Fungal Genomics

at Utrecht University

General Properties

Protein IDOphio5|6617
Gene name
Locationscaffold_59:35921..37882
Strand+
Gene length (bp)1961
Transcript length (bp)1749
Coding sequence length (bp)1746
Protein length (aa) 582

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF00481 PP2C Protein phosphatase 2C 6.8E-31 370 533

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|O14156|PP2C4_SCHPO Protein phosphatase 2C homolog 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc4 PE=1 SV=2 150 579 2.0E-48
sp|Q8BXN7|PPM1K_MOUSE Protein phosphatase 1K, mitochondrial OS=Mus musculus GN=Ppm1k PE=1 SV=1 366 550 3.0E-23
sp|P25646|PDP2_YEAST [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 2, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC6 PE=1 SV=2 397 550 6.0E-23
sp|Q6ING9|PPM1K_XENLA Protein phosphatase 1K, mitochondrial OS=Xenopus laevis GN=ppm1k PE=2 SV=1 366 550 2.0E-22
sp|Q2PC20|PPM1K_BOVIN Protein phosphatase 1K, mitochondrial OS=Bos taurus GN=PPM1K PE=2 SV=1 366 550 1.0E-21
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|O14156|PP2C4_SCHPO Protein phosphatase 2C homolog 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc4 PE=1 SV=2 150 579 2.0E-48
sp|Q8BXN7|PPM1K_MOUSE Protein phosphatase 1K, mitochondrial OS=Mus musculus GN=Ppm1k PE=1 SV=1 366 550 3.0E-23
sp|P25646|PDP2_YEAST [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 2, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC6 PE=1 SV=2 397 550 6.0E-23
sp|Q6ING9|PPM1K_XENLA Protein phosphatase 1K, mitochondrial OS=Xenopus laevis GN=ppm1k PE=2 SV=1 366 550 2.0E-22
sp|Q2PC20|PPM1K_BOVIN Protein phosphatase 1K, mitochondrial OS=Bos taurus GN=PPM1K PE=2 SV=1 366 550 1.0E-21
sp|Q8N3J5|PPM1K_HUMAN Protein phosphatase 1K, mitochondrial OS=Homo sapiens GN=PPM1K PE=1 SV=1 366 550 1.0E-21
sp|P40371|PP2C1_SCHPO Protein phosphatase 2C homolog 1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ptc1 PE=2 SV=1 372 547 1.0E-15
sp|Q8BHN0|PPM1L_MOUSE Protein phosphatase 1L OS=Mus musculus GN=Ppm1l PE=1 SV=1 370 547 2.0E-15
sp|Q5SGD2|PPM1L_HUMAN Protein phosphatase 1L OS=Homo sapiens GN=PPM1L PE=1 SV=1 370 547 2.0E-15
sp|Q4PSE8|P2C71_ARATH Probable protein phosphatase 2C 71 OS=Arabidopsis thaliana GN=At5g24940 PE=2 SV=1 397 547 6.0E-15
sp|A5PJZ2|PPM1L_BOVIN Protein phosphatase 1L OS=Bos taurus GN=PPM1L PE=2 SV=1 370 547 7.0E-15
sp|Q0JAA0|P2C44_ORYSJ Probable protein phosphatase 2C 44 OS=Oryza sativa subsp. japonica GN=Os04g0609600 PE=2 SV=1 371 547 7.0E-15
sp|Q8L7I4|P2C17_ARATH Probable protein phosphatase 2C 17 OS=Arabidopsis thaliana GN=At1g78200 PE=2 SV=1 371 547 1.0E-14
sp|Q8RXV3|P2C59_ARATH Probable protein phosphatase 2C 59 OS=Arabidopsis thaliana GN=WIN2 PE=1 SV=1 397 564 2.0E-14
sp|Q67UX7|P2C10_ORYSJ Probable protein phosphatase 2C 10 OS=Oryza sativa subsp. japonica GN=Os02g0149800 PE=2 SV=1 372 547 3.0E-13
sp|Q8VZN9|P2C11_ARATH Probable protein phosphatase 2C 11 OS=Arabidopsis thaliana GN=At1g43900 PE=2 SV=1 397 547 3.0E-13
