© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|581 |
| Gene name | |
| Location | Contig_1114:102..2947 |
| Strand | - |
| Gene length (bp) | 2845 |
| Transcript length (bp) | 2475 |
| Coding sequence length (bp) | 2475 |
| Protein length (aa) | 825 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00654 | Voltage_CLC | Voltage gated chloride channel | 2.7E-85 | 293 | 675 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9R279|CLCN3_CAVPO | H(+)/Cl(-) exchange transporter 3 OS=Cavia porcellus GN=CLCN3 PE=2 SV=1 | 158 | 821 | 5.0E-180 |
| sp|P51791|CLCN3_MOUSE | H(+)/Cl(-) exchange transporter 3 OS=Mus musculus GN=Clcn3 PE=1 SV=2 | 158 | 821 | 6.0E-180 |
| sp|O18894|CLCN3_RABIT | H(+)/Cl(-) exchange transporter 3 OS=Oryctolagus cuniculus GN=CLCN3 PE=2 SV=3 | 158 | 821 | 7.0E-180 |
| sp|P51790|CLCN3_HUMAN | H(+)/Cl(-) exchange transporter 3 OS=Homo sapiens GN=CLCN3 PE=1 SV=2 | 158 | 821 | 7.0E-180 |
| sp|P51792|CLCN3_RAT | H(+)/Cl(-) exchange transporter 3 OS=Rattus norvegicus GN=Clcn3 PE=2 SV=2 | 158 | 821 | 8.0E-180 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q9R279|CLCN3_CAVPO | H(+)/Cl(-) exchange transporter 3 OS=Cavia porcellus GN=CLCN3 PE=2 SV=1 | 158 | 821 | 5.0E-180 |
| sp|P51791|CLCN3_MOUSE | H(+)/Cl(-) exchange transporter 3 OS=Mus musculus GN=Clcn3 PE=1 SV=2 | 158 | 821 | 6.0E-180 |
| sp|O18894|CLCN3_RABIT | H(+)/Cl(-) exchange transporter 3 OS=Oryctolagus cuniculus GN=CLCN3 PE=2 SV=3 | 158 | 821 | 7.0E-180 |
| sp|P51790|CLCN3_HUMAN | H(+)/Cl(-) exchange transporter 3 OS=Homo sapiens GN=CLCN3 PE=1 SV=2 | 158 | 821 | 7.0E-180 |
| sp|P51792|CLCN3_RAT | H(+)/Cl(-) exchange transporter 3 OS=Rattus norvegicus GN=Clcn3 PE=2 SV=2 | 158 | 821 | 8.0E-180 |
| sp|P51793|CLCN4_HUMAN | H(+)/Cl(-) exchange transporter 4 OS=Homo sapiens GN=CLCN4 PE=1 SV=2 | 158 | 821 | 2.0E-172 |
| sp|Q61418|CLCN4_MOUSE | H(+)/Cl(-) exchange transporter 4 OS=Mus musculus GN=Clcn4 PE=2 SV=2 | 148 | 821 | 2.0E-172 |
| sp|P51794|CLCN4_RAT | H(+)/Cl(-) exchange transporter 4 OS=Rattus norvegicus GN=Clcn4 PE=2 SV=1 | 158 | 821 | 1.0E-171 |
| sp|Q9TTU3|CLCN5_RABIT | H(+)/Cl(-) exchange transporter 5 OS=Oryctolagus cuniculus GN=CLCN5 PE=2 SV=1 | 148 | 821 | 4.0E-171 |
| sp|Q99P66|CLCN5_CAVPO | H(+)/Cl(-) exchange transporter 5 OS=Cavia porcellus GN=CLCN5 PE=2 SV=1 | 148 | 821 | 9.0E-170 |
| sp|Q5RDJ7|CLCN3_PONAB | H(+)/Cl(-) exchange transporter 3 OS=Pongo abelii GN=CLCN3 PE=2 SV=1 | 158 | 821 | 2.0E-169 |
| sp|P51796|CLCN5_RAT | H(+)/Cl(-) exchange transporter 5 OS=Rattus norvegicus GN=Clcn5 PE=2 SV=1 | 148 | 821 | 3.0E-165 |
| sp|Q9GKE7|CLCN5_PIG | H(+)/Cl(-) exchange transporter 5 OS=Sus scrofa GN=CLCN5 PE=2 SV=1 | 148 | 821 | 4.0E-165 |
| sp|Q5RBK4|CLCN5_PONAB | H(+)/Cl(-) exchange transporter 5 OS=Pongo abelii GN=CLCN5 PE=2 SV=1 | 148 | 821 | 6.0E-165 |
| sp|P51795|CLCN5_HUMAN | H(+)/Cl(-) exchange transporter 5 OS=Homo sapiens GN=CLCN5 PE=1 SV=1 | 148 | 821 | 6.0E-165 |
