Fungal Genomics

at Utrecht University

General Properties

Protein IDOphauG2|1419
Gene name
LocationContig_1422:1490..3958
Strand-
Gene length (bp)2468
Transcript length (bp)2334
Coding sequence length (bp)2334
Protein length (aa) 778

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF13641 Glyco_tranf_2_3 Glycosyltransferase like family 2 5.1E-19 256 489
PF13632 Glyco_trans_2_3 Glycosyl transferase family group 2 3.6E-17 356 548
PF00535 Glycos_transf_2 Glycosyl transferase family 2 1.2E-14 258 437
PF03552 Cellulose_synt Cellulose synthase 6.7E-11 425 569
PF13506 Glyco_transf_21 Glycosyl transferase family 21 9.7E-12 353 488

Swissprot hits

[Show all]
Swissprot ID Swissprot Description Start End E-value
sp|O82859|BCSA2_KOMXY Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=3 SV=1 255 548 1.0E-29
sp|Q9WX61|BCSA3_KOMXY Cellulose synthase 1 catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsAI PE=3 SV=1 255 548 2.0E-29
sp|Q9WX75|BCSA5_KOMXY Putative cellulose synthase 3 OS=Komagataeibacter xylinus GN=bcsABII-B PE=3 SV=1 255 542 2.0E-29
sp|Q9RBJ2|BCSA4_KOMXY Putative cellulose synthase 2 OS=Komagataeibacter xylinus GN=bcsABII-A PE=3 SV=1 255 542 2.0E-29
sp|P0CW87|ACSA1_KOMXY Cellulose synthase 1 OS=Komagataeibacter xylinus GN=acsAB PE=1 SV=1 255 548 2.0E-29
[Show all]
[Show less]
Swissprot ID Swissprot Description Start End E-value
sp|O82859|BCSA2_KOMXY Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=3 SV=1 255 548 1.0E-29
sp|Q9WX61|BCSA3_KOMXY Cellulose synthase 1 catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsAI PE=3 SV=1 255 548 2.0E-29
sp|Q9WX75|BCSA5_KOMXY Putative cellulose synthase 3 OS=Komagataeibacter xylinus GN=bcsABII-B PE=3 SV=1 255 542 2.0E-29
sp|Q9RBJ2|BCSA4_KOMXY Putative cellulose synthase 2 OS=Komagataeibacter xylinus GN=bcsABII-A PE=3 SV=1 255 542 2.0E-29
sp|P0CW87|ACSA1_KOMXY Cellulose synthase 1 OS=Komagataeibacter xylinus GN=acsAB PE=1 SV=1 255 548 2.0E-29
sp|Q76KJ8|ACSA1_KOMHA Cellulose synthase 1 OS=Komagataeibacter hansenii GN=acsAB PE=1 SV=1 255 548 2.0E-29
sp|Q8Z291|BCSA_SALTI Cellulose synthase catalytic subunit [UDP-forming] OS=Salmonella typhi GN=bcsA PE=3 SV=1 255 552 4.0E-29
sp|Q93IN2|BCSA_SALTY Cellulose synthase catalytic subunit [UDP-forming] OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=bcsA PE=3 SV=1 255 552 9.0E-29
sp|P19449|BCSA1_KOMXY Cellulose synthase catalytic subunit [UDP-forming] OS=Komagataeibacter xylinus GN=bcsA PE=1 SV=1 255 548 2.0E-28
sp|P58931|BCSA_PSEFS Cellulose synthase catalytic subunit [UDP-forming] OS=Pseudomonas fluorescens (strain SBW25) GN=bcsA PE=3 SV=2 255 551 9.0E-28
