Protein ID | Ophio5|6408 |
Gene name | |
Location | scaffold_56:16778..18592 |
Strand | + |
Gene length (bp) | 1814 |
Transcript length (bp) | 1758 |
Coding sequence length (bp) | 1755 |
Protein length (aa) | 585 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF03155 | Alg6_Alg8 | ALG6, ALG8 glycosyltransferase family | 4.2E-78 | 64 | 291 |
PF03155 | Alg6_Alg8 | ALG6, ALG8 glycosyltransferase family | 1.9E-46 | 330 | 564 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O43053|ALG6_SCHPO | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg6 PE=3 SV=1 | 44 | 583 | 2.0E-127 |
sp|Q12001|ALG6_YEAST | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 | 16 | 567 | 5.0E-115 |
sp|Q802T2|ALG6_CHICK | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 | 48 | 556 | 1.0E-79 |
sp|Q9VKX7|ALG6_DROME | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 | 64 | 562 | 3.0E-79 |
sp|Q9Y672|ALG6_HUMAN | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 | 48 | 440 | 2.0E-77 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|O43053|ALG6_SCHPO | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg6 PE=3 SV=1 | 44 | 583 | 2.0E-127 |
sp|Q12001|ALG6_YEAST | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 | 16 | 567 | 5.0E-115 |
sp|Q802T2|ALG6_CHICK | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 | 48 | 556 | 1.0E-79 |
sp|Q9VKX7|ALG6_DROME | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 | 64 | 562 | 3.0E-79 |
sp|Q9Y672|ALG6_HUMAN | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 | 48 | 440 | 2.0E-77 |
sp|Q5NVS8|ALG6_PONAB | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 | 48 | 440 | 3.0E-76 |
sp|Q54QG6|ALG6_DICDI | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg6 PE=3 SV=1 | 46 | 484 | 3.0E-74 |
sp|Q3TAE8|ALG6_MOUSE | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg6 PE=2 SV=1 | 56 | 440 | 2.0E-73 |
sp|Q3T1L5|ALG6_RAT | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Rattus norvegicus GN=Alg6 PE=2 SV=1 | 48 | 440 | 8.0E-73 |
sp|Q9FF17|ALG6_ARATH | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At5g38460 PE=2 SV=1 | 12 | 491 | 7.0E-70 |
sp|Q09226|ALG6_CAEEL | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08B11.8 PE=3 SV=1 | 56 | 428 | 3.0E-65 |
