Protein ID | Ophio5|4673 |
Gene name | |
Location | scaffold_372:3173..7262 |
Strand | + |
Gene length (bp) | 4089 |
Transcript length (bp) | 4089 |
Coding sequence length (bp) | 4086 |
Protein length (aa) | 1362 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00069 | Pkinase | Protein kinase domain | 1.0E-20 | 98 | 289 |
PF12796 | Ank_2 | Ankyrin repeats (3 copies) | 3.2E-07 | 674 | 737 |
PF12796 | Ank_2 | Ankyrin repeats (3 copies) | 3.2E-07 | 679 | 751 |
PF07714 | PK_Tyr_Ser-Thr | Protein tyrosine and serine/threonine kinase | 2.4E-15 | 76 | 293 |
PF13606 | Ank_3 | Ankyrin repeat | 2.3E-03 | 711 | 737 |
PF13637 | Ank_4 | Ankyrin repeats (many copies) | 1.1E-04 | 676 | 730 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q7T6Y2|YR831_MIMIV | Putative serine/threonine-protein kinase/receptor R831 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R831 PE=3 SV=2 | 105 | 289 | 6.0E-11 |
sp|Q96S53|TESK2_HUMAN | Dual specificity testis-specific protein kinase 2 OS=Homo sapiens GN=TESK2 PE=1 SV=1 | 136 | 285 | 8.0E-11 |
sp|Q3U3Q1|ULK3_MOUSE | Serine/threonine-protein kinase ULK3 OS=Mus musculus GN=Ulk3 PE=2 SV=1 | 75 | 290 | 1.0E-10 |
sp|D3ZHP7|ULK3_RAT | Serine/threonine-protein kinase ULK3 OS=Rattus norvegicus GN=Ulk3 PE=1 SV=1 | 75 | 290 | 1.0E-10 |
sp|Q2MHE4|HT1_ARATH | Serine/threonine-protein kinase HT1 OS=Arabidopsis thaliana GN=HT1 PE=1 SV=1 | 135 | 286 | 3.0E-10 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q7T6Y2|YR831_MIMIV | Putative serine/threonine-protein kinase/receptor R831 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R831 PE=3 SV=2 | 105 | 289 | 6.0E-11 |
sp|Q96S53|TESK2_HUMAN | Dual specificity testis-specific protein kinase 2 OS=Homo sapiens GN=TESK2 PE=1 SV=1 | 136 | 285 | 8.0E-11 |
sp|Q3U3Q1|ULK3_MOUSE | Serine/threonine-protein kinase ULK3 OS=Mus musculus GN=Ulk3 PE=2 SV=1 | 75 | 290 | 1.0E-10 |
sp|D3ZHP7|ULK3_RAT | Serine/threonine-protein kinase ULK3 OS=Rattus norvegicus GN=Ulk3 PE=1 SV=1 | 75 | 290 | 1.0E-10 |
sp|Q2MHE4|HT1_ARATH | Serine/threonine-protein kinase HT1 OS=Arabidopsis thaliana GN=HT1 PE=1 SV=1 | 135 | 286 | 3.0E-10 |
sp|Q924U5|TESK2_RAT | Dual specificity testis-specific protein kinase 2 OS=Rattus norvegicus GN=Tesk2 PE=2 SV=1 | 136 | 285 | 4.0E-10 |
sp|Q12263|GIN4_YEAST | Serine/threonine-protein kinase GIN4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIN4 PE=1 SV=1 | 136 | 324 | 4.0E-10 |
sp|C0LGV1|RCH1_ARATH | LRR receptor-like serine/threonine-protein kinase RCH1 OS=Arabidopsis thaliana GN=RCH1 PE=2 SV=1 | 76 | 289 | 1.0E-09 |
sp|Q6PHR2|ULK3_HUMAN | Serine/threonine-protein kinase ULK3 OS=Homo sapiens GN=ULK3 PE=1 SV=2 | 75 | 290 | 1.0E-09 |
sp|Q8VCT9|TESK2_MOUSE | Dual specificity testis-specific protein kinase 2 OS=Mus musculus GN=Tesk2 PE=1 SV=1 | 136 | 285 | 2.0E-09 |
sp|Q5VJL3|GDT9_DICDI | Probable serine/threonine-protein kinase gdt9 OS=Dictyostelium discoideum GN=gdt9 PE=2 SV=2 | 184 | 291 | 2.0E-09 |
sp|P25389|KCC4_YEAST | Probable serine/threonine-protein kinase KCC4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=KCC4 PE=1 SV=3 | 136 | 324 | 3.0E-09 |
sp|C0LGJ1|Y1743_ARATH | Probable LRR receptor-like serine/threonine-protein kinase At1g74360 OS=Arabidopsis thaliana GN=At1g74360 PE=2 SV=1 | 136 | 284 | 3.0E-09 |
sp|Q55FT4|TSUA_DICDI | Probable serine/threonine-protein kinase tsuA OS=Dictyostelium discoideum GN=tsuA PE=1 SV=1 | 106 | 290 | 3.0E-09 |
sp|Q60855|RIPK1_MOUSE | Receptor-interacting serine/threonine-protein kinase 1 OS=Mus musculus GN=Ripk1 PE=1 SV=1 | 102 | 286 | 3.0E-09 |
sp|Q15569|TESK1_HUMAN | Dual specificity testis-specific protein kinase 1 OS=Homo sapiens GN=TESK1 PE=1 SV=2 | 136 | 285 | 3.0E-09 |
sp|O70146|TESK1_MOUSE | Dual specificity testis-specific protein kinase 1 OS=Mus musculus GN=Tesk1 PE=1 SV=3 | 109 | 285 | 4.0E-09 |
sp|Q63572|TESK1_RAT | Dual specificity testis-specific protein kinase 1 OS=Rattus norvegicus GN=Tesk1 PE=1 SV=1 | 109 | 285 | 5.0E-09 |
