCATACTCCCAGGATACCATTCTCGCCTACTCCTTGCCCTAC AGGCAGGCCCCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCCACGAGAATGCTGAAGAGACAATGACGCGCCAC GGCCGCGAAAAGAAAACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGCAGCACCCTCGGCCAGTGGCTCTAT AATGCCTGGACTGAGTTTATCGACCTGCTGAAAAACGCCGAGACTCTCGACATCTTCATCATGATCCTCGGCTAC ATATCCATGCACCTAACCTTTGTTTCCCTTTTCCTCTCCATGCGTCGCATGGGCTCCAACTTTTGGCTCGCAACG AGCACCCTATTGGCCTCCGTCTTTGCCTTCATCTTCGCCCTGTCCGTCACGACCAAGCTCGGCGTTCCCATCAGC TTCATCCTACTGTCTGAGGGCTTACCATTTCTTGTCGTCACCATTGGATTCGAGAAGAACATTGTCCTCACCCGC GCCGTTCTCTCCCGTGCCGTCGAATATCGTGCTCGCCGATCCAAACCCGACGCCGCCGAAAAAGCGCCAACGCAG AGCGTCATTCAGTACGCTATTCAGGCCGCCATCAAGGACAAAGGCTTTGACATTCTACGCGACTACGCCATTGAA ATCGCAATCCTCGTCCTGGGTGCTGCCTCTGGCGTCCAAGGAGGGCTGCAGCAGTTTTGCTTCCTCGCCGCCTGG ATTCTCTTCTTCGACTGCATCCTTCTCTTCACCTTTAGCACCGCCATCCTAAGCATCAAGCTGGAAATCAAGCGC ATCAAGCGCCATGTCGACATGCGTATGGCGCTCGAGGCCGATGGCGTCAGTCGCCGAGTGGCCGAGAACGTTGCC ACGGCCGAGGACGAGTGGCTGCTCTCAGGCGGACGGCCATCGGATGAGTCGTCTCTGTTCGGGCATAATGTAAAA AGCAGCAGCATCCCCAGGTTCAAGGTGCTCATGATCTCCGGCTTCTTCCTCGTCAACATCATCAATATCTGCACC ATCCCGTTCCGCAACACCGCTTCTCTATCGTCTCTCCGGTCCTGGGCCGGGGGACTGGGTGGCGTCGCTTCCAGC CCGCCCGTCGACCCCTTCAAGGTAGCCTCCAACGGGCTGGACGCCATCCTGGCGGCATCCAAGGCCAGCGGCAAG TCGGTGCTCGTCACCATCTTGACGCCGATCAAGTACGAGCTTCAGTACCCTTCGGTGCACTACGGGCTGTTATCT CCGCCCTGCGACGGCAACCTGGCCGCGTGCGACGGAGCGGGCCGGTTGGACCACTACGGCGTTGGCGGTCGCATG GTTGGCGGCCTCCTGAAGAGTCTGGAGGATCCCGTCCTGTCCAAGTGGATTGTCGTTGCCCTGGCCCTTAGCGTC GGTCTCAACGGGTACCTCTTCAACGCGGCTCGCAGCGGCATCAAGGACCCCAATATCCCCGAACGAGGCATCGAT CGCAAGGAGCTGGCGCGCGCACAGATGTTCAACGACTCGGAGCTGGCAACCCTGCCGCTCGGCGAGTACGTGCCA CGTACGCCAGTGCAGACCGAGCCCCCGACGCCATCTTCGTCTACCGACGACGAGGCCGATGTCACGTCTAAGACT AAGCCCATGCCCACCCCGGAGCATCGCTCGGCCACGGAGCTGGACCAGTTACTGGCGGAGAAGCGGGCGCACGAG ATGACGGATGACGAGATCGTCTCCTCGTCAATGCGGGGCAAGATTCCCGGCTACGCTCTGGAAAAGACGTTGAAT GACTTTACTCGCGCCGTCAAGATCAGGCGCATGATCATCTCCCGCACCAAGGTTACTGCGGCGCTCACCAACGGC CTGGATCGATCCAAGCTTCCCTACGAAAATTACAACTGGGAGCGCGTCTTCGGGGCCTGCTGCGAAAACGTCATC GGCTACCTGCCCCTACCAGTCGGCGTGGCGGGACCTCTCGTCGTCGACGGTCAGAGCTACTTCATTCCCATGGCG