sp|Q4IJT0|ALG8_GIBZE | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ALG8 PE=3 SV=1 | 83 | 468 | 6.0E-30 |
sp|Q9BVK2|ALG8_HUMAN | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG8 PE=1 SV=2 | 83 | 468 | 4.0E-28 |
sp|Q6BRE5|ALG8_DEBHA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=ALG8 PE=3 SV=1 | 83 | 468 | 2.0E-26 |
sp|Q5AJD2|ALG8_CANAL | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ALG8 PE=3 SV=1 | 83 | 484 | 1.0E-25 |
sp|Q5AWM9|ALG8_EMENI | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=alg8 PE=3 SV=1 | 83 | 503 | 1.0E-25 |
sp|Q2UB20|ALG8_ASPOR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=alg8 PE=3 SV=1 | 83 | 484 | 3.0E-25 |
sp|Q6P8H8|ALG8_MOUSE | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg8 PE=2 SV=2 | 83 | 468 | 1.0E-24 |
sp|Q2HA14|ALG8_CHAGB | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=ALG8 PE=3 SV=1 | 83 | 468 | 7.0E-24 |
sp|Q9W3V8|ALG8_DROME | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=xit PE=2 SV=1 | 83 | 476 | 2.0E-23 |
sp|Q0P5D9|ALG8_BOVIN | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Bos taurus GN=ALG8 PE=2 SV=1 | 83 | 442 | 2.0E-23 |
sp|Q759R3|ALG8_ASHGO | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ALG8 PE=3 SV=2 | 1 | 485 | 3.0E-23 |
sp|Q7RXP5|ALG8_NEUCR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-8 PE=3 SV=2 | 83 | 270 | 4.0E-23 |
sp|Q1DJR8|ALG8_COCIM | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 | 83 | 484 | 2.0E-22 |
sp|P40351|ALG8_YEAST | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG8 PE=1 SV=1 | 83 | 440 | 5.0E-22 |
sp|Q10479|ALG8_SCHPO | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg8 PE=3 SV=1 | 83 | 438 | 2.0E-21 |
sp|Q6CJR2|ALG8_KLULA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ALG8 PE=3 SV=1 | 83 | 439 | 3.0E-21 |
sp|Q6FKM3|ALG8_CANGA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=ALG8 PE=3 SV=1 | 83 | 447 | 7.0E-21 |
sp|P52887|ALG8_CAEEL | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08H9.3 PE=3 SV=3 | 83 | 494 | 1.0E-20 |
sp|O80505|ALG8_ARATH | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At2g44660 PE=2 SV=3 | 83 | 468 | 1.0E-18 |
sp|Q554E2|ALG8_DICDI | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 | 83 | 164 | 6.0E-09 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016758 | hexosyltransferase activity | Yes |