sp|Q9ESL4|MLTK_MOUSE | Mitogen-activated protein kinase kinase kinase MLT OS=Mus musculus GN=Zak PE=1 SV=1 | 136 | 289 | 1.0E-08 |
sp|Q4V7Q6|ULK3_XENLA | Serine/threonine-protein kinase ULK3 OS=Xenopus laevis GN=ulk3 PE=2 SV=1 | 105 | 290 | 1.0E-08 |
sp|A8R7E6|CERK1_ARATH | Chitin elicitor receptor kinase 1 OS=Arabidopsis thaliana GN=CERK1 PE=1 SV=1 | 119 | 289 | 2.0E-08 |
sp|Q8IYT8|ULK2_HUMAN | Serine/threonine-protein kinase ULK2 OS=Homo sapiens GN=ULK2 PE=1 SV=3 | 71 | 290 | 2.0E-08 |
sp|Q9NYL2|MLTK_HUMAN | Mitogen-activated protein kinase kinase kinase MLT OS=Homo sapiens GN=ZAK PE=1 SV=3 | 136 | 289 | 2.0E-08 |
sp|Q59W62|GIN4_CANAL | Serine/threonine-protein kinase GIN4 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GIN4 PE=1 SV=1 | 136 | 350 | 4.0E-08 |
sp|Q3EDL4|Y1154_ARATH | Probable serine/threonine-protein kinase At1g01540 OS=Arabidopsis thaliana GN=At1g01540 PE=1 SV=2 | 19 | 285 | 5.0E-08 |
sp|Q9QY01|ULK2_MOUSE | Serine/threonine-protein kinase ULK2 OS=Mus musculus GN=Ulk2 PE=1 SV=1 | 73 | 290 | 5.0E-08 |
sp|Q8S8S7|PUB34_ARATH | U-box domain-containing protein 34 OS=Arabidopsis thaliana GN=PUB34 PE=3 SV=1 | 103 | 289 | 6.0E-08 |
sp|O48814|BIK1_ARATH | Serine/threonine-protein kinase BIK1 OS=Arabidopsis thaliana GN=BIK1 PE=1 SV=1 | 60 | 289 | 6.0E-08 |
sp|Q90ZY4|SBK1_DANRE | Serine/threonine-protein kinase SBK1 OS=Danio rerio GN=sbk1 PE=1 SV=1 | 137 | 290 | 7.0E-08 |
sp|Q5ZJH6|ULK3_CHICK | Serine/threonine-protein kinase ULK3 OS=Gallus gallus GN=ULK3 PE=2 SV=1 | 75 | 290 | 7.0E-08 |
sp|Q7T6X2|YR826_MIMIV | Putative serine/threonine-protein kinase/receptor R826 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_R826 PE=3 SV=2 | 119 | 289 | 8.0E-08 |
sp|Q13546|RIPK1_HUMAN | Receptor-interacting serine/threonine-protein kinase 1 OS=Homo sapiens GN=RIPK1 PE=1 SV=3 | 102 | 286 | 9.0E-08 |
sp|C0LGF5|Y1341_ARATH | Probable LRR receptor-like serine/threonine-protein kinase At1g34110 OS=Arabidopsis thaliana GN=At1g34110 PE=2 SV=2 | 76 | 289 | 9.0E-08 |
sp|Q54TM7|DRKD_DICDI | Probable serine/threonine-protein kinase drkD OS=Dictyostelium discoideum GN=drkD PE=2 SV=1 | 136 | 289 | 9.0E-08 |
sp|P54744|PKNB_MYCLE | Serine/threonine-protein kinase PknB OS=Mycobacterium leprae (strain TN) GN=pknB PE=3 SV=3 | 136 | 289 | 1.0E-07 |
sp|Q9LFP7|Y5158_ARATH | Probable receptor-like protein kinase At5g15080 OS=Arabidopsis thaliana GN=At5g15080 PE=2 SV=1 | 105 | 285 | 1.0E-07 |
sp|Q8H186|Y3545_ARATH | Probable receptor-like protein kinase At3g55450 OS=Arabidopsis thaliana GN=At3g55450 PE=1 SV=1 | 60 | 289 | 1.0E-07 |
sp|Q8XJL8|PKN2_CLOPE | Probable serine/threonine-protein kinase CPE1738 OS=Clostridium perfringens (strain 13 / Type A) GN=CPE1738 PE=3 SV=1 | 136 | 289 | 2.0E-07 |
sp|O01427|AIR2_CAEEL | Aurora/IPL1-related protein kinase 2 OS=Caenorhabditis elegans GN=air-2 PE=1 SV=2 | 136 | 314 | 2.0E-07 |
sp|F4JTP5|STY46_ARATH | Serine/threonine-protein kinase STY46 OS=Arabidopsis thaliana GN=STY46 PE=1 SV=1 | 127 | 289 | 2.0E-07 |
sp|Q9SRH7|Y3130_ARATH | Receptor-like serine/threonine-protein kinase At3g01300 OS=Arabidopsis thaliana GN=At3g01300 PE=2 SV=1 | 24 | 285 | 2.0E-07 |
sp|F4I1N8|ATG1T_ARATH | Serine/threonine-protein kinase ATG1t OS=Arabidopsis thaliana GN=At1g49180 PE=2 SV=1 | 136 | 289 | 2.0E-07 |
sp|P57078|RIPK4_HUMAN | Receptor-interacting serine/threonine-protein kinase 4 OS=Homo sapiens GN=RIPK4 PE=1 SV=1 | 159 | 286 | 2.0E-07 |
sp|Q5XF57|Y5576_ARATH | Probable receptor-like serine/threonine-protein kinase At5g57670 OS=Arabidopsis thaliana GN=At5g57670 PE=2 SV=1 | 94 | 285 | 2.0E-07 |
sp|Q9ERK0|RIPK4_MOUSE | Receptor-interacting serine/threonine-protein kinase 4 OS=Mus musculus GN=Ripk4 PE=1 SV=2 | 159 | 286 | 3.0E-07 |
sp|Q55CY9|GDT8_DICDI | Probable serine/threonine-protein kinase gdt8 OS=Dictyostelium discoideum GN=gdt8 PE=3 SV=1 | 159 | 291 | 3.0E-07 |