sp|Q7XR06|P2C45_ORYSJ Probable protein phosphatase 2C 45 OS=Oryza sativa subsp. japonica GN=Os04g0659500 PE=2 SV=2 397 547 3.0E-13
sp|Q93YW5|P2C58_ARATH Probable protein phosphatase 2C 58 OS=Arabidopsis thaliana GN=At4g28400 PE=2 SV=1 370 547 4.0E-13
sp|Q53Q11|P2C74_ORYSJ Probable protein phosphatase 2C 74 OS=Oryza sativa subsp. japonica GN=Os11g0242200 PE=3 SV=1 370 530 4.0E-13
sp|Q5Z6F5|P2C59_ORYSJ Probable protein phosphatase 2C 59 OS=Oryza sativa subsp. japonica GN=Os06g0698300 PE=2 SV=1 372 547 8.0E-13
sp|Q6L5C4|P2C52_ORYSJ Probable protein phosphatase 2C 52 OS=Oryza sativa subsp. japonica GN=Os05g0587100 PE=2 SV=1 372 547 1.0E-12
sp|Q0JL75|P2C07_ORYSJ Probable protein phosphatase 2C 7 OS=Oryza sativa subsp. japonica GN=Os01g0618200 PE=2 SV=2 397 547 2.0E-12
sp|Q8LAY8|P2C69_ARATH Probable protein phosphatase 2C 69 OS=Arabidopsis thaliana GN=At5g10740 PE=2 SV=1 397 547 3.0E-12
sp|Q6Z8B9|P2C12_ORYSJ Probable protein phosphatase 2C 12 OS=Oryza sativa subsp. japonica GN=Os02g0224100 PE=2 SV=1 397 532 3.0E-12
sp|Q9LDA7|P2C39_ARATH Probable protein phosphatase 2C 39 OS=Arabidopsis thaliana GN=At3g15260 PE=2 SV=1 370 531 5.0E-12
sp|Q0D673|P2C62_ORYSJ Probable protein phosphatase 2C 62 OS=Oryza sativa subsp. japonica GN=Os07g0507000 PE=2 SV=1 370 547 7.0E-12
sp|Q6L482|P2C48_ORYSJ Probable protein phosphatase 2C 48 OS=Oryza sativa subsp. japonica GN=Os05g0358500 PE=2 SV=1 397 542 1.0E-11
sp|Q94AT1|P2C76_ARATH Probable protein phosphatase 2C 76 OS=Arabidopsis thaliana GN=At5g53140 PE=2 SV=1 397 547 2.0E-11
sp|Q9SIU8|P2C20_ARATH Probable protein phosphatase 2C 20 OS=Arabidopsis thaliana GN=PPC3-1.2 PE=1 SV=3 370 544 3.0E-11
sp|Q6EN45|P2C13_ORYSJ Probable protein phosphatase 2C 13 OS=Oryza sativa subsp. japonica GN=Os02g0255100 PE=2 SV=1 397 547 3.0E-11
sp|Q8RX37|P2C02_ARATH Probable protein phosphatase 2C 2 OS=Arabidopsis thaliana GN=At1g07160 PE=2 SV=1 370 531 1.0E-10
sp|Q653S3|P2C70_ORYSJ Probable protein phosphatase 2C 70 OS=Oryza sativa subsp. japonica GN=Os09g0558000 PE=2 SV=2 372 547 1.0E-10
sp|O81716|P2C21_ARATH Probable protein phosphatase 2C 21 OS=Arabidopsis thaliana GN=PPC4-2 PE=1 SV=1 372 541 1.0E-10
sp|Q2RBJ6|P2C73_ORYSJ Probable protein phosphatase 2C 73 OS=Oryza sativa subsp. japonica GN=Os11g0109000 PE=2 SV=1 397 531 2.0E-10
sp|Q0IIF0|ILKAP_BOVIN Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Bos taurus GN=ILKAP PE=2 SV=1 369 548 3.0E-10
sp|Q2R637|P2C75_ORYSJ Probable protein phosphatase 2C 75 OS=Oryza sativa subsp. japonica GN=Os11g0417400 PE=2 SV=1 397 532 5.0E-10
sp|Q2QWE3|P2C77_ORYSJ Probable protein phosphatase 2C 77 OS=Oryza sativa subsp. japonica GN=Os12g0198200 PE=3 SV=1 369 508 6.0E-10
sp|Q67UP9|P2C58_ORYSJ Probable protein phosphatase 2C 58 OS=Oryza sativa subsp. japonica GN=Os06g0651600 PE=2 SV=1 372 532 7.0E-10
sp|Q9XEE8|P2C30_ARATH Probable protein phosphatase 2C 30 OS=Arabidopsis thaliana GN=PP2C5 PE=2 SV=1 370 514 8.0E-10
sp|Q0WRB2|P2C73_ARATH Probable protein phosphatase 2C 73 OS=Arabidopsis thaliana GN=PPC6-7 PE=2 SV=1 396 531 9.0E-10