GO:0003824 | catalytic activity | No |
GO:0016740 | transferase activity | No |
GO:0003674 | molecular_function | No |
GO:0016757 | glycosyltransferase activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 49 | 0.5 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 52 | 74 | 22 |
2 | 152 | 174 | 22 |
3 | 181 | 203 | 22 |
4 | 207 | 229 | 22 |
5 | 236 | 258 | 22 |
6 | 273 | 295 | 22 |
7 | 405 | 424 | 19 |
8 | 449 | 468 | 19 |
9 | 473 | 495 | 22 |
10 | 508 | 530 | 22 |
11 | 543 | 565 | 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|6408 MATASPSPHKSRRKPRRSGVGSDGVRSLVRAPSFTLAAFLWPARCASSQWEVLPLVLMAVGLFRWAAGFWGYSGF QQPPLYGDYEAQRHWMELTTHLPVSQWYFHDLQWWGLDYPPLTAYHSWLMGKLGALINPAWFALFSSRGSDDPDL KIFMRASVIVSEYLIFIPAAVVFIRRFGRLNGVATWTSSIALVAFLMQPATILIDHVHFQYNSVMLGLVVASMNS MLAERYKSAAVFFVAALGFKQMALYYALTVFSYLLAKCLFPVNLTRLVAVSITTLLSLAVLLLPLVLGALYDSYR GIDLRPDLDARPPLPILPFLANYIDTRSGFYAVVEQLLQMVHRVFPFSRGLFEDKVANFWCAANVVFKLRDLPSS TLQKASLAATLLSILPPNAIVFFRPRKTTLPLAFAATAWGFFLFSYQVHEKSVLLPLMPMTLLLAGRHGLSGEVR AWVGFANLLGAWTLFPLLQRVSLGVPYAVLTLLWAYLLGLPPFSWDAIWDAPDGQSGLVRWATILIHGVFYGAMA LWHIIAASFHPPLDKPDLWVVANVGIGAVGFGICYLWCMWKLALESDLLPIGRAGKQKVN |
Coding | >Ophio5|6408 ATGGCCACAGCGAGCCCCTCGCCGCACAAGTCCCGGCGCAAGCCCCGACGGTCCGGCGTTGGCTCCGACGGGGTC CGGTCTCTGGTCCGCGCGCCCTCGTTCACGCTCGCTGCCTTCCTGTGGCCCGCACGCTGCGCCTCATCGCAGTGG GAGGTTCTGCCGCTCGTTCTCATGGCTGTCGGCTTGTTCCGCTGGGCGGCAGGCTTCTGGGGCTACTCGGGCTTT CAACAGCCTCCATTGTATGGCGACTACGAGGCTCAGCGCCACTGGATGGAGCTGACGACGCACCTGCCCGTTTCG CAATGGTATTTCCACGATCTGCAGTGGTGGGGGCTCGACTATCCGCCCCTTACGGCCTACCATAGCTGGCTGATG GGCAAGCTTGGCGCTCTCATCAACCCAGCTTGGTTTGCCCTCTTCTCTTCCCGTGGTTCCGACGACCCGGATTTG AAGATCTTCATGAGGGCATCTGTCATCGTTTCTGAGTATCTCATCTTCATCCCTGCTGCTGTTGTCTTCATCCGT CGCTTTGGCCGACTCAATGGTGTCGCCACTTGGACGAGCTCCATCGCCCTTGTCGCCTTTTTGATGCAGCCGGCT ACCATACTCATCGACCACGTTCACTTCCAGTACAACTCCGTCATGCTCGGCCTGGTCGTCGCTAGCATGAACAGC ATGCTGGCCGAGAGGTACAAGAGCGCCGCCGTCTTCTTCGTCGCCGCCCTCGGCTTCAAGCAGATGGCGCTCTAC TACGCCCTGACCGTCTTCTCCTATCTTCTGGCCAAGTGTCTCTTCCCAGTCAATCTCACGAGATTGGTTGCCGTC TCCATCACCACCCTGTTGTCTCTGGCCGTCTTGCTTCTTCCTCTCGTCCTCGGAGCCTTGTACGACAGCTACCGC GGCATCGACTTGAGGCCGGACTTGGATGCCCGCCCTCCACTGCCGATCCTCCCCTTCCTTGCCAATTACATTGAT