ACGACGGAGGGCGTCCTGGTGGCGAGTACTAGCAGAGGCTGCAAGGCTATCAACTCGGGGGGCGGCGCCATCACG GTCCTAACGGCGGATGGCATGACGCGCGGTCCGTGTATTAGCTTCGAGACGCTGGAGCGGGCCGGCGCGGCCAAG GTCTGGCTGGACTCGGATAAGGGCCAGATGCTAATGAAGGAGGCCTTCGACTCGACTAGTCGCTTTGCCCGACTA CAGACGATGAGGACGGCCCTCGCCGGCACGAACCTATATATCCGGTTCAAGACGACGACGGGCGACGCGATGGGC ATGAATATGATCTCTAAGGGCGTCGAGCAGGCGCTCAACGCTATGGCCGCGGAGGGCGGCTTCGAGGATATGATG GTGGTATCCCTATCCGGTAACTTTTGCATCGATAAGAAGCCGGCGGCTATTAACTGGATTGACGGGCGCGGCAAG AGTATCGTGGCCGAGGCTATTATCCCGGCCGAGGTGGTTAGGTCCGTGCTTAAGAGCGATGTCGATACCCTCGTG GAACTCAACGTATCGAAGAACCTCATCGGCTCGGCTATGGCCGGGTCTATTGGTGGGTTTAACGCGCATGCGGCC AATATCGTCGCTGCTGTCTTCATCGCGACGGGCCAGGACCCGGCACAGGTAGTGGAGAGTTCTAACTGCATTACC ACGATGAAGAACCTTCACGGATCTCTTCAAATCTCAGTTTCGATGCCATCGCTTGAAGTGGGCACACTGGGCGGC GGCACTATTCTCGAGCCGCAGAGCGCCATGCTCGACATACTAGGCGTTCGGGGCCCGCACCCGACTAATCCGGGC GACAACGCGCGGCGTCTGGCTCGTGTTATCGGCGCTGCCGTCCTGGCCGGCGAGTTGTCTCTATGCAGTGCTCTG GCGGCAGGGCATTTGGTGCGAGCACACATGCAGCACAACCGGAGCGCGGCTCCGTCGAGAAAGGCGACGCCCGCC CCGCCGCCGGCGACACCCGTTTCGCAGGCCTTGACGAGTGCGCACGAGAGGTCGACTCAACCGCTGAGCGCCGCG GCACAGCAGCGGTCGAGGCGT |
| Transcript | >Ophio5|8063 ATGATCTCCAACTCCATTCTCCCATCGCGCTTCCGCGGCGAATCGCGACACGATGAAAAGGCCATGCCCTCACCA CTGGCCAAGACAATCTCGCCCGTCCTTCAGGCCATGGCTAGGGTGGCCTGTCATCACCCCATTCACACCGCCGTC ATCGTCGCCCTCTTGGCAAGCACCTCGTACGTCAGCCTCCTTCAGGACAGCCTATTCGATGTCACTACCGGCATC GGCAAGGCAGACTGGTCGTCTCTGGTCGACGGCAGCAGAGACCTACTCGCCGGACCGGACACGGCATGGAGATGG CATAGCGTCGAGCACACCGCAGCCGCTACCGCCGCCGACGTCCAACACCTCGCTCTCCTGACCCTCGTCTTCCCG GACTCTCTCACCACCGACTCCTCCAACACGGCTCCGCAATCGCACGCCATTCCGACTCCGGCCAACCTCTCCATA ACGCCCCTTCCCACCACCGAAAACTCGTTTACCGCATACTCCCAGGATACCATTCTCGCCTACTCCTTGCCCTAC AGGCAGGCCCCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCCACGAGAATGCTGAAGAGACAATGACGCGCCAC GGCCGCGAAAAGAAAACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGCAGCACCCTCGGCCAGTGGCTCTAT AATGCCTGGACTGAGTTTATCGACCTGCTGAAAAACGCCGAGACTCTCGACATCTTCATCATGATCCTCGGCTAC ATATCCATGCACCTAACCTTTGTTTCCCTTTTCCTCTCCATGCGTCGCATGGGCTCCAACTTTTGGCTCGCAACG AGCACCCTATTGGCCTCCGTCTTTGCCTTCATCTTCGCCCTGTCCGTCACGACCAAGCTCGGCGTTCCCATCAGC TTCATCCTACTGTCTGAGGGCTTACCATTTCTTGTCGTCACCATTGGATTCGAGAAGAACATTGTCCTCACCCGC