© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|6385 |
| Gene name | |
| Location | scaffold_557:6723..8662 |
| Strand | + |
| Gene length (bp) | 1939 |
| Transcript length (bp) | 1767 |
| Coding sequence length (bp) | 1764 |
| Protein length (aa) | 588 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00534 | Glycos_transf_1 | Glycosyl transferases group 1 | 3.0E-10 | 224 | 292 |
| PF00534 | Glycos_transf_1 | Glycosyl transferases group 1 | 3.0E-19 | 315 | 412 |
| PF13439 | Glyco_transf_4 | Glycosyltransferase Family 4 | 7.9E-14 | 20 | 207 |
| PF13692 | Glyco_trans_1_4 | Glycosyl transferases group 1 | 2.4E-13 | 226 | 398 |
| PF13579 | Glyco_trans_4_4 | Glycosyl transferase 4-like domain | 2.8E-07 | 21 | 182 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q8X0H8|ALG2_NEUCR | Alpha-1,3/1,6-mannosyltransferase alg-2 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-2 PE=3 SV=1 | 10 | 434 | 8.0E-154 |
| sp|Q6CWQ0|ALG2_KLULA | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ALG2 PE=3 SV=1 | 1 | 467 | 1.0E-110 |
| sp|P43636|ALG2_YEAST | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG2 PE=1 SV=2 | 10 | 431 | 3.0E-109 |
| sp|Q96WW6|ALG2_SCHPO | Alpha-1,3/1,6-mannosyltransferase alg2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg2 PE=3 SV=2 | 13 | 492 | 3.0E-108 |
| sp|Q59LF2|ALG2_CANAL | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ALG2 PE=3 SV=1 | 13 | 434 | 3.0E-103 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q8X0H8|ALG2_NEUCR | Alpha-1,3/1,6-mannosyltransferase alg-2 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-2 PE=3 SV=1 | 10 | 434 | 8.0E-154 |
| sp|Q6CWQ0|ALG2_KLULA | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ALG2 PE=3 SV=1 | 1 | 467 | 1.0E-110 |
| sp|P43636|ALG2_YEAST | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG2 PE=1 SV=2 | 10 | 431 | 3.0E-109 |
| sp|Q96WW6|ALG2_SCHPO | Alpha-1,3/1,6-mannosyltransferase alg2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg2 PE=3 SV=2 | 13 | 492 | 3.0E-108 |
| sp|Q59LF2|ALG2_CANAL | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ALG2 PE=3 SV=1 | 13 | 434 | 3.0E-103 |
| sp|Q6FJJ9|ALG2_CANGA | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=ALG2 PE=3 SV=1 | 4 | 436 | 2.0E-100 |
| sp|Q6BVA4|ALG2_DEBHA | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=ALG2 PE=3 SV=2 | 6 | 427 | 2.0E-99 |
| sp|Q6C3V7|ALG2_YARLI | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=ALG2 PE=3 SV=1 | 13 | 434 | 6.0E-98 |
