Protein ID | Ophun1|784 |
Gene name | |
Location | Contig_127:20356..23060 |
Strand | - |
Gene length (bp) | 2704 |
Transcript length (bp) | 2586 |
Coding sequence length (bp) | 2586 |
Protein length (aa) | 862 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00493 | MCM | MCM P-loop domain | 1.5E-99 | 472 | 694 |
PF17207 | MCM_OB | MCM OB domain | 2.6E-39 | 305 | 431 |
PF17855 | MCM_lid | MCM AAA-lid domain | 5.3E-25 | 745 | 828 |
PF12619 | MCM2_N | Mini-chromosome maintenance protein 2 | 1.2E-24 | 63 | 192 |
PF14551 | MCM_N | MCM N-terminal domain | 5.8E-14 | 207 | 297 |
PF01078 | Mg_chelatase | Magnesium chelatase, subunit ChlI | 6.6E-06 | 582 | 647 |
PF07728 | AAA_5 | AAA domain (dynein-related subfamily) | 8.3E-06 | 529 | 647 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P29469|MCM2_YEAST | DNA replication licensing factor MCM2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM2 PE=1 SV=2 | 16 | 850 | 0.0E+00 |
sp|P40377|MCM2_SCHPO | DNA replication licensing factor mcm2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm2 PE=1 SV=1 | 62 | 850 | 0.0E+00 |
sp|P55861|MCM2_XENLA | DNA replication licensing factor mcm2 OS=Xenopus laevis GN=mcm2 PE=1 SV=2 | 85 | 852 | 0.0E+00 |
sp|P49736|MCM2_HUMAN | DNA replication licensing factor MCM2 OS=Homo sapiens GN=MCM2 PE=1 SV=4 | 88 | 848 | 0.0E+00 |
sp|P97310|MCM2_MOUSE | DNA replication licensing factor MCM2 OS=Mus musculus GN=Mcm2 PE=1 SV=3 | 85 | 848 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P29469|MCM2_YEAST | DNA replication licensing factor MCM2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM2 PE=1 SV=2 | 16 | 850 | 0.0E+00 |
sp|P40377|MCM2_SCHPO | DNA replication licensing factor mcm2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm2 PE=1 SV=1 | 62 | 850 | 0.0E+00 |
sp|P55861|MCM2_XENLA | DNA replication licensing factor mcm2 OS=Xenopus laevis GN=mcm2 PE=1 SV=2 | 85 | 852 | 0.0E+00 |
sp|P49736|MCM2_HUMAN | DNA replication licensing factor MCM2 OS=Homo sapiens GN=MCM2 PE=1 SV=4 | 88 | 848 | 0.0E+00 |
sp|P97310|MCM2_MOUSE | DNA replication licensing factor MCM2 OS=Mus musculus GN=Mcm2 PE=1 SV=3 | 85 | 848 | 0.0E+00 |
sp|Q6DIH3|MCM2_XENTR | DNA replication licensing factor mcm2 OS=Xenopus tropicalis GN=mcm2 PE=2 SV=1 | 67 | 852 | 0.0E+00 |
sp|Q2R482|MCM2_ORYSJ | DNA replication licensing factor MCM2 OS=Oryza sativa subsp. japonica GN=MCM2 PE=2 SV=1 | 85 | 848 | 0.0E+00 |
sp|B8BKI8|MCM2_ORYSI | DNA replication licensing factor MCM2 OS=Oryza sativa subsp. indica GN=OsI_36121 PE=3 SV=1 | 85 | 848 | 0.0E+00 |
sp|Q9LPD9|MCM2_ARATH | DNA replication licensing factor MCM2 OS=Arabidopsis thaliana GN=MCM2 PE=1 SV=1 | 85 | 848 | 0.0E+00 |
sp|P49735|MCM2_DROME | DNA replication licensing factor Mcm2 OS=Drosophila melanogaster GN=Mcm2 PE=1 SV=1 | 85 | 848 | 0.0E+00 |
sp|Q9UXG1|MCM_SULSO | Minichromosome maintenance protein MCM OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=MCM PE=1 SV=1 | 210 | 824 | 4.0E-121 |
sp|Q561P5|MCM5_XENTR | DNA replication licensing factor mcm5 OS=Xenopus tropicalis GN=mcm5 PE=2 SV=1 | 206 | 822 | 1.0E-104 |
sp|P55862|MCM5A_XENLA | DNA replication licensing factor mcm5-A OS=Xenopus laevis GN=mcm5-a PE=1 SV=2 | 206 | 822 | 4.0E-104 |
sp|Q6PCI7|MCM5B_XENLA | DNA replication licensing factor mcm5-B OS=Xenopus laevis GN=mcm5-b PE=2 SV=1 | 206 | 822 | 8.0E-104 |
sp|Q0V8B7|MCM5_BOVIN | DNA replication licensing factor MCM5 OS=Bos taurus GN=MCM5 PE=2 SV=1 | 206 | 822 | 2.0E-100 |
sp|Q5JKB0|MCM4_ORYSJ | DNA replication licensing factor MCM4 OS=Oryza sativa subsp. japonica GN=MCM4 PE=3 SV=2 | 233 | 822 | 9.0E-100 |