sp|P37653|BCSA_ECOLI Cellulose synthase catalytic subunit [UDP-forming] OS=Escherichia coli (strain K12) GN=bcsA PE=1 SV=3 255 552 2.0E-27
sp|Q59167|ACSA2_KOMHA Cellulose synthase 2 OS=Komagataeibacter hansenii GN=acsAII PE=3 SV=1 255 548 2.0E-27
sp|Q8X5L7|BCSA_ECO57 Cellulose synthase catalytic subunit [UDP-forming] OS=Escherichia coli O157:H7 GN=bcsA PE=3 SV=2 255 552 3.0E-27
sp|P58932|BCSA_XANAC Cellulose synthase catalytic subunit [UDP-forming] OS=Xanthomonas axonopodis pv. citri (strain 306) GN=bcsA PE=3 SV=1 255 537 3.0E-26
sp|Q9U720|DCSA_DICDI Cellulose synthase catalytic subunit A [UDP-forming] OS=Dictyostelium discoideum GN=dcsA PE=1 SV=1 313 549 9.0E-19
sp|Q69L19|CSLC2_ORYSJ Probable xyloglucan glycosyltransferase 2 OS=Oryza sativa subsp. japonica GN=CSLC2 PE=2 SV=2 251 490 4.0E-17
sp|Q7PC70|CSLC2_ORYSI Probable xyloglucan glycosyltransferase 2 OS=Oryza sativa subsp. indica GN=CSLC2 PE=2 SV=1 251 490 5.0E-17
sp|Q9SJA2|CSLC8_ARATH Probable xyloglucan glycosyltransferase 8 OS=Arabidopsis thaliana GN=CSLC8 PE=2 SV=1 247 490 1.0E-16
sp|Q9SB75|CSLC5_ARATH Probable xyloglucan glycosyltransferase 5 OS=Arabidopsis thaliana GN=CSLC5 PE=1 SV=1 251 490 2.0E-16
sp|Q9LZR3|CSLA9_ARATH Glucomannan 4-beta-mannosyltransferase 9 OS=Arabidopsis thaliana GN=CSLA9 PE=2 SV=1 274 506 6.0E-14
sp|Q7XIF5|CSLA7_ORYSJ Probable mannan synthase 7 OS=Oryza sativa subsp. japonica GN=CSLA7 PE=2 SV=1 274 498 6.0E-14
sp|Q9FNI7|CSLA2_ARATH Glucomannan 4-beta-mannosyltransferase 2 OS=Arabidopsis thaliana GN=CSLA2 PE=2 SV=1 274 534 1.0E-13
sp|Q9T0L2|CSLAF_ARATH Probable mannan synthase 15 OS=Arabidopsis thaliana GN=CSLA15 PE=3 SV=2 274 490 2.0E-13
sp|Q6UDF0|CSLA1_CYATE Mannan synthase 1 OS=Cyamopsis tetragonoloba GN=ManS PE=1 SV=1 222 490 4.0E-13
sp|Q7PC69|CSLC3_ORYSJ Probable xyloglucan glycosyltransferase 3 OS=Oryza sativa subsp. japonica GN=CSLC3 PE=2 SV=1 189 549 5.0E-13
sp|Q6Z2T9|CSLA6_ORYSJ Probable mannan synthase 6 OS=Oryza sativa subsp. japonica GN=CSLA6 PE=2 SV=2 274 490 7.0E-13
sp|Q6YWK8|CSLAB_ORYSJ Probable mannan synthase 11 OS=Oryza sativa subsp. japonica GN=CSLA11 PE=2 SV=1 274 540 1.0E-12
sp|Q9SRT3|CSLC6_ARATH Probable xyloglucan glycosyltransferase 6 OS=Arabidopsis thaliana GN=CSLC6 PE=1 SV=1 248 500 2.0E-12
sp|Q7PC67|CSLA2_ORYSJ Probable mannan synthase 2 OS=Oryza sativa subsp. japonica GN=CSLA2 PE=2 SV=2 274 498 2.0E-12
sp|Q9LJP4|CSLC4_ARATH Xyloglucan glycosyltransferase 4 OS=Arabidopsis thaliana GN=CSLC4 PE=1 SV=1 253 490 2.0E-12
sp|Q7PC76|CSLA1_ORYSJ Glucomannan 4-beta-mannosyltransferase 1 OS=Oryza sativa subsp. japonica GN=CSLA1 PE=3 SV=1 274 490 4.0E-12