GCCGTTCTCTCCCGTGCCGTCGAATATCGTGCTCGCCGATCCAAACCCGACGCCGCCGAAAAAGCGCCAACGCAG AGCGTCATTCAGTACGCTATTCAGGCCGCCATCAAGGACAAAGGCTTTGACATTCTACGCGACTACGCCATTGAA ATCGCAATCCTCGTCCTGGGTGCTGCCTCTGGCGTCCAAGGAGGGCTGCAGCAGTTTTGCTTCCTCGCCGCCTGG ATTCTCTTCTTCGACTGCATCCTTCTCTTCACCTTTAGCACCGCCATCCTAAGCATCAAGCTGGAAATCAAGCGC ATCAAGCGCCATGTCGACATGCGTATGGCGCTCGAGGCCGATGGCGTCAGTCGCCGAGTGGCCGAGAACGTTGCC ACGGCCGAGGACGAGTGGCTGCTCTCAGGCGGACGGCCATCGGATGAGTCGTCTCTGTTCGGGCATAATGTAAAA AGCAGCAGCATCCCCAGGTTCAAGGTGCTCATGATCTCCGGCTTCTTCCTCGTCAACATCATCAATATCTGCACC ATCCCGTTCCGCAACACCGCTTCTCTATCGTCTCTCCGGTCCTGGGCCGGGGGACTGGGTGGCGTCGCTTCCAGC CCGCCCGTCGACCCCTTCAAGGTAGCCTCCAACGGGCTGGACGCCATCCTGGCGGCATCCAAGGCCAGCGGCAAG TCGGTGCTCGTCACCATCTTGACGCCGATCAAGTACGAGCTTCAGTACCCTTCGGTGCACTACGGGCTGTTATCT CCGCCCTGCGACGGCAACCTGGCCGCGTGCGACGGAGCGGGCCGGTTGGACCACTACGGCGTTGGCGGTCGCATG GTTGGCGGCCTCCTGAAGAGTCTGGAGGATCCCGTCCTGTCCAAGTGGATTGTCGTTGCCCTGGCCCTTAGCGTC GGTCTCAACGGGTACCTCTTCAACGCGGCTCGCAGCGGCATCAAGGACCCCAATATCCCCGAACGAGGCATCGAT CGCAAGGAGCTGGCGCGCGCACAGATGTTCAACGACTCGGAGCTGGCAACCCTGCCGCTCGGCGAGTACGTGCCA CGTACGCCAGTGCAGACCGAGCCCCCGACGCCATCTTCGTCTACCGACGACGAGGCCGATGTCACGTCTAAGACT AAGCCCATGCCCACCCCGGAGCATCGCTCGGCCACGGAGCTGGACCAGTTACTGGCGGAGAAGCGGGCGCACGAG ATGACGGATGACGAGATCGTCTCCTCGTCAATGCGGGGCAAGATTCCCGGCTACGCTCTGGAAAAGACGTTGAAT GACTTTACTCGCGCCGTCAAGATCAGGCGCATGATCATCTCCCGCACCAAGGTTACTGCGGCGCTCACCAACGGC CTGGATCGATCCAAGCTTCCCTACGAAAATTACAACTGGGAGCGCGTCTTCGGGGCCTGCTGCGAAAACGTCATC GGCTACCTGCCCCTACCAGTCGGCGTGGCGGGACCTCTCGTCGTCGACGGTCAGAGCTACTTCATTCCCATGGCG ACGACGGAGGGCGTCCTGGTGGCGAGTACTAGCAGAGGCTGCAAGGCTATCAACTCGGGGGGCGGCGCCATCACG GTCCTAACGGCGGATGGCATGACGCGCGGTCCGTGTATTAGCTTCGAGACGCTGGAGCGGGCCGGCGCGGCCAAG GTCTGGCTGGACTCGGATAAGGGCCAGATGCTAATGAAGGAGGCCTTCGACTCGACTAGTCGCTTTGCCCGACTA CAGACGATGAGGACGGCCCTCGCCGGCACGAACCTATATATCCGGTTCAAGACGACGACGGGCGACGCGATGGGC ATGAATATGATCTCTAAGGGCGTCGAGCAGGCGCTCAACGCTATGGCCGCGGAGGGCGGCTTCGAGGATATGATG GTGGTATCCCTATCCGGTAACTTTTGCATCGATAAGAAGCCGGCGGCTATTAACTGGATTGACGGGCGCGGCAAG AGTATCGTGGCCGAGGCTATTATCCCGGCCGAGGTGGTTAGGTCCGTGCTTAAGAGCGATGTCGATACCCTCGTG