Protein ID | Hirsu2|7574 |
Gene name | |
Location | Contig_448:10958..13950 |
Strand | + |
Gene length (bp) | 2992 |
Transcript length (bp) | 2436 |
Coding sequence length (bp) | 2436 |
Protein length (aa) | 812 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF04082 | Fungal_trans | Fungal specific transcription factor domain | 2.8E-12 | 303 | 572 |
PF00172 | Zn_clus | Fungal Zn(2)-Cys(6) binuclear cluster domain | 9.7E-08 | 21 | 58 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1DIC0|XLNR_NEOFI | Xylanolytic transcriptional activator xlnR OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-116 |
sp|A2R5W7|XLNR_ASPNC | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-115 |
sp|B0XUL1|XLNR_ASPFC | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=xlnR PE=3 SV=1 | 16 | 811 | 9.0E-115 |
sp|O42804|XLNR_ASPNG | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger GN=xlnR PE=1 SV=2 | 16 | 811 | 2.0E-114 |
sp|Q4WZV6|XLNR_ASPFU | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=xlnR PE=3 SV=1 | 16 | 811 | 8.0E-114 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1DIC0|XLNR_NEOFI | Xylanolytic transcriptional activator xlnR OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-116 |
sp|A2R5W7|XLNR_ASPNC | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-115 |
sp|B0XUL1|XLNR_ASPFC | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=xlnR PE=3 SV=1 | 16 | 811 | 9.0E-115 |
sp|O42804|XLNR_ASPNG | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger GN=xlnR PE=1 SV=2 | 16 | 811 | 2.0E-114 |
sp|Q4WZV6|XLNR_ASPFU | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=xlnR PE=3 SV=1 | 16 | 811 | 8.0E-114 |
sp|Q96WP8|XLNR_ASPKA | Xylanolytic transcriptional activator xlnR OS=Aspergillus kawachii GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-113 |
sp|Q5AVS0|XLNR_EMENI | Xylanolytic transcriptional activator xlnR OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=xlnR PE=2 SV=2 | 16 | 811 | 2.0E-113 |
sp|A1C7P9|XLNR_ASPCL | Xylanolytic transcriptional activator xlnR OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=xlnR PE=3 SV=2 | 16 | 811 | 2.0E-109 |
sp|Q2UD93|XLNR_ASPOR | Xylanolytic transcriptional activator xlnR OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=xlnR PE=1 SV=2 | 255 | 811 | 9.0E-99 |