sp|Q9M9W9|P2C34_ARATH Probable protein phosphatase 2C 34 OS=Arabidopsis thaliana GN=At3g05640 PE=2 SV=1 396 542 1.0E-09
sp|Q7XQU7|P2C41_ORYSJ Probable protein phosphatase 2C 41 OS=Oryza sativa subsp. japonica GN=Os04g0452000 PE=2 SV=2 370 547 2.0E-09
sp|O80871|P2C25_ARATH Probable protein phosphatase 2C 25 OS=Arabidopsis thaliana GN=At2g30020 PE=1 SV=1 370 530 2.0E-09
sp|A0BLX0|PP2C2_PARTE Probable protein phosphatase 2C 2 OS=Paramecium tetraurelia GN=GSPATT00030171001 PE=3 SV=1 372 536 3.0E-09
sp|P49444|PP2C1_PARTE Protein phosphatase 2C 1 OS=Paramecium tetraurelia GN=GSPATT00029903001 PE=1 SV=2 372 536 3.0E-09
sp|Q5R522|PPM1K_PONAB Protein phosphatase 1K, mitochondrial OS=Pongo abelii GN=PPM1K PE=2 SV=1 366 509 3.0E-09
sp|Q8H4S6|P2C64_ORYSJ Probable protein phosphatase 2C 64 OS=Oryza sativa subsp. japonica GN=Os07g0566200 PE=2 SV=2 395 530 5.0E-09
sp|Q9H0C8|ILKAP_HUMAN Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Homo sapiens GN=ILKAP PE=1 SV=1 369 548 8.0E-09
sp|O82637|P2C61_ARATH Probable protein phosphatase 2C 61 OS=Arabidopsis thaliana GN=At4g32950 PE=3 SV=1 397 527 9.0E-09
sp|Q8R0F6|ILKAP_MOUSE Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Mus musculus GN=Ilkap PE=1 SV=1 369 548 1.0E-08
sp|Q9SA22|P2C06_ARATH Probable protein phosphatase 2C 6 OS=Arabidopsis thaliana GN=At1g16220 PE=2 SV=1 397 531 1.0E-08
sp|Q9XGZ9|P2C72_ARATH Probable protein phosphatase 2C 72 OS=Arabidopsis thaliana GN=At5g26010 PE=2 SV=2 397 513 1.0E-08
sp|Q9Z1Z6|ILKAP_RAT Integrin-linked kinase-associated serine/threonine phosphatase 2C OS=Rattus norvegicus GN=Ilkap PE=2 SV=1 369 548 1.0E-08
sp|P35182|PP2C1_YEAST Protein phosphatase 2C homolog 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC1 PE=1 SV=1 397 547 1.0E-08
sp|Q9SZ53|P2C60_ARATH Probable protein phosphatase 2C 60 OS=Arabidopsis thaliana GN=At4g31860 PE=2 SV=1 372 547 2.0E-08
sp|Q9FG61|P2C74_ARATH Probable protein phosphatase 2C 74 OS=Arabidopsis thaliana GN=At5g36250 PE=1 SV=1 397 531 2.0E-08
sp|P39966|PP2C2_YEAST Protein phosphatase 2C homolog 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC2 PE=1 SV=1 381 571 2.0E-08
sp|Q5JJY4|P2C04_ORYSJ Protein kinase and PP2C-like domain-containing protein OS=Oryza sativa subsp. japonica GN=Os01g0541900 PE=2 SV=1 389 547 2.0E-08
sp|Q8RXZ4|P2C18_ARATH Probable protein phosphatase 2C 18 OS=Arabidopsis thaliana GN=At1g79630 PE=2 SV=1 397 531 2.0E-08
sp|Q7XU84|P2C42_ORYSJ Probable protein phosphatase 2C 42 OS=Oryza sativa subsp. japonica GN=Os04g0500900 PE=3 SV=4 372 514 3.0E-08
sp|P35813|PPM1A_HUMAN Protein phosphatase 1A OS=Homo sapiens GN=PPM1A PE=1 SV=1 370 514 3.0E-08
sp|P35814|PPM1A_RABIT Protein phosphatase 1A OS=Oryctolagus cuniculus GN=PPM1A PE=2 SV=1 370 514 4.0E-08
sp|P20650|PPM1A_RAT Protein phosphatase 1A OS=Rattus norvegicus GN=Ppm1a PE=1 SV=1 370 514 4.0E-08
sp|Q9LNW3|P2C03_ARATH Protein phosphatase 2C 3 OS=Arabidopsis thaliana GN=AIP1 PE=1 SV=1 373 514 4.0E-08
sp|P49443|PPM1A_MOUSE Protein phosphatase 1A OS=Mus musculus GN=Ppm1a PE=1 SV=1 370 514 4.0E-08