ACCCGGTCCGGCTTCTACGCCGTCGTCGAGCAGCTTCTTCAGATGGTCCATCGCGTCTTTCCCTTTTCGAGAGGC CTGTTTGAGGACAAGGTGGCCAACTTTTGGTGCGCGGCCAATGTCGTCTTCAAGCTCCGCGACCTCCCCTCCTCA ACGCTGCAAAAGGCATCGCTGGCAGCAACACTACTCTCCATCCTGCCGCCCAACGCCATCGTGTTTTTCCGGCCG CGCAAAACGACGCTGCCCCTGGCCTTTGCCGCGACTGCGTGGGGATTTTTCCTCTTCAGCTACCAGGTTCACGAG AAGAGCGTCTTGCTGCCTTTGATGCCCATGACGCTTCTACTCGCTGGGAGGCACGGCCTGAGCGGAGAGGTTCGT GCCTGGGTGGGATTCGCGAACCTGCTGGGAGCGTGGACCTTGTTTCCGTTGCTGCAGCGCGTCAGCTTGGGCGTG CCCTACGCCGTCTTGACGCTTCTTTGGGCCTACCTCCTTGGACTCCCTCCCTTCTCGTGGGATGCTATTTGGGAC GCACCGGACGGACAATCTGGGTTGGTCCGGTGGGCGACCATCTTGATACACGGCGTCTTCTATGGTGCCATGGCG CTATGGCACATCATTGCCGCTTCCTTTCACCCGCCGCTCGACAAGCCAGATCTGTGGGTCGTGGCCAATGTCGGT ATCGGGGCGGTGGGCTTCGGCATTTGCTACCTGTGGTGTATGTGGAAGTTGGCATTGGAGAGCGATCTGTTACCA ATTGGTCGGGCGGGGAAGCAAAAGGTGAAT |
Transcript | >Ophio5|6408 ATGGCCACAGCGAGCCCCTCGCCGCACAAGTCCCGGCGCAAGCCCCGACGGTCCGGCGTTGGCTCCGACGGGGTC CGGTCTCTGGTCCGCGCGCCCTCGTTCACGCTCGCTGCCTTCCTGTGGCCCGCACGCTGCGCCTCATCGCAGTGG GAGGTTCTGCCGCTCGTTCTCATGGCTGTCGGCTTGTTCCGCTGGGCGGCAGGCTTCTGGGGCTACTCGGGCTTT CAACAGCCTCCATTGTATGGCGACTACGAGGCTCAGCGCCACTGGATGGAGCTGACGACGCACCTGCCCGTTTCG CAATGGTATTTCCACGATCTGCAGTGGTGGGGGCTCGACTATCCGCCCCTTACGGCCTACCATAGCTGGCTGATG GGCAAGCTTGGCGCTCTCATCAACCCAGCTTGGTTTGCCCTCTTCTCTTCCCGTGGTTCCGACGACCCGGATTTG AAGATCTTCATGAGGGCATCTGTCATCGTTTCTGAGTATCTCATCTTCATCCCTGCTGCTGTTGTCTTCATCCGT CGCTTTGGCCGACTCAATGGTGTCGCCACTTGGACGAGCTCCATCGCCCTTGTCGCCTTTTTGATGCAGCCGGCT ACCATACTCATCGACCACGTTCACTTCCAGTACAACTCCGTCATGCTCGGCCTGGTCGTCGCTAGCATGAACAGC ATGCTGGCCGAGAGGTACAAGAGCGCCGCCGTCTTCTTCGTCGCCGCCCTCGGCTTCAAGCAGATGGCGCTCTAC TACGCCCTGACCGTCTTCTCCTATCTTCTGGCCAAGTGTCTCTTCCCAGTCAATCTCACGAGATTGGTTGCCGTC TCCATCACCACCCTGTTGTCTCTGGCCGTCTTGCTTCTTCCTCTCGTCCTCGGAGCCTTGTACGACAGCTACCGC GGCATCGACTTGAGGCCGGACTTGGATGCCCGCCCTCCACTGCCGATCCTCCCCTTCCTTGCCAATTACATTGAT ACCCGGTCCGGCTTCTACGCCGTCGTCGAGCAGCTTCTTCAGATGGTCCATCGCGTCTTTCCCTTTTCGAGAGGC CTGTTTGAGGACAAGGTGGCCAACTTTTGGTGCGCGGCCAATGTCGTCTTCAAGCTCCGCGACCTCCCCTCCTCA ACGCTGCAAAAGGCATCGCTGGCAGCAACACTACTCTCCATCCTGCCGCCCAACGCCATCGTGTTTTTCCGGCCG CGCAAAACGACGCTGCCCCTGGCCTTTGCCGCGACTGCGTGGGGATTTTTCCTCTTCAGCTACCAGGTTCACGAG AAGAGCGTCTTGCTGCCTTTGATGCCCATGACGCTTCTACTCGCTGGGAGGCACGGCCTGAGCGGAGAGGTTCGT