sp|Q3UHC2|LRRK1_MOUSE | Leucine-rich repeat serine/threonine-protein kinase 1 OS=Mus musculus GN=Lrrk1 PE=1 SV=1 | 136 | 289 | 3.0E-07 |
sp|P0C5E2|Y1839_ARATH | Probable serine/threonine-protein kinase At1g18390 OS=Arabidopsis thaliana GN=At1g18390 PE=2 SV=2 | 136 | 285 | 3.0E-07 |
sp|Q64261|CDK6_MOUSE | Cyclin-dependent kinase 6 OS=Mus musculus GN=Cdk6 PE=1 SV=2 | 95 | 264 | 3.0E-07 |
sp|P54736|PKN2_MYXXA | Serine/threonine-protein kinase pkn2 OS=Myxococcus xanthus GN=pkn2 PE=3 SV=1 | 136 | 289 | 4.0E-07 |
sp|Q3ECH2|Y1670_ARATH | Probable receptor-like protein kinase At1g67000 OS=Arabidopsis thaliana GN=At1g67000 PE=2 SV=2 | 136 | 285 | 4.0E-07 |
sp|Q9C5S8|CRK5_ARATH | Cysteine-rich receptor-like protein kinase 5 OS=Arabidopsis thaliana GN=CRK5 PE=1 SV=1 | 56 | 285 | 4.0E-07 |
sp|Q9Z2P5|RIPK3_RAT | Receptor-interacting serine/threonine-protein kinase 3 OS=Rattus norvegicus GN=Ripk3 PE=1 SV=3 | 136 | 289 | 5.0E-07 |
sp|Q6XHA5|ROC11_DICDI | Probable serine/threonine-protein kinase roco11 OS=Dictyostelium discoideum GN=roco11 PE=3 SV=1 | 136 | 321 | 5.0E-07 |
sp|Q9XEC7|CRK37_ARATH | Cysteine-rich receptor-like protein kinase 37 OS=Arabidopsis thaliana GN=CRK37 PE=3 SV=1 | 66 | 285 | 5.0E-07 |
sp|Q00534|CDK6_HUMAN | Cyclin-dependent kinase 6 OS=Homo sapiens GN=CDK6 PE=1 SV=1 | 95 | 264 | 5.0E-07 |
sp|Q39203|SD22_ARATH | G-type lectin S-receptor-like serine/threonine-protein kinase SD2-2 OS=Arabidopsis thaliana GN=SD22 PE=1 SV=1 | 63 | 285 | 5.0E-07 |
sp|Q9FID6|Y5392_ARATH | Probable receptor-like protein kinase At5g39020 OS=Arabidopsis thaliana GN=At5g39020 PE=2 SV=1 | 136 | 285 | 6.0E-07 |
sp|O65405|CRK28_ARATH | Cysteine-rich receptor-like protein kinase 28 OS=Arabidopsis thaliana GN=CRK28 PE=3 SV=2 | 103 | 285 | 7.0E-07 |
sp|Q54L00|LIMKA_DICDI | Probable LIM domain-containing serine/threonine-protein kinase DDB_G0287001 OS=Dictyostelium discoideum GN=DDB_G0287001 PE=3 SV=1 | 136 | 286 | 7.0E-07 |
sp|Q8SSS9|QKGA_DICDI | Probable serine/threonine-protein kinase qkgA OS=Dictyostelium discoideum GN=qkgA-1 PE=3 SV=2 | 136 | 289 | 7.0E-07 |
sp|Q5JPF3|AN36C_HUMAN | Ankyrin repeat domain-containing protein 36C OS=Homo sapiens GN=ANKRD36C PE=2 SV=3 | 665 | 822 | 7.0E-07 |
sp|Q05609|CTR1_ARATH | Serine/threonine-protein kinase CTR1 OS=Arabidopsis thaliana GN=CTR1 PE=1 SV=1 | 73 | 301 | 7.0E-07 |
sp|Q54H05|KINY_DICDI | Probable serine/threonine-protein kinase kinY OS=Dictyostelium discoideum GN=kinY PE=2 SV=1 | 136 | 290 | 8.0E-07 |
sp|Q54TA1|DRKC_DICDI | Probable serine/threonine-protein kinase drkC OS=Dictyostelium discoideum GN=drkC PE=3 SV=1 | 136 | 287 | 8.0E-07 |
sp|Q6C3J2|IPL1_YARLI | Spindle assembly checkpoint kinase OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=IPL1 PE=3 SV=1 | 136 | 289 | 8.0E-07 |
sp|Q21017|KIN29_CAEEL | Serine/threonine-protein kinase kin-29 OS=Caenorhabditis elegans GN=kin-29 PE=1 SV=2 | 136 | 322 | 9.0E-07 |
sp|Q9FII5|TDR_ARATH | Leucine-rich repeat receptor-like protein kinase TDR OS=Arabidopsis thaliana GN=TDR PE=1 SV=1 | 76 | 285 | 9.0E-07 |
sp|Q5S007|LRRK2_HUMAN | Leucine-rich repeat serine/threonine-protein kinase 2 OS=Homo sapiens GN=LRRK2 PE=1 SV=2 | 116 | 286 | 9.0E-07 |
sp|Q9FID9|Y5389_ARATH | Probable receptor-like protein kinase At5g38990 OS=Arabidopsis thaliana GN=At5g38990 PE=2 SV=1 | 136 | 289 | 1.0E-06 |
sp|Q9ZP16|CRK11_ARATH | Cysteine-rich receptor-like protein kinase 11 OS=Arabidopsis thaliana GN=CRK11 PE=2 SV=2 | 63 | 285 | 1.0E-06 |
sp|Q6CWQ4|IPL1_KLULA | Spindle assembly checkpoint kinase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=IPL1 PE=3 SV=1 | 136 | 290 | 1.0E-06 |
sp|Q8W4G6|CRK15_ARATH | Cysteine-rich receptor-like protein kinase 15 OS=Arabidopsis thaliana GN=CRK15 PE=2 SV=2 | 54 | 285 | 1.0E-06 |
sp|Q9LHP4|RCH2_ARATH | Receptor-like protein kinase 2 OS=Arabidopsis thaliana GN=RCH2 PE=1 SV=1 | 136 | 289 | 1.0E-06 |