GAACTCAACGTATCGAAGAACCTCATCGGCTCGGCTATGGCCGGGTCTATTGGTGGGTTTAACGCGCATGCGGCC AATATCGTCGCTGCTGTCTTCATCGCGACGGGCCAGGACCCGGCACAGGTAGTGGAGAGTTCTAACTGCATTACC ACGATGAAGAACCTTCACGGATCTCTTCAAATCTCAGTTTCGATGCCATCGCTTGAAGTGGGCACACTGGGCGGC GGCACTATTCTCGAGCCGCAGAGCGCCATGCTCGACATACTAGGCGTTCGGGGCCCGCACCCGACTAATCCGGGC GACAACGCGCGGCGTCTGGCTCGTGTTATCGGCGCTGCCGTCCTGGCCGGCGAGTTGTCTCTATGCAGTGCTCTG GCGGCAGGGCATTTGGTGCGAGCACACATGCAGCACAACCGGAGCGCGGCTCCGTCGAGAAAGGCGACGCCCGCC CCGCCGCCGGCGACACCCGTTTCGCAGGCCTTGACGAGTGCGCACGAGAGGTCGACTCAACCGCTGAGCGCCGCG GCACAGCAGCGGTCGAGGCGTTAA |
| Gene | >Ophio5|8063 ATGATCTCCAACTCCATTCTCCCATCGCGCTTCCGCGGCGAATCGCGACACGATGAAAAGGCCATGCCCTCACCA CTGGCCAAGACAATCTCGCCCGTCCTTCAGGCCATGGCTAGGGTGGCCTGTCATCACCCCATTCACACCGCCGTC ATCGTCGCCCTCTTGGCAAGCACCTCGTACGTCAGCCTCCTTCAGGACAGCCTATTCGATGTCACTACCGGCATC GGCAAGGCAGACTGGTCGTCTCTGGTCGACGGCAGCAGAGACCTACTCGCCGGACCGGACACGGCATGGAGATGG CATAGCGTCGAGCACACCGCAGCCGCTACCGCCGCCGACGTCCAACACCTCGCTCTCCTGACCCTCGTCTTCCCG GACTCTCTCACCACCGACTCCTCCAACACGGCTCCGCAATCGCACGCCATTCCGACTCCGGCCAACCTCTCCATA ACGCCCCTTCCCACCACCGAAAACTCGTTTACCGCATACTCCCAGGATACCATTCTCGCCTACTCCTTGCCCTAC AGGCAGGCCCCCGAGTTCGTCTCCGCCATCCAGGAGATCCCCCACGAGAATGCTGAAGAGACAATGACGCGCCAC GGCCGCGAAAAGAAAACGTGGATCATGAAGGCCGCCAAGGTCGACACCCGCAGCACCCTCGGCCAGTGGCTCTAT AATGCCTGGACTGAGTTTATCGACCTGCTGAAAAACGCCGAGACTCTCGACATCTTCATCATGATCCTCGGCTAC ATATCCATGCACCTAACCTTTGTTTCCCTTTTCCTCTCCATGCGTCGCATGGGCTCCAACTTTTGGCTCGCAACG AGCACCCTATTGGCCTCCGTCTTTGCCTTCATCTTCGCCCTGTCCGTCACGACCAAGCTCGGCGTTCCCATCAGC TTCATCCTACTGTCTGAGGGCTTACCATTTCTTGTCGTCACCATTGGATTCGAGAAGAACATTGTCCTCACCCGC GCCGTTCTCTCCCGTGCCGTCGAATATCGTGCTCGCCGATCCAAACCCGACGCCGCCGAAAAAGCGCCAACGCAG AGCGTCATTCAGTACGCTATTCAGGCCGCCATCAAGGACAAAGGCTTTGACATTCTACGCGACTACGCCATTGAA ATCGCAATCCTCGTCCTGGGTGCTGCCTCTGGCGTCCAAGGAGGGCTGCAGCAGTTTTGCTTCCTCGCCGCCTGG ATTCTCTTCTTCGACTGCATCCTTCTCTTCACCTTTAGCACCGCCATCCTAAGCATCAAGCTGGAAATCAAGCGC ATCAAGCGCCATGTCGACATGCGTATGGCGCTCGAGGCCGATGGCGTCAGTCGCCGAGTGGCCGAGAACGTTGCC ACGGCCGAGGACGAGTGGCTGCTCTCAGGCGGACGGCCATCGGATGAGTCGTCTCTGTTCGGGCATAATGTAAAA AGCAGCAGCATCCCCAGGTTCAAGGTGCTCATGATCTCCGGCTTCTTCCTCGTCAACATCATCAATATCTGCACC