Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|3481
Gene name
Locationscaffold_276:9578..13191
Strand-
Gene length (bp)3613
Transcript length (bp)2979
Coding sequence length (bp)2976
Protein length (aa) 992

Overview

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF01301 Glyco_hydro_35 Glycosyl hydrolases family 35 2.5E-93 47 378
PF10435 BetaGal_dom2 Beta-galactosidase, domain 2 1.3E-58 392 569
PF13364 BetaGal_dom4_5 Beta-galactosidase jelly roll domain 2.0E-23 684 797
PF13363 BetaGal_dom3 Beta-galactosidase, domain 3 3.3E-21 570 650

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|A2QAN3|BGALA_ASPNC Probable beta-galactosidase A OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=lacA PE=3 SV=1 30 992 0.0E+00
sp|B8QGZ3|BGALA_PENEN Probable beta-galactosidase A OS=Penicillium expansum GN=lacA PE=2 SV=1 30 992 0.0E+00
sp|A1DJ58|BGALE_NEOFI Probable beta-galactosidase E OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=lacE PE=3 SV=1 32 992 0.0E+00
sp|B0XXE7|BGALE_ASPFC Probable beta-galactosidase E OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=lacE PE=3 SV=1 32 992 0.0E+00
sp|Q4WG05|BGALE_ASPFU Probable beta-galactosidase E OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=lacE PE=3 SV=1 32 992 0.0E+00
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|A2QAN3|BGALA_ASPNC Probable beta-galactosidase A OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=lacA PE=3 SV=1 30 992 0.0E+00
sp|B8QGZ3|BGALA_PENEN Probable beta-galactosidase A OS=Penicillium expansum GN=lacA PE=2 SV=1 30 992 0.0E+00
sp|A1DJ58|BGALE_NEOFI Probable beta-galactosidase E OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=lacE PE=3 SV=1 32 992 0.0E+00
sp|B0XXE7|BGALE_ASPFC Probable beta-galactosidase E OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=lacE PE=3 SV=1 32 992 0.0E+00
sp|Q4WG05|BGALE_ASPFU Probable beta-galactosidase E OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=lacE PE=3 SV=1 32 992 0.0E+00
sp|Q5BFC4|BGALA_EMENI Probable beta-galactosidase A OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=lacA PE=3 SV=2 30 992 0.0E+00
sp|Q700S9|BGALA_PENSQ Probable beta-galactosidase A OS=Penicillium sp. GN=lacA PE=1 SV=1 30 992 0.0E+00
sp|P29853|BGAL_ASPNG Beta-galactosidase OS=Aspergillus niger GN=lacA PE=1 SV=2 30 992 0.0E+00
sp|Q4WS33|BGALA_ASPFU Probable beta-galactosidase A OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=lacA PE=3 SV=2 30 992 0.0E+00
sp|B0XMP7|BGALA_ASPFC Probable beta-galactosidase A OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=lacA PE=3 SV=2 30 992 0.0E+00
sp|Q4ZHV7|BGALA_ASPPH Probable beta-galactosidase A OS=Aspergillus phoenicis GN=lacA PE=2 SV=1 30 992 0.0E+00
sp|Q2UCU3|BGALA_ASPOR Probable beta-galactosidase A OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=lacA PE=1 SV=1 30 992 0.0E+00
sp|B8N6V7|BGALA_ASPFN Probable beta-galactosidase A OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=lacA PE=3 SV=1 30 992 0.0E+00
sp|A1D1Z9|BGALA_NEOFI Probable beta-galactosidase A OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=lacA PE=3 SV=1 30 992 0.0E+00
sp|Q4WRD3|BGALB_ASPFU Probable beta-galactosidase B OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=lacB PE=3 SV=1 37 963 5.0E-153
sp|B0XNY2|BGALB_ASPFC Probable beta-galactosidase B OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=lacB PE=3 SV=1 37 963 5.0E-153
sp|A1D199|BGALB_NEOFI Probable beta-galactosidase B OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=lacB PE=3 SV=1 37 963 1.0E-149
sp|B6H5X9|BGALC_PENRW Probable beta-galactosidase C OS=Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) GN=lacC PE=3 SV=1 1 959 1.0E-146
sp|A1CE56|BGALC_ASPCL Probable beta-galactosidase C OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=lacC PE=3 SV=1 41 959 3.0E-142
sp|Q4WNE4|BGALC_ASPFU Probable beta-galactosidase C OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=lacC PE=3 SV=1 41 959 4.0E-142
sp|B0Y752|BGALC_ASPFC Probable beta-galactosidase C OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=lacC PE=3 SV=1 41 959 4.0E-142