sp|Q8S7W0|CSLA4_ORYSJ Probable mannan synthase 4 OS=Oryza sativa subsp. japonica GN=CSLA4 PE=2 SV=1 274 498 8.0E-12
sp|Q9LQC9|CSLA3_ARATH Probable mannan synthase 3 OS=Arabidopsis thaliana GN=CSLA3 PE=2 SV=1 274 490 1.0E-11
sp|Q9LF09|CSLAB_ARATH Probable mannan synthase 11 OS=Arabidopsis thaliana GN=CSLA11 PE=2 SV=2 274 490 2.0E-11
sp|Q67X45|CSLA3_ORYSJ Probable mannan synthase 3 OS=Oryza sativa subsp. japonica GN=CSLA3 PE=2 SV=1 274 544 2.0E-11
sp|Q8LIY0|CSLC1_ORYSJ Probable xyloglucan glycosyltransferase 1 OS=Oryza sativa subsp. japonica GN=CSLC1 PE=3 SV=1 255 500 2.0E-11
sp|Q9ZQN8|CSLA7_ARATH Probable mannan synthase 7 OS=Arabidopsis thaliana GN=CSLA7 PE=2 SV=2 267 511 8.0E-11
sp|Q7PC73|CSLA5_ORYSJ Probable mannan synthase 5 OS=Oryza sativa subsp. japonica GN=CSLA5 PE=2 SV=1 274 498 1.0E-10
sp|Q9ZQB9|CSLCC_ARATH Probable xyloglucan glycosyltransferase 12 OS=Arabidopsis thaliana GN=CSLC12 PE=1 SV=1 251 490 2.0E-10
sp|Q6L538|CSLC7_ORYSJ Probable xyloglucan glycosyltransferase 7 OS=Oryza sativa subsp. japonica GN=CSLC7 PE=2 SV=1 255 500 2.0E-10
sp|Q8XAR5|PGAC_ECO57 Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Escherichia coli O157:H7 GN=pgaC PE=3 SV=1 255 534 3.0E-10
sp|P75905|PGAC_ECOLI Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Escherichia coli (strain K12) GN=pgaC PE=1 SV=1 255 534 3.0E-10
sp|Q6AU53|CSLC9_ORYSJ Probable xyloglucan glycosyltransferase 9 OS=Oryza sativa subsp. japonica GN=CSLC9 PE=2 SV=2 255 490 4.0E-10
sp|Q67VS7|CSLA9_ORYSJ Probable mannan synthase 9 OS=Oryza sativa subsp. japonica GN=CSLA9 PE=2 SV=1 274 490 5.0E-10
sp|Q84W54|CSLA1_ARATH Probable mannan synthase 1 OS=Arabidopsis thaliana GN=CSLA1 PE=2 SV=1 274 490 5.0E-10
sp|Q84W06|CSLAE_ARATH Probable mannan synthase 14 OS=Arabidopsis thaliana GN=CSLA14 PE=2 SV=2 274 512 9.0E-10
sp|Q8NUI7|ICAA_STAAW Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MW2) GN=icaA PE=3 SV=1 227 490 5.0E-09
sp|Q6G608|ICAA_STAAS Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MSSA476) GN=icaA PE=3 SV=1 227 490 5.0E-09
sp|Q3MB01|BMGDS_ANAVT Beta-monoglucosyldiacylglycerol synthase OS=Anabaena variabilis (strain ATCC 29413 / PCC 7937) GN=Ava_2217 PE=1 SV=1 240 543 7.0E-09
sp|Q84Z01|CSLCA_ORYSJ Putative xyloglucan glycosyltransferase 10 OS=Oryza sativa subsp. japonica GN=CSLC10 PE=3 SV=1 251 490 1.0E-08
sp|A2YHR9|CSLCA_ORYSI Putative xyloglucan glycosyltransferase 10 OS=Oryza sativa subsp. indica GN=CSLC10 PE=3 SV=1 251 490 1.0E-08
sp|P74165|BMGDS_SYNY3 Beta-monoglucosyldiacylglycerol synthase OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=sll1377 PE=1 SV=1 254 490 1.0E-08