sp|B8N6M6|XLNR_ASPFN | Xylanolytic transcriptional activator xlnR OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=xlnR PE=3 SV=1 | 255 | 811 | 9.0E-99 |
sp|G4MZJ4|XLNR_MAGO7 | Xylanolytic transcriptional activator xlnR homolog OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=xlr1 PE=3 SV=1 | 255 | 811 | 5.0E-98 |
sp|Q0CV52|XLNR_ASPTN | Xylanolytic transcriptional activator xlnR OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=xlnR PE=3 SV=2 | 255 | 811 | 2.0E-97 |
sp|A2QJX5|ARAR_ASPNC | Arabinanolytic transcriptional activator araR OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=araR PE=3 SV=1 | 17 | 811 | 1.0E-81 |
sp|Q5BGE2|ARAR_EMENI | Arabinolytic transcriptional activator araR OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=AN0388 PE=3 SV=1 | 17 | 811 | 1.0E-80 |
sp|G4MZJ4|XLNR_MAGO7 | Xylanolytic transcriptional activator xlnR homolog OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=xlr1 PE=3 SV=1 | 16 | 67 | 2.0E-10 |
sp|P38157|MAL33_YEAST | Maltose fermentation regulatory protein MAL33 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MAL33 PE=3 SV=1 | 19 | 66 | 4.0E-07 |
sp|P40467|ASG1_YEAST | Activator of stress genes 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ASG1 PE=1 SV=1 | 4 | 57 | 5.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0006351 | transcription, DNA-templated | Yes |
GO:0008270 | zinc ion binding | Yes |
GO:0003677 | DNA binding | Yes |
GO:0006355 | regulation of transcription, DNA-templated | Yes |
GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific | Yes |
GO:0097159 | organic cyclic compound binding | No |
GO:0034654 | nucleobase-containing compound biosynthetic process | No |
GO:0009987 | cellular process | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0140110 | transcription regulator activity | No |
GO:0006139 | nucleobase-containing compound metabolic process | No |
GO:0051252 | regulation of RNA metabolic process | No |
GO:1903506 | regulation of nucleic acid-templated transcription | No |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
GO:0032774 | RNA biosynthetic process | No |
GO:0031323 | regulation of cellular metabolic process | No |
GO:0003676 | nucleic acid binding | No |
GO:0008152 | metabolic process | No |
GO:0034641 | cellular nitrogen compound metabolic process | No |