sp|A1DM65|BGALC_NEOFI Probable beta-galactosidase C OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=lacC PE=3 SV=1 41 959 9.0E-142
sp|Q5BEQ0|BGALB_EMENI Probable beta-galactosidase B OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=lacB PE=3 SV=2 37 989 1.0E-140
sp|A2QL84|BGALC_ASPNC Probable beta-galactosidase C OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=lacC PE=3 SV=1 37 991 3.0E-139
sp|A2QA64|BGALB_ASPNC Probable beta-galactosidase B OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=lacB PE=3 SV=2 41 963 1.0E-138
sp|Q2UMD5|BGALC_ASPOR Probable beta-galactosidase C OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=lacC PE=3 SV=1 41 965 2.0E-138
sp|B8N2I5|BGALC_ASPFN Probable beta-galactosidase C OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=lacC PE=3 SV=1 41 965 2.0E-138
sp|B6QLF0|BGALB_TALMQ Probable beta-galactosidase B OS=Talaromyces marneffei (strain ATCC 18224 / CBS 334.59 / QM 7333) GN=lacB PE=3 SV=1 37 957 7.0E-138
sp|B8NKI4|BGALB_ASPFN Probable beta-galactosidase B OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=lacB PE=3 SV=2 1 963 1.0E-137
sp|B6QHA9|BGALC_TALMQ Probable beta-galactosidase C OS=Talaromyces marneffei (strain ATCC 18224 / CBS 334.59 / QM 7333) GN=lacC PE=3 SV=1 41 918 2.0E-135
sp|Q2U6P1|BGALB_ASPOR Probable beta-galactosidase B OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=lacB PE=3 SV=2 1 963 2.0E-135
sp|B6GW04|BGALB_PENRW Probable beta-galactosidase B OS=Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) GN=lacB PE=3 SV=2 36 963 4.0E-135
sp|Q0CMF3|BGALB_ASPTN Probable beta-galactosidase B OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=lacB PE=3 SV=2 32 963 1.0E-133
sp|A7EZS5|BGALC_SCLS1 Probable beta-galactosidase C OS=Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) GN=lacC PE=3 SV=1 37 959 2.0E-131
sp|A6RPN7|BGALB_BOTFB Probable beta-galactosidase B OS=Botryotinia fuckeliana (strain B05.10) GN=lacB PE=3 SV=1 37 977 9.0E-130
sp|B2W791|BGALB_PYRTR Probable beta-galactosidase B OS=Pyrenophora tritici-repentis (strain Pt-1C-BFP) GN=lacB PE=3 SV=1 37 959 6.0E-128
sp|A7EBU5|BGALB_SCLS1 Probable beta-galactosidase B OS=Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) GN=lacB PE=3 SV=1 37 977 7.0E-126
sp|Q5XIL5|GLBL3_RAT Beta-galactosidase-1-like protein 3 OS=Rattus norvegicus GN=Glb1l3 PE=2 SV=1 50 377 4.0E-39
sp|A2RSQ1|GLBL3_MOUSE Beta-galactosidase-1-like protein 3 OS=Mus musculus GN=Glb1l3 PE=1 SV=1 50 377 2.0E-37
sp|Q8NCI6|GLBL3_HUMAN Beta-galactosidase-1-like protein 3 OS=Homo sapiens GN=GLB1L3 PE=2 SV=3 50 413 3.0E-33
sp|Q9SCV0|BGA12_ARATH Beta-galactosidase 12 OS=Arabidopsis thaliana GN=BGAL12 PE=2 SV=1 37 398 1.0E-29
sp|Q9MAJ7|BGAL5_ARATH Beta-galactosidase 5 OS=Arabidopsis thaliana GN=BGAL5 PE=2 SV=1 41 399 3.0E-29
sp|Q9SCV9|BGAL3_ARATH Beta-galactosidase 3 OS=Arabidopsis thaliana GN=BGAL3 PE=1 SV=1 37 392 8.0E-29
sp|Q93Z24|BGA17_ARATH Beta-galactosidase 17 OS=Arabidopsis thaliana GN=BGAL17 PE=2 SV=1 45 432 7.0E-28
sp|Q54MV6|BGAL2_DICDI Probable beta-galactosidase 2 OS=Dictyostelium discoideum GN=glb2 PE=3 SV=1 41 385 9.0E-28
sp|Q9LFA6|BGAL2_ARATH Beta-galactosidase 2 OS=Arabidopsis thaliana GN=BGAL2 PE=2 SV=2 38 398 2.0E-26
sp|Q0DGD7|BGAL8_ORYSJ Beta-galactosidase 8 OS=Oryza sativa subsp. japonica GN=Os05g0539400 PE=2 SV=1 44 377 2.0E-26
sp|Q8IW92|GLBL2_HUMAN Beta-galactosidase-1-like protein 2 OS=Homo sapiens GN=GLB1L2 PE=2 SV=1 57 366 3.0E-26
sp|Q9SCW1|BGAL1_ARATH Beta-galactosidase 1 OS=Arabidopsis thaliana GN=BGAL1 PE=1 SV=1 11 399 5.0E-26
sp|Q9SCV1|BGA11_ARATH Beta-galactosidase 11 OS=Arabidopsis thaliana GN=BGAL11 PE=2 SV=1 41 377 6.0E-26
sp|Q9SCV8|BGAL4_ARATH Beta-galactosidase 4 OS=Arabidopsis thaliana GN=BGAL4 PE=1 SV=1 41 398 1.0E-25
sp|Q9SCU9|BGA13_ARATH Beta-galactosidase 13 OS=Arabidopsis thaliana GN=BGAL13 PE=2 SV=1 41 377 1.0E-25
sp|Q9SCV3|BGAL9_ARATH Beta-galactosidase 9 OS=Arabidopsis thaliana GN=BGAL9 PE=2 SV=1 41 406 3.0E-25
sp|Q3UPY5|GLBL2_MOUSE Beta-galactosidase-1-like protein 2 OS=Mus musculus GN=Glb1l2 PE=1 SV=1 60 377 3.0E-25
sp|Q7XFK2|BGA14_ORYSJ Beta-galactosidase 14 OS=Oryza sativa subsp. japonica GN=Os10g0340600 PE=2 SV=1 40 377 1.0E-24
