Protein ID | OphauG2|2511 |
Gene name | |
Location | Contig_1916:38..1719 |
Strand | + |
Gene length (bp) | 1681 |
Transcript length (bp) | 1377 |
Coding sequence length (bp) | 1377 |
Protein length (aa) | 459 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00534 | Glycos_transf_1 | Glycosyl transferases group 1 | 1.7E-33 | 208 | 395 |
PF13439 | Glyco_transf_4 | Glycosyltransferase Family 4 | 3.1E-17 | 16 | 199 |
PF13692 | Glyco_trans_1_4 | Glycosyl transferases group 1 | 4.3E-14 | 217 | 382 |
PF13579 | Glyco_trans_4_4 | Glycosyl transferase 4-like domain | 5.6E-10 | 17 | 177 |
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 | 5 | 419 | 7.0E-170 |
sp|Q96WW6|ALG2_SCHPO | Alpha-1,3/1,6-mannosyltransferase alg2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg2 PE=3 SV=2 | 4 | 448 | 2.0E-112 |
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 | 1 | 417 | 1.0E-109 |
sp|P43636|ALG2_YEAST | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG2 PE=1 SV=2 | 5 | 434 | 3.0E-109 |
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 | 5 | 427 | 3.0E-109 |
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 | 5 | 419 | 7.0E-170 |
sp|Q96WW6|ALG2_SCHPO | Alpha-1,3/1,6-mannosyltransferase alg2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg2 PE=3 SV=2 | 4 | 448 | 2.0E-112 |
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 | 1 | 417 | 1.0E-109 |
sp|P43636|ALG2_YEAST | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG2 PE=1 SV=2 | 5 | 434 | 3.0E-109 |
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 | 5 | 427 | 3.0E-109 |
sp|O94738|ALG2_RHIPU | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Rhizomucor pusillus GN=ALG2 PE=1 SV=1 | 2 | 454 | 2.0E-103 |
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 | 7 | 419 | 7.0E-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 | 2 | 417 | 2.0E-102 |
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 | 5 | 453 | 2.0E-102 |
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 | 1 | 412 | 2.0E-94 |
sp|Q7KWM5|ALG2_DICDI | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Dictyostelium discoideum GN=alg2 PE=3 SV=1 | 2 | 419 | 4.0E-89 |
sp|Q9H553|ALG2_HUMAN | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Homo sapiens GN=ALG2 PE=1 SV=1 | 6 | 420 | 2.0E-83 |
sp|Q9DBE8|ALG2_MOUSE | Alpha-1,3/1,6-mannosyltransferase ALG2 OS=Mus musculus GN=Alg2 PE=1 SV=2 | 6 | 420 | 1.0E-82 |