sp|Q6GDD8|ICAA_STAAR Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain MRSA252) GN=icaA PE=3 SV=1 227 490 2.0E-08
sp|Q9LR87|CSLAA_ARATH Probable mannan synthase 10 OS=Arabidopsis thaliana GN=CSLA10 PE=2 SV=2 255 490 2.0E-08
sp|Q9RQP9|ICAA_STAA8 Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain NCTC 8325) GN=icaA PE=3 SV=2 227 490 2.0E-08
sp|Q5HCN1|ICAA_STAAC Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain COL) GN=icaA PE=3 SV=1 227 490 2.0E-08
sp|Q99QX3|ICAA_STAAM Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=icaA PE=3 SV=1 227 490 2.0E-08
sp|Q7A351|ICAA_STAAN Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus aureus (strain N315) GN=icaA PE=3 SV=1 227 490 2.0E-08
sp|Q8YMK0|BMGDS_NOSS1 Beta-monoglucosyldiacylglycerol synthase OS=Nostoc sp. (strain PCC 7120 / UTEX 2576) GN=all4933 PE=1 SV=1 240 543 4.0E-08
sp|Q84ZN6|CESA8_ORYSJ Probable cellulose synthase A catalytic subunit 8 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA8 PE=2 SV=1 412 561 5.0E-08
sp|Q84M43|CESA2_ORYSJ Probable cellulose synthase A catalytic subunit 2 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA2 PE=2 SV=1 412 561 2.0E-07
sp|A2XN66|CESA2_ORYSI Probable cellulose synthase A catalytic subunit 2 [UDP-forming] OS=Oryza sativa subsp. indica GN=CESA2 PE=3 SV=1 412 561 2.0E-07
sp|Q8GLC5|ICAA_STAEP Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus epidermidis GN=icaA PE=3 SV=1 260 490 4.0E-07
sp|Q84JA6|CESA4_ARATH Cellulose synthase A catalytic subunit 4 [UDP-forming] OS=Arabidopsis thaliana GN=CESA4 PE=1 SV=1 412 541 5.0E-07
sp|Q9SWW6|CESA7_ARATH Cellulose synthase A catalytic subunit 7 [UDP-forming] OS=Arabidopsis thaliana GN=CESA7 PE=1 SV=1 412 546 7.0E-07
sp|Q5HKQ0|ICAA_STAEQ Poly-beta-1,6-N-acetyl-D-glucosamine synthase OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=icaA PE=1 SV=1 260 490 7.0E-07
sp|Q941L0|CESA3_ARATH Cellulose synthase A catalytic subunit 3 [UDP-forming] OS=Arabidopsis thaliana GN=CESA3 PE=1 SV=2 412 533 2.0E-06
sp|A2WV32|CESA4_ORYSI Cellulose synthase A catalytic subunit 4 [UDP-forming] OS=Oryza sativa subsp. indica GN=CESA4 PE=2 SV=2 412 573 6.0E-06
sp|Q5JN63|CESA4_ORYSJ Cellulose synthase A catalytic subunit 4 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA4 PE=2 SV=1 412 573 6.0E-06
sp|Q9AV71|CESA7_ORYSJ Cellulose synthase A catalytic subunit 7 [UDP-forming] OS=Oryza sativa subsp. japonica GN=CESA7 PE=2 SV=1 412 630 7.0E-06
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GO

GO Term Description Terminal node