sp|Q0IZZ8|BGA12_ORYSJ Beta-galactosidase 12 OS=Oryza sativa subsp. japonica GN=Os09g0539200 PE=2 SV=2 40 377 2.0E-24
sp|P48981|BGAL_MALDO Beta-galactosidase OS=Malus domestica PE=1 SV=1 41 410 2.0E-24
sp|Q10RB4|BGAL5_ORYSJ Beta-galactosidase 5 OS=Oryza sativa subsp. japonica GN=Os03g0165400 PE=2 SV=1 41 398 6.0E-24
sp|Q9SCU8|BGA14_ARATH Beta-galactosidase 14 OS=Arabidopsis thaliana GN=BGAL14 PE=2 SV=2 41 390 7.0E-24
sp|O19015|BGAL_FELCA Beta-galactosidase OS=Felis catus GN=GLB1 PE=2 SV=1 52 390 7.0E-24
sp|Q9SCV5|BGAL7_ARATH Beta-galactosidase 7 OS=Arabidopsis thaliana GN=BGAL7 PE=2 SV=2 40 423 8.0E-24
sp|P45582|BGAL_ASPOF Beta-galactosidase OS=Asparagus officinalis PE=2 SV=1 41 196 9.0E-24
sp|Q5Z7L0|BGAL9_ORYSJ Beta-galactosidase 9 OS=Oryza sativa subsp. japonica GN=Os06g0573600 PE=2 SV=1 42 376 1.0E-23
sp|P23780|BGAL_MOUSE Beta-galactosidase OS=Mus musculus GN=Glb1 PE=1 SV=1 52 388 1.0E-23
sp|Q9C6W4|BGA15_ARATH Beta-galactosidase 15 OS=Arabidopsis thaliana GN=BGAL15 PE=2 SV=1 40 377 1.0E-23
sp|Q9TRY9|BGAL_CANLF Beta-galactosidase OS=Canis lupus familiaris GN=GLB1 PE=2 SV=3 52 390 1.0E-23
sp|Q0INM3|BGA15_ORYSJ Beta-galactosidase 15 OS=Oryza sativa subsp. japonica GN=Os12g0429200 PE=2 SV=1 41 396 3.0E-23
sp|P48980|BGAL_SOLLC Beta-galactosidase OS=Solanum lycopersicum PE=1 SV=1 41 403 4.0E-23
sp|Q95LV1|GLB1L_MACFA Beta-galactosidase-1-like protein OS=Macaca fascicularis GN=GLB1L PE=2 SV=1 40 366 5.0E-23
sp|Q8GX69|BGA16_ARATH Beta-galactosidase 16 OS=Arabidopsis thaliana GN=BGAL16 PE=2 SV=2 41 377 5.0E-23
sp|P48982|BGAL_XANMN Beta-galactosidase OS=Xanthomonas manihotis GN=bga PE=1 SV=1 49 366 8.0E-23
sp|Q6UWU2|GLB1L_HUMAN Beta-galactosidase-1-like protein OS=Homo sapiens GN=GLB1L PE=2 SV=1 59 366 8.0E-23
sp|Q9FN08|BGA10_ARATH Beta-galactosidase 10 OS=Arabidopsis thaliana GN=BGAL10 PE=2 SV=1 41 392 8.0E-23
sp|Q8RUV9|BGAL1_ORYSJ Beta-galactosidase 1 OS=Oryza sativa subsp. japonica GN=Os01g0533400 PE=2 SV=1 41 391 1.0E-22
sp|Q58D55|BGAL_BOVIN Beta-galactosidase OS=Bos taurus GN=GLB1 PE=2 SV=1 52 415 1.0E-22
sp|P49676|BGAL_BRAOL Beta-galactosidase OS=Brassica oleracea PE=2 SV=1 40 406 2.0E-22
sp|Q60HF6|BGAL_MACFA Beta-galactosidase OS=Macaca fascicularis GN=GLB1 PE=2 SV=1 46 388 4.0E-22
sp|Q8VC60|GLB1L_MOUSE Beta-galactosidase-1-like protein OS=Mus musculus GN=Glb1l PE=1 SV=1 59 366 5.0E-22
sp|Q7G3T8|BGA13_ORYSJ Beta-galactosidase 13 OS=Oryza sativa subsp. japonica GN=Os10g0330600 PE=2 SV=1 41 428 5.0E-22
sp|Q10NX8|BGAL6_ORYSJ Beta-galactosidase 6 OS=Oryza sativa subsp. japonica GN=Os03g0255100 PE=1 SV=2 41 425 9.0E-22
sp|Q5R7P4|BGAL_PONAB Beta-galactosidase OS=Pongo abelii GN=GLB1 PE=2 SV=1 46 388 1.0E-21
sp|Q9SCV4|BGAL8_ARATH Beta-galactosidase 8 OS=Arabidopsis thaliana GN=BGAL8 PE=2 SV=2 41 196 1.0E-21
sp|Q00662|BGAL_DIACA Putative beta-galactosidase OS=Dianthus caryophyllus GN=CARSR12 PE=2 SV=1 41 422 2.0E-21
sp|P16278|BGAL_HUMAN Beta-galactosidase OS=Homo sapiens GN=GLB1 PE=1 SV=2 41 388 3.0E-21
sp|Q9FFN4|BGAL6_ARATH Beta-galactosidase 6 OS=Arabidopsis thaliana GN=BGAL6 PE=2 SV=1 41 197 2.0E-20
sp|Q8W0A1|BGAL2_ORYSJ Beta-galactosidase 2 OS=Oryza sativa subsp. japonica GN=Os01g0580200 PE=2 SV=1 42 196 2.0E-20
sp|Q6ZJJ0|BGA11_ORYSJ Beta-galactosidase 11 OS=Oryza sativa subsp. japonica GN=Os08g0549200 PE=2 SV=1 40 384 2.0E-20
sp|Q6Z6K4|BGAL4_ORYSJ Beta-galactosidase 4 OS=Oryza sativa subsp. japonica GN=Os02g0219200 PE=2 SV=1 41 196 2.0E-19
sp|A2X2H7|BGAL4_ORYSI Beta-galactosidase 4 OS=Oryza sativa subsp. indica GN=OsI_006270 PE=3 SV=1 41 196 2.0E-19
sp|Q54GE1|BGAL1_DICDI Beta-galactosidase 1 OS=Dictyostelium discoideum GN=glb1 PE=3 SV=1 1 470 3.0E-19
sp|Q75HQ3|BGAL7_ORYSJ Beta-galactosidase 7 OS=Oryza sativa subsp. japonica GN=Os05g0428100 PE=3 SV=1 35 197 4.0E-19
sp|Q67VU7|BGA10_ORYSJ Putative beta-galactosidase 10 OS=Oryza sativa subsp. japonica GN=Os06g0628500 PE=3 SV=1 41 227 6.0E-19
sp|Q5N8X6|BGAL3_ORYSJ Beta-galactosidase 3 OS=Oryza sativa subsp. japonica GN=Os01g0875500 PE=3 SV=1 41 377 2.0E-18
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GO