sp|Q0WVF5|MCM4_ARATH | DNA replication licensing factor MCM4 OS=Arabidopsis thaliana GN=MCM4 PE=1 SV=1 | 188 | 822 | 1.0E-99 |
sp|Q9FL33|MCM3_ARATH | DNA replication licensing factor MCM3 OS=Arabidopsis thaliana GN=MCM3 PE=1 SV=1 | 276 | 824 | 3.0E-99 |
sp|P33992|MCM5_HUMAN | DNA replication licensing factor MCM5 OS=Homo sapiens GN=MCM5 PE=1 SV=5 | 206 | 822 | 1.0E-98 |
sp|Q9VGW6|MCM5_DROME | DNA replication licensing factor Mcm5 OS=Drosophila melanogaster GN=Mcm5 PE=1 SV=1 | 198 | 822 | 1.0E-98 |
sp|Q0DHC4|MCM3_ORYSJ | DNA replication licensing factor MCM3 OS=Oryza sativa subsp. japonica GN=MCM3 PE=2 SV=1 | 211 | 824 | 2.0E-98 |
sp|B8AZ99|MCM3_ORYSI | DNA replication licensing factor MCM3 OS=Oryza sativa subsp. indica GN=MCM3 PE=3 SV=1 | 211 | 824 | 2.0E-98 |
sp|Q9SX04|MCM32_MAIZE | DNA replication licensing factor MCM3 homolog 2 OS=Zea mays GN=ROA2 PE=2 SV=1 | 211 | 824 | 5.0E-98 |
sp|Q43704|MCM31_MAIZE | DNA replication licensing factor MCM3 homolog 1 OS=Zea mays GN=ROA1 PE=2 SV=2 | 211 | 824 | 6.0E-98 |
sp|Q9SX03|MCM33_MAIZE | DNA replication licensing factor MCM3 homolog 3 OS=Zea mays GN=ROA3 PE=2 SV=1 | 211 | 824 | 8.0E-98 |
sp|B8AEH3|MCM5_ORYSI | DNA replication licensing factor MCM5 OS=Oryza sativa subsp. indica GN=MCM5 PE=3 SV=1 | 209 | 822 | 4.0E-97 |
sp|Q6KAJ4|MCM5_ORYSJ | DNA replication licensing factor MCM5 OS=Oryza sativa subsp. japonica GN=MCM5 PE=2 SV=1 | 209 | 822 | 5.0E-97 |
sp|Q54CP4|MCM5_DICDI | DNA replication licensing factor mcm5 OS=Dictyostelium discoideum GN=mcm5 PE=3 SV=1 | 205 | 822 | 1.0E-96 |
sp|P49718|MCM5_MOUSE | DNA replication licensing factor MCM5 OS=Mus musculus GN=Mcm5 PE=1 SV=1 | 206 | 822 | 2.0E-95 |
sp|Q21902|MCM5_CAEEL | DNA replication licensing factor mcm-5 OS=Caenorhabditis elegans GN=mcm-5 PE=3 SV=1 | 204 | 822 | 7.0E-95 |
sp|Q9XYU1|MCM3_DROME | DNA replication licensing factor Mcm3 OS=Drosophila melanogaster GN=Mcm3 PE=1 SV=1 | 204 | 858 | 1.0E-94 |
sp|O80786|MCM5_ARATH | DNA replication licensing factor MCM5 OS=Arabidopsis thaliana GN=MCM5 PE=1 SV=1 | 236 | 824 | 3.0E-94 |
sp|P41389|MCM5_SCHPO | DNA replication licensing factor mcm5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm5 PE=1 SV=2 | 241 | 832 | 5.0E-94 |
sp|P43299|MCM7_ARATH | DNA replication licensing factor MCM7 OS=Arabidopsis thaliana GN=MCM7 PE=1 SV=2 | 304 | 822 | 7.0E-94 |
sp|P33993|MCM7_HUMAN | DNA replication licensing factor MCM7 OS=Homo sapiens GN=MCM7 PE=1 SV=4 | 304 | 833 | 2.0E-93 |
sp|Q6NX31|MCM7_XENTR | DNA replication licensing factor mcm7 OS=Xenopus tropicalis GN=mcm7 PE=2 SV=1 | 289 | 833 | 3.0E-93 |
sp|B8BMI1|MCM7_ORYSI | DNA replication licensing factor MCM7 OS=Oryza sativa subsp. indica GN=MCM7 PE=3 SV=1 | 291 | 822 | 3.0E-93 |
sp|Q2QNM1|MCM7_ORYSJ | DNA replication licensing factor MCM7 OS=Oryza sativa subsp. japonica GN=MCM7 PE=2 SV=1 | 291 | 822 | 3.0E-93 |
sp|P29496|MCM5_YEAST | Minichromosome maintenance protein 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM5 PE=1 SV=1 | 305 | 822 | 4.0E-93 |
sp|Q3ZBH9|MCM7_BOVIN | DNA replication licensing factor MCM7 OS=Bos taurus GN=MCM7 PE=2 SV=1 | 304 | 833 | 5.0E-93 |
sp|Q7ZXB1|MCM7B_XENLA | DNA replication licensing factor mcm7-B OS=Xenopus laevis GN=mcm7-b PE=2 SV=1 | 289 | 825 | 2.0E-92 |
sp|Q91876|MCM7A_XENLA | DNA replication licensing factor mcm7-A OS=Xenopus laevis GN=mcm7-a PE=1 SV=2 | 304 | 833 | 2.0E-92 |
sp|Q6GL41|MCM4_XENTR | DNA replication licensing factor mcm4 OS=Xenopus tropicalis GN=mcm4 PE=2 SV=1 | 193 | 821 | 2.0E-92 |
sp|P30665|MCM4_YEAST | DNA replication licensing factor MCM4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM4 PE=1 SV=2 | 196 | 822 | 3.0E-92 |