GO:0016757 glycosyltransferase activity Yes
GO:0016020 membrane Yes
GO:0016760 cellulose synthase (UDP-forming) activity Yes
GO:0030244 cellulose biosynthetic process Yes
GO:0035251 UDP-glucosyltransferase activity No
GO:0009059 macromolecule biosynthetic process No
GO:0016759 cellulose synthase activity No
GO:1901576 organic substance biosynthetic process No
GO:0044264 cellular polysaccharide metabolic process No
GO:0009058 biosynthetic process No
GO:0008152 metabolic process No
GO:0008150 biological_process No
GO:0005975 carbohydrate metabolic process No
GO:0044042 glucan metabolic process No
GO:0005575 cellular_component No
GO:0000271 polysaccharide biosynthetic process No
GO:0046527 glucosyltransferase activity No
GO:0044238 primary metabolic process No
GO:0030243 cellulose metabolic process No
GO:0009250 glucan biosynthetic process No
GO:0005976 polysaccharide metabolic process No
GO:0034645 cellular macromolecule biosynthetic process No
GO:0008194 UDP-glycosyltransferase activity No
GO:0003674 molecular_function No
GO:0051274 beta-glucan biosynthetic process No
GO:0003824 catalytic activity No
GO:0051273 beta-glucan metabolic process No
GO:0044237 cellular metabolic process No
GO:0016051 carbohydrate biosynthetic process No
GO:0044260 cellular macromolecule metabolic process No
GO:0016758 hexosyltransferase activity No
GO:0110165 cellular anatomical entity No
GO:0006073 cellular glucan metabolic process No
GO:0016740 transferase activity No
GO:0034637 cellular carbohydrate biosynthetic process No
GO:0044249 cellular biosynthetic process No
GO:0071704 organic substance metabolic process No
GO:0044262 cellular carbohydrate metabolic process No
GO:0033692 cellular polysaccharide biosynthetic process No
GO:0043170 macromolecule metabolic process No
GO:0009987 cellular process No

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 37 0.45

Transmembrane Domains

Domain # Start End Length
1 181 203 22
2 210 232 22
3 521 543 22
4 650 672 22
5 695 717 22
6 754 776 22

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

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 >OphauG2|1419
MRPYPDHAEHDEKLDPAAYQGRNQPSPEQQFSGLSRPARANVRYPPANSPYSSPYSHNDGFSPEWPPSVAGRSDS
QTLYESNPYDSRSSLRSWRTDQHTPVDMGASPRFMPSFADSSPSMTPMNQSTISLAALLPHQHSKTHPAREEFVD
LNDSVAILDNRDDVDIWHGWKRYLFKLVPFLTFANTAVYLAYLALRIACVIWSQQQQGQVFIAAWIFIAVEIAVA
IPSLMHNSWTMWSMKSRNRQKFRLKGYAVPTVDVFITCCGEDDDLVIDTVRAACDLDYPYDRFRVVILDDAKSEG
LSAAASRLAMQYPNIYYMAREKIPGKPHHFKAGNLNYGLDQVHLLPGGAGQFMAALDADMIPERDWLRAVLPHLL
VDPKMALACPPQLFYNTPTSDPLAQSLDFFVHVIEPIKDALGVAWCTGSGYVVRREALEEIGNFPLGSLAEDVAT