| sp|Q9WVD4|CLCN5_MOUSE | H(+)/Cl(-) exchange transporter 5 OS=Mus musculus GN=Clcn5 PE=1 SV=1 | 148 | 821 | 1.0E-164 |
| sp|P0C197|CLCNX_USTMA | Probable chloride channel protein UM03490-D OS=Ustilago maydis (strain 521 / FGSC 9021) GN=UMAG_11084 PE=3 SV=1 | 254 | 796 | 1.0E-128 |
| sp|O60159|YHYB_SCHPO | Putative anion/proton exchange transporter C19C7.11 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC19C7.11 PE=3 SV=2 | 111 | 817 | 1.0E-112 |
| sp|P37020|GEF1_YEAST | Anion/proton exchange transporter GEF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GEF1 PE=1 SV=2 | 190 | 811 | 6.0E-84 |
| sp|O94287|YOO2_SCHPO | Uncharacterized chloride channel protein C887.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.02 PE=3 SV=2 | 231 | 811 | 2.0E-65 |
| sp|P35525|CLCN2_RAT | Chloride channel protein 2 OS=Rattus norvegicus GN=Clcn2 PE=1 SV=1 | 279 | 776 | 2.0E-56 |
| sp|Q54C67|CLCF_DICDI | Chloride channel protein F OS=Dictyostelium discoideum GN=clcF PE=3 SV=1 | 277 | 779 | 3.0E-56 |
| sp|P51788|CLCN2_HUMAN | Chloride channel protein 2 OS=Homo sapiens GN=CLCN2 PE=1 SV=2 | 279 | 776 | 2.0E-55 |
| sp|Q9R0A1|CLCN2_MOUSE | Chloride channel protein 2 OS=Mus musculus GN=Clcn2 PE=1 SV=2 | 279 | 776 | 3.0E-55 |
| sp|P51789|CLCN2_RABIT | Chloride channel protein 2 OS=Oryctolagus cuniculus GN=CLCN2 PE=2 SV=1 | 259 | 764 | 7.0E-55 |
| sp|Q9WU45|CLCN2_CAVPO | Chloride channel protein 2 OS=Cavia porcellus GN=CLCN2 PE=2 SV=1 | 259 | 764 | 2.0E-54 |
| sp|Q9BMK9|CLH3_CAEEL | Chloride channel protein clh-3 OS=Caenorhabditis elegans GN=clh-3 PE=1 SV=1 | 280 | 765 | 3.0E-54 |
| sp|P35524|CLCN1_RAT | Chloride channel protein 1 OS=Rattus norvegicus GN=Clcn1 PE=1 SV=1 | 280 | 769 | 3.0E-52 |
| sp|Q86AZ6|CLCB_DICDI | Chloride channel protein B OS=Dictyostelium discoideum GN=clcB PE=3 SV=1 | 160 | 751 | 4.0E-52 |
| sp|P35523|CLCN1_HUMAN | Chloride channel protein 1 OS=Homo sapiens GN=CLCN1 PE=1 SV=3 | 280 | 783 | 5.0E-52 |
| sp|Q75JF3|CLCC_DICDI | Chloride channel protein C OS=Dictyostelium discoideum GN=clcC PE=3 SV=1 | 201 | 811 | 5.0E-52 |
| sp|Q64347|CLCN1_MOUSE | Chloride channel protein 1 OS=Mus musculus GN=Clcn1 PE=1 SV=3 | 280 | 778 | 2.0E-51 |
| sp|Q9MZT1|CLCN1_CANLF | Chloride channel protein 1 OS=Canis lupus familiaris GN=CLCN1 PE=1 SV=1 | 280 | 778 | 6.0E-51 |
| sp|Q9VGH7|CLCN2_DROME | Chloride channel protein 2 OS=Drosophila melanogaster GN=ClC-a PE=2 SV=3 | 279 | 764 | 1.0E-50 |
| sp|P92941|CLCA_ARATH | Chloride channel protein CLC-a OS=Arabidopsis thaliana GN=CLC-A PE=1 SV=2 | 268 | 817 | 4.0E-48 |
| sp|P35522|CICH_TORCA | Chloride channel protein OS=Torpedo californica PE=1 SV=3 | 276 | 765 | 1.0E-46 |
| sp|P21564|CICH_TORMA | Chloride channel protein OS=Torpedo marmorata PE=1 SV=1 | 280 | 765 | 3.0E-46 |
| sp|Q54AX6|CLCA_DICDI | Chloride channel protein A OS=Dictyostelium discoideum GN=clcA PE=2 SV=1 | 201 | 751 | 1.0E-45 |