GCCTGGGTGGGATTCGCGAACCTGCTGGGAGCGTGGACCTTGTTTCCGTTGCTGCAGCGCGTCAGCTTGGGCGTG CCCTACGCCGTCTTGACGCTTCTTTGGGCCTACCTCCTTGGACTCCCTCCCTTCTCGTGGGATGCTATTTGGGAC GCACCGGACGGACAATCTGGGTTGGTCCGGTGGGCGACCATCTTGATACACGGCGTCTTCTATGGTGCCATGGCG CTATGGCACATCATTGCCGCTTCCTTTCACCCGCCGCTCGACAAGCCAGATCTGTGGGTCGTGGCCAATGTCGGT ATCGGGGCGGTGGGCTTCGGCATTTGCTACCTGTGGTGTATGTGGAAGTTGGCATTGGAGAGCGATCTGTTACCA ATTGGTCGGGCGGGGAAGCAAAAGGTGAATTGA |
Gene | >Ophio5|6408 ATGGCCACAGCGAGCCCCTCGCCGCACAAGTCCCGGCGCAAGCCCCGACGGTCCGGCGTTGGCTCCGACGGGGTC CGGTCTCTGGTCCGCGCGCCCTCGTTCACGCTCGCTGCCTTCCTGTGGCCCGCACGCTGCGCCTCATCGCAGTGG GAGGTTCTGCCGCTCGTTCTCATGGCTGTCGGCTTGTTCCGCTGGGCGGCAGGCTTCTGGGGCTACTCGGGTAAA GAAAATGTCCCTCATCCGCTCCCGGGAAAAGCCAAGCTGACGCGGCCATAGGCTTTCAACAGCCTCCATTGTATG GCGACTACGAGGCTCAGCGCCACTGGATGGAGCTGACGACGCACCTGCCCGTTTCGCAATGGTATTTCCACGATC TGCAGTGGTGGGGGCTCGACTATCCGCCCCTTACGGCCTACCATAGCTGGCTGATGGGCAAGCTTGGCGCTCTCA TCAACCCAGCTTGGTTTGCCCTCTTCTCTTCCCGTGGTTCCGACGACCCGGATTTGAAGATCTTCATGAGGGCAT CTGTCATCGTTTCTGAGTATCTCATCTTCATCCCTGCTGCTGTTGTCTTCATCCGTCGCTTTGGCCGACTCAATG GTGTCGCCACTTGGACGAGCTCCATCGCCCTTGTCGCCTTTTTGATGCAGCCGGCTACCATACTCATCGACCACG TTCACTTCCAGTACAACTCCGTCATGCTCGGCCTGGTCGTCGCTAGCATGAACAGCATGCTGGCCGAGAGGTACA AGAGCGCCGCCGTCTTCTTCGTCGCCGCCCTCGGCTTCAAGCAGATGGCGCTCTACTACGCCCTGACCGTCTTCT CCTATCTTCTGGCCAAGTGTCTCTTCCCAGTCAATCTCACGAGATTGGTTGCCGTCTCCATCACCACCCTGTTGT CTCTGGCCGTCTTGCTTCTTCCTCTCGTCCTCGGAGCCTTGTACGACAGCTACCGCGGCATCGACTTGAGGCCGG ACTTGGATGCCCGCCCTCCACTGCCGATCCTCCCCTTCCTTGCCAATTACATTGATACCCGGTCCGGCTTCTACG CCGTCGTCGAGCAGCTTCTTCAGATGGTCCATCGCGTCTTTCCCTTTTCGAGAGGCCTGTTTGAGGACAAGGTGG CCAACTTTTGGTGCGCGGCCAATGTCGTCTTCAAGCTCCGCGACCTCCCCTCCTCAACGCTGCAAAAGGCATCGC TGGCAGCAACACTACTCTCCATCCTGCCGCCCAACGCCATCGTGTTTTTCCGGCCGCGCAAAACGACGCTGCCCC TGGCCTTTGCCGCGACTGCGTGGGGATTTTTCCTCTTCAGCTACCAGGTTCACGAGAAGAGCGTCTTGCTGCCTT TGATGCCCATGACGCTTCTACTCGCTGGGAGGCACGGCCTGAGCGGAGAGGTTCGTGCCTGGGTGGGATTCGCGA ACCTGCTGGGAGCGTGGACCTTGTTTCCGTTGCTGCAGCGCGTCAGCTTGGGCGTGCCCTACGCCGTCTTGACGC TTCTTTGGGCCTACCTCCTTGGACTCCCTCCCTTCTCGTGGGATGCTATTTGGGACGCACCGGACGGACAATCTG GGTTGGTCCGGTGGGCGACCATCTTGATACACGGCGTCTTCTATGGTGCCATGGCGCTATGGCACATCATTGCCG CTTCCTTTCACCCGCCGCTCGACAAGCCAGATCTGTGGGTCGTGGCCAATGTCGGTATCGGGGCGGTGGGCTTCG GCATTTGCTACCTGTGGTGTATGTGGAAGTTGGCATTGGAGAGCGATCTGTTACCAATTGGTCGGGCGGGGAAGC AAAAGGTGAATTGA |