sp|A3A8W2|P2C21_ORYSJ Probable protein phosphatase 2C 21 OS=Oryza sativa subsp. japonica GN=Os02g0606900 PE=2 SV=2 372 547 5.0E-08
sp|P34221|PP2C3_YEAST Protein phosphatase 2C homolog 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PTC3 PE=1 SV=4 372 513 5.0E-08
sp|A3CCP9|P2C76_ORYSJ Putative protein phosphatase 2C 76 OS=Oryza sativa subsp. japonica GN=Os11g0586001 PE=3 SV=2 367 548 5.0E-08
sp|Q9LME4|P2C09_ARATH Probable protein phosphatase 2C 9 OS=Arabidopsis thaliana GN=At1g22280 PE=1 SV=1 370 547 5.0E-08
sp|Q9LRZ4|P2C41_ARATH Probable protein phosphatase 2C 41 OS=Arabidopsis thaliana GN=At3g16800 PE=2 SV=1 397 533 5.0E-08
sp|Q5UPZ7|YR307_MIMIV PP2C-like domain-containing protein R307 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R307 PE=1 SV=1 392 515 7.0E-08
sp|P49596|PP2C2_CAEEL Probable protein phosphatase 2C T23F11.1 OS=Caenorhabditis elegans GN=ppm-2 PE=3 SV=2 372 515 7.0E-08
sp|P36993|PPM1B_MOUSE Protein phosphatase 1B OS=Mus musculus GN=Ppm1b PE=1 SV=1 370 535 1.0E-07
sp|O62829|PPM1A_BOVIN Protein phosphatase 1A OS=Bos taurus GN=PPM1A PE=2 SV=1 370 514 2.0E-07
sp|Q8GY60|P2C52_ARATH Probable protein phosphatase 2C 52 OS=Arabidopsis thaliana GN=At4g03415 PE=2 SV=1 395 513 2.0E-07
sp|Q3EAF9|P2C49_ARATH Probable protein phosphatase 2C 49 OS=Arabidopsis thaliana GN=At3g62260 PE=2 SV=1 397 552 2.0E-07
sp|Q7XW27|P2C38_ORYSJ Probable protein phosphatase 2C 38 OS=Oryza sativa subsp. japonica GN=Os04g0321800 PE=2 SV=2 397 530 3.0E-07
sp|Q54WS9|Y9461_DICDI Probable protein phosphatase DDB_G0279461 OS=Dictyostelium discoideum GN=DDB_G0279461 PE=3 SV=2 372 547 4.0E-07
sp|Q9FXE4|P2C14_ARATH Probable protein phosphatase 2C 14 OS=Arabidopsis thaliana GN=At1g67820 PE=2 SV=2 397 534 6.0E-07
sp|Q10MX1|P2C32_ORYSJ Probable protein phosphatase 2C 32 OS=Oryza sativa subsp. japonica GN=Os03g0292100 PE=2 SV=1 397 514 9.0E-07
sp|Q84JD5|P2C68_ARATH Probable protein phosphatase 2C 68 OS=Arabidopsis thaliana GN=At5g06750 PE=2 SV=1 394 534 1.0E-06
sp|Q65XK7|P2C51_ORYSJ Probable protein phosphatase 2C 51 OS=Oryza sativa subsp. japonica GN=Os05g0572700 PE=2 SV=1 372 514 1.0E-06
sp|Q9FLI3|P2C75_ARATH Probable protein phosphatase 2C 75 OS=Arabidopsis thaliana GN=AHG1 PE=2 SV=1 397 514 1.0E-06
sp|Q940A2|P2C31_ARATH Protein kinase and PP2C-like domain-containing protein OS=Arabidopsis thaliana GN=At2g40860/At2g40870 PE=2 SV=1 389 547 1.0E-06
sp|Q9FIF5|P2C78_ARATH Probable protein phosphatase 2C 78 OS=Arabidopsis thaliana GN=At5g59220 PE=2 SV=1 373 514 1.0E-06
sp|Q8H2T0|P2C65_ORYSJ Probable protein phosphatase 2C 65 OS=Oryza sativa subsp. japonica GN=Os07g0646100 PE=2 SV=1 399 541 3.0E-06
sp|Q84JI0|P2C30_ORYSJ Probable protein phosphatase 2C 30 OS=Oryza sativa subsp. japonica GN=Os03g0268600 PE=2 SV=1 397 514 5.0E-06
sp|Q9ZW21|P2C24_ARATH Probable protein phosphatase 2C 24 OS=Arabidopsis thaliana GN=At2g29380 PE=2 SV=1 373 507 6.0E-06
sp|Q9LR65|P2C01_ARATH Probable protein phosphatase 2C 1 OS=Arabidopsis thaliana GN=PPC6-6 PE=1 SV=1 395 531 6.0E-06
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GO