| sp|P92943|CLCD_ARATH | Chloride channel protein CLC-d OS=Arabidopsis thaliana GN=CLC-D PE=1 SV=2 | 261 | 801 | 5.0E-45 |
| sp|P92942|CLCB_ARATH | Chloride channel protein CLC-b OS=Arabidopsis thaliana GN=CLC-B PE=1 SV=1 | 201 | 817 | 3.0E-44 |
| sp|Q9TT16|CLCN6_RABIT | Chloride transport protein 6 OS=Oryctolagus cuniculus GN=CLCN6 PE=2 SV=1 | 288 | 751 | 2.0E-42 |
| sp|Q9W701|CLCKB_XENLA | Chloride channel protein ClC-Kb OS=Xenopus laevis GN=clcnkb PE=1 SV=1 | 257 | 783 | 3.0E-41 |
| sp|Q54LQ4|CLCE_DICDI | Chloride channel protein E OS=Dictyostelium discoideum GN=clcE PE=3 SV=1 | 279 | 768 | 4.0E-41 |
| sp|O35454|CLCN6_MOUSE | Chloride transport protein 6 OS=Mus musculus GN=Clcn6 PE=1 SV=1 | 288 | 751 | 6.0E-41 |
| sp|P51797|CLCN6_HUMAN | Chloride transport protein 6 OS=Homo sapiens GN=CLCN6 PE=1 SV=2 | 288 | 751 | 9.0E-41 |
| sp|P51799|CLCN7_RAT | H(+)/Cl(-) exchange transporter 7 OS=Rattus norvegicus GN=Clcn7 PE=2 SV=1 | 201 | 817 | 6.0E-40 |
| sp|O70496|CLCN7_MOUSE | H(+)/Cl(-) exchange transporter 7 OS=Mus musculus GN=Clcn7 PE=1 SV=1 | 201 | 817 | 2.0E-39 |
| sp|Q4PKH3|CLCN7_BOVIN | H(+)/Cl(-) exchange transporter 7 OS=Bos taurus GN=CLCN7 PE=2 SV=1 | 201 | 817 | 9.0E-36 |
| sp|P51798|CLCN7_HUMAN | H(+)/Cl(-) exchange transporter 7 OS=Homo sapiens GN=CLCN7 PE=1 SV=2 | 201 | 817 | 1.0E-34 |
| sp|Q96282|CLCC_ARATH | Chloride channel protein CLC-c OS=Arabidopsis thaliana GN=CLC-C PE=1 SV=1 | 277 | 750 | 4.0E-34 |
| sp|P51804|CLCKB_RABIT | Chloride channel protein ClC-Kb OS=Oryctolagus cuniculus GN=CLCNKB PE=2 SV=1 | 275 | 777 | 2.0E-27 |
| sp|P51803|CLCKA_RABIT | Chloride channel protein ClC-Ka OS=Oryctolagus cuniculus GN=CLCNKA PE=2 SV=1 | 275 | 777 | 2.0E-27 |
| sp|Q06393|CLCKA_RAT | Chloride channel protein ClC-Ka OS=Rattus norvegicus GN=Clcnka PE=1 SV=3 | 275 | 787 | 2.0E-25 |
| sp|P51800|CLCKA_HUMAN | Chloride channel protein ClC-Ka OS=Homo sapiens GN=CLCNKA PE=1 SV=1 | 275 | 820 | 1.0E-24 |
| sp|Q9WUB7|CLCKA_MOUSE | Chloride channel protein ClC-Ka OS=Mus musculus GN=Clcnka PE=1 SV=2 | 280 | 787 | 7.0E-24 |
| sp|Q9WUB6|CLCKB_MOUSE | Chloride channel protein ClC-Kb OS=Mus musculus GN=Clcnkb PE=1 SV=2 | 275 | 780 | 8.0E-23 |
| sp|P51801|CLCKB_HUMAN | Chloride channel protein ClC-Kb OS=Homo sapiens GN=CLCNKB PE=1 SV=3 | 275 | 780 | 2.0E-22 |
| sp|P51802|CLCKB_RAT | Chloride channel protein ClC-Kb OS=Rattus norvegicus GN=Clcnkb PE=1 SV=1 | 275 | 770 | 6.0E-22 |
| sp|Q1ZXJ0|CLCD_DICDI | Chloride channel protein D OS=Dictyostelium discoideum GN=clcD PE=3 SV=1 | 558 | 788 | 1.0E-21 |
| sp|Q1ZXJ0|CLCD_DICDI | Chloride channel protein D OS=Dictyostelium discoideum GN=clcD PE=3 SV=1 | 279 | 511 | 8.0E-21 |
| sp|P60300|CLCG_ARATH | Putative chloride channel-like protein CLC-g OS=Arabidopsis thaliana GN=CBSCLC6 PE=3 SV=2 | 285 | 448 | 9.0E-20 |
| sp|B5Y1L4|CLCA_KLEP3 | H(+)/Cl(-) exchange transporter ClcA OS=Klebsiella pneumoniae (strain 342) GN=clcA PE=3 SV=1 | 277 | 689 | 2.0E-17 |