| sp|O94738|ALG2_RHIPU | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Rhizomucor pusillus GN=ALG2 PE=1 SV=1 | 6 | 433 | 9.0E-98 |
| sp|Q755C1|ALG2_ASHGO | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ALG2 PE=3 SV=1 | 15 | 431 | 6.0E-96 |
| sp|Q7KWM5|ALG2_DICDI | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Dictyostelium discoideum GN=alg2 PE=3 SV=1 | 15 | 434 | 1.0E-77 |
| sp|Q9H553|ALG2_HUMAN | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Homo sapiens GN=ALG2 PE=1 SV=1 | 3 | 429 | 3.0E-74 |
| sp|Q9DBE8|ALG2_MOUSE | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Mus musculus GN=Alg2 PE=1 SV=2 | 8 | 429 | 2.0E-71 |
| sp|Q7ZW24|ALG11_DANRE | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Danio rerio GN=alg11 PE=2 SV=2 | 7 | 418 | 2.0E-14 |
| sp|Q08B22|ALG11_XENLA | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Xenopus laevis GN=alg11 PE=2 SV=2 | 13 | 422 | 1.0E-13 |
| sp|Q54DM9|ALG11_DICDI | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Dictyostelium discoideum GN=alg11 PE=3 SV=1 | 13 | 381 | 8.0E-10 |
| sp|Q73SU4|MSHA_MYCPA | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium paratuberculosis (strain ATCC BAA-968 / K-10) GN=mshA PE=3 SV=1 | 197 | 394 | 1.0E-09 |
| sp|A0QLK5|MSHA_MYCA1 | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium avium (strain 104) GN=mshA PE=3 SV=1 | 197 | 394 | 1.0E-09 |
| sp|P9WMY7|MSHA_MYCTU | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=mshA PE=1 SV=1 | 197 | 420 | 4.0E-09 |
| sp|P64708|MSHA_MYCBO | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|A1KFW0|MSHA_MYCBP | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|C1AKG4|MSHA_MYCBT | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium bovis (strain BCG / Tokyo 172 / ATCC 35737 / TMC 1019) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|A5TZL4|MSHA_MYCTA | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|A5WJJ8|MSHA_MYCTF | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium tuberculosis (strain F11) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|C6DT68|MSHA_MYCTK | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium tuberculosis (strain KZN 1435 / MDR) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|P9WMY6|MSHA_MYCTO | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=mshA PE=3 SV=1 | 197 | 420 | 4.0E-09 |
| sp|C4LLD6|MSHA_CORK4 | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium kroppenstedtii (strain DSM 44385 / CCUG 35717) GN=mshA PE=3 SV=1 | 197 | 412 | 1.0E-08 |
| sp|Q6P312|ALG11_XENTR | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Xenopus tropicalis GN=alg11 PE=2 SV=1 | 13 | 422 | 3.0E-08 |