GO Term Description Terminal node
GO:0004722 protein serine/threonine phosphatase activity Yes
GO:0004721 phosphoprotein phosphatase activity No
GO:0016791 phosphatase activity No
GO:0016787 hydrolase activity No
GO:0140096 catalytic activity, acting on a protein No
GO:0003824 catalytic activity No
GO:0042578 phosphoric ester hydrolase activity No
GO:0003674 molecular_function No
GO:0016788 hydrolase activity, acting on ester bonds No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)		 D score
(significance: > 0.45)
No 1 - 61 0.45

Transmembrane Domains

(None)

Transcription Factor Class

(None)

Expression data

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

Expression values

Label Description Expression (RPKM) Confidence interval (low) Confidence interval (high)
SC16a Pure fungal culture 21.94 10.75 33.13
CcL In ants, during behavior modification 36.98 19.90 54.07
CcD In ants, recently dead 49.77 27.25 72.30

Differential expression

Label1 Label2 Q-value Significant difference
SC16a CcL 0.026849 yes
SC16a CcD 0.000535 yes
CcL CcD 0.198863 no

Sequences

Type of sequenceSequence
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|6617
MFHDASSASLSPNSRPHSPLHLPPIFSSSSTSARRWTRFIPWTCHAPAALDFNRARAAEAHPPPPNHPLPSSSSM
ASVANRLAGHASPTVFIRAFHTYFVTHLPSSSLHPDSPVSPHKLPRDASTPHTPSPGAAPAVVLPNMPGRDLTVV
RIPLRRAKHHFGSYTCRGSRPYNEDADQAGIVEMPAFATRAPLSVKQKPGEATSADGASGDPQIFYFALFDGHGG
SQCSHFLRDELHGYIEEAAARLGLQSSLRKKKPGRDTHARPPSNDTTPARLEQELVAEYKNSIGGYYRRFSPDHF
GERAAGDESAPSIEASLTYAFLRADLDFVAAQARKPDPDDFDMPVNHDEILGVPHATPSGHGIGGATRFKGGSTA
SIALVSTPTPTPFWHPAARSTLLVAHVGDSRILICDTASGRAHPLTSDHHPSTPTESRRLRRYGPTGSMVSGDSF
GEERIAGLANSRAFGDVGSKRLGVSAEPEIVRVDLGPAQYAFLVLVSDGVSGSLADQEMVDIIKEAPTPEQGARN
VVDYAVEVSVDGDNATCQVVRLGGWERRSEGGLGSLGTKEIRDARRAEAQDPRRGKQ
Coding >Ophio5|6617
ATGTTCCATGACGCTTCATCTGCCTCCCTAAGTCCCAACAGTCGCCCTCATTCGCCGCTTCACCTTCCACCTATT