sp|Q6XHB2|ROCO4_DICDI | Probable serine/threonine-protein kinase roco4 OS=Dictyostelium discoideum GN=roco4 PE=1 SV=1 | 136 | 289 | 2.0E-06 |
sp|Q54VC0|Y9865_DICDI | Probable serine/threonine-protein kinase DDB_G0280461 OS=Dictyostelium discoideum GN=DDB_G0280461 PE=3 SV=1 | 118 | 291 | 2.0E-06 |
sp|Q9LP24|Y1571_ARATH | Probable leucine-rich repeat receptor-like protein kinase At1g35710 OS=Arabidopsis thaliana GN=At1g35710 PE=2 SV=1 | 107 | 290 | 2.0E-06 |
sp|Q38SD2|LRRK1_HUMAN | Leucine-rich repeat serine/threonine-protein kinase 1 OS=Homo sapiens GN=LRRK1 PE=1 SV=3 | 179 | 289 | 2.0E-06 |
sp|Q54Y90|Y0133_DICDI | Probable serine/threonine-protein kinase DDB_G0278665 OS=Dictyostelium discoideum GN=DDB_G0278665 PE=3 SV=1 | 117 | 291 | 2.0E-06 |
sp|Q9XEC8|CRK38_ARATH | Cysteine-rich receptor-like protein kinase 38 OS=Arabidopsis thaliana GN=CRK38 PE=3 SV=1 | 103 | 285 | 2.0E-06 |
sp|Q55GG4|Y9847_DICDI | Probable serine/threonine-protein kinase DDB_G0267686 OS=Dictyostelium discoideum GN=DDB_G0267686 PE=3 SV=1 | 75 | 292 | 2.0E-06 |
sp|P0CD62|LIMKB_DICDI | Probable LIM domain-containing serine/threonine-protein kinase DDB_G0286997 OS=Dictyostelium discoideum GN=DDB_G0286997 PE=3 SV=1 | 136 | 289 | 2.0E-06 |
sp|Q54RZ7|Y1199_DICDI | Probable serine/threonine-protein kinase DDB_G0282895 OS=Dictyostelium discoideum GN=DDB_G0282895 PE=3 SV=1 | 108 | 287 | 3.0E-06 |
sp|Q54H46|DRKA_DICDI | Probable serine/threonine-protein kinase drkA OS=Dictyostelium discoideum GN=drkA PE=3 SV=1 | 129 | 307 | 3.0E-06 |
sp|Q9S9M3|WAKLC_ARATH | Wall-associated receptor kinase-like 3 OS=Arabidopsis thaliana GN=WAKL3 PE=2 SV=2 | 65 | 285 | 4.0E-06 |
sp|Q09892|HOG1_SCHPO | Mitogen-activated protein kinase sty1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=sty1 PE=1 SV=1 | 105 | 271 | 4.0E-06 |
sp|Q6NKZ9|Y4345_ARATH | Probable receptor-like serine/threonine-protein kinase At4g34500 OS=Arabidopsis thaliana GN=At4g34500 PE=2 SV=1 | 66 | 307 | 4.0E-06 |
sp|Q54HW1|PSD10_DICDI | 26S proteasome non-ATPase regulatory subunit 10 OS=Dictyostelium discoideum GN=psmD10 PE=2 SV=1 | 679 | 856 | 4.0E-06 |
sp|Q8RZV7|MSP1_ORYSJ | Leucine-rich repeat receptor protein kinase MSP1 OS=Oryza sativa subsp. japonica GN=MSP1 PE=1 SV=1 | 136 | 289 | 5.0E-06 |
sp|O70405|ULK1_MOUSE | Serine/threonine-protein kinase ULK1 OS=Mus musculus GN=Ulk1 PE=1 SV=1 | 105 | 289 | 5.0E-06 |
sp|Q9Y572|RIPK3_HUMAN | Receptor-interacting serine/threonine-protein kinase 3 OS=Homo sapiens GN=RIPK3 PE=1 SV=2 | 145 | 286 | 5.0E-06 |
sp|Q9SGP2|HSL1_ARATH | Receptor-like protein kinase HSL1 OS=Arabidopsis thaliana GN=HSL1 PE=2 SV=1 | 76 | 285 | 6.0E-06 |
sp|Q9LRP3|Y3174_ARATH | Probable receptor-like protein kinase At3g17420 OS=Arabidopsis thaliana GN=At3g17420 PE=1 SV=1 | 94 | 289 | 7.0E-06 |
sp|Q9SHI2|Y1723_ARATH | Leucine-rich repeat receptor-like serine/threonine-protein kinase At1g17230 OS=Arabidopsis thaliana GN=At1g17230 PE=2 SV=2 | 65 | 365 | 7.0E-06 |
sp|O75385|ULK1_HUMAN | Serine/threonine-protein kinase ULK1 OS=Homo sapiens GN=ULK1 PE=1 SV=2 | 77 | 289 | 8.0E-06 |
sp|Q8GUQ5|BRI1_SOLLC | Brassinosteroid LRR receptor kinase OS=Solanum lycopersicum GN=CURL3 PE=1 SV=1 | 63 | 289 | 9.0E-06 |
sp|P43298|TMK1_ARATH | Receptor protein kinase TMK1 OS=Arabidopsis thaliana GN=TMK1 PE=1 SV=1 | 71 | 285 | 9.0E-06 |
sp|O70511|ANK3_RAT | Ankyrin-3 OS=Rattus norvegicus GN=Ank3 PE=1 SV=3 | 671 | 1051 | 9.0E-06 |
sp|Q23023|UNC51_CAEEL | Serine/threonine-protein kinase unc-51 OS=Caenorhabditis elegans GN=unc-51 PE=1 SV=1 | 71 | 289 | 9.0E-06 |
sp|Q8L899|BRI1_SOLPE | Systemin receptor SR160 OS=Solanum peruvianum PE=1 SV=1 | 63 | 289 | 9.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0005515 | protein binding | Yes |
GO:0005524 | ATP binding | Yes |
GO:0004672 | protein kinase activity | Yes |
GO:0006468 | protein phosphorylation | Yes |
GO:0016310 | phosphorylation | No |
GO:0071704 | organic substance metabolic process | No |
GO:0032555 | purine ribonucleotide binding | No |