| sp|A8ALD3|CLCA_CITK8 | H(+)/Cl(-) exchange transporter ClcA OS=Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) GN=clcA PE=3 SV=1 | 285 | 675 | 2.0E-16 |
| sp|A6T4V9|CLCA_KLEP7 | H(+)/Cl(-) exchange transporter ClcA OS=Klebsiella pneumoniae subsp. pneumoniae (strain ATCC 700721 / MGH 78578) GN=clcA PE=3 SV=1 | 278 | 675 | 7.0E-16 |
| sp|B5BL83|CLCA_SALPK | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella paratyphi A (strain AKU_12601) GN=clcA PE=3 SV=1 | 285 | 675 | 5.0E-15 |
| sp|Q5PD50|CLCA_SALPA | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella paratyphi A (strain ATCC 9150 / SARB42) GN=clcA PE=3 SV=1 | 285 | 675 | 5.0E-15 |
| sp|B5RHE1|CLCA_SALG2 | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella gallinarum (strain 287/91 / NCTC 13346) GN=clcA PE=3 SV=1 | 285 | 675 | 9.0E-15 |
| sp|B4TK31|CLCA_SALHS | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella heidelberg (strain SL476) GN=clcA PE=3 SV=1 | 285 | 675 | 1.0E-14 |
| sp|B5FJ02|CLCA_SALDC | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella dublin (strain CT_02021853) GN=clcA PE=3 SV=1 | 285 | 675 | 1.0E-14 |
| sp|B5F8R6|CLCA_SALA4 | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella agona (strain SL483) GN=clcA PE=3 SV=1 | 285 | 675 | 1.0E-14 |
| sp|A9MPK6|CLCA_SALAR | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella arizonae (strain ATCC BAA-731 / CDC346-86 / RSK2980) GN=clcA PE=3 SV=1 | 285 | 675 | 2.0E-14 |
| sp|B4TXQ7|CLCA_SALSV | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella schwarzengrund (strain CVM19633) GN=clcA PE=3 SV=1 | 285 | 675 | 3.0E-14 |
| sp|A9N0Q1|CLCA_SALPB | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella paratyphi B (strain ATCC BAA-1250 / SPB7) GN=clcA PE=3 SV=1 | 285 | 675 | 3.0E-14 |
| sp|B4SUY5|CLCA_SALNS | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella newport (strain SL254) GN=clcA PE=3 SV=1 | 285 | 675 | 3.0E-14 |
| sp|B5R3G7|CLCA_SALEP | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella enteritidis PT4 (strain P125109) GN=clcA PE=3 SV=1 | 285 | 675 | 3.0E-14 |
| sp|C0Q5R6|CLCA_SALPC | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella paratyphi C (strain RKS4594) GN=clcA PE=3 SV=1 | 285 | 675 | 4.0E-14 |
| sp|Q57T52|CLCA_SALCH | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella choleraesuis (strain SC-B67) GN=clcA PE=3 SV=1 | 285 | 675 | 4.0E-14 |
| sp|Q8ZRP8|CLCA_SALTY | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=clcA PE=1 SV=1 | 285 | 675 | 6.0E-14 |
| sp|Q8Z9B3|CLCA_SALTI | H(+)/Cl(-) exchange transporter ClcA OS=Salmonella typhi GN=clcA PE=3 SV=1 | 285 | 675 | 8.0E-14 |
| sp|P60300|CLCG_ARATH | Putative chloride channel-like protein CLC-g OS=Arabidopsis thaliana GN=CBSCLC6 PE=3 SV=2 | 563 | 821 | 1.0E-12 |