sp|P33991|MCM4_HUMAN | DNA replication licensing factor MCM4 OS=Homo sapiens GN=MCM4 PE=1 SV=5 | 171 | 821 | 6.0E-92 |
sp|P30666|MCM3_SCHPO | DNA replication licensing factor mcm3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm3 PE=1 SV=2 | 302 | 821 | 9.0E-92 |
sp|P30664|MCM4B_XENLA | DNA replication licensing factor mcm4-B OS=Xenopus laevis GN=mcm4-b PE=1 SV=3 | 193 | 821 | 1.0E-91 |
sp|Q26454|MCM4_DROME | DNA replication licensing factor MCM4 OS=Drosophila melanogaster GN=dpa PE=1 SV=2 | 189 | 821 | 2.0E-91 |
sp|Q61881|MCM7_MOUSE | DNA replication licensing factor MCM7 OS=Mus musculus GN=Mcm7 PE=1 SV=1 | 304 | 833 | 2.0E-91 |
sp|Q5XK83|MCM4A_XENLA | DNA replication licensing factor mcm4-A OS=Xenopus laevis GN=mcm4-a PE=1 SV=1 | 207 | 821 | 2.0E-91 |
sp|P24279|MCM3_YEAST | DNA replication licensing factor MCM3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM3 PE=1 SV=1 | 306 | 831 | 2.0E-91 |
sp|Q5R8G6|MCM3_PONAB | DNA replication licensing factor MCM3 OS=Pongo abelii GN=MCM3 PE=2 SV=1 | 211 | 822 | 4.0E-91 |
sp|P25205|MCM3_HUMAN | DNA replication licensing factor MCM3 OS=Homo sapiens GN=MCM3 PE=1 SV=3 | 211 | 822 | 1.0E-90 |
sp|P49717|MCM4_MOUSE | DNA replication licensing factor MCM4 OS=Mus musculus GN=Mcm4 PE=1 SV=1 | 171 | 821 | 6.0E-90 |
sp|P29458|MCM4_SCHPO | DNA replication licensing factor mcm4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm4 PE=1 SV=2 | 196 | 818 | 8.0E-90 |
sp|B8AZX3|MCM6_ORYSI | DNA replication licensing factor MCM6 OS=Oryza sativa subsp. indica GN=MCM6 PE=3 SV=1 | 291 | 809 | 8.0E-90 |
sp|P49739|MCM3M_XENLA | Maternal DNA replication licensing factor mcm3 OS=Xenopus laevis GN=mmcm3 PE=1 SV=2 | 302 | 825 | 8.0E-90 |
sp|O75001|MCM7_SCHPO | DNA replication licensing factor mcm7 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm7 PE=1 SV=1 | 303 | 822 | 3.0E-89 |
sp|Q28BS0|MCM3Z_XENTR | Zygotic DNA replication licensing factor mcm3 OS=Xenopus tropicalis GN=zmcm3 PE=2 SV=1 | 211 | 858 | 5.0E-89 |
sp|F4KAB8|MCM6_ARATH | DNA replication licensing factor MCM6 OS=Arabidopsis thaliana GN=MCM6 PE=1 SV=1 | 291 | 809 | 1.0E-88 |
sp|P25206|MCM3_MOUSE | DNA replication licensing factor MCM3 OS=Mus musculus GN=Mcm3 PE=1 SV=2 | 211 | 822 | 1.0E-88 |
sp|A4FUD9|MCM3_BOVIN | DNA replication licensing factor MCM3 OS=Bos taurus GN=MCM3 PE=2 SV=1 | 211 | 822 | 1.0E-88 |
sp|Q7ZY18|MC6ZB_XENLA | Zygotic DNA replication licensing factor mcm6-B OS=Xenopus laevis GN=zmcm6-b PE=1 SV=1 | 197 | 830 | 2.0E-88 |
sp|Q6P1V8|MCM6Z_XENTR | Zygotic DNA replication licensing factor mcm6 OS=Xenopus tropicalis GN=zmcm6 PE=2 SV=1 | 291 | 830 | 3.0E-88 |
sp|Q7Q0Q1|MCM6_ANOGA | DNA replication licensing factor Mcm6 OS=Anopheles gambiae GN=Mcm6 PE=3 SV=3 | 210 | 830 | 4.0E-88 |
sp|P38132|MCM7_YEAST | DNA replication licensing factor MCM7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM7 PE=1 SV=4 | 304 | 822 | 8.0E-88 |
sp|Q2KIZ8|MCM6_BOVIN | DNA replication licensing factor MCM6 OS=Bos taurus GN=MCM6 PE=2 SV=1 | 291 | 830 | 1.0E-87 |
sp|Q7ZXZ0|MCM3Z_XENLA | Zygotic DNA replication licensing factor mcm3 OS=Xenopus laevis GN=zmcm3 PE=1 SV=1 | 211 | 822 | 3.0E-87 |
sp|Q28CM3|MCM6M_XENTR | Maternal DNA replication licensing factor mcm6 OS=Xenopus tropicalis GN=mmcm6 PE=2 SV=1 | 291 | 830 | 3.0E-87 |
sp|Q14566|MCM6_HUMAN | DNA replication licensing factor MCM6 OS=Homo sapiens GN=MCM6 PE=1 SV=1 | 291 | 830 | 5.0E-87 |
sp|Q498J7|MC6ZA_XENLA | Zygotic DNA replication licensing factor mcm6-A OS=Xenopus laevis GN=zmcm6-a PE=1 SV=1 | 197 | 830 | 9.0E-87 |
sp|Q5FWY4|MCM6M_XENLA | Maternal DNA replication licensing factor mcm6 OS=Xenopus laevis GN=mmcm6 PE=1 SV=1 | 291 | 830 | 9.0E-87 |