GO:0050794 | regulation of cellular process | No |
GO:2001141 | regulation of RNA biosynthetic process | No |
GO:0009059 | macromolecule biosynthetic process | No |
GO:0071704 | organic substance metabolic process | No |
GO:0044271 | cellular nitrogen compound biosynthetic process | No |
GO:0005488 | binding | No |
GO:0044249 | cellular biosynthetic process | No |
GO:0009058 | biosynthetic process | No |
GO:0010468 | regulation of gene expression | No |
GO:0008150 | biological_process | No |
GO:0046483 | heterocycle metabolic process | No |
GO:0009889 | regulation of biosynthetic process | No |
GO:0046872 | metal ion binding | No |
GO:0090304 | nucleic acid metabolic process | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0044237 | cellular metabolic process | No |
GO:0080090 | regulation of primary metabolic process | No |
GO:0046914 | transition metal ion binding | No |
GO:1901576 | organic substance biosynthetic process | No |
GO:0006725 | cellular aromatic compound metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0019438 | aromatic compound biosynthetic process | No |
GO:0018130 | heterocycle biosynthetic process | No |
GO:0060255 | regulation of macromolecule metabolic process | No |
GO:0097659 | nucleic acid-templated transcription | No |
GO:0051171 | regulation of nitrogen compound metabolic process | No |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0043167 | ion binding | No |
GO:0044238 | primary metabolic process | No |
GO:0065007 | biological regulation | No |
GO:0043169 | cation binding | No |
GO:0016070 | RNA metabolic process | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:1901362 | organic cyclic compound biosynthetic process | No |
GO:0031326 | regulation of cellular biosynthetic process | No |
GO:0003700 | DNA-binding transcription factor activity | No |
GO:0019222 | regulation of metabolic process | No |
GO:0050789 | regulation of biological process | No |
GO:0010556 | regulation of macromolecule biosynthetic process | No |
Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
---|---|---|---|---|---|---|---|---|---|---|---|
Nucleus | Nuclear localization signal | 0.4178 | 0.7542 | 0.0489 | 0.0636 | 0.0461 | 0.0057 | 0.0581 | 0.0319 | 0.0756 | 0.1235 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 708 | 730 | 22 |