GO:0006793 | phosphorus metabolic process | No |
GO:0016740 | transferase activity | No |
GO:0003674 | molecular_function | No |
GO:0044237 | cellular metabolic process | No |
GO:0008152 | metabolic process | No |
GO:0043167 | ion binding | No |
GO:0043412 | macromolecule modification | No |
GO:0140096 | catalytic activity, acting on a protein | No |
GO:0044238 | primary metabolic process | No |
GO:0006796 | phosphate-containing compound metabolic process | No |
GO:1901564 | organonitrogen compound metabolic process | No |
GO:0043168 | anion binding | No |
GO:0008150 | biological_process | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0000166 | nucleotide binding | No |
GO:0035639 | purine ribonucleoside triphosphate binding | No |
GO:0003824 | catalytic activity | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0032559 | adenyl ribonucleotide binding | No |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | No |
GO:0036094 | small molecule binding | No |
GO:0016301 | kinase activity | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0097367 | carbohydrate derivative binding | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:0032553 | ribonucleotide binding | No |
GO:0036211 | protein modification process | No |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | No |
GO:0019538 | protein metabolic process | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0017076 | purine nucleotide binding | No |
GO:0030554 | adenyl nucleotide binding | No |
GO:0009987 | cellular process | No |
GO:0005488 | binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 44 | 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 | >Ophio5|4673 MVETTAYAYPSTFAAESETSGNAASSSSGASAAKASLAGGAFASFICHVAHLEKGLQSEKSFFDEAQRKASSRTR LGHGTSFLVDRVELPSSSGDATKESRFAVIKTVRQKGQSPTQWRDVLLEIRVLLHKPIRYHPNIVRLLDIGWDNS SEIASPFPALIQEYAEFGTLARLQADSRPLPFPIKQKLCYDVGRGLSILHACGIIHGDLKHENVLVFANRYPSPA GQPYTAKVADFGGSIMDVLDGSGSHSILMNTFPYEAPEIGQKLSVDGVKKTDAFSYGMLIWRCMLDCDDVLAAIG FALPPGQPSDEDRTAMNKLKLSDQLLEGAIASLSKHATTRDLPSQSLGLIVTSLLFTLRGDPAQRALDRAQARTR GMSASASQAYVYVKEAANKKLAESQERRTPGSHGIDMDSVGYALGRVAGDDYDAQNNLPGYRPDLPHPEKGGFLF EPLKLRRLLDWEQQKDMVAEFMAAAAAPRSRGSAAGLEPWSASFFLYQSFLSGFGVSVDGAEACRWLRSAAQASE ETATVDYLAGAWLVRAHGALNVPNPLTPDEQMSFLFWGRIRGHRHCSTDAQSMIQAEPETSKRTYWESRMMNACA NYLSRTGGTGMPFFISRRLTRQWDTEDVVALDETVKAELGDAYGSCLRPEPYSMTNEPTPDGGYRFDAIYVNNKG HGLLHLAATLGDVEILKHLHGKYKCNINLSNQSHSDTPLTCACRSGNLSCALYLLENGADANGTEFGEESPLHCI ANFVDADMDVIVPKLMAAGADMEKLSQPSRKDVRGILADWEDSGSMKLTPLGRAVLFQNLHAVEILLRYGANPWG YRTDSKLASVQPMQLAAVLTLPDILQTMLSHTEEAESAPLFDECGMLQRAHSCQLTPYDALTLQSRIIRCGSLYK PYLAQTLRILRDRRRKLGLAAQESSPGAQLCAEIALGNKDIVEALLHLGHDVDGSACTRPIRAAVMANDEDMFFS VLLRRGASLSISHDEESGQPSLLSAAATRPHYTPRGTRIVEYLLSQGVSPEPKTQQQPCALALAVRNGYFELADL FLSGTSIESLNAFHTWSDGRDSESVLGSLLSSHTNSSARAVAYLAAVHGDSTWRLEMGPQVNKVKRLSAVHVVAQ CPSSEWNDYSQISARIVQHVLNMFPKPETLGEHHIHPIVGTPLSAAVLAGNKSMVALLMDSPYREDVDKSVPIEY QLGGVKTKESLTPRELASKITQDLMQRLSSVVTAATPIGLTKLRDASEIMLQLIKTDGSDQDQSPNPEEMRLVVR NRLDKVKMETDEVGSHDPSAMLPVDLSVICEEKPSGWHEGVEMTEVMAHRTFLKTFRSAEASFGDGITGVMDKAF NKRSPELRSTGG |
Coding | >Ophio5|4673 ATGGTAGAAACAACAGCCTACGCCTATCCGTCCACCTTCGCCGCCGAATCCGAAACGTCTGGCAACGCCGCCTCC AGCTCAAGCGGCGCGTCAGCGGCCAAAGCGAGTCTCGCCGGAGGAGCCTTTGCCTCGTTCATCTGCCACGTCGCC CACCTGGAAAAAGGTCTTCAGTCGGAAAAGTCCTTCTTTGACGAAGCGCAGCGGAAAGCGAGTTCGAGAACGCGA CTCGGCCACGGCACCTCGTTTCTCGTCGACCGAGTAGAGTTGCCGTCCAGCAGCGGAGATGCCACCAAAGAGTCC CGATTCGCCGTCATCAAGACGGTCCGGCAGAAGGGTCAGAGCCCGACGCAGTGGCGAGATGTTCTCCTGGAGATA AGGGTGCTGTTGCACAAGCCGATTCGCTATCACCCCAACATCGTCCGTCTTCTCGACATAGGGTGGGATAATTCC AGTGAGATTGCGTCACCCTTTCCGGCTCTGATTCAAGAGTATGCCGAGTTTGGAACGTTGGCCAGGCTGCAGGCA GACAGCAGGCCGCTTCCGTTCCCTATCAAGCAGAAGCTTTGCTACGATGTTGGCCGGGGGTTGTCCATCTTACAC GCCTGTGGCATCATTCACGGGGACCTGAAGCACGAGAATGTTCTCGTCTTTGCTAACCGATATCCGAGTCCGGCC GGCCAACCATACACGGCAAAGGTGGCTGATTTCGGAGGGAGTATCATGGACGTCTTGGATGGCAGCGGTTCGCAC