sp|P97311|MCM6_MOUSE | DNA replication licensing factor MCM6 OS=Mus musculus GN=Mcm6 PE=1 SV=1 | 291 | 830 | 2.0E-86 |
sp|Q5ZMN2|MCM3_CHICK | DNA replication licensing factor MCM3 OS=Gallus gallus GN=MCM3 PE=2 SV=1 | 211 | 825 | 5.0E-86 |
sp|Q9CWV1|MCM8_MOUSE | DNA helicase MCM8 OS=Mus musculus GN=Mcm8 PE=1 SV=3 | 210 | 832 | 6.0E-85 |
sp|Q6F353|MCM6_ORYSJ | DNA replication licensing factor MCM6 OS=Oryza sativa subsp. japonica GN=Os05g0235800 PE=3 SV=1 | 291 | 809 | 9.0E-85 |
sp|D3ZVK1|MCM8_RAT | DNA helicase MCM8 OS=Rattus norvegicus GN=Mcm8 PE=3 SV=1 | 292 | 832 | 2.0E-84 |
sp|P34647|MCM6_CAEEL | DNA replication licensing factor mcm-6 OS=Caenorhabditis elegans GN=mcm-6 PE=1 SV=1 | 206 | 830 | 6.0E-84 |
sp|Q5F310|MCM8_XENLA | DNA helicase MCM8 OS=Xenopus laevis GN=mcm8 PE=2 SV=2 | 292 | 832 | 2.0E-83 |
sp|Q0V9Q6|MCM8_XENTR | DNA helicase MCM8 OS=Xenopus tropicalis GN=mcm8 PE=2 SV=1 | 292 | 832 | 3.0E-83 |
sp|Q24849|MCM3_ENTHI | DNA replication licensing factor MCM3 OS=Entamoeba histolytica GN=MCM3 PE=3 SV=1 | 302 | 824 | 3.0E-83 |
sp|Q9V461|MCM6_DROME | DNA replication licensing factor Mcm6 OS=Drosophila melanogaster GN=Mcm6 PE=1 SV=1 | 210 | 822 | 4.0E-83 |
sp|Q9XYU0|MCM7_DROME | DNA replication licensing factor Mcm7 OS=Drosophila melanogaster GN=Mcm7 PE=1 SV=1 | 303 | 822 | 8.0E-83 |
sp|Q29JI9|MCM6_DROPS | DNA replication licensing factor Mcm6 OS=Drosophila pseudoobscura pseudoobscura GN=Mcm6 PE=3 SV=1 | 210 | 822 | 1.0E-82 |
sp|I0IUP3|MCM8_CHICK | DNA helicase MCM8 OS=Gallus gallus GN=MCM8 PE=1 SV=1 | 292 | 832 | 2.0E-82 |
sp|Q61J08|MCM6_CAEBR | DNA replication licensing factor mcm-6 OS=Caenorhabditis briggsae GN=mcm-6 PE=3 SV=1 | 206 | 830 | 4.0E-82 |
sp|Q9SF37|MCM8_ARATH | Probable DNA helicase MCM8 OS=Arabidopsis thaliana GN=MCM8 PE=2 SV=2 | 240 | 829 | 7.0E-82 |
sp|Q9UJA3|MCM8_HUMAN | DNA helicase MCM8 OS=Homo sapiens GN=MCM8 PE=1 SV=2 | 210 | 832 | 2.0E-81 |
sp|B8AZ14|MCM8_ORYSI | Probable DNA helicase MCM8 OS=Oryza sativa subsp. indica GN=MCM8 PE=3 SV=1 | 240 | 829 | 3.0E-81 |
sp|B9FKM7|MCM8_ORYSJ | Probable DNA helicase MCM8 OS=Oryza sativa subsp. japonica GN=MCM8 PE=2 SV=1 | 240 | 829 | 2.0E-80 |
sp|P49731|MCM6_SCHPO | DNA replication licensing factor mcm6 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=mcm6 PE=1 SV=2 | 205 | 806 | 2.0E-80 |
sp|E1BPX4|MCM8_BOVIN | DNA helicase MCM8 OS=Bos taurus GN=MCM8 PE=3 SV=2 | 292 | 832 | 6.0E-77 |
sp|B8B406|MCM9_ORYSI | Probable DNA helicase MCM9 OS=Oryza sativa subsp. indica GN=MCM9 PE=3 SV=1 | 241 | 832 | 1.0E-72 |
sp|Q69QA6|MCM9_ORYSJ | Probable DNA helicase MCM9 OS=Oryza sativa subsp. japonica GN=MCM9 PE=2 SV=1 | 241 | 832 | 2.0E-72 |
sp|P53091|MCM6_YEAST | DNA replication licensing factor MCM6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM6 PE=1 SV=2 | 434 | 806 | 3.0E-72 |
sp|Q9NXL9|MCM9_HUMAN | DNA helicase MCM9 OS=Homo sapiens GN=MCM9 PE=1 SV=4 | 248 | 845 | 5.0E-72 |
sp|F1N2W9|MCM9_BOVIN | DNA helicase MCM9 OS=Bos taurus GN=MCM9 PE=3 SV=2 | 248 | 852 | 6.0E-72 |
sp|F6RIX4|MCM9_XENTR | DNA helicase MCM9 OS=Xenopus tropicalis GN=mcm9 PE=3 SV=1 | 240 | 845 | 2.0E-70 |
sp|Q6NRM6|MCM9_XENLA | DNA helicase MCM9 OS=Xenopus laevis GN=mcm9 PE=1 SV=1 | 240 | 845 | 2.0E-70 |
sp|Q2KHI9|MCM9_MOUSE | DNA helicase MCM9 OS=Mus musculus GN=Mcm9 PE=1 SV=2 | 243 | 845 | 2.0E-70 |
sp|F4IFF3|MCM9_ARATH | Probable DNA helicase MCM9 OS=Arabidopsis thaliana GN=MCM9 PE=3 SV=1 | 269 | 822 | 2.0E-70 |
sp|Q62724|MCM6_RAT | DNA replication licensing factor MCM6 (Fragment) OS=Rattus norvegicus GN=Mcm6 PE=1 SV=2 | 466 | 830 | 9.0E-70 |
sp|I0IUP4|MCM9_CHICK | DNA helicase MCM9 OS=Gallus gallus GN=MCM9 PE=1 SV=2 | 248 | 852 | 1.0E-69 |