ATCCCGTTCCGCAACACCGCTTCTCTATCGTCTCTCCGGTCCTGGGCCGGGGGACTGGGTGGCGTCGCTTCCAGC CCGCCCGTCGACCCCTTCAAGGTAGCCTCCAACGGGCTGGACGCCATCCTGGCGGCATCCAAGGCCAGCGGCAAG TCGGTGCTCGTCACCATCTTGACGCCGATCAAGTACGAGCTTCAGTACCCTTCGGTGCACTACGGGCTGTTATCT CCGCCCTGCGACGGCAACCTGGCCGCGTGCGACGGAGCGGGCCGGTTGGACCACTACGGCGTTGGCGGTCGCATG GTTGGCGGCCTCCTGAAGAGTCTGGAGGATCCCGTCCTGTCCAAGTGGATTGTCGTTGCCCTGGCCCTTAGCGTC GGTCTCAACGGGTACCTCTTCAACGCGGCTCGCAGCGGCATCAAGGACCCCAATATCCCCGAACGAGGCATCGAT CGCAAGGAGCTGGCGCGCGCACAGATGTTCAACGACTCGGAGCTGGCAACCCTGCCGCTCGGCGAGTACGTGCCA CGTACGCCAGTGCAGACCGAGCCCCCGACGCCATCTTCGTCTACCGACGACGAGGCCGATGTCACGTCTAAGACT AAGCCCATGCCCACCCCGGAGCATCGCTCGGCCACGGAGCTGGACCAGTTACTGGCGGAGAAGCGGGCGCACGAG ATGACGGATGACGAGATCGTCTCCTCGTCAATGCGGGGCAAGATTCCCGGCTACGCTCTGGAAAAGACGTTGAAT GACTTTACTCGCGCCGTCAAGATCAGGCGCATGATCATCTCCCGCACCAAGGTTACTGCGGCGCTCACCAACGGC CTGGATCGATCCAAGCTTCCCTACGAAAATTACAACTGGGAGCGCGTCTTCGGGGCCTGCTGCGAAAACGTCATC GGCTACCTGCCCCTACCAGTCGGCGTGGCGGGACCTCTCGTCGTCGACGGTCAGAGCTACTTCATTCCCATGGCG ACGACGGAGGGCGTCCTGGTGGCGAGTACTAGCAGAGGCTGCAAGGCTATCAACTCGGGGGGCGGCGCCATCACG GTCCTAACGGCGGATGGCATGACGCGCGGTCCGTGTATTAGCTTCGAGACGCTGGAGCGGGCCGGCGCGGCCAAG GTCTGGCTGGACTCGGATAAGGGCCAGATGCTAATGAAGGAGGCCTTCGACTCGACTAGTCGCTTTGCCCGACTA CAGACGATGAGGACGGCCCTCGCCGGCACGAACCTATATATCCGGTTCAAGACGACGACGGGCGACGCGATGGGC ATGAATATGATCTCTAAGGGCGTCGAGCAGGCGCTCAACGCTATGGCCGCGGAGGGCGGCTTCGAGGATATGATG GTGGTATCCCTATCCGGTAACTTTTGCATCGATAAGAAGCCGGCGGCTATTAACTGGATTGACGGGCGCGGCAAG AGTATCGTGGCCGAGGCTATTATCCCGGCCGAGGTGGTTAGGTCCGTGCTTAAGAGCGATGTCGATACCCTCGTG GAACTCAACGTATCGAAGAACCTCATCGGCTCGGCTATGGCCGGGTCTATTGGTGGGTTTAACGCGCATGCGGCC AATATCGTCGCTGCTGTCTTCATCGCGACGGGCCAGGACCCGGCACAGGTAGTGGAGAGTTCTAACTGCATTACC ACGATGAAGAAGTAAGCCCGTCGTATTTCGGTCTAGCTAGTGGACGTTGCTGACGCGTGATAGCCTTCACGGATC TCTTCAAATCTCAGTTTCGATGCCATCGCTTGAAGTGGGCACACTGGGCGGCGGCACTATTCTCGAGCCGCAGAG CGCCATGCTCGACATACTAGGCGTTCGGGGCCCGCACCCGACTAATCCGGGCGACAACGCGCGGCGTCTGGCTCG TGTTATCGGCGCTGCCGTCCTGGCCGGCGAGTTGTCTCTATGCAGTGCTCTGGCGGCAGGGCATTTGGTGCGAGC ACACATGCAGCACAACCGGAGCGCGGCTCCGTCGAGAAAGGCGACGCCCGCCCCGCCGCCGGCGACACCCGTTTC GCAGGCCTTGACGAGTGCGCACGAGAGGTCGACTCAACCGCTGAGCGCCGCGGCACAGCAGCGGTCGAGGCGTTA A |