| sp|A7MGR4|CLCA_CROS8 | H(+)/Cl(-) exchange transporter ClcA OS=Cronobacter sakazakii (strain ATCC BAA-894) GN=clcA PE=3 SV=1 | 299 | 676 | 2.0E-10 |
| sp|Q8XTT4|CLCL_RALSO | Putative chloride channel protein ClcB-like OS=Ralstonia solanacearum (strain GMI1000) GN=RSp0020 PE=3 SV=2 | 343 | 692 | 4.0E-10 |
| sp|Q8RXR2|CLCF_ARATH | Chloride channel protein CLC-f OS=Arabidopsis thaliana GN=CLC-F PE=2 SV=2 | 327 | 764 | 2.0E-08 |
| sp|Q87GZ9|CLCA_VIBPA | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) GN=clcA PE=3 SV=1 | 286 | 438 | 3.0E-07 |
| sp|B2U300|CLCA_SHIB3 | H(+)/Cl(-) exchange transporter ClcA OS=Shigella boydii serotype 18 (strain CDC 3083-94 / BS512) GN=clcA PE=3 SV=1 | 287 | 675 | 4.0E-07 |
| sp|Q325Y4|CLCA_SHIBS | H(+)/Cl(-) exchange transporter ClcA OS=Shigella boydii serotype 4 (strain Sb227) GN=clcA PE=3 SV=1 | 287 | 675 | 7.0E-07 |
| sp|Q8ZEB3|CLCB_YERPE | Voltage-gated ClC-type chloride channel ClcB OS=Yersinia pestis GN=clcB PE=3 SV=2 | 334 | 674 | 9.0E-07 |
| sp|Q3Z5K2|CLCA_SHISS | H(+)/Cl(-) exchange transporter ClcA OS=Shigella sonnei (strain Ss046) GN=clcA PE=1 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B6HZD1|CLCA_ECOSE | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain SE11) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B7N824|CLCA_ECOLU | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|P37019|CLCA_ECOLI | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain K12) GN=clcA PE=1 SV=2 | 287 | 675 | 1.0E-06 |
| sp|B1IQI5|CLCA_ECOLC | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain ATCC 8739 / DSM 1576 / Crooks) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B1XD25|CLCA_ECODH | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain K12 / DH10B) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|C4ZRP8|CLCA_ECOBW | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain K12 / MC4100 / BW2952) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B7M196|CLCA_ECO8A | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O8 (strain IAI1) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B7LGL7|CLCA_ECO55 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain 55989 / EAEC) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|B7UIK2|CLCA_ECO27 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O127:H6 (strain E2348/69 / EPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|A7ZHP7|CLCA_ECO24 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O139:H28 (strain E24377A / ETEC) GN=clcA PE=3 SV=1 | 287 | 675 | 1.0E-06 |
| sp|A7ZWA3|CLCA_ECOHS | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O9:H4 (strain HS) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|Q1RG33|CLCA_ECOUT | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain UTI89 / UPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|Q8FL15|CLCA_ECOL6 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|A1A7K1|CLCA_ECOK1 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O1:K1 / APEC GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|B7MBD8|CLCA_ECO45 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O45:K1 (strain S88 / ExPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|Q9AGD5|CLCB_YERPS | Voltage-gated ClC-type chloride channel ClcB OS=Yersinia pseudotuberculosis serotype I (strain IP32953) GN=clcB PE=3 SV=3 | 334 | 674 | 2.0E-06 |