sp|P53993|YMP8_CAEEL | Uncharacterized glycosyltransferase B0361.8 OS=Caenorhabditis elegans GN=B0361.8 PE=3 SV=3 | 3 | 416 | 2.0E-15 |
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 | 419 | 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 | 9 | 412 | 1.0E-12 |
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 | 145 | 424 | 3.0E-12 |
sp|O74878|ALG11_SCHPO | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg11 PE=3 SV=1 | 5 | 374 | 6.0E-12 |
sp|D0L476|MSHA_GORB4 | D-inositol 3-phosphate glycosyltransferase OS=Gordonia bronchialis (strain ATCC 25592 / DSM 43247 / JCM 3198 / NCTC 10667) GN=mshA PE=3 SV=1 | 197 | 428 | 4.0E-10 |
sp|Q3TZM9|ALG11_MOUSE | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Mus musculus GN=Alg11 PE=2 SV=1 | 2 | 416 | 5.0E-10 |
sp|Q8X092|ALG11_NEUCR | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-11 PE=3 SV=1 | 7 | 352 | 6.0E-09 |
sp|Q59002|Y1607_METJA | Uncharacterized glycosyltransferase MJ1607 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ1607 PE=3 SV=1 | 217 | 417 | 8.0E-09 |
sp|Q2TAA5|ALG11_HUMAN | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Homo sapiens GN=ALG11 PE=1 SV=2 | 163 | 417 | 1.0E-08 |
sp|Q5R7Z6|ALG11_PONAB | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Pongo abelii GN=ALG11 PE=2 SV=2 | 163 | 417 | 3.0E-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 | 3 | 412 | 3.0E-08 |
sp|Q8NTA6|MSHA_CORGL | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / JCM 1318 / LMG 3730 / NCIMB 10025) GN=mshA PE=1 SV=1 | 115 | 401 | 4.0E-08 |
sp|A4QB40|MSHA_CORGB | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium glutamicum (strain R) GN=mshA PE=3 SV=1 | 115 | 401 | 4.0E-08 |
sp|A8LZG1|MSHA_SALAI | D-inositol 3-phosphate glycosyltransferase OS=Salinispora arenicola (strain CNS-205) GN=mshA PE=3 SV=1 | 209 | 423 | 4.0E-08 |
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 | 209 | 423 | 6.0E-08 |
sp|Q9XEE9|ALG11_ARATH | GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase OS=Arabidopsis thaliana GN=ALG11 PE=1 SV=2 | 2 | 417 | 1.0E-07 |
sp|A1SP12|MSHA_NOCSJ | D-inositol 3-phosphate glycosyltransferase OS=Nocardioides sp. (strain BAA-499 / JS614) GN=mshA PE=3 SV=1 | 185 | 418 | 2.0E-07 |
sp|P26470|WAAK_SALTY | Lipopolysaccharide 1,2-N-acetylglucosaminetransferase OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=waaK PE=3 SV=1 | 166 | 417 | 5.0E-07 |
sp|Q73SU4|MSHA_MYCPA | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium paratuberculosis (strain ATCC BAA-968 / K-10) GN=mshA PE=3 SV=1 | 192 | 381 | 9.0E-07 |