(None)

Deeploc

[Help with interpreting the results of Deeploc 2.0]
Localizations Signals Cytoplasm Nucleus Extracellular Cell membrane Mitochondrion Plastid Endoplasmic reticulum Lysosome vacuole Golgi apparatus Peroxisome
Extracellular Signal peptide 0.1292 0.0842 0.93 0.0989 0.1286 0.0179 0.3454 0.3699 0.164 0.0065

SignalP

SignalP signal predicted Location Score
Yes 1 - 18 0.999562

Transmembrane Domains

(None)

Transcription Factor Class

(None)

CAZymes

CAZyme category E-value Start End
GH35 2.4E-91 48 378

Secondary Metabolism

(None)

Expression data

Analysis 1: Expression analysis during behavioral modification. Published in De Bekker et al., 2017.

Click here for more information

Orthologs

Orthofinder run ID4
Orthogroup4214
Change Orthofinder run
Species Protein ID
Ophiocordyceps australis 1348a (Ghana) OphauG2|2094
Ophiocordyceps australis map64 (Brazil) OphauB2|3071
Ophiocordyceps camponoti-floridani Ophcf2|00868
Ophiocordyceps camponoti-rufipedis Ophun1|208
Ophiocordyceps kimflemingae Ophio5|3481 (this protein)
Ophiocordyceps subramaniannii Hirsu2|860