STLMLGRGWKTAYVHEPLQFGTVPDDYGSHLKQRTRWAIGTVDTSFKLNFCLWGEKVREMNFAQRFSGFMYAMLS
IYTIPLVISMFAIPIILVMRKPLVAYANDDQLRWLIWAAFAATMTNRLCEYVMSIPAGFNTGQRSSRYQLWMSPY
IAICILRSFVLPKWLGGQVQAFKPTGSLASALNERDPVLKKNMLGRLRGILFSYMGIFHLFFVYFTLVGVTLTSF
GCFMTEKGVRELLICLVTHAFWPPLTFIFLCSSLWIPVAYAIDPPMMPEREQLLDRDPKTLVAHPTAKSKKIAFG
GQAAWLNLELIVSTGFTILIFVASFIV*
Coding >OphauG2|1419
ATGAGACCGTATCCAGACCACGCAGAGCATGACGAGAAGCTCGACCCTGCAGCATACCAAGGCCGCAACCAGCCG
TCTCCCGAACAGCAATTCTCGGGCTTGTCTCGGCCGGCCAGAGCAAACGTCAGATACCCTCCCGCCAACTCGCCA
TACTCGTCGCCATACTCGCACAATGACGGCTTCTCCCCCGAGTGGCCTCCCTCGGTAGCAGGCCGCTCCGACTCG
CAGACTCTGTACGAGAGCAATCCATATGACAGCAGATCAAGCTTGCGCTCGTGGCGCACTGACCAACACACCCCC
GTCGACATGGGCGCTTCCCCAAGATTTATGCCCTCGTTTGCCGATTCGAGTCCTTCAATGACACCCATGAACCAA
AGCACCATCAGTCTCGCTGCCCTGCTCCCCCATCAGCATTCCAAGACACATCCTGCCAGGGAAGAGTTTGTTGAT
CTCAACGACTCCGTCGCCATCTTGGACAACCGCGACGATGTAGACATCTGGCACGGCTGGAAGCGTTACCTCTTC
AAGCTGGTTCCCTTCTTGACCTTTGCCAATACCGCCGTCTACTTGGCATATCTCGCTCTGCGCATCGCCTGTGTC
ATATGGTCTCAGCAGCAACAAGGCCAAGTCTTCATCGCCGCATGGATATTCATTGCTGTTGAAATCGCCGTTGCT
ATTCCCTCACTCATGCATAATTCCTGGACCATGTGGTCCATGAAGTCGCGCAACCGCCAGAAATTTCGCCTCAAA
GGCTATGCTGTGCCCACGGTCGACGTCTTCATCACTTGCTGTGGCGAGGATGACGATTTGGTCATTGACACTGTC
CGCGCTGCCTGCGACCTCGATTATCCCTATGACCGCTTCAGGGTTGTTATTCTTGACGACGCCAAGTCTGAGGGT
CTGAGCGCCGCTGCATCGCGTCTCGCTATGCAATACCCCAACATCTATTACATGGCCCGCGAAAAGATTCCTGGA
AAGCCCCACCATTTCAAGGCTGGAAATCTCAACTATGGCTTGGATCAGGTCCACCTGCTTCCAGGCGGTGCCGGC
CAATTCATGGCTGCTCTTGATGCCGACATGATTCCCGAGCGGGACTGGCTGCGGGCCGTGCTGCCTCATCTTCTT
GTCGATCCCAAGATGGCTCTCGCCTGCCCACCACAGCTCTTTTATAACACGCCCACTTCTGATCCGCTGGCGCAA
AGTCTCGACTTTTTTGTCCACGTCATTGAGCCCATCAAGGACGCGCTAGGCGTTGCCTGGTGTACCGGCTCTGGA
TATGTTGTTCGTCGCGAGGCTTTGGAAGAGATTGGCAACTTTCCCCTGGGCTCGCTGGCCGAGGACGTGGCCACG
TCTACGCTCATGCTGGGCCGAGGATGGAAGACGGCCTATGTGCACGAGCCCCTGCAGTTTGGCACCGTGCCTGAT
GACTATGGCAGCCACTTGAAACAGCGTACTCGATGGGCTATTGGAACCGTTGACACGTCGTTCAAGCTCAACTTT
TGCCTGTGGGGTGAAAAGGTTCGCGAGATGAACTTTGCCCAGCGCTTCTCGGGCTTCATGTACGCCATGCTCAGC
ATCTACACGATTCCCCTCGTCATTTCCATGTTTGCCATTCCCATTATTCTCGTCATGAGGAAGCCCCTGGTCGCC
TATGCCAATGACGACCAGCTGCGTTGGCTCATTTGGGCCGCCTTTGCCGCCACCATGACGAACCGACTATGCGAA
TACGTCATGTCCATTCCCGCTGGCTTCAACACGGGACAGCGAAGCTCGAGATACCAGCTCTGGATGTCGCCATAT
ATTGCCATTTGCATCCTCCGCTCCTTTGTCCTGCCCAAGTGGCTTGGCGGCCAAGTCCAGGCCTTTAAGCCGACG
GGCTCTCTGGCCTCGGCACTCAATGAGCGCGATCCCGTGCTCAAGAAGAATATGCTTGGACGCTTGCGCGGCATT
CTCTTTAGCTACATGGGCATCTTCCACCTCTTCTTTGTCTACTTTACTCTGGTTGGAGTGACATTGACGTCATTT
GGCTGCTTCATGACGGAAAAGGGCGTTCGCGAGCTTCTCATTTGCCTGGTGACGCACGCGTTTTGGCCGCCCTTG
ACCTTTATCTTTCTCTGCAGCTCTCTGTGGATTCCCGTGGCCTACGCCATTGACCCTCCAATGATGCCGGAACGC