| sp|P54138|MSHA_MYCLE | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium leprae (strain TN) GN=mshA PE=3 SV=2 | 197 | 401 | 5.0E-08 |
| sp|B8ZT88|MSHA_MYCLB | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium leprae (strain Br4923) GN=mshA PE=3 SV=1 | 197 | 401 | 5.0E-08 |
| sp|A1SP12|MSHA_NOCSJ | D-inositol 3-phosphate glycosyltransferase OS=Nocardioides sp. (strain BAA-499 / JS614) GN=mshA PE=3 SV=1 | 288 | 430 | 6.0E-08 |
| sp|C3PK12|MSHA_CORA7 | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium aurimucosum (strain ATCC 700975 / DSM 44827 / CN-1) GN=mshA PE=3 SV=1 | 121 | 436 | 2.0E-07 |
| sp|Q4JSW2|MSHA_CORJK | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium jeikeium (strain K411) GN=mshA PE=3 SV=1 | 192 | 432 | 3.0E-06 |
| sp|A4X1R6|MSHA_SALTO | D-inositol 3-phosphate glycosyltransferase OS=Salinispora tropica (strain ATCC BAA-916 / DSM 44818 / CNB-440) GN=mshA PE=3 SV=1 | 330 | 420 | 7.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016757 | glycosyltransferase activity | Yes |
| GO:0003824 | catalytic activity | No |
| GO:0016740 | transferase activity | No |
| GO:0003674 | molecular_function | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 24 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 450 | 472 | 22 |
| 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|6385 MPPAPSGSGTLIFFHPDLGIGGAERLIVDAAVGLQQRGHRVIIFTNRCDADHCFDECRDGTLDVRVRANSPIPSS VCNRLAILCAITRQLQLILQLSLSGELSSLKPRAFIVDQLSAALPLLRSLYTDIPILFYCHFPDLLLARGRTASL VKRIYRLPFDWLEEWSMTFSHMVAVNSRFTRSVVCATWPRLAHVVAIDVVYPCVDTDPDPPAEDWATAVALLGNL VLSINRFERKKDIALAIRAFAALPTADRDGVRLVLAGGHDRRVSENAEYHAELQTLSDSLRLSHQTIDSPDSATA LTSATSSCSSSSSPPQVLFLLSIPNGLKAALLASANLVVYTPANEHFGIVPLEAMLASRPVLAADSGGPVETVRD GTTGWLRDPDDVSAWSAAMREALTLSDTDRAAMGAEAAARVRKSFGRHVMAQRLDHLLSLADVVAKMRAPARLAS PITLGLLVLFFLFGTTLSAAFVHHGKRIAAVKPIFTFVYTHIFYSQSPTCFAGDPETRDDVISTPPSTTGDRLSP RSRLQVDSEIHLSTASSSNLIQFPAPKGQTLTAPSPIPNYASTHSSTTPTHQMARLNQPPRSP |
| Coding | >Ophio5|6385 ATGCCGCCCGCCCCCAGCGGCAGCGGCACCCTCATCTTCTTTCATCCAGACCTCGGCATCGGCGGCGCAGAACGA CTCATCGTCGACGCCGCCGTCGGTCTCCAGCAACGAGGTCACCGGGTGATAATTTTCACGAACCGCTGCGACGCC GACCATTGCTTTGACGAGTGCCGCGATGGAACGCTCGACGTCCGCGTCCGCGCAAACAGCCCGATCCCATCATCC GTCTGCAACCGCCTCGCCATCCTCTGCGCCATCACGCGCCAACTGCAACTAATTCTCCAACTCTCCCTCAGCGGC GAGCTCTCAAGCTTGAAACCACGGGCCTTCATCGTCGACCAACTCTCGGCCGCGCTGCCGCTTCTTCGCAGCCTC TATACCGATATCCCCATTCTCTTTTACTGCCACTTCCCTGACCTCCTCCTCGCCCGCGGTCGTACCGCTTCGCTC GTCAAGCGTATATATCGTCTCCCTTTTGACTGGCTCGAGGAATGGAGCATGACTTTTTCGCACATGGTTGCGGTG