sp|Q8FSH1|MSHA_COREF | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium efficiens (strain DSM 44549 / YS-314 / AJ 12310 / JCM 11189 / NBRC 100395) GN=mshA PE=3 SV=1 | 115 | 418 | 1.0E-06 |
sp|B8HCF8|MSHA_ARTCA | D-inositol 3-phosphate glycosyltransferase OS=Arthrobacter chlorophenolicus (strain ATCC 700700 / DSM 12829 / JCM 12360 / NCIMB 13794 / A6) GN=mshA PE=3 SV=1 | 293 | 429 | 1.0E-06 |
sp|A0QQZ8|MSHA_MYCS2 | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=mshA PE=1 SV=1 | 185 | 416 | 2.0E-06 |
sp|A6W6D9|MSHA_KINRD | D-inositol 3-phosphate glycosyltransferase OS=Kineococcus radiotolerans (strain ATCC BAA-149 / DSM 14245 / SRS30216) GN=mshA PE=3 SV=1 | 185 | 351 | 2.0E-06 |
sp|C8XA09|MSHA_NAKMY | D-inositol 3-phosphate glycosyltransferase OS=Nakamurella multipartita (strain ATCC 700099 / DSM 44233 / JCM 9543 / Y-104) GN=mshA PE=3 SV=1 | 192 | 417 | 4.0E-06 |
sp|A0QLK5|MSHA_MYCA1 | D-inositol 3-phosphate glycosyltransferase OS=Mycobacterium avium (strain 104) GN=mshA PE=3 SV=1 | 192 | 381 | 5.0E-06 |
sp|C7R101|MSHA_JONDD | D-inositol 3-phosphate glycosyltransferase OS=Jonesia denitrificans (strain ATCC 14870 / DSM 20603 / CIP 55134) GN=mshA PE=3 SV=1 | 190 | 418 | 6.0E-06 |
sp|B1VEI4|MSHA_CORU7 | D-inositol 3-phosphate glycosyltransferase OS=Corynebacterium urealyticum (strain ATCC 43042 / DSM 7109) GN=mshA PE=3 SV=1 | 313 | 419 | 7.0E-06 |
sp|Q82G92|MSHA_STRAW | D-inositol 3-phosphate glycosyltransferase OS=Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) GN=mshA PE=3 SV=1 | 309 | 425 | 8.0E-06 |
sp|D1A4Q3|MSHA_THECD | D-inositol 3-phosphate glycosyltransferase OS=Thermomonospora curvata (strain ATCC 19995 / DSM 43183 / JCM 3096 / NCIMB 10081) GN=mshA PE=3 SV=1 | 209 | 430 | 8.0E-06 |
sp|B7F7B9|SPSA2_ORYSJ | Probable sucrose-phosphate synthase 2 OS=Oryza sativa subsp. japonica GN=SPS2 PE=2 SV=2 | 195 | 381 | 9.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016757 | glycosyltransferase activity | Yes |
GO:0003674 | molecular_function | No |
GO:0003824 | catalytic activity | No |
GO:0016740 | transferase activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 22 | 0.45 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 434 | 456 | 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 | >OphauG2|2511 MAKPQTIVFFHPDLGIGGAERLVVDAAVGLQRLGHRVVIYTNHCDANHCFDECRNGTLQVRVAGNSIFPPSINSR LSILCALARHVHLVLSTTAQLAALAPDAFFVDQLSGGLPLLRLLYPRVPILFYCHYPDLLLVRGRASWLKRAYRL PFDALEQWSMRFAHAVAVNSQFTKSVVQATWPRLAQSSPLIVIYPCVDTHPPSPSKASRLPFNKKAKMLLSINRF EPKKDIGLAIKAFAALPPAKRRHARLILAGGYDSRVAENVSYHAHLQSLATALHLSHQTMHPNDSYVDAALDADV IFLLSISNPTKQALLAAASCVIYTPANEHFGIVPLEAMLANCPVLAADSGGPVETVTPGRSGWLCDPANVDAWTQ VLARVLDMPHNDLRKMGQDGATRVKSQFSRDQMANTLDKVMRRLVHSHMGHKPPVRLGLVPLLLAALMVLAAFAL ALLCCFVS* |