| sp|A7FHW4|CLCB_YERP3 | Voltage-gated ClC-type chloride channel ClcB OS=Yersinia pseudotuberculosis serotype O:1b (strain IP 31758) GN=clcB PE=3 SV=1 | 334 | 674 | 2.0E-06 |
| sp|B7LWB6|CLCA_ESCF3 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CDC 0568-73) GN=clcA PE=3 SV=1 | 206 | 675 | 2.0E-06 |
| sp|Q32JV3|CLCA_SHIDS | H(+)/Cl(-) exchange transporter ClcA OS=Shigella dysenteriae serotype 1 (strain Sd197) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|B1LGV8|CLCA_ECOSM | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli (strain SMS-3-5 / SECEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|Q0TLH6|CLCA_ECOL5 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O6:K15:H31 (strain 536 / UPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|B7MP17|CLCA_ECO81 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O81 (strain ED1a) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|B7NIB8|CLCA_ECO7I | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O7:K1 (strain IAI39 / ExPEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|B5Z0D5|CLCA_ECO5E | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O157:H7 (strain EC4115 / EHEC) GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|P58244|CLCA_ECO57 | H(+)/Cl(-) exchange transporter ClcA OS=Escherichia coli O157:H7 GN=clcA PE=3 SV=1 | 287 | 675 | 2.0E-06 |
| sp|C3LVE3|CLCA_VIBCM | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain M66-2) GN=clcA PE=3 SV=1 | 287 | 415 | 2.0E-06 |
| sp|Q9KM62|CLCA_VIBCH | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=clcA PE=3 SV=1 | 287 | 415 | 2.0E-06 |
| sp|A5F0D5|CLCA_VIBC3 | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) GN=clcA PE=3 SV=1 | 287 | 415 | 2.0E-06 |
| sp|Q8GX93|CLCE_ARATH | Chloride channel protein CLC-e OS=Arabidopsis thaliana GN=CLC-E PE=2 SV=2 | 580 | 681 | 2.0E-06 |
| sp|A5F0D5|CLCA_VIBC3 | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) GN=clcA PE=3 SV=1 | 547 | 689 | 5.0E-06 |
| sp|C3LVE3|CLCA_VIBCM | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain M66-2) GN=clcA PE=3 SV=1 | 547 | 689 | 7.0E-06 |
| sp|Q9KM62|CLCA_VIBCH | H(+)/Cl(-) exchange transporter ClcA OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=clcA PE=3 SV=1 | 547 | 689 | 7.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0005247 | voltage-gated chloride channel activity | Yes |
| GO:0055085 | transmembrane transport | Yes |
| GO:0016020 | membrane | Yes |
| GO:0006821 | chloride transport | Yes |
| GO:0015267 | channel activity | No |