TTCTCCTCCTCCTCCACGTCGGCTCGGCGCTGGACTCGCTTCATCCCATGGACCTGCCACGCACCGGCCGCACTC
GATTTCAACCGCGCGAGAGCTGCTGAGGCTCACCCGCCGCCGCCGAATCATCCTCTTCCCTCCTCCAGCTCAATG
GCCTCTGTGGCAAACCGCCTCGCCGGCCATGCTTCGCCCACCGTCTTCATCCGCGCCTTTCACACTTACTTCGTC
ACTCACCTCCCATCCTCGTCTCTTCACCCGGACTCGCCCGTCTCTCCTCACAAGCTTCCCCGCGATGCTTCGACA
CCTCATACGCCCAGTCCCGGCGCCGCGCCGGCCGTCGTGCTGCCCAACATGCCAGGCCGAGACCTGACCGTCGTG
CGTATCCCGCTGCGGCGGGCCAAGCATCACTTCGGCTCCTACACATGCAGGGGTAGCCGACCTTACAACGAGGAC
GCCGACCAGGCCGGTATCGTCGAGATGCCTGCCTTCGCCACCAGGGCTCCCCTGAGCGTCAAACAGAAGCCGGGC
GAGGCCACCTCCGCAGACGGCGCTTCCGGCGACCCCCAGATCTTCTACTTTGCCCTCTTTGACGGCCACGGCGGG
TCGCAGTGCTCTCATTTCCTTCGCGATGAGCTGCACGGATATATAGAGGAGGCCGCCGCTCGTCTGGGCCTGCAG
AGCAGCCTGCGCAAGAAGAAACCCGGGCGCGACACACACGCACGCCCGCCGTCAAACGACACGACGCCCGCCCGG
CTCGAGCAGGAGCTGGTGGCGGAATACAAAAACTCCATCGGCGGCTACTACAGACGCTTCAGCCCGGACCACTTT
GGCGAGCGCGCTGCAGGCGACGAATCGGCCCCCAGCATCGAAGCCAGCCTCACCTACGCCTTTCTCCGCGCCGAC
CTCGATTTCGTGGCGGCTCAGGCGCGAAAGCCCGACCCCGACGATTTCGACATGCCCGTCAACCACGACGAGATC
CTCGGCGTCCCCCACGCCACGCCCTCGGGCCACGGCATCGGCGGCGCAACCCGCTTCAAGGGCGGCTCCACGGCC
TCCATCGCCCTCGTCTCGACGCCGACGCCGACGCCGTTTTGGCACCCGGCCGCCCGGTCGACACTGCTGGTGGCG
CACGTCGGCGACAGTCGCATCCTCATCTGCGACACGGCCTCGGGAAGAGCCCACCCGCTGACGTCGGATCATCAC
CCGTCGACGCCGACGGAGAGCCGCCGGCTTCGGCGCTACGGCCCCACCGGCTCCATGGTCTCGGGCGACAGCTTC
GGCGAGGAGCGCATCGCCGGCCTGGCAAACAGTCGCGCCTTCGGTGACGTGGGCAGCAAACGGCTCGGCGTATCC
GCCGAACCGGAAATCGTCCGTGTCGACCTGGGCCCCGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTC
TCGGGCTCGCTGGCCGATCAAGAGATGGTCGATATCATCAAGGAGGCTCCGACCCCGGAACAGGGCGCCCGAAAC
GTCGTCGACTACGCCGTAGAGGTCTCCGTCGACGGCGATAACGCTACCTGCCAGGTCGTCCGTCTCGGCGGCTGG
GAGCGCCGCTCCGAGGGTGGCCTCGGCAGCCTCGGCACCAAGGAGATTCGCGATGCTAGGAGGGCTGAGGCTCAA
GACCCGCGCAGGGGGAAACAA
Transcript >Ophio5|6617
ATGTTCCATGACGCTTCATCTGCCTCCCTAAGTCCCAACAGTCGCCCTCATTCGCCGCTTCACCTTCCACCTATT
TTCTCCTCCTCCTCCACGTCGGCTCGGCGCTGGACTCGCTTCATCCCATGGACCTGCCACGCACCGGCCGCACTC