Coding | >OphauG2|2511 ATGGCAAAACCCCAAACCATCGTCTTTTTCCACCCCGACCTCGGCATTGGCGGCGCCGAGCGCCTCGTCGTCGAC GCCGCCGTCGGCCTGCAGCGCCTGGGCCATCGCGTCGTCATCTACACCAACCACTGCGATGCTAACCACTGCTTT GACGAATGCCGCAACGGAACCCTCCAGGTCCGCGTCGCCGGCAATTCCATCTTTCCCCCCTCCATCAACTCGCGC CTCTCCATTCTCTGCGCTCTCGCTCGCCATGTCCATCTCGTCCTCTCCACCACGGCCCAACTCGCCGCTCTCGCC CCCGATGCCTTCTTTGTCGACCAGTTGTCCGGCGGCCTCCCTCTTCTCCGCCTCCTCTACCCCAGAGTCCCCATT CTCTTCTACTGCCATTATCCCGACTTGCTCCTTGTCAGGGGCCGCGCCTCATGGCTCAAGCGCGCCTACCGCCTA CCCTTTGATGCCCTCGAGCAATGGAGCATGCGCTTTGCTCACGCCGTCGCCGTCAACTCGCAATTCACAAAGTCT GTCGTACAAGCCACCTGGCCACGCCTTGCCCAATCCTCACCCCTCATCGTCATCTATCCATGCGTCGACACCCAC CCCCCCTCCCCCTCCAAAGCCTCCCGCCTGCCCTTCAACAAAAAGGCCAAAATGCTGCTGAGCATCAATCGCTTC GAGCCCAAAAAGGACATTGGCCTTGCCATCAAGGCCTTTGCTGCCCTCCCCCCCGCCAAGCGCCGCCACGCTCGT CTCATCCTCGCAGGCGGTTACGACTCGAGAGTCGCAGAAAACGTCTCCTACCATGCTCACCTCCAATCTCTCGCC ACCGCCCTCCACCTCTCTCATCAAACCATGCATCCCAACGACTCCTACGTCGATGCCGCCCTCGATGCCGACGTC ATTTTCCTCCTCTCAATATCAAACCCTACAAAGCAAGCCCTTCTCGCCGCCGCCAGCTGCGTCATCTACACCCCC GCCAACGAACACTTTGGCATCGTCCCCCTCGAAGCCATGCTCGCAAACTGTCCCGTCCTTGCTGCAGACTCTGGC GGCCCCGTAGAAACTGTCACTCCCGGTCGTTCCGGCTGGCTGTGCGACCCTGCCAATGTCGACGCCTGGACACAA GTCTTGGCCCGCGTCCTCGACATGCCACACAATGACCTGCGCAAAATGGGCCAAGATGGCGCCACTCGCGTCAAG TCCCAATTTAGCCGTGATCAAATGGCCAACACTCTCGACAAGGTTATGCGCCGGCTTGTCCACTCGCACATGGGC CATAAACCGCCTGTCCGACTTGGACTCGTCCCTTTGTTGCTTGCTGCCCTCATGGTACTGGCAGCATTTGCCTTG GCTCTCCTGTGCTGCTTCGTCTCTTAA |
Transcript | >OphauG2|2511 ATGGCAAAACCCCAAACCATCGTCTTTTTCCACCCCGACCTCGGCATTGGCGGCGCCGAGCGCCTCGTCGTCGAC GCCGCCGTCGGCCTGCAGCGCCTGGGCCATCGCGTCGTCATCTACACCAACCACTGCGATGCTAACCACTGCTTT GACGAATGCCGCAACGGAACCCTCCAGGTCCGCGTCGCCGGCAATTCCATCTTTCCCCCCTCCATCAACTCGCGC CTCTCCATTCTCTGCGCTCTCGCTCGCCATGTCCATCTCGTCCTCTCCACCACGGCCCAACTCGCCGCTCTCGCC CCCGATGCCTTCTTTGTCGACCAGTTGTCCGGCGGCCTCCCTCTTCTCCGCCTCCTCTACCCCAGAGTCCCCATT CTCTTCTACTGCCATTATCCCGACTTGCTCCTTGTCAGGGGCCGCGCCTCATGGCTCAAGCGCGCCTACCGCCTA CCCTTTGATGCCCTCGAGCAATGGAGCATGCGCTTTGCTCACGCCGTCGCCGTCAACTCGCAATTCACAAAGTCT GTCGTACAAGCCACCTGGCCACGCCTTGCCCAATCCTCACCCCTCATCGTCATCTATCCATGCGTCGACACCCAC CCCCCCTCCCCCTCCAAAGCCTCCCGCCTGCCCTTCAACAAAAAGGCCAAAATGCTGCTGAGCATCAATCGCTTC