GAGCAGCTGCTTGATCGTGACCCCAAGACGCTGGTTGCGCACCCCACGGCCAAGAGCAAGAAGATTGCATTTGGC
GGCCAGGCCGCGTGGCTTAATCTGGAGCTCATTGTATCGACTGGATTCACCATTTTGATATTTGTCGCGTCGTTT
ATTGTTTGA
Transcript >OphauG2|1419
ATGAGACCGTATCCAGACCACGCAGAGCATGACGAGAAGCTCGACCCTGCAGCATACCAAGGCCGCAACCAGCCG
TCTCCCGAACAGCAATTCTCGGGCTTGTCTCGGCCGGCCAGAGCAAACGTCAGATACCCTCCCGCCAACTCGCCA
TACTCGTCGCCATACTCGCACAATGACGGCTTCTCCCCCGAGTGGCCTCCCTCGGTAGCAGGCCGCTCCGACTCG
CAGACTCTGTACGAGAGCAATCCATATGACAGCAGATCAAGCTTGCGCTCGTGGCGCACTGACCAACACACCCCC
GTCGACATGGGCGCTTCCCCAAGATTTATGCCCTCGTTTGCCGATTCGAGTCCTTCAATGACACCCATGAACCAA
AGCACCATCAGTCTCGCTGCCCTGCTCCCCCATCAGCATTCCAAGACACATCCTGCCAGGGAAGAGTTTGTTGAT
CTCAACGACTCCGTCGCCATCTTGGACAACCGCGACGATGTAGACATCTGGCACGGCTGGAAGCGTTACCTCTTC
AAGCTGGTTCCCTTCTTGACCTTTGCCAATACCGCCGTCTACTTGGCATATCTCGCTCTGCGCATCGCCTGTGTC
ATATGGTCTCAGCAGCAACAAGGCCAAGTCTTCATCGCCGCATGGATATTCATTGCTGTTGAAATCGCCGTTGCT
ATTCCCTCACTCATGCATAATTCCTGGACCATGTGGTCCATGAAGTCGCGCAACCGCCAGAAATTTCGCCTCAAA
GGCTATGCTGTGCCCACGGTCGACGTCTTCATCACTTGCTGTGGCGAGGATGACGATTTGGTCATTGACACTGTC
CGCGCTGCCTGCGACCTCGATTATCCCTATGACCGCTTCAGGGTTGTTATTCTTGACGACGCCAAGTCTGAGGGT
CTGAGCGCCGCTGCATCGCGTCTCGCTATGCAATACCCCAACATCTATTACATGGCCCGCGAAAAGATTCCTGGA
AAGCCCCACCATTTCAAGGCTGGAAATCTCAACTATGGCTTGGATCAGGTCCACCTGCTTCCAGGCGGTGCCGGC
CAATTCATGGCTGCTCTTGATGCCGACATGATTCCCGAGCGGGACTGGCTGCGGGCCGTGCTGCCTCATCTTCTT
GTCGATCCCAAGATGGCTCTCGCCTGCCCACCACAGCTCTTTTATAACACGCCCACTTCTGATCCGCTGGCGCAA
AGTCTCGACTTTTTTGTCCACGTCATTGAGCCCATCAAGGACGCGCTAGGCGTTGCCTGGTGTACCGGCTCTGGA
TATGTTGTTCGTCGCGAGGCTTTGGAAGAGATTGGCAACTTTCCCCTGGGCTCGCTGGCCGAGGACGTGGCCACG
TCTACGCTCATGCTGGGCCGAGGATGGAAGACGGCCTATGTGCACGAGCCCCTGCAGTTTGGCACCGTGCCTGAT
GACTATGGCAGCCACTTGAAACAGCGTACTCGATGGGCTATTGGAACCGTTGACACGTCGTTCAAGCTCAACTTT
TGCCTGTGGGGTGAAAAGGTTCGCGAGATGAACTTTGCCCAGCGCTTCTCGGGCTTCATGTACGCCATGCTCAGC
ATCTACACGATTCCCCTCGTCATTTCCATGTTTGCCATTCCCATTATTCTCGTCATGAGGAAGCCCCTGGTCGCC
TATGCCAATGACGACCAGCTGCGTTGGCTCATTTGGGCCGCCTTTGCCGCCACCATGACGAACCGACTATGCGAA
TACGTCATGTCCATTCCCGCTGGCTTCAACACGGGACAGCGAAGCTCGAGATACCAGCTCTGGATGTCGCCATAT
ATTGCCATTTGCATCCTCCGCTCCTTTGTCCTGCCCAAGTGGCTTGGCGGCCAAGTCCAGGCCTTTAAGCCGACG
GGCTCTCTGGCCTCGGCACTCAATGAGCGCGATCCCGTGCTCAAGAAGAATATGCTTGGACGCTTGCGCGGCATT
CTCTTTAGCTACATGGGCATCTTCCACCTCTTCTTTGTCTACTTTACTCTGGTTGGAGTGACATTGACGTCATTT
GGCTGCTTCATGACGGAAAAGGGCGTTCGCGAGCTTCTCATTTGCCTGGTGACGCACGCGTTTTGGCCGCCCTTG
ACCTTTATCTTTCTCTGCAGCTCTCTGTGGATTCCCGTGGCCTACGCCATTGACCCTCCAATGATGCCGGAACGC
GAGCAGCTGCTTGATCGTGACCCCAAGACGCTGGTTGCGCACCCCACGGCCAAGAGCAAGAAGATTGCATTTGGC
GGCCAGGCCGCGTGGCTTAATCTGGAGCTCATTGTATCGACTGGATTCACCATTTTGATATTTGTCGCGTCGTTT
ATTGTTTGA
Gene >OphauG2|1419