Sequences

Type of sequenceSequence
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|3481
MKLSSTLLAALAMAMSHALSLAGRPVKVLDVDKRAPLQDLVTWDDQSLFIRGERVMMYSGEFHPFRLPVPSLYLD
IFQKIRALGFNLVSFYVDWALLEGKPGEFRADGIFDLEPFFDAAKKAGIYLLARPGPYINAEVSGGGFPGWLQRI
KGILRTDAGDFLSTTDNYMAHICAIIAKHQITQGGPVVLFQPENEYSYGYRIPFPNGNYMQYVIDQARKAGIVVP
TINNDIGPGGNYAPGTGRGAMDIYGHDNYPLGFDCANPSTWPSEKFPTNFHELHMKQSPNTPFSIIEFQGGSYDP
WGGTGLEQCSALINHEFERVYYKNNMAAGVRIFNVYMIFGGTNWGNLGHPGGYTSYDYGAAIRENGVIDREKYSE
LKLEAEFLRVSPGYLVTTPGSATRGVYSANQDITVTPLLSQDAGSFFVVRHTNFANTGSTTYTLRLPTSAGTLSI
PQSGGELTLLGRDSKMLVTDYPVGGYTLLYSTAEVFTWKRFADRTVLVLYGGGPDETNEFAVHGDDDQQVTQLEG
SGVSLDSLAGVAVVVKWKTSSGRQVIKMGDLVVHLLDRNSAYKYWVPVLPSNGSAYGSSVMNPESLIVSGGYLVR
SATISGSVLSLKADFNASTSLEIMGVPPGVSQLIVNGRPTRYSLSALGDWMAEPDIGIPKMVVPDLRALSWRRID
SLPEVQAGYDDSAWPVADKKKSSNTAFPSKTPVSLYGSDYGFHTGTLVFRGHFVARGNESRLFLRTAGGSGFASS
VWLDDTFLGSFTNTEAAAEENNSTYRVPSLVSGRRHVLTVVVDNMGLNEVVNPGTETMKSPRGILDYALLSGDAS
ANEPSVTDISPWKLTGNLGGEDYVDKSRGPLNEGGLFFERQAYHVPPTPSSSSSSSSSSSSSSPLLDRFTSASPW
QGLDRAGIAFYAAELTLNYPSDKSNTFADFPVPEGILNYRGANWIGLAVWALDAGGAKVPGFWLKVGTAVVTGRE
PVEVVNATAYAERFGAY
Coding >Ophio5|3481
ATGAAGCTCTCGTCGACGCTGCTGGCCGCGCTGGCGATGGCCATGTCCCATGCCCTGAGCCTCGCCGGCCGGCCG
GTCAAGGTCCTGGACGTCGACAAGCGCGCGCCTCTCCAGGACTTGGTCACTTGGGATGACCAGTCGCTGTTCATC
CGCGGAGAGCGTGTCATGATGTACTCGGGCGAATTCCACCCCTTTCGCTTGCCTGTGCCGTCGCTATACCTCGAC
ATATTCCAAAAGATAAGGGCCCTCGGCTTCAACCTGGTGTCCTTCTACGTCGATTGGGCTCTCCTCGAGGGCAAG
CCGGGTGAATTTCGCGCCGATGGCATCTTTGATCTCGAGCCCTTCTTCGACGCGGCCAAGAAGGCGGGCATCTAT
CTCCTCGCCCGGCCGGGACCTTACATCAACGCCGAGGTTTCTGGCGGCGGCTTCCCCGGCTGGCTCCAGAGGATC
AAGGGAATCTTGCGGACCGATGCCGGCGACTTTCTTAGCACGACGGACAACTACATGGCTCACATCTGCGCCATC
ATTGCAAAGCACCAGATCACTCAGGGCGGACCAGTCGTCTTGTTCCAGCCGGAAAACGAGTATAGCTACGGCTAT
AGGATCCCGTTTCCCAACGGCAACTACATGCAGTACGTCATCGACCAGGCTCGCAAGGCCGGCATCGTCGTCCCC
ACCATCAACAATGATATTGGCCCCGGAGGCAACTATGCTCCCGGCACCGGCAGAGGCGCCATGGACATTTACGGA
CACGACAACTATCCCCTGGGCTTCGACTGTGCGAACCCGTCCACTTGGCCTTCTGAAAAGTTCCCTACCAACTTC
CATGAGCTGCACATGAAGCAAAGTCCCAACACACCCTTCTCCATCATCGAGTTCCAAGGTGGCTCCTATGATCCA
TGGGGCGGCACTGGCCTCGAGCAATGCTCCGCCCTCATCAACCACGAGTTCGAGCGCGTCTACTACAAGAACAAC
ATGGCGGCCGGCGTGAGAATCTTCAACGTATACATGATCTTCGGGGGGACCAACTGGGGCAACCTTGGACATCCA
GGCGGCTACACCTCGTACGACTACGGCGCGGCAATTCGGGAAAACGGAGTCATCGATCGCGAAAAGTACTCGGAG
CTCAAGCTCGAGGCCGAGTTCCTCAGGGTCTCACCGGGATACCTCGTCACGACGCCCGGAAGCGCGACCCGAGGT
GTCTACAGCGCCAACCAGGACATCACGGTCACGCCCCTCCTTTCCCAGGACGCGGGGAGTTTCTTCGTGGTGCGG
CACACCAACTTTGCCAATACCGGGTCGACGACGTACACGCTGAGGCTGCCTACATCGGCCGGAACGCTGTCGATT
CCTCAGAGCGGCGGCGAGCTGACGCTTCTCGGTCGGGACTCGAAGATGCTCGTAACCGACTACCCAGTCGGTGGT
TACACTCTGCTGTACTCGACGGCCGAGGTCTTTACGTGGAAGAGGTTTGCCGACAGGACGGTGCTCGTCCTGTAC
GGCGGAGGTCCCGACGAGACCAACGAGTTTGCCGTGCACGGTGACGACGACCAACAGGTGACGCAGCTCGAGGGC