GAGCCCAAAAAGGACATTGGCCTTGCCATCAAGGCCTTTGCTGCCCTCCCCCCCGCCAAGCGCCGCCACGCTCGT CTCATCCTCGCAGGCGGTTACGACTCGAGAGTCGCAGAAAACGTCTCCTACCATGCTCACCTCCAATCTCTCGCC ACCGCCCTCCACCTCTCTCATCAAACCATGCATCCCAACGACTCCTACGTCGATGCCGCCCTCGATGCCGACGTC ATTTTCCTCCTCTCAATATCAAACCCTACAAAGCAAGCCCTTCTCGCCGCCGCCAGCTGCGTCATCTACACCCCC GCCAACGAACACTTTGGCATCGTCCCCCTCGAAGCCATGCTCGCAAACTGTCCCGTCCTTGCTGCAGACTCTGGC GGCCCCGTAGAAACTGTCACTCCCGGTCGTTCCGGCTGGCTGTGCGACCCTGCCAATGTCGACGCCTGGACACAA GTCTTGGCCCGCGTCCTCGACATGCCACACAATGACCTGCGCAAAATGGGCCAAGATGGCGCCACTCGCGTCAAG TCCCAATTTAGCCGTGATCAAATGGCCAACACTCTCGACAAGGTTATGCGCCGGCTTGTCCACTCGCACATGGGC CATAAACCGCCTGTCCGACTTGGACTCGTCCCTTTGTTGCTTGCTGCCCTCATGGTACTGGCAGCATTTGCCTTG GCTCTCCTGTGCTGCTTCGTCTCTTAA |
Gene | >OphauG2|2511 ATGGCAAAACCCCAAACCATCGTCTTTTTCCACCCCGACCTCGGCATTGGCGGCGCCGAGCGCCTCGTCGTCGAC GCCGCCGTCGGCCTGCAGCGCCTGGGCCATCGCGTCGTCATCTACACCAACCACTGCGATGCTAACCACTGCTTT GACGAATGCCGCAACGGTCTGTCCTTGAATGCAGCAGAGCGACCAAGCAATCCCCATTAATCAAGACCACAAAAA AAAAAAAANNTACAGAGCACACCCTACAGATCCCCGATAGCTGGCGCTCCGTCCGTAGTTGGCTCGGCACCACGT CTTTTCTTCCTCGGTTCCAAATTTCAATTGACAGTCATGATTTGCCCGTGCAGACCACAAAAAAAAAAAAAAACC CCCAAAAAACAAAAATTAACAAGCCTCTCTCCCTCGCAGGAACCCTCCAGGTCCGCGTCGCCGGCAATTCCATCT TTCCCCCCTCCATCAACTCGCGCCTCTCCATTCTCTGCGCTCTCGCTCGCCATGTCCATCTCGTCCTCTCCACCA CGGCCCAACTCGCCGCTCTCGCCCCCGATGCCTTCTTTGTCGACCAGTTGTCCGGCGGCCTCCCTCTTCTCCGCC TCCTCTACCCCAGAGTCCCCATTCTCTTCTACTGCCATTATCCCGACTTGCTCCTTGTCAGGGGCCGCGCCTCAT GGCTCAAGCGCGCCTACCGCCTACCCTTTGATGCCCTCGAGCAATGGAGCATGCGCTTTGCTCACGCCGTCGCCG TCAACTCGCAATTCACAAAGTCTGTCGTACAAGCCACCTGGCCACGCCTTGCCCAATCCTCACCCCTCATCGTCA TCTATCCATGCGTCGACACCCACCCCCCCTCCCCCTCCAAAGCCTCCCGCCTGCCCTTCAACAAAAAGGCCAAAA TGCTGCTGAGCATCAATCGCTTCGAGCCCAAAAAGGACATTGGCCTTGCCATCAAGGCCTTTGCTGCCCTCCCCC CCGCCAAGCGCCGCCACGCTCGTCTCATCCTCGCAGGTTCACTTGTCCCCTCTATTGGAATCCCTCCTCCTCTAA TCTAATGCCATTCCTAGGCGGTTACGACTCGAGAGTCGCAGAAAACGTCTCCTACCATGCTCACCTCCAATCTCT CGCCACCGCCCTCCACCTCTCTCATCAAACCATGCATCCCAACGACTCCTACGTCGATGCCGCCCTCGATGCCGA CGTCATTTTCCTCCTCTCAATATCAAACCCTACAAAGCAAGCCCTTCTCGCCGCCGCCAGCTGCGTCATCTACAC CCCCGCCAACGAACACTTTGGCATCGTCCCCCTCGAAGCCATGCTCGCAAACTGTCCCGTCCTTGCTGCAGACTC TGGCGGCCCCGTAGAAACTGTCACTCCCGGTCGTTCCGGCTGGCTGTGCGACCCTGCCAATGTCGACGCCTGGAC ACAAGTCTTGGCCCGCGTCCTCGACATGCCACACAATGACCTGCGCAAAATGGGCCAAGATGGCGCCACTCGCGT CAAGTCCCAATTTAGCCGTGATCAAATGGCCAACACTCTCGACAAGGTTATGCGCCGGCTTGTCCACTCGCACAT GGGCCATAAACCGCCTGTCCGACTTGGACTCGTCCCTTTGTTGCTTGCTGCCCTCATGGTACTGGCAGCATTTGC CTTGGCTCTCCTGTGCTGCTTCGTCTCTTAA |