| GO:0022836 | gated channel activity | No |
| GO:0009987 | cellular process | No |
| GO:0008509 | anion transmembrane transporter activity | No |
| GO:0015108 | chloride transmembrane transporter activity | No |
| GO:0015103 | inorganic anion transmembrane transporter activity | No |
| GO:0022832 | voltage-gated channel activity | No |
| GO:0022857 | transmembrane transporter activity | No |
| GO:0005216 | ion channel activity | No |
| GO:0008308 | voltage-gated anion channel activity | No |
| GO:0008150 | biological_process | No |
| GO:0005244 | voltage-gated ion channel activity | No |
| GO:0051179 | localization | No |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | No |
| GO:0006820 | anion transport | No |
| GO:0051234 | establishment of localization | No |
| GO:0022803 | passive transmembrane transporter activity | No |
| GO:0006811 | ion transport | No |
| GO:0005215 | transporter activity | No |
| GO:0015075 | ion transmembrane transporter activity | No |
| GO:0015698 | inorganic anion transport | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0006810 | transport | No |
| GO:0003674 | molecular_function | No |
| GO:0005575 | cellular_component | No |
| GO:0005253 | anion channel activity | No |
| GO:0005254 | chloride channel activity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 21 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 200 | 222 | 22 |
| 2 | 278 | 300 | 22 |
| 3 | 327 | 349 | 22 |
| 4 | 354 | 371 | 17 |
| 5 | 384 | 406 | 22 |
| 6 | 456 | 478 | 22 |
| 7 | 491 | 513 | 22 |
| 8 | 552 | 574 | 22 |
| 9 | 581 | 603 | 22 |
| 10 | 623 | 640 | 17 |
| 11 | 647 | 669 | 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 | >Hirsu2|581 MNRTMSRAIQSDYAFASASSSSHSPPANTPPPSDDRDELDFPDDADDQEDGDSVHVRRSGDDEILDDDPTRDDMS VPLSFKRRPAPSLLSAPARFLSSLGGSRSPRRDFASSQPRRSPGLAGSSAAPQRTGLNSLNSTAKDALSHDWYTE GPGRRVGYEDLTAIDWIFEYTKERQRQRVLSSSATGILGYAQRLLDASQIWVVLILTGLLVGVIAAGIDITTDWL ADLKLGFCSSGPEGGHFYLNKSFCCYGYDQGSKCLGWKYWSDALGVHAAGGKWFIEYIFFILFSVTLAYCAAVLV QEYAMYAKHSGIPEIKTVLGGFVIRRFLGTWTLVTKALGLVLAVGSGMWLGKEGPLVHVACCCASLFIKLFGNIR DNEARKREVLSAAAAAGISVAFGSPIGGVLFSLEQLSYYFPDKTMWQSFVCAMTAAVVLQAFDPFRSGKLVLYQT KYSVDWHGFEIVPYALLGIFGGVYGGLFIKANMAVARWKTARAWLPSPIAQVLAVALLTALINYPNSYMKVQSSE LVSNLFADCARVLDDQVGLCKTGAASAGTIILLILAAVLGFLLATITFGLQIPAGIILPSMAIGALAGRAVGIIM EIWVSNHADFFVFSSCAPDAPCITPGTYAIIGAAAALAGVTRMTVSIVVITFELTGALTYVLPIMVAVMISKWVG DAFSRRGIYESWIHFNEYPFLDNSEEMVVPDVPVSQIMTRIEDLVVLTATGHSIASLNAILETHPYRGFPVISDP RDAILLGYISRGELSYNLRTATQPPRSLAPETEAFFSHQPLADPRSTLDLRPWMDQTPLTLLSRTSLHLAVSAS* |