sp|F1M5F3|MCM9_RAT | DNA helicase MCM9 OS=Rattus norvegicus GN=Mcm9 PE=3 SV=2 | 241 | 845 | 5.0E-69 |
sp|F1QDI9|MCM9_DANRE | DNA helicase MCM9 OS=Danio rerio GN=mcm9 PE=3 SV=2 | 284 | 811 | 2.0E-65 |
sp|Q86B14|MCM6_DICDI | DNA replication licensing factor mcm6 OS=Dictyostelium discoideum GN=mcm6 PE=3 SV=1 | 467 | 809 | 4.0E-65 |
sp|Q58884|Y1489_METJA | Uncharacterized MCM-type protein MJ1489 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ1489 PE=3 SV=1 | 303 | 829 | 6.0E-52 |
sp|Q58371|Y961_METJA | Uncharacterized MCM-type protein MJ0961 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ0961 PE=3 SV=1 | 440 | 826 | 3.0E-37 |
sp|Q9VF30|MCMR_DROME | DNA replication licensing factor REC OS=Drosophila melanogaster GN=rec PE=1 SV=2 | 291 | 829 | 9.0E-33 |
sp|Q57809|Y363_METJA | Uncharacterized MCM-type protein MJ0363 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ0363 PE=3 SV=1 | 284 | 822 | 2.0E-32 |
sp|Q60275|Y3513_METJA | Uncharacterized MCM-type protein MJECL13 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJECL13 PE=3 SV=1 | 293 | 826 | 4.0E-18 |
sp|P53091|MCM6_YEAST | DNA replication licensing factor MCM6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MCM6 PE=1 SV=2 | 292 | 428 | 5.0E-17 |
sp|Q86B14|MCM6_DICDI | DNA replication licensing factor mcm6 OS=Dictyostelium discoideum GN=mcm6 PE=3 SV=1 | 223 | 427 | 6.0E-13 |
GO Term | Description | Terminal node |
---|---|---|
GO:0005524 | ATP binding | Yes |
GO:0003677 | DNA binding | Yes |
GO:0042555 | MCM complex | Yes |
GO:0006270 | DNA replication initiation | Yes |
GO:0005634 | nucleus | Yes |
GO:1905775 | negative regulation of DNA helicase activity | Yes |
GO:0032508 | DNA duplex unwinding | Yes |
GO:0016887 | ATP hydrolysis activity | Yes |
GO:0008152 | metabolic process | No |
GO:0048523 | negative regulation of cellular process | No |
GO:0051128 | regulation of cellular component organization | No |
GO:0051129 | negative regulation of cellular component organization | No |
GO:1905774 | regulation of DNA helicase activity | No |
GO:0043167 | ion binding | No |
GO:0051276 | chromosome organization | No |
GO:0017111 | nucleoside-triphosphatase activity | No |
GO:2001251 | negative regulation of chromosome organization | No |
GO:0010639 | negative regulation of organelle organization | No |
GO:0008150 | biological_process | No |
GO:0051097 | negative regulation of helicase activity | No |
GO:0065007 | biological regulation | No |
GO:0017076 | purine nucleotide binding | No |
GO:0003824 | catalytic activity | No |
GO:0034641 | cellular nitrogen compound metabolic process | No |
GO:0050789 | regulation of biological process | No |
GO:0051095 | regulation of helicase activity | No |
GO:0006725 | cellular aromatic compound metabolic process | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0032780 | negative regulation of ATP-dependent activity | No |
GO:0035639 | purine ribonucleoside triphosphate binding | No |
GO:0005575 | cellular_component | No |
GO:1905463 | negative regulation of DNA duplex unwinding | No |
GO:0050790 | regulation of catalytic activity | No |
GO:0043227 | membrane-bounded organelle | No |
GO:0071704 | organic substance metabolic process | No |
GO:0006996 | organelle organization | No |
GO:0033043 | regulation of organelle organization | No |
GO:0043086 | negative regulation of catalytic activity | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0032555 | purine ribonucleotide binding | No |
GO:0044238 | primary metabolic process | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0036094 | small molecule binding | No |
GO:0032559 | adenyl ribonucleotide binding | No |