AGCGGCGTCTCGCTAGATTCGTTGGCCGGAGTGGCTGTCGTCGTCAAGTGGAAAACATCGTCTGGTCGACAGGTC
ATCAAGATGGGCGACCTCGTCGTCCATCTTCTTGACCGCAACTCGGCGTACAAGTACTGGGTGCCGGTGCTCCCC
AGCAACGGCAGCGCCTACGGCAGCTCCGTCATGAACCCCGAGTCCCTCATCGTCAGCGGCGGCTATCTCGTACGG
TCAGCAACCATCAGCGGCTCCGTGCTTTCCCTCAAGGCCGACTTCAACGCGTCTACGTCGCTCGAGATCATGGGC
GTTCCCCCCGGCGTTTCGCAGCTCATCGTCAACGGCCGGCCAACGCGGTACAGCCTGTCTGCGTTGGGCGACTGG
ATGGCGGAACCGGATATCGGCATCCCCAAGATGGTGGTGCCGGATCTGCGCGCCCTGTCGTGGCGTCGGATCGAC
TCGCTGCCCGAGGTTCAGGCCGGCTACGACGATTCCGCCTGGCCGGTAGCCGACAAGAAGAAGTCGAGCAACACG
GCCTTTCCGTCCAAGACGCCCGTGTCGTTGTACGGATCCGATTACGGTTTCCACACCGGCACCCTCGTCTTTCGC
GGTCACTTCGTCGCCCGCGGCAACGAGTCTCGCCTCTTCCTCCGGACAGCGGGCGGAAGCGGCTTTGCGAGCTCG
GTCTGGCTCGACGACACCTTCCTCGGCTCCTTTACGAATACCGAAGCGGCGGCGGAGGAGAACAACTCGACGTAT
CGGGTACCGTCTCTGGTCAGCGGTCGGCGTCACGTCTTGACCGTCGTCGTCGACAACATGGGCCTCAACGAGGTG
GTCAACCCGGGCACGGAAACGATGAAGTCTCCGCGCGGAATCCTCGACTACGCCCTCTTGTCCGGAGACGCTTCC
GCCAACGAGCCCTCCGTGACGGACATTTCTCCCTGGAAGCTGACGGGTAACCTCGGCGGGGAGGACTACGTCGAC
AAGTCCCGCGGCCCCCTCAACGAGGGAGGCCTCTTCTTCGAACGGCAGGCGTACCATGTCCCCCCCACCCCTTCA
TCATCATCATCATCATCATCATCATCATCATCATCATCCCCACTACTAGACCGCTTCACCTCTGCCTCCCCCTGG
CAAGGCCTCGACCGGGCGGGAATCGCCTTTTACGCCGCCGAGCTGACGCTCAACTACCCGTCGGACAAAAGCAAC
ACTTTCGCCGACTTTCCCGTTCCCGAGGGCATCCTCAACTACCGCGGTGCCAACTGGATCGGTCTCGCCGTCTGG
GCCCTCGACGCGGGCGGCGCAAAGGTGCCCGGCTTTTGGCTCAAGGTTGGCACCGCCGTCGTGACGGGGAGGGAA
CCTGTCGAGGTCGTGAATGCGACGGCCTACGCCGAGCGCTTCGGTGCGTAC
Transcript >Ophio5|3481
ATGAAGCTCTCGTCGACGCTGCTGGCCGCGCTGGCGATGGCCATGTCCCATGCCCTGAGCCTCGCCGGCCGGCCG
GTCAAGGTCCTGGACGTCGACAAGCGCGCGCCTCTCCAGGACTTGGTCACTTGGGATGACCAGTCGCTGTTCATC
CGCGGAGAGCGTGTCATGATGTACTCGGGCGAATTCCACCCCTTTCGCTTGCCTGTGCCGTCGCTATACCTCGAC
ATATTCCAAAAGATAAGGGCCCTCGGCTTCAACCTGGTGTCCTTCTACGTCGATTGGGCTCTCCTCGAGGGCAAG
CCGGGTGAATTTCGCGCCGATGGCATCTTTGATCTCGAGCCCTTCTTCGACGCGGCCAAGAAGGCGGGCATCTAT
CTCCTCGCCCGGCCGGGACCTTACATCAACGCCGAGGTTTCTGGCGGCGGCTTCCCCGGCTGGCTCCAGAGGATC
AAGGGAATCTTGCGGACCGATGCCGGCGACTTTCTTAGCACGACGGACAACTACATGGCTCACATCTGCGCCATC
ATTGCAAAGCACCAGATCACTCAGGGCGGACCAGTCGTCTTGTTCCAGCCGGAAAACGAGTATAGCTACGGCTAT
AGGATCCCGTTTCCCAACGGCAACTACATGCAGTACGTCATCGACCAGGCTCGCAAGGCCGGCATCGTCGTCCCC
ACCATCAACAATGATATTGGCCCCGGAGGCAACTATGCTCCCGGCACCGGCAGAGGCGCCATGGACATTTACGGA
CACGACAACTATCCCCTGGGCTTCGACTGTGCGAACCCGTCCACTTGGCCTTCTGAAAAGTTCCCTACCAACTTC
CATGAGCTGCACATGAAGCAAAGTCCCAACACACCCTTCTCCATCATCGAGTTCCAAGGTGGCTCCTATGATCCA
TGGGGCGGCACTGGCCTCGAGCAATGCTCCGCCCTCATCAACCACGAGTTCGAGCGCGTCTACTACAAGAACAAC
ATGGCGGCCGGCGTGAGAATCTTCAACGTATACATGATCTTCGGGGGGACCAACTGGGGCAACCTTGGACATCCA
GGCGGCTACACCTCGTACGACTACGGCGCGGCAATTCGGGAAAACGGAGTCATCGATCGCGAAAAGTACTCGGAG
CTCAAGCTCGAGGCCGAGTTCCTCAGGGTCTCACCGGGATACCTCGTCACGACGCCCGGAAGCGCGACCCGAGGT
GTCTACAGCGCCAACCAGGACATCACGGTCACGCCCCTCCTTTCCCAGGACGCGGGGAGTTTCTTCGTGGTGCGG