AGCATCCTCATGAACACGTTCCCCTACGAAGCACCCGAGATCGGCCAGAAGCTTTCGGTGGACGGGGTGAAGAAG ACGGATGCCTTTTCGTACGGTATGCTCATCTGGCGATGTATGCTGGATTGTGATGATGTCTTGGCCGCCATAGGC TTCGCCCTTCCGCCGGGCCAGCCGAGCGACGAAGACCGGACAGCGATGAACAAGCTCAAGCTATCCGACCAACTG CTCGAGGGCGCCATTGCCAGCCTCTCGAAGCATGCCACTACTCGTGACCTGCCAAGTCAAAGCCTCGGCCTCATC GTCACCTCCCTCCTCTTCACTCTTCGCGGTGACCCAGCCCAGAGGGCTCTGGATCGCGCCCAGGCTCGTACCCGG GGCATGTCTGCCTCGGCTTCTCAGGCTTACGTCTACGTCAAGGAGGCGGCCAACAAGAAACTGGCGGAAAGTCAA GAGCGACGCACGCCCGGCAGCCATGGCATAGACATGGACAGCGTAGGCTATGCTCTCGGACGCGTAGCTGGGGAC GACTACGATGCGCAGAATAACCTTCCTGGTTACCGGCCGGATCTCCCACATCCGGAAAAGGGCGGTTTTCTATTC GAGCCCCTGAAGCTTCGCCGGCTGCTTGACTGGGAGCAGCAAAAGGACATGGTGGCCGAGTTCATGGCGGCGGCC GCGGCCCCTCGTTCTCGTGGCAGCGCCGCCGGTCTCGAGCCCTGGTCTGCTTCCTTCTTCCTGTACCAGAGCTTC TTGAGCGGCTTCGGAGTCTCGGTCGACGGCGCTGAAGCCTGTCGCTGGCTCCGGTCTGCCGCTCAGGCGAGCGAG GAGACGGCGACGGTGGATTACTTGGCCGGTGCCTGGCTCGTGCGGGCCCATGGTGCGCTCAACGTTCCCAACCCC TTGACGCCGGACGAGCAGATGAGTTTTTTGTTCTGGGGCCGAATCAGGGGTCATCGACACTGTTCCACGGATGCC CAGTCCATGATCCAAGCCGAGCCGGAGACGAGCAAGCGGACTTATTGGGAGAGCCGGATGATGAATGCTTGCGCC AACTATCTATCTCGCACCGGTGGCACGGGCATGCCCTTTTTCATCTCTCGGAGGTTGACGCGCCAGTGGGACACG GAAGACGTTGTAGCTCTCGACGAGACAGTCAAGGCCGAGCTGGGCGATGCGTACGGATCGTGTCTGCGTCCGGAG CCATACTCAATGACCAACGAGCCAACTCCAGACGGCGGGTACAGATTCGATGCCATCTACGTTAACAACAAAGGC CACGGGCTCCTCCATCTCGCCGCCACGCTGGGCGACGTCGAGATATTGAAGCATCTGCACGGCAAGTACAAGTGC AACATCAACCTCAGCAACCAATCTCACAGCGACACGCCCCTGACATGTGCCTGCCGGTCTGGAAACCTGAGCTGT GCCTTGTATCTGCTGGAGAACGGGGCGGATGCGAACGGGACCGAGTTTGGAGAGGAGTCTCCGCTGCACTGCATC GCCAACTTCGTCGACGCCGACATGGACGTCATCGTCCCCAAGCTGATGGCCGCAGGGGCAGACATGGAGAAGCTT TCCCAGCCGTCTAGAAAGGACGTCCGCGGCATATTGGCAGACTGGGAAGACAGCGGCTCGATGAAGCTGACGCCC CTGGGCAGAGCAGTCCTGTTCCAGAACTTGCACGCAGTCGAGATTCTGCTTCGATACGGAGCCAATCCATGGGGG TATCGGACTGACTCGAAGCTCGCCAGCGTTCAGCCCATGCAGCTGGCAGCCGTCCTGACGCTGCCCGATATCTTG CAGACCATGCTCTCTCACACCGAAGAAGCAGAGTCGGCTCCGCTGTTCGATGAGTGCGGTATGCTACAAAGGGCT CATTCCTGTCAACTTACCCCCTACGATGCCCTCACACTGCAGAGCCGCATCATCCGGTGTGGGAGTCTATACAAG CCATATTTGGCGCAGACGCTTCGCATACTAAGAGACAGGAGACGCAAACTCGGCCTTGCGGCACAGGAGTCGTCA CCCGGCGCTCAACTATGCGCAGAGATTGCGCTGGGAAACAAAGACATTGTCGAAGCTTTGCTCCATCTCGGCCAC GACGTCGACGGCTCCGCATGTACTCGACCTATACGAGCTGCTGTCATGGCCAACGACGAGGACATGTTCTTCTCC GTGCTTCTCCGTCGCGGAGCTTCCTTATCCATCTCACACGATGAGGAGTCCGGCCAGCCGTCGCTGCTGTCTGCG GCCGCCACCCGTCCGCATTACACGCCGCGAGGCACACGCATTGTAGAGTATCTTCTCAGTCAGGGGGTTTCCCCG GAGCCCAAGACTCAGCAGCAGCCGTGTGCTCTGGCTTTAGCCGTCAGAAACGGCTATTTTGAACTTGCCGACCTC TTCCTTTCCGGCACCTCGATCGAGAGTCTCAACGCTTTTCACACTTGGTCAGATGGAAGAGACTCCGAGTCCGTT CTGGGCTCTCTTCTCTCCAGTCACACCAACTCCAGCGCGCGGGCCGTTGCTTATCTTGCAGCTGTCCATGGCGAC TCGACTTGGCGCCTCGAGATGGGCCCTCAGGTGAACAAGGTCAAGAGATTATCAGCCGTACACGTTGTGGCTCAG TGTCCGTCGAGCGAATGGAACGACTATTCTCAGATCTCGGCGAGGATTGTGCAGCATGTGTTGAACATGTTTCCG AAGCCCGAAACGCTGGGAGAGCACCACATACATCCCATCGTCGGCACACCGCTAAGTGCGGCCGTGCTCGCTGGG AATAAGAGTATGGTAGCCTTGTTGATGGACTCCCCCTATCGAGAAGATGTAGACAAGTCGGTCCCGATCGAGTAT CAGCTTGGTGGCGTCAAGACCAAGGAATCGTTGACGCCCAGGGAACTGGCATCCAAGATTACACAGGACTTGATG CAACGCCTGAGCAGCGTCGTCACTGCTGCCACCCCCATCGGCCTCACCAAGCTTAGGGATGCGTCGGAAATCATG CTTCAGCTCATCAAGACGGATGGCAGCGATCAAGACCAGTCACCGAATCCGGAGGAGATGCGACTGGTGGTGAGA AACAGGCTCGACAAGGTCAAGATGGAAACTGACGAGGTCGGGTCTCACGATCCGTCTGCCATGCTGCCCGTGGAT TTGTCCGTGATTTGTGAAGAGAAGCCGAGCGGATGGCACGAGGGGGTGGAAATGACGGAGGTCATGGCACACAGA ACCTTTCTCAAGACCTTCCGGAGCGCTGAGGCATCTTTCGGGGATGGCATCACTGGTGTTATGGACAAGGCTTTT AACAAGAGGTCGCCAGAGCTTCGAAGTACGGGGGGA |