GO:0016462 | pyrophosphatase activity | No |
GO:0016787 | hydrolase activity | No |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0016043 | cellular component organization | No |
GO:0000166 | nucleotide binding | No |
GO:0044237 | cellular metabolic process | No |
GO:0032553 | ribonucleotide binding | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0071840 | cellular component organization or biogenesis | No |
GO:0050794 | regulation of cellular process | No |
GO:0030554 | adenyl nucleotide binding | No |
GO:0032392 | DNA geometric change | No |
GO:0003674 | molecular_function | No |
GO:0065009 | regulation of molecular function | No |
GO:0044092 | negative regulation of molecular function | No |
GO:0048519 | negative regulation of biological process | No |
GO:0043168 | anion binding | No |
GO:0046483 | heterocycle metabolic process | No |
GO:0003676 | nucleic acid binding | No |
GO:0016817 | hydrolase activity, acting on acid anhydrides | No |
GO:0071103 | DNA conformation change | No |
GO:0033044 | regulation of chromosome organization | No |
GO:0097367 | carbohydrate derivative binding | No |
GO:0009987 | cellular process | No |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | No |
GO:0043462 | regulation of ATP-dependent activity | No |
GO:0032991 | protein-containing complex | No |
GO:0044260 | cellular macromolecule metabolic process | No |
GO:0006259 | DNA metabolic process | No |
GO:0043231 | intracellular membrane-bounded organelle | No |
GO:0006139 | nucleobase-containing compound metabolic process | No |
GO:0043229 | intracellular organelle | No |
GO:0090304 | nucleic acid metabolic process | No |
GO:0043226 | organelle | No |
GO:1905462 | regulation of DNA duplex unwinding | No |
GO:0110165 | cellular anatomical entity | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:0005488 | binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 11 | 0.45 |
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 | >Ophun1|784 MSSPLRDNPSSANRGLPPRSGLKRSRGVGDDGPSPADFGSSPSHMPSSPPNMAHGADDDDDIEEDAEIPDDLDEL DEQAGDEIDLFHEGYEADYADAEGDAYEGEGIDDEGDHEELDIGTRRRIDANLDKRDRNVRQRIPAAFLPDEEDG DIDPTALQRRHRHHYDEVAMDGGDIMDEVLSLEALSDVKATSLTDWLAQASVQRSIKHEFRAFLTSYTDSHGKSV YGDRINTMSTENGESLEVSYEHLSESKAILAYFLANAPTEMLALMDKVAMEVVLLQFSDYASIRSEIHVRITDLP VHYTLRQLRQSHLNCLVRVSGVVTRRTGVFPQLKYVKFDCAKCGVTLGPFQQENNVEVKISFCQNCQSRGPFSVN SEKTVYRNYQKLTLQESPGTVPAGRLPRHRDIILLWDLIDRAKPGEEVEITGIYRNNYDAQLNNRNGFPVFATVL EANNVVKSHDQLAGFRLTEEDEREIRRLSREPNIIDRLVRSMAPSIYGHTDIKTAVALSLFGGVAKTTKGAHHVR GDINVLLLGDPGTAKSQVLKYVEKTAHRAVFATGQGASAVGLTASVRRDPLTSEWTLEGGALVLADRGTCLIDEF DKMNDQDRTSIHEAMEQQTISISKAGIVTTLQARCGIIAAANPLGGRYNSTIPFSANVQLTEPILSRFDILCVVR DTVEPEEDERLARFIVGSHGRSHPDREAADGNEAPSASQGPDSMEVEHESHPRSRQQQRSGSDLEEIPQELLRKY ILYARERCSPKLYHMEEDKVARLFADMRRESITTGAYPITVRHLEAIIRISEAFCRMRLSEYCSTQDMDRAIAVT VDSFIGSQKLSCKKALSRAFAKYTLSRPAPRRRGRP* |
Coding | >Ophun1|784 ATGAGCTCCCCCCTCCGAGACAATCCATCCTCGGCCAACCGCGGTCTCCCTCCGCGATCCGGCCTCAAGCGCTCG CGCGGCGTCGGCGACGATGGTCCTTCGCCGGCAGACTTCGGCTCAAGCCCGAGTCACATGCCGTCGTCGCCGCCC AACATGGCGCACGGGGCGGACGACGACGACGACATCGAGGAGGACGCCGAGATCCCGGATGACCTTGACGAACTT GATGAGCAGGCTGGAGATGAGATCGACCTGTTTCACGAGGGCTATGAAGCCGATTATGCAGATGCTGAGGGAGAC GCATACGAGGGCGAGGGCATTGACGATGAAGGCGACCACGAAGAACTCGACATCGGCACCCGTCGTCGGATCGAC GCCAACCTCGACAAGCGGGACAGGAACGTACGGCAGAGAATCCCAGCCGCCTTTCTCCCAGACGAAGAGGATGGC GATATCGACCCCACAGCCCTGCAGCGAAGACATCGTCATCACTACGACGAGGTGGCCATGGACGGCGGCGACATC ATGGACGAGGTGCTCTCGCTCGAAGCACTAAGCGACGTCAAGGCAACAAGCCTAACGGACTGGCTCGCACAAGCC TCGGTGCAGCGATCCATCAAGCACGAGTTCCGCGCGTTCCTAACCTCCTACACCGACTCCCACGGCAAGTCCGTC TACGGCGACCGCATCAACACCATGAGCACGGAGAACGGCGAGTCTCTCGAGGTGTCGTACGAGCACCTGTCGGAA