ATGAGACCGTATCCAGACCACGCAGAGCATGACGAGAAGCTCGACCCTGCAGCATACCAAGGCCGCAACCAGCCG
TCTCCCGAACAGCAATTCTCGGGCTTGTCTCGGCCGGCCAGAGCAAACGTCAGATACCCTCCCGCCAACTCGCCA
TACTCGTCGCCATACTCGCACAATGACGGCTTCTCCCCCGAGTGGCCTCCCTCGGTAGCAGGCCGCTCCGACTCG
CAGACTCTGTACGAGAGCAATCCATATGACAGCAGATCAAGCTTGCGCTCGTGGCGCACTGACCAACACACCCCC
GTCGACATGGGCGCTTCCCCAAGATTTATGCCCTCGTTTGCCGATTCGAGTCCTTCAATGACACCCATGGTTGGT
CTGCTGCAGCTTCTTGCATGCCCTCATTGCTCTTTTGCTGACTGCCTTGCTTTGTTGTCCATAGAACCAAAGCAC
CATCAGTCTCGCTGCCCTGCTCCCCCATCAGCATTCCAAGACACATCCTGCCAGGGAAGAGTTTGTTGATCTCAA
CGACTCCGTCGCCATCTTGGACAACCGCGACGATGTAGACATCTGGCACGGCTGGAAGCGTTACCTCTTCAAGCT
GGTTCCCTTCTTGACCTTTGCCAATACCGCCGTCTACTTGGCATATCTCGCTCTGCGCATCGCCTGTGTCATATG
GTCTCAGCAGCAACAAGGCCAAGTCTTCATCGCCGCATGGATATTCATTGCTGTTGAAATCGCCGTTGCTATTCC
CTCACTCATGCATAATTCCTGGACCATGTGGTCCATGAAGTCGCGCAACCGCCAGAAATTTCGCCTCAAAGGCTA
TGCTGTGCCCACGGTCGACGTCTTCATCACTTGCTGTGGCGAGGATGACGATTTGGTCATTGACACTGTCCGCGC
TGCCTGCGACCTCGATTATCCCTATGACCGCTTCAGGGTTGTTATTCTTGACGACGCCAAGTCTGAGGGTCTGAG
CGCCGCTGCATCGCGTCTCGCTATGCAATACCCCAACATCTATTACATGGCCCGCGAAAAGATTCCTGGAAAGCC
CCACCATTTCAAGGCTGGAAATCTCAACTATGGCTTGGATCAGGTCCACCTGCTTCCAGGCGGTGCCGGCCAATT
CATGGCTGCTCTTGATGCCGACATGGTTTGTCCTCTGCGTCTTGTTTTGCCTTGCAAGTCGGTGCTAATGTTTGA
TGTCCGTTTTTTAGATTCCCGAGCGGGACTGGCTGCGGGCCGTGCTGCCTCATCTTCTTGTCGATCCCAAGATGG
CTCTCGCCTGCCCACCACAGCTCTTTTATAACACGCCCACTTCTGATCCGCTGGCGCAAAGTCTCGACTTTTTTG
TCCACGTCATTGAGCCCATCAAGGACGCGCTAGGCGTTGCCTGGTGTACCGGCTCTGGATATGTTGTTCGTCGCG
AGGCTTTGGAAGAGATTGGCAACTTTCCCCTGGGCTCGCTGGCCGAGGACGTGGCCACGTCTACGCTCATGCTGG
GCCGAGGATGGAAGACGGCCTATGTGCACGAGCCCCTGCAGTTTGGCACCGTGCCTGATGACTATGGCAGCCACT
TGAAACAGCGTACTCGATGGGCTATTGGAACCGTTGACACGTCGTTCAAGCTCAACTTTTGCCTGTGGGGTGAAA
AGGTTCGCGAGATGAACTTTGCCCAGCGCTTCTCGGGCTTCATGTACGCCATGCTCAGCATCTACACGATTCCCC
TCGTCATTTCCATGTTTGCCATTCCCATTATTCTCGTCATGAGGAAGCCCCTGGTCGCCTATGCCAATGACGACC
AGCTGCGTTGGCTCATTTGGGCCGCCTTTGCCGCCACCATGACGAACCGACTATGCGAATACGTCATGTCCATTC
CCGCTGGCTTCAACACGGGACAGCGAAGCTCGAGATACCAGCTCTGGATGTCGCCATATATTGCCATTTGCATCC
TCCGCTCCTTTGTCCTGCCCAAGTGGCTTGGCGGCCAAGTCCAGGCCTTTAAGCCGACGGGCTCTCTGGCCTCGG
CACTCAATGAGCGCGATCCCGTGCTCAAGAAGAATATGCTTGGACGCTTGCGCGGCATTCTCTTTAGCTACATGG
GCATCTTCCACCTCTTCTTTGTCTACTTTACTCTGGTTGGAGTGACATTGACGTCATTTGGCTGCTTCATGACGG
AAAAGGGCGTTCGCGAGCTTCTCATTTGCCTGGTGACGCACGCGTTTTGGCCGCCCTTGACCTTTATCTTTCTCT
GCAGCTCTCTGTGGATTCCCGTGGCCTACGCCATTGACCCTCCAATGATGCCGGAACGCGAGCAGCTGCTTGATC
GTGACCCCAAGACGCTGGTTGCGCACCCCACGGCCAAGAGCAAGAAGATTGCATTTGGCGGCCAGGCCGCGTGGC
TTAATCTGGAGCTCATTGTATCGACTGGATTCACCATTTTGATATTTGTCGCGTCGTTTATTGTTTGA

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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