GATTTCAACCGCGCGAGAGCTGCTGAGGCTCACCCGCCGCCGCCGAATCATCCTCTTCCCTCCTCCAGCTCAATG
GCCTCTGTGGCAAACCGCCTCGCCGGCCATGCTTCGCCCACCGTCTTCATCCGCGCCTTTCACACTTACTTCGTC
ACTCACCTCCCATCCTCGTCTCTTCACCCGGACTCGCCCGTCTCTCCTCACAAGCTTCCCCGCGATGCTTCGACA
CCTCATACGCCCAGTCCCGGCGCCGCGCCGGCCGTCGTGCTGCCCAACATGCCAGGCCGAGACCTGACCGTCGTG
CGTATCCCGCTGCGGCGGGCCAAGCATCACTTCGGCTCCTACACATGCAGGGGTAGCCGACCTTACAACGAGGAC
GCCGACCAGGCCGGTATCGTCGAGATGCCTGCCTTCGCCACCAGGGCTCCCCTGAGCGTCAAACAGAAGCCGGGC
GAGGCCACCTCCGCAGACGGCGCTTCCGGCGACCCCCAGATCTTCTACTTTGCCCTCTTTGACGGCCACGGCGGG
TCGCAGTGCTCTCATTTCCTTCGCGATGAGCTGCACGGATATATAGAGGAGGCCGCCGCTCGTCTGGGCCTGCAG
AGCAGCCTGCGCAAGAAGAAACCCGGGCGCGACACACACGCACGCCCGCCGTCAAACGACACGACGCCCGCCCGG
CTCGAGCAGGAGCTGGTGGCGGAATACAAAAACTCCATCGGCGGCTACTACAGACGCTTCAGCCCGGACCACTTT
GGCGAGCGCGCTGCAGGCGACGAATCGGCCCCCAGCATCGAAGCCAGCCTCACCTACGCCTTTCTCCGCGCCGAC
CTCGATTTCGTGGCGGCTCAGGCGCGAAAGCCCGACCCCGACGATTTCGACATGCCCGTCAACCACGACGAGATC
CTCGGCGTCCCCCACGCCACGCCCTCGGGCCACGGCATCGGCGGCGCAACCCGCTTCAAGGGCGGCTCCACGGCC
TCCATCGCCCTCGTCTCGACGCCGACGCCGACGCCGTTTTGGCACCCGGCCGCCCGGTCGACACTGCTGGTGGCG
CACGTCGGCGACAGTCGCATCCTCATCTGCGACACGGCCTCGGGAAGAGCCCACCCGCTGACGTCGGATCATCAC
CCGTCGACGCCGACGGAGAGCCGCCGGCTTCGGCGCTACGGCCCCACCGGCTCCATGGTCTCGGGCGACAGCTTC
GGCGAGGAGCGCATCGCCGGCCTGGCAAACAGTCGCGCCTTCGGTGACGTGGGCAGCAAACGGCTCGGCGTATCC
GCCGAACCGGAAATCGTCCGTGTCGACCTGGGCCCCGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTC
TCGGGCTCGCTGGCCGATCAAGAGATGGTCGATATCATCAAGGAGGCTCCGACCCCGGAACAGGGCGCCCGAAAC
GTCGTCGACTACGCCGTAGAGGTCTCCGTCGACGGCGATAACGCTACCTGCCAGGTCGTCCGTCTCGGCGGCTGG
GAGCGCCGCTCCGAGGGTGGCCTCGGCAGCCTCGGCACCAAGGAGATTCGCGATGCTAGGAGGGCTGAGGCTCAA
GACCCGCGCAGGGGGAAACAATGA
Gene >Ophio5|6617
ATGTTGTACGAATAGACTTTCGATTAGTCACCCTGCATGCATCGTCAAGGCTTCTGATTGGTCATCACAGACTGC
ACGCCTCTCGACCAGGTGGAAGCGAAGCTAGTTCCTAGGCATCTATTCCCCCTACCATCTCCAGCCATGACGCTT
CATCTGCCTCCCTAAGGTTAGACATCACCTCGTCCGTCGCCTCGTCCAATCGTCTCGTCCGTCATCCATGACGAC