Transcription Factor Class (based on PFAM domains) |
---|
Fungal Specific TF |
Orthofinder run ID | 4 |
Orthogroup | 5600 |
Change Orthofinder run |
Type of sequence | Sequence |
---|---|
Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
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 | >Hirsu2|7574 MDAPLRSRLQEHARPRRRTRRACDKCSTSRTRCDGEYPCRRCEEYGYTCRYNREVKKRGRLPASTRDSDQASHGS PPATPPKTMASISAPDGDPKYSSEPVAIPRRSESVNDDKARETVARESTDAPQPMAPRTVHAMSIPSLTQIGIHQ SPRPPPLSVDDRSSQPRAASSSAGALDGHLAESEAPISDESAGYPSPANAAPSIELGRRSRRRTSFRSAASNDRP RASIISTPTTAPDGSIPDVLHRAPTEECCYKFLDPVLPFIRRIIPASVACELLDIFLTDPGSSLFRGASPYILTR VFRKKSILHPTSPRYTTPALLATILWCVAQTADVMLLHVPGTRARVVNDLYDLATSLVSERDPDRWRRIHGGLRA EHESPHPSLPSSSSVPMTTAANEPAGVIDDVLTFILLSIAVSGGDFKSDCYKWWSKAVRLALSLRLNREDERCSA PVSPCANPLCSCHRNTAEVSLPDRERREERRRVFWLLYSLDRHLSLSFNTVLSMPDSYCDVYAPLPESAWENLDI IMPRDLPMRTMGPPTLASGSGFFEYFLPMMAILGDIIEVHHRRRHPRLGEQDDSHSVAVIQELLANYELSLNSLT APGVPSLGAPVHANRDLVTGLSTPALYQDGMRLASCDAADLTKVRLVKAYSTHILHVLHVLLHGKWDAISMLDDG DDWITSKRFTECAAHAISASQSVSTILAIDPELTFMSYLFGIYLLQGSFILLLFADRMPQLGPNESVEQACENII RAHEVCVVTLSTEFQKNFRKVVRSTLYSVRGSGTTNWEEHRARRRALSLYRWTRGAKGLAL* |
Coding | >Hirsu2|7574 ATGGATGCGCCGCTGCGGTCGCGCTTGCAGGAGCATGCGAGGCCGAGGAGGAGGACGCGGCGGGCATGCGACAAG TGCAGCACTTCGAGGACGCGATGCGACGGGGAGTACCCGTGTCGCCGCTGTGAAGAGTACGGATACACTTGTCGC TACAACCGCGAGGTGAAGAAGCGAGGGCGTCTGCCCGCTTCGACCCGCGACAGCGATCAAGCCAGCCACGGCTCG CCTCCCGCAACGCCTCCAAAGACGATGGCCTCGATCTCGGCCCCTGATGGCGATCCGAAGTATTCGAGTGAGCCC GTTGCGATACCACGCCGGTCGGAGTCGGTCAACGACGACAAGGCGCGAGAGACTGTAGCCCGGGAGAGCACCGAT GCTCCGCAGCCGATGGCGCCTCGTACTGTCCACGCCATGTCGATCCCGTCGCTGACGCAGATTGGCATTCATCAA TCGCCACGTCCACCGCCTCTTTCTGTCGATGACCGTTCAAGCCAGCCGCGGGCGGCCTCGTCGTCCGCCGGGGCC TTGGACGGACACCTTGCCGAATCGGAGGCTCCCATCTCAGATGAGAGCGCCGGCTATCCCTCGCCGGCCAACGCG GCTCCGTCGATCGAACTCGGGAGGAGGAGCCGCCGCCGGACCTCGTTCCGCTCGGCGGCCAGCAACGACCGGCCG AGGGCGTCCATCATCAGCACGCCCACGACGGCCCCGGACGGATCCATCCCGGACGTCTTGCATCGGGCTCCGACC GAAGAATGCTGCTACAAGTTTCTCGACCCCGTCCTGCCCTTCATCCGCCGCATCATCCCGGCCTCGGTTGCGTGC GAACTTCTCGACATCTTTCTCACCGACCCGGGCAGCTCCCTCTTTCGAGGCGCTTCTCCGTATATTCTGACTAGA GTCTTCCGCAAAAAGTCCATCCTCCATCCGACGAGCCCGAGATATACGACACCGGCCCTTCTGGCCACTATTCTG TGGTGTGTCGCCCAAACAGCCGATGTTATGCTGCTTCACGTCCCCGGGACGCGTGCCAGAGTAGTCAACGATTTG TACGACTTGGCCACCTCTCTCGTTTCCGAGCGGGATCCAGACAGATGGCGGCGCATTCACGGCGGCCTGCGAGCC