CACACCAACTTTGCCAATACCGGGTCGACGACGTACACGCTGAGGCTGCCTACATCGGCCGGAACGCTGTCGATT
CCTCAGAGCGGCGGCGAGCTGACGCTTCTCGGTCGGGACTCGAAGATGCTCGTAACCGACTACCCAGTCGGTGGT
TACACTCTGCTGTACTCGACGGCCGAGGTCTTTACGTGGAAGAGGTTTGCCGACAGGACGGTGCTCGTCCTGTAC
GGCGGAGGTCCCGACGAGACCAACGAGTTTGCCGTGCACGGTGACGACGACCAACAGGTGACGCAGCTCGAGGGC
AGCGGCGTCTCGCTAGATTCGTTGGCCGGAGTGGCTGTCGTCGTCAAGTGGAAAACATCGTCTGGTCGACAGGTC
ATCAAGATGGGCGACCTCGTCGTCCATCTTCTTGACCGCAACTCGGCGTACAAGTACTGGGTGCCGGTGCTCCCC
AGCAACGGCAGCGCCTACGGCAGCTCCGTCATGAACCCCGAGTCCCTCATCGTCAGCGGCGGCTATCTCGTACGG
TCAGCAACCATCAGCGGCTCCGTGCTTTCCCTCAAGGCCGACTTCAACGCGTCTACGTCGCTCGAGATCATGGGC
GTTCCCCCCGGCGTTTCGCAGCTCATCGTCAACGGCCGGCCAACGCGGTACAGCCTGTCTGCGTTGGGCGACTGG
ATGGCGGAACCGGATATCGGCATCCCCAAGATGGTGGTGCCGGATCTGCGCGCCCTGTCGTGGCGTCGGATCGAC
TCGCTGCCCGAGGTTCAGGCCGGCTACGACGATTCCGCCTGGCCGGTAGCCGACAAGAAGAAGTCGAGCAACACG
GCCTTTCCGTCCAAGACGCCCGTGTCGTTGTACGGATCCGATTACGGTTTCCACACCGGCACCCTCGTCTTTCGC
GGTCACTTCGTCGCCCGCGGCAACGAGTCTCGCCTCTTCCTCCGGACAGCGGGCGGAAGCGGCTTTGCGAGCTCG
GTCTGGCTCGACGACACCTTCCTCGGCTCCTTTACGAATACCGAAGCGGCGGCGGAGGAGAACAACTCGACGTAT
CGGGTACCGTCTCTGGTCAGCGGTCGGCGTCACGTCTTGACCGTCGTCGTCGACAACATGGGCCTCAACGAGGTG
GTCAACCCGGGCACGGAAACGATGAAGTCTCCGCGCGGAATCCTCGACTACGCCCTCTTGTCCGGAGACGCTTCC
GCCAACGAGCCCTCCGTGACGGACATTTCTCCCTGGAAGCTGACGGGTAACCTCGGCGGGGAGGACTACGTCGAC
AAGTCCCGCGGCCCCCTCAACGAGGGAGGCCTCTTCTTCGAACGGCAGGCGTACCATGTCCCCCCCACCCCTTCA
TCATCATCATCATCATCATCATCATCATCATCATCATCCCCACTACTAGACCGCTTCACCTCTGCCTCCCCCTGG
CAAGGCCTCGACCGGGCGGGAATCGCCTTTTACGCCGCCGAGCTGACGCTCAACTACCCGTCGGACAAAAGCAAC
ACTTTCGCCGACTTTCCCGTTCCCGAGGGCATCCTCAACTACCGCGGTGCCAACTGGATCGGTCTCGCCGTCTGG
GCCCTCGACGCGGGCGGCGCAAAGGTGCCCGGCTTTTGGCTCAAGGTTGGCACCGCCGTCGTGACGGGGAGGGAA
CCTGTCGAGGTCGTGAATGCGACGGCCTACGCCGAGCGCTTCGGTGCGTACTAG
Gene >Ophio5|3481
ATGAAGCTCTCGTCGACGCTGCTGGCCGCGCTGGCGATGGCCATGTCCCATGCCCTGAGCCTCGCCGGCCGGCCG
GTCAAGGTCCTGGACGTCGACAAGCGCGCGCCTCTCCAGGACTTGGTCACTTGGGATGACCAGTCGCTGTTCATC
CGCGGAGAGCGTGTCATGATGTACTCGGGCGAATTCCACCCCTTTCGCTTGCCTGTGCCGTCGCTATACCTCGAC
ATATTCCAAAAGATAAGGGCCCTCGGCTTCAACCTGGTGTCCTTCTACGTCGATTGGGCTCTCCTCGAGGGCAAG
CCGGGTGAATTTCGCGCCGATGGCATCTTTGATCTCGAGCCCTTCTTCGACGCGGCCAAGAAGGCGGGCATCTAT
CTCCTCGCCCGGCCGGGACCTTACATCAACGCCGAGGTTTCTGGCGGCGGCTTCCCCGGCTGGCTCCAGAGGATC
AAGGGAATCTTGCGGACCGATGCCGGCGACTTTCTTAGCACGACGGACAAGTGAGCCGACTCGCGGCACTCTTGT
TCGTGCATGTGCCGCTAACACACGTAACACCAGCTACATGGCTCACATCTGCGCCATCATTGCAAAGCACCAGAT
CACTCAGGGCGGACCAGTCGTCTTGTTCCAGCCGGAAAACGAGTATAGCTACGGCTATAGGATCCCGTTTCCCAA
CGGCAACTACATGCAGTACGTCATCGACCAGGCTCGCAAGGCCGGCATCGTCGTCCCCACCATCAACAATGATAT
TGGCCCCGGAGGCAACTATGCTCCCGGCACCGGCAGAGGCGCCATGGACATTTACGTCGGTAGCATCTTCTGCAA
CCGCCGGAGCAAGATGCTGACTCTCGACAGGGACACGACAACTATCCCCTGGGCTTCGACTGTGTCGGTCAAGAC
GTCCGAGCCACTCGCGGCTGAAAGATTGCTGATGGTAACGCAGGCGAACCCGTCCACTTGGCCTTCTGAAAAGTT
CCCTACCAACTTCCATGAGCTGCACATGAAGCAAAGTCCCAACACACCCTTCTCCATCATCGAGGTGAGCGGGGT