Transcript | >Ophio5|4673 ATGGTAGAAACAACAGCCTACGCCTATCCGTCCACCTTCGCCGCCGAATCCGAAACGTCTGGCAACGCCGCCTCC AGCTCAAGCGGCGCGTCAGCGGCCAAAGCGAGTCTCGCCGGAGGAGCCTTTGCCTCGTTCATCTGCCACGTCGCC CACCTGGAAAAAGGTCTTCAGTCGGAAAAGTCCTTCTTTGACGAAGCGCAGCGGAAAGCGAGTTCGAGAACGCGA CTCGGCCACGGCACCTCGTTTCTCGTCGACCGAGTAGAGTTGCCGTCCAGCAGCGGAGATGCCACCAAAGAGTCC CGATTCGCCGTCATCAAGACGGTCCGGCAGAAGGGTCAGAGCCCGACGCAGTGGCGAGATGTTCTCCTGGAGATA AGGGTGCTGTTGCACAAGCCGATTCGCTATCACCCCAACATCGTCCGTCTTCTCGACATAGGGTGGGATAATTCC AGTGAGATTGCGTCACCCTTTCCGGCTCTGATTCAAGAGTATGCCGAGTTTGGAACGTTGGCCAGGCTGCAGGCA GACAGCAGGCCGCTTCCGTTCCCTATCAAGCAGAAGCTTTGCTACGATGTTGGCCGGGGGTTGTCCATCTTACAC GCCTGTGGCATCATTCACGGGGACCTGAAGCACGAGAATGTTCTCGTCTTTGCTAACCGATATCCGAGTCCGGCC GGCCAACCATACACGGCAAAGGTGGCTGATTTCGGAGGGAGTATCATGGACGTCTTGGATGGCAGCGGTTCGCAC AGCATCCTCATGAACACGTTCCCCTACGAAGCACCCGAGATCGGCCAGAAGCTTTCGGTGGACGGGGTGAAGAAG ACGGATGCCTTTTCGTACGGTATGCTCATCTGGCGATGTATGCTGGATTGTGATGATGTCTTGGCCGCCATAGGC TTCGCCCTTCCGCCGGGCCAGCCGAGCGACGAAGACCGGACAGCGATGAACAAGCTCAAGCTATCCGACCAACTG CTCGAGGGCGCCATTGCCAGCCTCTCGAAGCATGCCACTACTCGTGACCTGCCAAGTCAAAGCCTCGGCCTCATC GTCACCTCCCTCCTCTTCACTCTTCGCGGTGACCCAGCCCAGAGGGCTCTGGATCGCGCCCAGGCTCGTACCCGG GGCATGTCTGCCTCGGCTTCTCAGGCTTACGTCTACGTCAAGGAGGCGGCCAACAAGAAACTGGCGGAAAGTCAA GAGCGACGCACGCCCGGCAGCCATGGCATAGACATGGACAGCGTAGGCTATGCTCTCGGACGCGTAGCTGGGGAC GACTACGATGCGCAGAATAACCTTCCTGGTTACCGGCCGGATCTCCCACATCCGGAAAAGGGCGGTTTTCTATTC GAGCCCCTGAAGCTTCGCCGGCTGCTTGACTGGGAGCAGCAAAAGGACATGGTGGCCGAGTTCATGGCGGCGGCC GCGGCCCCTCGTTCTCGTGGCAGCGCCGCCGGTCTCGAGCCCTGGTCTGCTTCCTTCTTCCTGTACCAGAGCTTC TTGAGCGGCTTCGGAGTCTCGGTCGACGGCGCTGAAGCCTGTCGCTGGCTCCGGTCTGCCGCTCAGGCGAGCGAG GAGACGGCGACGGTGGATTACTTGGCCGGTGCCTGGCTCGTGCGGGCCCATGGTGCGCTCAACGTTCCCAACCCC TTGACGCCGGACGAGCAGATGAGTTTTTTGTTCTGGGGCCGAATCAGGGGTCATCGACACTGTTCCACGGATGCC CAGTCCATGATCCAAGCCGAGCCGGAGACGAGCAAGCGGACTTATTGGGAGAGCCGGATGATGAATGCTTGCGCC AACTATCTATCTCGCACCGGTGGCACGGGCATGCCCTTTTTCATCTCTCGGAGGTTGACGCGCCAGTGGGACACG GAAGACGTTGTAGCTCTCGACGAGACAGTCAAGGCCGAGCTGGGCGATGCGTACGGATCGTGTCTGCGTCCGGAG CCATACTCAATGACCAACGAGCCAACTCCAGACGGCGGGTACAGATTCGATGCCATCTACGTTAACAACAAAGGC CACGGGCTCCTCCATCTCGCCGCCACGCTGGGCGACGTCGAGATATTGAAGCATCTGCACGGCAAGTACAAGTGC AACATCAACCTCAGCAACCAATCTCACAGCGACACGCCCCTGACATGTGCCTGCCGGTCTGGAAACCTGAGCTGT GCCTTGTATCTGCTGGAGAACGGGGCGGATGCGAACGGGACCGAGTTTGGAGAGGAGTCTCCGCTGCACTGCATC GCCAACTTCGTCGACGCCGACATGGACGTCATCGTCCCCAAGCTGATGGCCGCAGGGGCAGACATGGAGAAGCTT TCCCAGCCGTCTAGAAAGGACGTCCGCGGCATATTGGCAGACTGGGAAGACAGCGGCTCGATGAAGCTGACGCCC CTGGGCAGAGCAGTCCTGTTCCAGAACTTGCACGCAGTCGAGATTCTGCTTCGATACGGAGCCAATCCATGGGGG TATCGGACTGACTCGAAGCTCGCCAGCGTTCAGCCCATGCAGCTGGCAGCCGTCCTGACGCTGCCCGATATCTTG CAGACCATGCTCTCTCACACCGAAGAAGCAGAGTCGGCTCCGCTGTTCGATGAGTGCGGTATGCTACAAAGGGCT CATTCCTGTCAACTTACCCCCTACGATGCCCTCACACTGCAGAGCCGCATCATCCGGTGTGGGAGTCTATACAAG CCATATTTGGCGCAGACGCTTCGCATACTAAGAGACAGGAGACGCAAACTCGGCCTTGCGGCACAGGAGTCGTCA CCCGGCGCTCAACTATGCGCAGAGATTGCGCTGGGAAACAAAGACATTGTCGAAGCTTTGCTCCATCTCGGCCAC GACGTCGACGGCTCCGCATGTACTCGACCTATACGAGCTGCTGTCATGGCCAACGACGAGGACATGTTCTTCTCC GTGCTTCTCCGTCGCGGAGCTTCCTTATCCATCTCACACGATGAGGAGTCCGGCCAGCCGTCGCTGCTGTCTGCG GCCGCCACCCGTCCGCATTACACGCCGCGAGGCACACGCATTGTAGAGTATCTTCTCAGTCAGGGGGTTTCCCCG GAGCCCAAGACTCAGCAGCAGCCGTGTGCTCTGGCTTTAGCCGTCAGAAACGGCTATTTTGAACTTGCCGACCTC TTCCTTTCCGGCACCTCGATCGAGAGTCTCAACGCTTTTCACACTTGGTCAGATGGAAGAGACTCCGAGTCCGTT CTGGGCTCTCTTCTCTCCAGTCACACCAACTCCAGCGCGCGGGCCGTTGCTTATCTTGCAGCTGTCCATGGCGAC TCGACTTGGCGCCTCGAGATGGGCCCTCAGGTGAACAAGGTCAAGAGATTATCAGCCGTACACGTTGTGGCTCAG TGTCCGTCGAGCGAATGGAACGACTATTCTCAGATCTCGGCGAGGATTGTGCAGCATGTGTTGAACATGTTTCCG AAGCCCGAAACGCTGGGAGAGCACCACATACATCCCATCGTCGGCACACCGCTAAGTGCGGCCGTGCTCGCTGGG AATAAGAGTATGGTAGCCTTGTTGATGGACTCCCCCTATCGAGAAGATGTAGACAAGTCGGTCCCGATCGAGTAT CAGCTTGGTGGCGTCAAGACCAAGGAATCGTTGACGCCCAGGGAACTGGCATCCAAGATTACACAGGACTTGATG CAACGCCTGAGCAGCGTCGTCACTGCTGCCACCCCCATCGGCCTCACCAAGCTTAGGGATGCGTCGGAAATCATG CTTCAGCTCATCAAGACGGATGGCAGCGATCAAGACCAGTCACCGAATCCGGAGGAGATGCGACTGGTGGTGAGA AACAGGCTCGACAAGGTCAAGATGGAAACTGACGAGGTCGGGTCTCACGATCCGTCTGCCATGCTGCCCGTGGAT TTGTCCGTGATTTGTGAAGAGAAGCCGAGCGGATGGCACGAGGGGGTGGAAATGACGGAGGTCATGGCACACAGA ACCTTTCTCAAGACCTTCCGGAGCGCTGAGGCATCTTTCGGGGATGGCATCACTGGTGTTATGGACAAGGCTTTT AACAAGAGGTCGCCAGAGCTTCGAAGTACGGGGGGATGA |