AATTCGCGTTTTACCCGCTCCGTTGTCTGCGCTACTTGGCCCCGTCTTGCCCATGTTGTTGCTATAGACGTCGTT TATCCCTGCGTCGATACCGATCCGGATCCGCCGGCTGAGGACTGGGCTACTGCTGTCGCCCTTCTTGGTAATCTG GTCCTCAGTATAAACCGCTTCGAGCGCAAAAAGGATATCGCCCTCGCTATCCGCGCCTTTGCCGCCTTGCCCACC GCAGATCGAGACGGTGTCCGCCTCGTCCTCGCCGGCGGCCACGACCGACGCGTATCGGAAAACGCAGAATATCAC GCCGAACTACAAACACTCTCCGACTCACTCCGTCTCTCACATCAAACCATCGACAGCCCAGACTCAGCCACGGCG CTAACATCCGCAACCTCCTCCTGCTCCTCCTCCTCTTCCCCTCCACAAGTCCTCTTCCTCCTCTCCATCCCCAAC GGCCTCAAAGCCGCCCTCCTCGCCAGCGCCAACCTCGTCGTCTACACCCCGGCAAACGAACACTTCGGCATCGTC CCCCTCGAAGCCATGCTCGCCTCCCGTCCCGTCCTGGCCGCTGACTCGGGCGGGCCCGTCGAGACGGTCCGCGAC GGTACCACCGGTTGGCTTCGCGACCCGGACGACGTCTCCGCTTGGTCGGCTGCCATGCGGGAAGCCCTCACCTTG TCGGATACGGATCGCGCTGCTATGGGCGCCGAGGCTGCGGCCCGGGTCCGCAAGTCTTTTGGGAGGCATGTCATG GCCCAGCGGCTTGATCATCTACTCTCCCTGGCTGATGTTGTGGCCAAGATGAGGGCTCCCGCAAGGCTTGCTAGT CCAATTACTCTTGGTCTTTTGGTCTTGTTCTTTCTCTTTGGCACCACCTTGTCTGCTGCCTTTGTGCATCACGGC AAGCGGATAGCTGCGGTAAAGCCAATCTTCACCTTTGTCTATACACACATCTTCTACTCTCAGTCTCCGACATGT TTCGCAGGTGACCCAGAGACCAGAGACGATGTCATCTCCACCCCTCCCTCCACGACCGGAGACCGCCTCTCACCA CGGTCACGACTCCAAGTTGATAGTGAAATCCATCTCTCTACCGCGTCTTCTTCAAACCTCATTCAATTTCCCGCC CCCAAGGGCCAAACCCTCACCGCCCCCTCTCCTATCCCCAACTATGCTTCCACTCACTCGTCCACCACACCCACG CATCAAATGGCCAGGCTCAACCAACCCCCCCGATCGCCA |
| Transcript | >Ophio5|6385 ATGCCGCCCGCCCCCAGCGGCAGCGGCACCCTCATCTTCTTTCATCCAGACCTCGGCATCGGCGGCGCAGAACGA CTCATCGTCGACGCCGCCGTCGGTCTCCAGCAACGAGGTCACCGGGTGATAATTTTCACGAACCGCTGCGACGCC GACCATTGCTTTGACGAGTGCCGCGATGGAACGCTCGACGTCCGCGTCCGCGCAAACAGCCCGATCCCATCATCC GTCTGCAACCGCCTCGCCATCCTCTGCGCCATCACGCGCCAACTGCAACTAATTCTCCAACTCTCCCTCAGCGGC GAGCTCTCAAGCTTGAAACCACGGGCCTTCATCGTCGACCAACTCTCGGCCGCGCTGCCGCTTCTTCGCAGCCTC TATACCGATATCCCCATTCTCTTTTACTGCCACTTCCCTGACCTCCTCCTCGCCCGCGGTCGTACCGCTTCGCTC GTCAAGCGTATATATCGTCTCCCTTTTGACTGGCTCGAGGAATGGAGCATGACTTTTTCGCACATGGTTGCGGTG AATTCGCGTTTTACCCGCTCCGTTGTCTGCGCTACTTGGCCCCGTCTTGCCCATGTTGTTGCTATAGACGTCGTT TATCCCTGCGTCGATACCGATCCGGATCCGCCGGCTGAGGACTGGGCTACTGCTGTCGCCCTTCTTGGTAATCTG GTCCTCAGTATAAACCGCTTCGAGCGCAAAAAGGATATCGCCCTCGCTATCCGCGCCTTTGCCGCCTTGCCCACC GCAGATCGAGACGGTGTCCGCCTCGTCCTCGCCGGCGGCCACGACCGACGCGTATCGGAAAACGCAGAATATCAC GCCGAACTACAAACACTCTCCGACTCACTCCGTCTCTCACATCAAACCATCGACAGCCCAGACTCAGCCACGGCG CTAACATCCGCAACCTCCTCCTGCTCCTCCTCCTCTTCCCCTCCACAAGTCCTCTTCCTCCTCTCCATCCCCAAC GGCCTCAAAGCCGCCCTCCTCGCCAGCGCCAACCTCGTCGTCTACACCCCGGCAAACGAACACTTCGGCATCGTC CCCCTCGAAGCCATGCTCGCCTCCCGTCCCGTCCTGGCCGCTGACTCGGGCGGGCCCGTCGAGACGGTCCGCGAC GGTACCACCGGTTGGCTTCGCGACCCGGACGACGTCTCCGCTTGGTCGGCTGCCATGCGGGAAGCCCTCACCTTG