GAGCACGAGTCCCCCCATCCCAGCCTGCCGAGCTCGAGCTCTGTGCCGATGACGACGGCGGCTAACGAGCCGGCC GGCGTCATTGACGACGTGCTGACCTTCATTCTGTTGTCGATTGCCGTGTCCGGGGGCGACTTCAAGTCTGACTGC TACAAATGGTGGTCCAAGGCTGTCCGGCTGGCTCTCTCCCTGAGGCTCAACCGCGAGGACGAGCGCTGCTCGGCT CCCGTCTCTCCCTGCGCCAATCCTCTCTGTTCCTGTCACAGGAACACGGCCGAAGTGTCCTTGCCTGATCGCGAG CGACGCGAGGAACGGAGACGAGTGTTTTGGCTGCTGTACAGCCTCGACCGCCACCTCAGCCTTTCTTTCAACACG GTGCTCTCCATGCCGGACTCCTACTGCGACGTCTACGCGCCGCTTCCCGAGAGCGCTTGGGAGAACCTCGACATC ATCATGCCGCGAGACCTACCGATGAGGACCATGGGGCCTCCGACGCTGGCCAGCGGCTCGGGCTTCTTCGAGTAT TTCCTGCCCATGATGGCCATCCTGGGCGACATCATCGAGGTTCATCACCGGCGCCGCCACCCGCGGCTCGGCGAG CAGGACGACTCCCACTCGGTGGCCGTCATACAGGAGCTGCTGGCAAACTACGAGCTCAGCCTCAACTCTCTGACC GCGCCCGGTGTTCCTTCGCTCGGGGCGCCCGTCCACGCCAACAGGGACCTTGTCACCGGACTCTCGACCCCGGCC CTGTACCAAGACGGGATGCGCCTGGCATCGTGCGATGCGGCCGACCTCACCAAAGTGCGTCTTGTCAAGGCGTAC AGCACGCACATCCTTCACGTGTTGCACGTGCTGCTGCACGGCAAATGGGACGCTATATCCATGCTGGACGACGGC GATGACTGGATCACGTCGAAGCGCTTCACCGAGTGCGCAGCCCATGCCATCTCTGCGTCACAGTCGGTATCGACC ATCCTGGCCATCGACCCGGAGCTCACCTTCATGTCGTACCTGTTCGGCATATACCTACTACAGGGGAGCTTTATC CTGCTGCTTTTTGCGGATCGCATGCCTCAGCTCGGCCCCAACGAGTCGGTCGAGCAGGCGTGCGAGAACATCATC CGGGCGCACGAGGTTTGCGTCGTTACTCTCAGCACGGAGTTCCAGAAAAACTTCCGCAAGGTGGTGCGCTCTACA CTATACAGCGTGCGAGGGTCGGGCACGACGAACTGGGAGGAGCACCGAGCGAGACGACGAGCGTTGTCTCTGTAT CGGTGGACAAGGGGCGCCAAAGGATTAGCCCTATGA |
Transcript | >Hirsu2|7574 ATGGATGCGCCGCTGCGGTCGCGCTTGCAGGAGCATGCGAGGCCGAGGAGGAGGACGCGGCGGGCATGCGACAAG TGCAGCACTTCGAGGACGCGATGCGACGGGGAGTACCCGTGTCGCCGCTGTGAAGAGTACGGATACACTTGTCGC TACAACCGCGAGGTGAAGAAGCGAGGGCGTCTGCCCGCTTCGACCCGCGACAGCGATCAAGCCAGCCACGGCTCG CCTCCCGCAACGCCTCCAAAGACGATGGCCTCGATCTCGGCCCCTGATGGCGATCCGAAGTATTCGAGTGAGCCC GTTGCGATACCACGCCGGTCGGAGTCGGTCAACGACGACAAGGCGCGAGAGACTGTAGCCCGGGAGAGCACCGAT GCTCCGCAGCCGATGGCGCCTCGTACTGTCCACGCCATGTCGATCCCGTCGCTGACGCAGATTGGCATTCATCAA TCGCCACGTCCACCGCCTCTTTCTGTCGATGACCGTTCAAGCCAGCCGCGGGCGGCCTCGTCGTCCGCCGGGGCC TTGGACGGACACCTTGCCGAATCGGAGGCTCCCATCTCAGATGAGAGCGCCGGCTATCCCTCGCCGGCCAACGCG GCTCCGTCGATCGAACTCGGGAGGAGGAGCCGCCGCCGGACCTCGTTCCGCTCGGCGGCCAGCAACGACCGGCCG AGGGCGTCCATCATCAGCACGCCCACGACGGCCCCGGACGGATCCATCCCGGACGTCTTGCATCGGGCTCCGACC GAAGAATGCTGCTACAAGTTTCTCGACCCCGTCCTGCCCTTCATCCGCCGCATCATCCCGGCCTCGGTTGCGTGC GAACTTCTCGACATCTTTCTCACCGACCCGGGCAGCTCCCTCTTTCGAGGCGCTTCTCCGTATATTCTGACTAGA