Gene | >Ophio5|4673 ATGGTAGAAACAACAGCCTACGCCTATCCGTCCACCTTCGCCGCCGAATCCGAAACGTCTGGCAACGCCGCCTCC AGCTCAAGCGGCGCGTCAGCGGCCAAAGCGAGTCTCGCCGGAGGAGCCTTTGCCTCGTTCATCTGCCACGTCGCC CACCTGGAAAAAGGTCTTCAGTCGGAAAAGTCCTTCTTTGACGAAGCGCAGCGGAAAGCGAGTTCGAGAACGCGA CTCGGCCACGGCACCTCGTTTCTCGTCGACCGAGTAGAGTTGCCGTCCAGCAGCGGAGATGCCACCAAAGAGTCC CGATTCGCCGTCATCAAGACGGTCCGGCAGAAGGGTCAGAGCCCGACGCAGTGGCGAGATGTTCTCCTGGAGATA AGGGTGCTGTTGCACAAGCCGATTCGCTATCACCCCAACATCGTCCGTCTTCTCGACATAGGGTGGGATAATTCC AGTGAGATTGCGTCACCCTTTCCGGCTCTGATTCAAGAGTATGCCGAGTTTGGAACGTTGGCCAGGCTGCAGGCA GACAGCAGGCCGCTTCCGTTCCCTATCAAGCAGAAGCTTTGCTACGATGTTGGCCGGGGGTTGTCCATCTTACAC GCCTGTGGCATCATTCACGGGGACCTGAAGCACGAGAATGTTCTCGTCTTTGCTAACCGATATCCGAGTCCGGCC GGCCAACCATACACGGCAAAGGTGGCTGATTTCGGAGGGAGTATCATGGACGTCTTGGATGGCAGCGGTTCGCAC AGCATCCTCATGAACACGTTCCCCTACGAAGCACCCGAGATCGGCCAGAAGCTTTCGGTGGACGGGGTGAAGAAG ACGGATGCCTTTTCGTACGGTATGCTCATCTGGCGATGTATGCTGGATTGTGATGATGTCTTGGCCGCCATAGGC TTCGCCCTTCCGCCGGGCCAGCCGAGCGACGAAGACCGGACAGCGATGAACAAGCTCAAGCTATCCGACCAACTG CTCGAGGGCGCCATTGCCAGCCTCTCGAAGCATGCCACTACTCGTGACCTGCCAAGTCAAAGCCTCGGCCTCATC GTCACCTCCCTCCTCTTCACTCTTCGCGGTGACCCAGCCCAGAGGGCTCTGGATCGCGCCCAGGCTCGTACCCGG GGCATGTCTGCCTCGGCTTCTCAGGCTTACGTCTACGTCAAGGAGGCGGCCAACAAGAAACTGGCGGAAAGTCAA GAGCGACGCACGCCCGGCAGCCATGGCATAGACATGGACAGCGTAGGCTATGCTCTCGGACGCGTAGCTGGGGAC GACTACGATGCGCAGAATAACCTTCCTGGTTACCGGCCGGATCTCCCACATCCGGAAAAGGGCGGTTTTCTATTC GAGCCCCTGAAGCTTCGCCGGCTGCTTGACTGGGAGCAGCAAAAGGACATGGTGGCCGAGTTCATGGCGGCGGCC GCGGCCCCTCGTTCTCGTGGCAGCGCCGCCGGTCTCGAGCCCTGGTCTGCTTCCTTCTTCCTGTACCAGAGCTTC TTGAGCGGCTTCGGAGTCTCGGTCGACGGCGCTGAAGCCTGTCGCTGGCTCCGGTCTGCCGCTCAGGCGAGCGAG GAGACGGCGACGGTGGATTACTTGGCCGGTGCCTGGCTCGTGCGGGCCCATGGTGCGCTCAACGTTCCCAACCCC TTGACGCCGGACGAGCAGATGAGTTTTTTGTTCTGGGGCCGAATCAGGGGTCATCGACACTGTTCCACGGATGCC CAGTCCATGATCCAAGCCGAGCCGGAGACGAGCAAGCGGACTTATTGGGAGAGCCGGATGATGAATGCTTGCGCC AACTATCTATCTCGCACCGGTGGCACGGGCATGCCCTTTTTCATCTCTCGGAGGTTGACGCGCCAGTGGGACACG GAAGACGTTGTAGCTCTCGACGAGACAGTCAAGGCCGAGCTGGGCGATGCGTACGGATCGTGTCTGCGTCCGGAG CCATACTCAATGACCAACGAGCCAACTCCAGACGGCGGGTACAGATTCGATGCCATCTACGTTAACAACAAAGGC CACGGGCTCCTCCATCTCGCCGCCACGCTGGGCGACGTCGAGATATTGAAGCATCTGCACGGCAAGTACAAGTGC AACATCAACCTCAGCAACCAATCTCACAGCGACACGCCCCTGACATGTGCCTGCCGGTCTGGAAACCTGAGCTGT GCCTTGTATCTGCTGGAGAACGGGGCGGATGCGAACGGGACCGAGTTTGGAGAGGAGTCTCCGCTGCACTGCATC GCCAACTTCGTCGACGCCGACATGGACGTCATCGTCCCCAAGCTGATGGCCGCAGGGGCAGACATGGAGAAGCTT TCCCAGCCGTCTAGAAAGGACGTCCGCGGCATATTGGCAGACTGGGAAGACAGCGGCTCGATGAAGCTGACGCCC CTGGGCAGAGCAGTCCTGTTCCAGAACTTGCACGCAGTCGAGATTCTGCTTCGATACGGAGCCAATCCATGGGGG TATCGGACTGACTCGAAGCTCGCCAGCGTTCAGCCCATGCAGCTGGCAGCCGTCCTGACGCTGCCCGATATCTTG CAGACCATGCTCTCTCACACCGAAGAAGCAGAGTCGGCTCCGCTGTTCGATGAGTGCGGTATGCTACAAAGGGCT CATTCCTGTCAACTTACCCCCTACGATGCCCTCACACTGCAGAGCCGCATCATCCGGTGTGGGAGTCTATACAAG CCATATTTGGCGCAGACGCTTCGCATACTAAGAGACAGGAGACGCAAACTCGGCCTTGCGGCACAGGAGTCGTCA CCCGGCGCTCAACTATGCGCAGAGATTGCGCTGGGAAACAAAGACATTGTCGAAGCTTTGCTCCATCTCGGCCAC GACGTCGACGGCTCCGCATGTACTCGACCTATACGAGCTGCTGTCATGGCCAACGACGAGGACATGTTCTTCTCC GTGCTTCTCCGTCGCGGAGCTTCCTTATCCATCTCACACGATGAGGAGTCCGGCCAGCCGTCGCTGCTGTCTGCG GCCGCCACCCGTCCGCATTACACGCCGCGAGGCACACGCATTGTAGAGTATCTTCTCAGTCAGGGGGTTTCCCCG GAGCCCAAGACTCAGCAGCAGCCGTGTGCTCTGGCTTTAGCCGTCAGAAACGGCTATTTTGAACTTGCCGACCTC TTCCTTTCCGGCACCTCGATCGAGAGTCTCAACGCTTTTCACACTTGGTCAGATGGAAGAGACTCCGAGTCCGTT CTGGGCTCTCTTCTCTCCAGTCACACCAACTCCAGCGCGCGGGCCGTTGCTTATCTTGCAGCTGTCCATGGCGAC TCGACTTGGCGCCTCGAGATGGGCCCTCAGGTGAACAAGGTCAAGAGATTATCAGCCGTACACGTTGTGGCTCAG TGTCCGTCGAGCGAATGGAACGACTATTCTCAGATCTCGGCGAGGATTGTGCAGCATGTGTTGAACATGTTTCCG AAGCCCGAAACGCTGGGAGAGCACCACATACATCCCATCGTCGGCACACCGCTAAGTGCGGCCGTGCTCGCTGGG AATAAGAGTATGGTAGCCTTGTTGATGGACTCCCCCTATCGAGAAGATGTAGACAAGTCGGTCCCGATCGAGTAT CAGCTTGGTGGCGTCAAGACCAAGGAATCGTTGACGCCCAGGGAACTGGCATCCAAGATTACACAGGACTTGATG CAACGCCTGAGCAGCGTCGTCACTGCTGCCACCCCCATCGGCCTCACCAAGCTTAGGGATGCGTCGGAAATCATG CTTCAGCTCATCAAGACGGATGGCAGCGATCAAGACCAGTCACCGAATCCGGAGGAGATGCGACTGGTGGTGAGA AACAGGCTCGACAAGGTCAAGATGGAAACTGACGAGGTCGGGTCTCACGATCCGTCTGCCATGCTGCCCGTGGAT TTGTCCGTGATTTGTGAAGAGAAGCCGAGCGGATGGCACGAGGGGGTGGAAATGACGGAGGTCATGGCACACAGA ACCTTTCTCAAGACCTTCCGGAGCGCTGAGGCATCTTTCGGGGATGGCATCACTGGTGTTATGGACAAGGCTTTT AACAAGAGGTCGCCAGAGCTTCGAAGTACGGGGGGATGA |