TCGGATACGGATCGCGCTGCTATGGGCGCCGAGGCTGCGGCCCGGGTCCGCAAGTCTTTTGGGAGGCATGTCATG GCCCAGCGGCTTGATCATCTACTCTCCCTGGCTGATGTTGTGGCCAAGATGAGGGCTCCCGCAAGGCTTGCTAGT CCAATTACTCTTGGTCTTTTGGTCTTGTTCTTTCTCTTTGGCACCACCTTGTCTGCTGCCTTTGTGCATCACGGC AAGCGGATAGCTGCGGTAAAGCCAATCTTCACCTTTGTCTATACACACATCTTCTACTCTCAGTCTCCGACATGT TTCGCAGGTGACCCAGAGACCAGAGACGATGTCATCTCCACCCCTCCCTCCACGACCGGAGACCGCCTCTCACCA CGGTCACGACTCCAAGTTGATAGTGAAATCCATCTCTCTACCGCGTCTTCTTCAAACCTCATTCAATTTCCCGCC CCCAAGGGCCAAACCCTCACCGCCCCCTCTCCTATCCCCAACTATGCTTCCACTCACTCGTCCACCACACCCACG CATCAAATGGCCAGGCTCAACCAACCCCCCCGATCGCCATGA |
| Gene | >Ophio5|6385 ATGCCGCCCGCCCCCAGCGGCAGCGGCACCCTCATCTTCTTTCATCCAGACCTCGGCATCGGCGGCGCAGAACGA CTCATCGTCGACGCCGCCGTCGGTCTCCAGCAACGAGGTCACCGGGTGATAATTTTCACGAACCGCTGCGACGCC GACCATTGCTTTGACGAGTGCCGCGATGGTAAAACAATTCCTCTTCACAGTTTGGCTTTTTATTCGATACATCTG GCTGAAGTTTGTCGATAGGAACGCTCGACGTCCGCGTCCGCGCAAACAGCCCGATCCCATCATCCGTCTGCAACC GCCTCGCCATCCTCTGCGCCATCACGCGCCAACTGCAACTAATTCTCCAACTCTCCCTCAGCGGCGAGCTCTCAA GCTTGAAACCACGGGCCTTCATCGTCGACCAACTCTCGGCCGCGCTGCCGCTTCTTCGCAGCCTCTATACCGATA TCCCCATTCTCTTTTACTGCCACTTCCCTGACCTCCTCCTCGCCCGCGGTCGTACCGCTTCGCTCGTCAAGCGTA TATATCGTCTCCCTTTTGACTGGCTCGAGGAATGGAGCATGACTTTTTCGCACATGGTTGCGGTGAATTCGCGTT TTACCCGCTCCGTTGTCTGCGCTACTTGGCCCCGTCTTGCCCATGTTGTTGCTATAGACGTCGTTTATCCCTGCG TCGATACCGATCCGGATCCGCCGGCTGAGGACTGGGCTACTGCTGTCGCCCTTCTTGGTAATCTGGTCCTCAGTA TAAACCGCTTCGAGCGCAAAAAGGATATCGCCCTCGCTATCCGCGCCTTTGCCGCCTTGCCCACCGCAGATCGAG ACGGTGTCCGCCTCGTCCTCGCCGGCGGCCACGACCGACGCGTATCGGAAAACGCAGAATATCACGCCGAACTAC AAACACTCTCCGACTCACTCCGTCTCTCACATCAAACCATCGACAGCCCAGACTCAGCCACGGCGCTAACATCCG CAACCTCCTCCTGCTCCTCCTCCTCTTCCCCTCCACAAGTCCTCTTCCTCCTCTCCATCCCCAACGGCCTCAAAG CCGCCCTCCTCGCCAGCGCCAACCTCGTCGTCTACACCCCGGCAAACGAACACTTCGGCATCGTCCCCCTCGAAG CCATGCTCGCCTCCCGTCCCGTCCTGGCCGCTGACTCGGGCGGGCCCGTCGAGACGGTCCGCGACGGTACCACCG GTTGGCTTCGCGACCCGGACGACGTCTCCGCTTGGTCGGCTGCCATGCGGGAAGCCCTCACCTTGTCGGATACGG ATCGCGCTGCTATGGGCGCCGAGGCTGCGGCCCGGGTCCGCAAGTCTTTTGGGAGGCATGTCATGGCCCAGCGGC TTGATCATCTACTCTCCCTGGCTGATGTTGTGGCCAAGATGAGGGCTCCCGCAAGGCTTGCTAGTCCAATTACTC TTGGTCTTTTGGTCTTGTTCTTTCTCTTTGGCACCACCTTGTCTGCTGCCTTTGTGCGTCTGTTTCGGCCTTGAA GGTTCTATTCTTCTTGTCGTCTTCTTGCCTTCACTTTGGACGACCGGCGTCGGGAGACGGAGCGTGGAAGTTAGA TGATTTCCCCATAGATCACGGCAAGCGGATAGCTGCGGTAAAGCCAATCTTCACCTTTGTCTATACACACATCTT CTACTCTCAGTCTCCGACATGTTTCGCAGGTGACCCAGAGACCAGAGACGATGTCATCTCCACCCCTCCCTCCAC GACCGGAGACCGCCTCTCACCACGGTCACGACTCCAAGTTGATAGTGAAATCCATCTCTCTACCGCGTCTTCTTC AAACCTCATTCAATTTCCCGCCCCCAAGGGCCAAACCCTCACCGCCCCCTCTCCTATCCCCAACTATGCTTCCAC TCACTCGTCCACCACACCCACGCATCAAATGGCCAGGCTCAACCAACCCCCCCGATCGCCATGA |