GTCTTCCGCAAAAAGTCCATCCTCCATCCGACGAGCCCGAGATATACGACACCGGCCCTTCTGGCCACTATTCTG TGGTGTGTCGCCCAAACAGCCGATGTTATGCTGCTTCACGTCCCCGGGACGCGTGCCAGAGTAGTCAACGATTTG TACGACTTGGCCACCTCTCTCGTTTCCGAGCGGGATCCAGACAGATGGCGGCGCATTCACGGCGGCCTGCGAGCC GAGCACGAGTCCCCCCATCCCAGCCTGCCGAGCTCGAGCTCTGTGCCGATGACGACGGCGGCTAACGAGCCGGCC GGCGTCATTGACGACGTGCTGACCTTCATTCTGTTGTCGATTGCCGTGTCCGGGGGCGACTTCAAGTCTGACTGC TACAAATGGTGGTCCAAGGCTGTCCGGCTGGCTCTCTCCCTGAGGCTCAACCGCGAGGACGAGCGCTGCTCGGCT CCCGTCTCTCCCTGCGCCAATCCTCTCTGTTCCTGTCACAGGAACACGGCCGAAGTGTCCTTGCCTGATCGCGAG CGACGCGAGGAACGGAGACGAGTGTTTTGGCTGCTGTACAGCCTCGACCGCCACCTCAGCCTTTCTTTCAACACG GTGCTCTCCATGCCGGACTCCTACTGCGACGTCTACGCGCCGCTTCCCGAGAGCGCTTGGGAGAACCTCGACATC ATCATGCCGCGAGACCTACCGATGAGGACCATGGGGCCTCCGACGCTGGCCAGCGGCTCGGGCTTCTTCGAGTAT TTCCTGCCCATGATGGCCATCCTGGGCGACATCATCGAGGTTCATCACCGGCGCCGCCACCCGCGGCTCGGCGAG CAGGACGACTCCCACTCGGTGGCCGTCATACAGGAGCTGCTGGCAAACTACGAGCTCAGCCTCAACTCTCTGACC GCGCCCGGTGTTCCTTCGCTCGGGGCGCCCGTCCACGCCAACAGGGACCTTGTCACCGGACTCTCGACCCCGGCC CTGTACCAAGACGGGATGCGCCTGGCATCGTGCGATGCGGCCGACCTCACCAAAGTGCGTCTTGTCAAGGCGTAC AGCACGCACATCCTTCACGTGTTGCACGTGCTGCTGCACGGCAAATGGGACGCTATATCCATGCTGGACGACGGC GATGACTGGATCACGTCGAAGCGCTTCACCGAGTGCGCAGCCCATGCCATCTCTGCGTCACAGTCGGTATCGACC ATCCTGGCCATCGACCCGGAGCTCACCTTCATGTCGTACCTGTTCGGCATATACCTACTACAGGGGAGCTTTATC CTGCTGCTTTTTGCGGATCGCATGCCTCAGCTCGGCCCCAACGAGTCGGTCGAGCAGGCGTGCGAGAACATCATC CGGGCGCACGAGGTTTGCGTCGTTACTCTCAGCACGGAGTTCCAGAAAAACTTCCGCAAGGTGGTGCGCTCTACA CTATACAGCGTGCGAGGGTCGGGCACGACGAACTGGGAGGAGCACCGAGCGAGACGACGAGCGTTGTCTCTGTAT CGGTGGACAAGGGGCGCCAAAGGATTAGCCCTATGA |
Gene | >Hirsu2|7574 ATGGATGCGCCGCTGCGGTCGCGCTTGCAGGAGCATGCGAGGCCGAGGAGGAGGACGCGGCGGGCATGCGACAAG TGCAGCACTTCGAGGACGCGATGCGACGGGGAGTAGTGAGTCCATGCCTTCCCCCGCCCTTCCTCTCATCGCCTG CTGACCGCGGCGTTGGCATCATGGCAGCCCGTGTCGCCGCTGTGAAGGTGAGCCTCATCTCCATTGCTGGGCCTG CATTGTCGATTCGCTCCCGATATGTATCCGGAGCCTTCCAACCATTTGAGCTGGACTGCCGAGCGTGACGAAGCA ACATGAAGACTCGCGCCGCCGCGTAGCCGATCTGCGCTGATTCACTCGTTGTCTTGTCGCGCGCTCTTCTGTGCC GCTGAAGAGTACGGATACACTTGTCGCTACAACCGCGAGGTGAAGAAGCGAGGGCGTCTGCCCGCTTCGACGTAC GTGCGACCCGAGCCCGATTCACTCGGCCGAGGTTCCCTGCCCCCGAGAGCACCGAGGACTCACGCGCCAGCAGCC GCGACAGCGATCAAGCCAGCCACGGCTCGCCTCCCGCAACGCCTCCAAAGACGATGGCCTCGATCTCGGCCCCTG ATGGCGATCCGAAGTATTCGAGTGAGCCCGTTGCGATACCACGCCGGTCGGAGTCGGTCAACGACGACAAGGCGC GAGAGACTGTAGCCCGGGAGAGCACCGATGCTCCGCAGCCGATGGCGCCTCGTACTGTCCACGCCATGTCGATCC