GGTGGGATCCACGCTGGCCGACGTCGGGCTTACTGTCTGGCTCAGTTCCAAGGTGGCTCCTATGATCCATGGGGC
GGCACTGGCCTCGAGCAATGCTCCGCCCTCATCAACCACGAGTTCGAGCGCGTCTACTACAAGAACAACATGGCG
GCCGGCGTGAGAATCTTCAACGTATACATGGTAAGGCGATCTGTCGTCGTCTAAGCTTCGCGCTGATGGGCCCAG
ATCTTCGGGGGGACCAACTGGGGCAACCTTGGACATCCAGGCGGCTACACCTCGTACGACTACGGCGCGGTAAGG
GCCAACCCCCGGACCATGGACGCAGAAGCTCACTGATGGTCGTAGGCAATTCGGGAAAACGGAGTCATCGATCGC
GAAAAGTACTCGGAGCTCAAGCTCGAGGCCGAGTTCCTCAGGGTCTCACCGGGATACCTCGTCACGACGCCCGGA
AGCGCGACCCGAGGTGTCTACAGCGCCAACCAGGACATCACGGTCACGCCCCTCCTTTCCCAGGACGCGGGGAGT
TTCTTCGTGGTGCGGCACACCAACTTTGCCAATACCGGGTCGACGACGTACACGCTGAGGCTGCCTACATCGGCC
GGAACGCTGTCGATTCCTCAGAGCGGCGGCGAGCTGACGCTTCTCGGTCGGGACTCGAAGATGCTCGTAACCGAC
TACCCAGTCGGTGGTTACACTCTGCTGTACTCGACGGCCGAGGTCTTTACGTGGAAGAGGTTTGCCGACAGGACG
GTGCTCGTCCTGTACGGCGGAGGTCCCGACGAGACCAACGAGTTTGCCGTGCACGGTGACGACGACCAACAGGTG
ACGCAGCTCGAGGGCAGCGGCGTCTCGCTAGATTCGTTGGCCGGAGTGGCTGTCGTCGTCAAGTGGAAAACATCG
TCTGGTCGACAGGTCATCAAGATGGGCGACCTCGTCGTCCATCTTCTTGGTGAGTTGAAACCCTCACCCCCCCCC
CCCCAAAAAAAAAAAAAAAAAAAAAAATAGGGTCTACCATGCCTATATAGGGAAAAAAAAAAAAAAAAAAAAAAA
AAAAAAAAGAAAAGGTCTTCGGTTCAGCGTGCTGATGAGGGCAAAAAATGGAAAAAAAAAAACAAAAAACCATAC
AATAACATAAGACCGCAACTCGGCGTACAAGTACTGGGTGCCGGTGCTCCCCAGCAACGGCAGCGCCTACGGCAG
CTCCGTCATGAACCCCGAGTCCCTCATCGTCAGCGGCGGCTATCTCGTACGGTCAGCAACCATCAGCGGCTCCGT
GCTTTCCCTCAAGGCCGACTTCAACGCGTCTACGTCGCTCGAGATCATGGGCGTTCCCCCCGGCGTTTCGCAGCT
CATCGTCAACGGCCGGCCAACGCGGTACAGCCTGTCTGCGTTGGGCGACTGGATGGCGGAACCGGATATCGGCAT
CCCCAAGATGGTGGTGCCGGATCTGCGCGCCCTGTCGTGGCGTCGGATCGACTCGCTGCCCGAGGTTCAGGCCGG
CTACGACGATTCCGCCTGGCCGGTAGCCGACAAGAAGAAGTCGAGCAACACGGCCTTTCCGTCCAAGACGCCCGT
GTCGTTGTACGGATCCGATTACGGTTTCCACACCGGCACCCTCGTCTTTCGCGGTCACTTCGTCGCCCGCGGCAA
CGAGTCTCGCCTCTTCCTCCGGACAGCGGGCGGAAGCGGCTTTGCGAGCTCGGTCTGGCTCGACGACACCTTCCT
CGGCTCCTTTACGAATACCGAAGCGGCGGCGGAGGAGAACAACTCGACGTATCGGGTACCGTCTCTGGTCAGCGG
TCGGCGTCACGTCTTGACCGTCGTCGTCGACAACATGGGCCTCAACGAGGTGGTCAACCCGGGCACGGAAACGAT
GAAGTCTCCGCGCGGAATCCTCGACTACGCCCTCTTGTCCGGAGACGCTTCCGCCAACGAGCCCTCCGTGACGGA
CATTTCTCCCTGGAAGCTGACGGGTAACCTCGGCGGGGAGGACTACGTCGACAAGTCCCGCGGCCCCCTCAACGA
GGGAGGCCTCTTCTTCGAACGGCAGGCGTACCATGTCCCCCCCACCCCTTCATCATCATCATCATCATCATCATC
ATCATCATCATCATCCCCACTACTAGACCGCTTCACCTCTGCCTCCCCCTGGCAAGGCCTCGACCGGGCGGGAAT
CGCCTTTTACGCCGCCGAGCTGACGCTCAACTACCCGTCGGACAAGTACGACATACCCATCTCCTTTGTCTTTGA
CAATGTCTTTGACAATGTCTTGAACCGACACTCTGCCAAGAAGCAACACTTTCGTGCCACCCTCTTCGTCAACGG
CTTTCAGTACGGCAAGTACGCCAGCAACATCGGCCCCCAGGCCGACTTTCCCGTTCCCGAGGGCATCCTCAACTA
CCGCGGTGCCAACTGGATCGGTCTCGCCGTCTGGGCCCTCGACGCGGGCGGCGCAAAGGTGCCCGGCTTTTGGCT
CAAGGTTGGCACCGCCGTCGTGACGGGGAGGGAACCTGTCGAGGTCGTGAATGCGACGGCCTACGCCGAGCGCTT
CGGTGCGTACTAG

© 2023 - Robin Ohm - Utrecht University - The Netherlands

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