AGCAAGGCCATCCTCGCCTACTTCCTAGCCAACGCCCCGACCGAGATGCTCGCCCTCATGGACAAGGTGGCCATG GAAGTGGTGCTTCTTCAGTTCAGCGACTACGCCAGCATCCGGTCCGAGATCCACGTCCGGATCACGGACCTACCA GTCCACTACACGCTGCGACAGCTCCGTCAGTCGCATCTCAACTGCCTGGTACGGGTCAGCGGCGTCGTCACCCGC CGAACAGGCGTCTTCCCCCAGCTCAAATACGTAAAGTTCGACTGCGCAAAGTGCGGCGTCACGCTGGGCCCCTTT CAGCAGGAGAACAACGTCGAGGTCAAGATCTCGTTCTGCCAGAACTGCCAGTCTCGCGGGCCCTTTTCCGTCAAC TCGGAGAAGACGGTCTACCGCAACTACCAGAAGCTCACGCTGCAGGAGTCGCCGGGGACGGTGCCGGCCGGTCGT CTGCCCCGTCACCGAGACATCATCCTCCTCTGGGACCTGATAGACCGCGCCAAGCCCGGTGAGGAGGTGGAGATA ACGGGCATCTATCGCAACAACTACGACGCCCAGCTCAATAACCGCAATGGCTTCCCCGTCTTCGCCACCGTGCTC GAGGCCAACAACGTGGTCAAGTCACACGATCAGCTGGCCGGCTTCCGCCTGACCGAGGAAGACGAGCGAGAGATT CGCCGCCTGTCGCGCGAGCCCAACATCATCGACCGCCTGGTCCGGTCCATGGCGCCCAGCATCTACGGCCACACC GACATCAAGACAGCCGTCGCCCTCTCGCTCTTCGGCGGCGTGGCAAAGACGACAAAGGGCGCCCACCACGTCCGC GGCGACATCAACGTCCTGCTCCTCGGAGACCCGGGAACGGCAAAGTCCCAGGTGCTCAAGTACGTGGAGAAGACG GCGCACCGAGCCGTCTTCGCTACCGGTCAGGGAGCCAGCGCCGTCGGTCTGACGGCCAGCGTTCGCCGCGATCCC TTGACCAGCGAGTGGACGCTCGAGGGAGGCGCCCTTGTCCTGGCCGATCGCGGAACCTGCCTGATCGACGAGTTC GACAAGATGAACGACCAGGATCGTACCTCTATCCACGAGGCCATGGAGCAGCAGACCATCTCCATCTCAAAAGCC GGCATCGTCACCACCCTCCAGGCCCGCTGCGGCATCATCGCCGCCGCCAACCCGCTGGGAGGCCGCTACAACTCC ACCATCCCCTTCTCCGCCAACGTCCAGCTGACAGAGCCCATCCTCTCGCGCTTCGACATCCTATGCGTCGTCCGC GACACCGTCGAGCCAGAGGAAGACGAGCGTCTGGCCCGCTTCATCGTCGGCTCCCATGGCCGCAGCCACCCAGAC AGAGAAGCAGCGGACGGCAACGAAGCCCCCTCCGCTTCGCAGGGTCCGGATTCCATGGAGGTTGAGCACGAGTCG CATCCTCGTTCGCGACAGCAGCAGCGTTCCGGCTCGGATCTCGAGGAGATTCCGCAGGAGCTGCTGCGCAAGTAC ATCCTCTACGCGCGCGAACGCTGCAGTCCAAAGCTGTATCACATGGAAGAAGACAAGGTAGCGCGCCTCTTCGCA GACATGCGCCGCGAATCCATCACCACAGGAGCCTACCCCATCACGGTCCGCCACCTGGAAGCCATCATCCGCATC AGCGAAGCCTTCTGCCGCATGCGCCTCTCGGAATACTGCTCAACCCAGGACATGGATCGCGCCATCGCCGTGACG GTCGATAGCTTCATTGGCAGCCAGAAGCTGAGCTGCAAGAAGGCGCTCTCGCGCGCCTTCGCCAAGTACACGCTT TCTCGGCCGGCGCCGCGTCGGAGGGGGAGGCCTTAG |
Transcript | >Ophun1|784 ATGAGCTCCCCCCTCCGAGACAATCCATCCTCGGCCAACCGCGGTCTCCCTCCGCGATCCGGCCTCAAGCGCTCG CGCGGCGTCGGCGACGATGGTCCTTCGCCGGCAGACTTCGGCTCAAGCCCGAGTCACATGCCGTCGTCGCCGCCC AACATGGCGCACGGGGCGGACGACGACGACGACATCGAGGAGGACGCCGAGATCCCGGATGACCTTGACGAACTT GATGAGCAGGCTGGAGATGAGATCGACCTGTTTCACGAGGGCTATGAAGCCGATTATGCAGATGCTGAGGGAGAC GCATACGAGGGCGAGGGCATTGACGATGAAGGCGACCACGAAGAACTCGACATCGGCACCCGTCGTCGGATCGAC GCCAACCTCGACAAGCGGGACAGGAACGTACGGCAGAGAATCCCAGCCGCCTTTCTCCCAGACGAAGAGGATGGC GATATCGACCCCACAGCCCTGCAGCGAAGACATCGTCATCACTACGACGAGGTGGCCATGGACGGCGGCGACATC ATGGACGAGGTGCTCTCGCTCGAAGCACTAAGCGACGTCAAGGCAACAAGCCTAACGGACTGGCTCGCACAAGCC TCGGTGCAGCGATCCATCAAGCACGAGTTCCGCGCGTTCCTAACCTCCTACACCGACTCCCACGGCAAGTCCGTC TACGGCGACCGCATCAACACCATGAGCACGGAGAACGGCGAGTCTCTCGAGGTGTCGTACGAGCACCTGTCGGAA AGCAAGGCCATCCTCGCCTACTTCCTAGCCAACGCCCCGACCGAGATGCTCGCCCTCATGGACAAGGTGGCCATG GAAGTGGTGCTTCTTCAGTTCAGCGACTACGCCAGCATCCGGTCCGAGATCCACGTCCGGATCACGGACCTACCA GTCCACTACACGCTGCGACAGCTCCGTCAGTCGCATCTCAACTGCCTGGTACGGGTCAGCGGCGTCGTCACCCGC CGAACAGGCGTCTTCCCCCAGCTCAAATACGTAAAGTTCGACTGCGCAAAGTGCGGCGTCACGCTGGGCCCCTTT CAGCAGGAGAACAACGTCGAGGTCAAGATCTCGTTCTGCCAGAACTGCCAGTCTCGCGGGCCCTTTTCCGTCAAC TCGGAGAAGACGGTCTACCGCAACTACCAGAAGCTCACGCTGCAGGAGTCGCCGGGGACGGTGCCGGCCGGTCGT CTGCCCCGTCACCGAGACATCATCCTCCTCTGGGACCTGATAGACCGCGCCAAGCCCGGTGAGGAGGTGGAGATA ACGGGCATCTATCGCAACAACTACGACGCCCAGCTCAATAACCGCAATGGCTTCCCCGTCTTCGCCACCGTGCTC GAGGCCAACAACGTGGTCAAGTCACACGATCAGCTGGCCGGCTTCCGCCTGACCGAGGAAGACGAGCGAGAGATT CGCCGCCTGTCGCGCGAGCCCAACATCATCGACCGCCTGGTCCGGTCCATGGCGCCCAGCATCTACGGCCACACC GACATCAAGACAGCCGTCGCCCTCTCGCTCTTCGGCGGCGTGGCAAAGACGACAAAGGGCGCCCACCACGTCCGC GGCGACATCAACGTCCTGCTCCTCGGAGACCCGGGAACGGCAAAGTCCCAGGTGCTCAAGTACGTGGAGAAGACG GCGCACCGAGCCGTCTTCGCTACCGGTCAGGGAGCCAGCGCCGTCGGTCTGACGGCCAGCGTTCGCCGCGATCCC