CGTCGCTGACGCAGATTGGCATTCATCAATCGCCACGTCCACCGCCTCTTTCTGTCGATGACCGTTCAAGCCAGC CGCGGGCGGCCTCGTCGTCCGCCGGGGCCTTGGACGGACACCTTGCCGAATCGGAGGCTCCCATCTCAGATGAGA GCGCCGGCTATCCCTCGCCGGCCAACGCGGCTCCGTCGATCGAACTCGGGAGGAGGAGCCGCCGCCGGACCTCGT TCCGCTCGGCGGCCAGCAACGACCGGCCGAGGGCGTCCATCATCAGCACGCCCACGACGGCCCCGGACGGATCCA TCCCGGACGTCTTGCATCGGGCTCCGACCGAAGAATGCTGCTACAAGTTTCTCGACCCCGTCCTGCCCTTCATCC GCCGCATCATCCCGGCCTCGGTTGCGTGCGAACTTCTCGACATCTTTCTCACCGACCCGGGCAGCTCCCTCTTTC GAGGCGCTTCTCCGTATATTCTGACTAGAGTCTTCCGCAAAAAGTCCATCCTCCATCCGACGAGCCCGAGATATA CGACACCGGCCCTTCTGGCCACTATTCTGTGGTGTGTCGCCCAAACAGCCGATGTTATGCTGCTTCACGTCCCCG GGACGCGTGCCAGAGTAGTCAACGATTTGTACGACTTGGCCACCTCTCTCGTTTCCGAGCGGGATCCAGACAGAT GGCGGCGCATTCACGGTCTGTGCCTGGCGGAGATCTTGGCCCTTGGGCCCCTCTTAGAGAGAGCTGACAGTGTGG TCAGGCGGCCTGCGAGCCGAGCACGAGTCCCCCCATCCCAGCCTGCCGAGCTCGAGCTCTGTGCCGATGACGACG GCGGCTAACGAGCCGGCCGGCGTCATTGACGACGTGCTGACCTTCATTCTGTTGTCGATTGCCGTGTCCGGGGGC GACTTCAAGTCTGACTGCTACAAATGGTGGTCCAAGGCTGTCCGGCTGGCTCTCTCCCTGAGGCTCAACCGCGAG GACGAGCGCTGCTCGGCTCCCGTCTCTCCCTGCGCCAATCCTCTCTGTTCCTGTCACAGGAACACGGCCGAAGTG TCCTTGCCTGATCGCGAGCGACGCGAGGAACGGAGACGAGTGTTTTGGCTGCTGTACAGCCTCGACCGCCACCTC AGCCTTTCTTTCAACACGGTGCTCTCCATGCCGGACTCCTACTGCGACGTCTACGGTGAGTTCTTTCCACCGCCG GAGTCGTTGGCGAAATGCCTCGGCACGATACAGAGACTGACTGTGTCTTGTTATGCCGGTGTGATGTTGAAGCGC CGCTTCCCGAGAGCGCTTGGGAGAACCTCGACATCATCATGCCGCGAGACCTACCGATGAGGACCATGGGGCCTC CGACGCTGGCCAGCGGCTCGGGCTTCTTCGAGTATTTCCTGCCCATGATGGCCATCCTGGGCGACATCATCGAGG TTCATCACCGGCGCCGCCACCCGCGGCTCGGCGAGCAGGACGACTCCCACTCGGTGGCCGTCATACAGGAGCTGC TGGCAAACTACGAGCTCAGCCTCAACTCTCTGACCGCGCCCGGTGTTCCTTCGCTCGGGGCGCCCGTCCACGCCA ACAGGGACCTTGTCACCGGACTCTCGACCCCGGCCCTGTACCAAGACGGGATGCGCCTGGCATCGTGCGATGCGG CCGACCTCACCAAAGTGCGTCTTGTCAAGGCGTACAGCACGCACATCCTTCACGTGTTGCACGTGCTGCTGCACG GCAAATGGGACGCTATATCCATGCTGGACGACGGCGATGACTGGATCACGTCGAAGCGCTTCACCGAGTGCGCAG CCCATGCCATCTCTGCGTCACAGTCGGTATCGACCATCCTGGCCATCGACCCGGAGCTCACCTTCATGTCGTACC TGTTCGGCATATACCTACTACAGGGGAGCTTTATCCTGCTGCTTTTTGCGGATCGCATGCCTCAGCTCGGCCCCA ACGAGTCGGTCGAGCAGGCGTGCGAGAACATCATCCGGGCGCACGAGGTTTGCGTCGTTACTCTCAGCACGGAGT TCCAGGTAAGAGTCTCGTTGCCGAGTATTCGAGCCTCTTGGATCCGTCTCAAGGGCTAACGAAGAGCGATGGACA GAAAAACTTCCGCAAGGTGGTGCGCTCTACACTATACAGCGTGCGAGGGTCGGGCACGACGAACTGGGAGGAGCA CCGAGCGAGACGACGAGCGTTGTCTCTGTATCGGTGGACAAGGGGCGCCAAAGGATTAGCCCTATGA |