CGCACTCACAGACCAACAGTCCCAACAGTCGCCCTCATTCGCCGCTTCACCTTCCACCTATTTTCTCCTCCTCCT
CCACGTCGGCTCGGCGCTGGACTCGCTTCATCCCATGGACCTGCCACGCACCGGCCGCACTCGATTTCAACCGCG
CGAGAGCTGCTGAGGCTCACCCGCCGCCGCCGAATCATCCTCTTCCCTCCTCCAGCTCAATGGCCTCTGTGGCAA
ACCGCCTCGCCGGCCATGCTTCGCCCACCGTCTTCATCCGCGCCTTTCACACTTACTTCGTCACTCACCTCCCAT
CCTCGTCTCTTCACCCGGACTCGCCCGTCTCTCCTCACAAGCTTCCCCGCGATGCTTCGACACCTCATACGCCCA
GTCCCGGCGCCGCGCCGGCCGTCGTGCTGCCCAACATGCCAGGCCGAGACCTGACCGTCGTGCGTATCCCGCTGC
GGCGGGCCAAGCATCACTTCGGCTCCTACACATGCAGGGGTAGCCGACCTTACAACGAGGACGCCGACCAGGCCG
GTATCGTCGAGATGCCTGCCTTCGCCACCAGGGCTCCCCTGAGCGTCAAACAGAAGCCGGGCGAGGCCACCTCCG
CAGACGGCGCTTCCGGCGACCCCCAGATCTTCTACTTTGCCCTCTTTGACGGCCACGGCGGGTCGCAGTGCTCTC
ATTTCCTTCGCGATGAGCTGCACGGATATATAGAGGAGGCCGCCGCTCGTCTGGGCCTGCAGAGCAGCCTGCGCA
AGAAGAAACCCGGGCGCGACACACACGCACGCCCGCCGTCAAACGACACGACGCCCGCCCGGCTCGAGCAGGAGC
TGGTGGCGGAATACAAAAACTCCATCGGCGGCTACTACAGACGCTTCAGCCCGGACCACTTTGGCGAGCGCGCTG
CAGGCGACGAATCGGCCCCCAGCATCGAAGCCAGCCTCACCTACGCCTTTCTCCGCGCCGACCTCGATTTCGTGG
CGGCTCAGGCGCGAAAGCCCGACCCCGACGATTTCGACATGCCCGTCAACCACGACGAGATCCTCGGCGTCCCCC
ACGCCACGCCCTCGGGCCACGGCATCGGCGGCGCAACCCGCTTCAAGGGCGGCTCCACGGCCTCCATCGCCCTCG
TCTCGACGCCGACGCCGACGCCGTTTTGGCACCCGGCCGCCCGGTCGACACTGCTGGTGGCGCACGTCGGCGACA
GTCGCATCCTCATCTGCGACACGGCCTCGGGAAGAGCCCACCCGCTGACGTCGGATCATCACCCGTCGACGCCGA
CGGAGAGCCGCCGGCTTCGGCGCTACGGCCCCACCGGCTCCATGGTCTCGGGCGACAGCTTCGGCGAGGAGCGCA
TCGCCGGCCTGGCAAACAGTCGCGCCTTCGGTGACGTGGGCAGCAAACGGCTCGGCGTATCCGCCGAACCGGAAA
TCGTCCGTGTCGACCTGGGCCCCGCCCAGTACGCCTTCCTCGTCCTCGTCAGCGACGGCGTCTCGGGCTCGCTGG
CCGATCAAGAGATGGTCGATATCATCAAGGAGGCTCCGACCCCGGAACAGGGCGCCCGAAACGTCGTCGACTACG
CCGTAGAGGTCTCCGTCGACGGCGATAACGCTACCTGCCAGGTCGTCCGTCTCGGCGGCTGGGAGCGCCGCTCCG
AGGGTGGCCTCGGCAGCCTCGGCACCAAGGAGATTCGCGATGCTAGGAGGGCTGAGGCTCAAGACCCGCGCAGGG
GGAAACAATGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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