TTGACCAGCGAGTGGACGCTCGAGGGAGGCGCCCTTGTCCTGGCCGATCGCGGAACCTGCCTGATCGACGAGTTC GACAAGATGAACGACCAGGATCGTACCTCTATCCACGAGGCCATGGAGCAGCAGACCATCTCCATCTCAAAAGCC GGCATCGTCACCACCCTCCAGGCCCGCTGCGGCATCATCGCCGCCGCCAACCCGCTGGGAGGCCGCTACAACTCC ACCATCCCCTTCTCCGCCAACGTCCAGCTGACAGAGCCCATCCTCTCGCGCTTCGACATCCTATGCGTCGTCCGC GACACCGTCGAGCCAGAGGAAGACGAGCGTCTGGCCCGCTTCATCGTCGGCTCCCATGGCCGCAGCCACCCAGAC AGAGAAGCAGCGGACGGCAACGAAGCCCCCTCCGCTTCGCAGGGTCCGGATTCCATGGAGGTTGAGCACGAGTCG CATCCTCGTTCGCGACAGCAGCAGCGTTCCGGCTCGGATCTCGAGGAGATTCCGCAGGAGCTGCTGCGCAAGTAC ATCCTCTACGCGCGCGAACGCTGCAGTCCAAAGCTGTATCACATGGAAGAAGACAAGGTAGCGCGCCTCTTCGCA GACATGCGCCGCGAATCCATCACCACAGGAGCCTACCCCATCACGGTCCGCCACCTGGAAGCCATCATCCGCATC AGCGAAGCCTTCTGCCGCATGCGCCTCTCGGAATACTGCTCAACCCAGGACATGGATCGCGCCATCGCCGTGACG GTCGATAGCTTCATTGGCAGCCAGAAGCTGAGCTGCAAGAAGGCGCTCTCGCGCGCCTTCGCCAAGTACACGCTT TCTCGGCCGGCGCCGCGTCGGAGGGGGAGGCCTTAG |
Gene | >Ophun1|784 ATGAGGTATCGCATCATGAAGCGTCCGATCACTCATCTTCCCTCGCTAATGTCATCCCAGCTCCCCCCTCCGAGA CAATCCATCCTCGGCCAACCGCGGTCTCCCTCCGCGATCCGGCCTCAAGCGCTCGCGCGGCGTCGGCGACGATGG TCCTTCGCCGGCAGACTTCGGCTCAAGCCCGAGTCACATGCCGTCGTCGCCGCCCAACATGGCGCACGGGGCGGA CGACGACGACGACATCGAGGAGGACGCCGAGATCCCGGATGACCTTGACGAACTTGATGAGCAGGCTGGAGATGA GATCGACCTGTTTCACGAGGGCTATGAAGCCGATTATGCAGATGCTGAGGGAGACGCATACGAGGGCGAGGGCAT TGACGATGAAGGCGACCACGAAGAACTCGACATCGGCACCCGTCGTCGGATCGACGCCAACCTCGACAAGCGGGA CAGGAACGTACGGCAGAGAATCCCAGCCGCCTTTCTCCCAGACGAAGAGGATGGCGATATCGACCCCACAGCCCT GCAGCGAAGACATCGTCATCACTACGACGAGGTGGCCATGGACGGCGGCGACATCATGGACGAGGTGCTCTCGCT CGAAGCACTAAGCGACGTCAAGGCAACAAGCCTAACGGACTGGCTCGCACAAGCCTCGGTGCAGCGATCCATCAA GCACGAGTTCCGCGCGTTCCTAACCTCCTACACCGACTCCCACGGCAAGTCCGTCTACGGCGACCGCATCAACAC CATGAGCACGGAGAACGGCGAGTCTCTCGAGGTGTCGTACGAGCACCTGTCGGAAAGCAAGGCCATCCTCGCCTA CTTCCTAGCCAACGCCCCGACCGAGATGCTCGCCCTCATGGACAAGGTGGCCATGGAAGTGGTGCTTCTTCAGTT CAGCGACTACGCCAGCATCCGGTCCGAGATCCACGTCCGGATCACGGACCTACCAGTCCACTACACGCTGCGACA GCTCCGTCAGTCGCATCTCAACTGCCTGGTACGGGTCAGCGGCGTCGTCACCCGCCGAACAGGCGTCTTCCCCCA GCTCAAATACGTAAAGTTCGACTGCGCAAAGTGCGGCGTCACGCTGGGCCCCTTTCAGCAGGAGAACAACGTCGA GGTCAAGATCTCGTTCTGCCAGAACTGCCAGTCTCGCGGGCCCTTTTCCGTCAACTCGGAGAAGACGGTCTACCG CAACTACCAGAAGCTCACGCTGCAGGAGTCGCCGGGGACGGTGCCGGCCGGTCGTCTGCCCCGTCACCGAGACAT CATCCTCCTCTGGGACCTGATAGACCGCGCCAAGCCCGGTGAGGAGGTGGAGATAACGGGCATCTATCGCAACAA CTACGACGCCCAGCTCAATAACCGCAATGGCTTCCCCGTCTTCGCCACCGTGCTCGAGGCCAACAACGTGGTCAA GTCACACGATCAGCTGGCCGGCTTCCGCCTGACCGAGGAAGACGAGCGAGAGATTCGCCGCCTGTCGCGCGAGCC CAACATCATCGACCGCCTGGTCCGGTCCATGGCGCCCAGCATCTACGGCCACACCGACATCAAGACAGCCGTCGC CCTCTCGCTCTTCGGCGGCGTGGCAAAGACGACAAAGGGCGCCCACCACGTCCGCGGCGACATCAACGTCCTGCT CCTCGGAGACCCGGGAACGGCAAAGTCCCAGGTGCTCAAGTACGTGGAGAAGACGGCGCACCGAGCCGTCTTCGC TACCGGTCAGGGAGCCAGCGCCGTCGGTCTGACGGCCAGCGTTCGCCGCGATCCCTTGACCAGCGAGTGGACGCT CGAGGGAGGCGCCCTTGTCCTGGCCGATCGCGGAACCTGCCTGATCGACGAGTTCGACAAGATGAACGACCAGGA TCGTACCTCTATCCACGAGGCCATGGAGCAGCAGACCATCTCCATCTCAAAAGCCGGCATCGTCACCACCCTCCA GGCCCGCTGCGGCATCATCGCCGCCGCCAACCCGCTGGGAGGCCGCTACAACTCCACCATCCCCTTCTCCGCCAA CGTCCAGCTGACAGAGCCCATCCTCTCGCGCTTCGACATCCTATGCGTCGTCCGCGACACCGTCGAGCCAGAGGA AGACGAGCGTCTGGCCCGCTTCATCGTCGGCTCCCATGGCCGCAGCCACCCAGACAGAGAAGCAGCGGACGGCAA CGAAGCCCCCTCCGCTTCGCAGGGTCCGGATTCCATGGAGGTTGAGCACGAGTCGCATCCTCGTTCGCGACAGCA GCAGCGTTCCGGCTCGGATCTCGAGGAGATTCCGCAGGAGCTGCTGCGCAAGTACATCCTCTACGCGCGCGAACG CTGCAGTCCAAAGCTGTATCACATGGAAGAAGACAAGGTAGCGCGCCTCTTCGCAGACATGCGCCGCGAATCCAT CACCACAGGAGCCTACCCCATCACGGTATAGTCTTTGACCCCCCCCCTGATAACCAACCTCCCTCTCTAACCAAC CCTTCTTCTGCAGGTCCGCCACCTGGAAGCCATCATCCGCATCAGCGAAGCCTTCTGCCGCATGCGCCTCTCGGA ATACTGCTCAACCCAGGACATGGATCGCGCCATCGCCGTGACGGTCGATAGCTTCATTGGCAGCCAGAAGCTGAG CTGCAAGAAGGCGCTCTCGCGCGCCTTCGCCAAGTACACGCTTTCTCGGCCGGCGCCGCGTCGGAGGGGGAGGCC TTAG |