| Coding | >Hirsu2|581 ATGAACCGAACCATGTCTAGGGCCATTCAGAGCGACTATGCATTTGCTTCCGCCTCATCGTCTTCCCACTCCCCT CCGGCTAACACGCCGCCCCCTTCCGACGACCGCGACGAGCTCGACTTCCCGGACGACGCCGACGACCAAGAAGAT GGCGATAGCGTCCATGTCCGCCGTTCGGGCGACGATGAAATCCTCGACGACGACCCTACGCGCGACGACATGAGC GTTCCCCTATCCTTCAAGCGAAGGCCGGCTCCCTCGCTGCTCTCCGCGCCGGCCCGCTTCCTCTCCTCCCTTGGC GGCTCGCGATCGCCTCGCCGCGACTTTGCGTCTTCCCAGCCGCGCCGTTCCCCCGGGCTCGCGGGATCCTCCGCC GCGCCGCAAAGAACCGGCCTGAACAGCCTCAACTCAACCGCCAAGGACGCACTGTCGCACGACTGGTATACTGAG GGCCCCGGCCGACGCGTCGGATACGAGGACCTGACGGCCATCGACTGGATCTTCGAATACACGAAGGAACGGCAG CGGCAGCGAGTGCTGTCCTCCAGTGCAACTGGAATCCTTGGCTATGCACAGCGGCTTCTGGACGCCAGCCAGATC TGGGTCGTCTTGATCCTGACCGGTCTTCTCGTCGGTGTCATAGCTGCGGGCATCGACATAACTACCGACTGGCTG GCCGATCTGAAGCTGGGCTTTTGCTCAAGCGGTCCCGAGGGGGGGCACTTCTATCTGAACAAGAGCTTCTGCTGC TACGGCTACGACCAAGGTTCCAAGTGCTTGGGGTGGAAGTACTGGAGCGATGCGCTCGGTGTCCACGCTGCCGGC GGCAAATGGTTCATCGAATACATCTTTTTCATTCTCTTCTCGGTGACGCTGGCATATTGCGCTGCTGTGCTTGTT CAGGAGTATGCCATGTATGCCAAGCACAGCGGCATCCCGGAGATCAAGACGGTTCTTGGAGGATTCGTCATCCGC AGGTTTCTCGGCACATGGACCCTGGTCACCAAAGCTCTCGGCCTGGTGCTGGCTGTCGGCTCTGGCATGTGGCTT GGAAAGGAGGGGCCACTGGTCCATGTTGCCTGCTGTTGCGCGAGTCTCTTCATTAAGCTCTTCGGCAACATTAGG GACAATGAAGCTCGAAAGCGAGAAGTGCTCTCGGCTGCGGCCGCAGCGGGCATTTCGGTTGCCTTTGGCTCCCCA ATCGGCGGCGTCCTGTTCAGCCTCGAGCAACTCTCGTATTACTTTCCAGACAAAACCATGTGGCAGAGCTTTGTC TGCGCCATGACGGCGGCCGTCGTGCTCCAGGCTTTTGACCCCTTTCGCTCGGGCAAACTTGTCCTCTACCAGACC AAGTACAGCGTAGACTGGCACGGTTTCGAGATTGTCCCTTATGCGCTTCTCGGCATCTTTGGGGGTGTGTACGGT GGCCTGTTTATCAAGGCCAACATGGCTGTTGCGCGATGGAAGACGGCCAGGGCCTGGCTCCCCAGTCCCATTGCC CAGGTCTTGGCCGTGGCCCTGCTGACTGCGCTCATCAACTACCCAAACTCGTATATGAAAGTGCAGTCTTCGGAG CTCGTCTCCAACCTCTTCGCCGACTGCGCGCGCGTCCTCGACGACCAGGTCGGCCTGTGCAAGACGGGTGCGGCG TCTGCCGGCACCATCATTCTCCTGATCCTGGCCGCCGTGCTGGGCTTCCTGCTCGCGACCATCACCTTTGGCCTG CAGATCCCCGCGGGCATCATCCTCCCGTCCATGGCCATCGGCGCCCTGGCCGGGCGCGCCGTGGGCATCATCATG GAGATCTGGGTCAGCAACCACGCCGACTTCTTCGTGTTCTCGTCGTGCGCGCCCGACGCGCCGTGCATCACGCCC GGGACGTACGCCATCATCGGCGCGGCCGCCGCACTCGCGGGCGTCACGCGGATGACGGTGTCCATCGTCGTCATC ACGTTCGAGCTCACCGGGGCGCTCACGTACGTCCTCCCTATCATGGTGGCCGTCATGATCTCCAAGTGGGTCGGC GACGCCTTTTCGCGACGCGGCATCTACGAGTCCTGGATCCATTTCAACGAGTACCCCTTCCTCGACAACAGCGAG GAGATGGTGGTGCCGGACGTGCCCGTCTCGCAGATCATGACGCGCATCGAGGACCTGGTCGTCCTGACCGCCACG GGCCACAGCATCGCCTCGCTCAACGCGATCCTCGAGACGCACCCGTACCGCGGCTTCCCCGTCATCTCGGACCCG CGCGATGCCATCCTACTGGGCTACATCTCGCGCGGCGAGCTGAGCTACAACCTCCGGACGGCGACGCAGCCGCCG CGGTCGCTGGCGCCGGAGACGGAGGCCTTCTTCTCGCACCAGCCGCTGGCGGACCCGCGCTCGACGCTCGACCTG CGCCCCTGGATGGACCAGACGCCGCTGACGCTGCTGTCGCGCACGAGCCTGCACCTCGCCGTCTCGGCCTCCTGA |
| Transcript | >Hirsu2|581 ATGAACCGAACCATGTCTAGGGCCATTCAGAGCGACTATGCATTTGCTTCCGCCTCATCGTCTTCCCACTCCCCT CCGGCTAACACGCCGCCCCCTTCCGACGACCGCGACGAGCTCGACTTCCCGGACGACGCCGACGACCAAGAAGAT GGCGATAGCGTCCATGTCCGCCGTTCGGGCGACGATGAAATCCTCGACGACGACCCTACGCGCGACGACATGAGC GTTCCCCTATCCTTCAAGCGAAGGCCGGCTCCCTCGCTGCTCTCCGCGCCGGCCCGCTTCCTCTCCTCCCTTGGC GGCTCGCGATCGCCTCGCCGCGACTTTGCGTCTTCCCAGCCGCGCCGTTCCCCCGGGCTCGCGGGATCCTCCGCC GCGCCGCAAAGAACCGGCCTGAACAGCCTCAACTCAACCGCCAAGGACGCACTGTCGCACGACTGGTATACTGAG GGCCCCGGCCGACGCGTCGGATACGAGGACCTGACGGCCATCGACTGGATCTTCGAATACACGAAGGAACGGCAG CGGCAGCGAGTGCTGTCCTCCAGTGCAACTGGAATCCTTGGCTATGCACAGCGGCTTCTGGACGCCAGCCAGATC TGGGTCGTCTTGATCCTGACCGGTCTTCTCGTCGGTGTCATAGCTGCGGGCATCGACATAACTACCGACTGGCTG GCCGATCTGAAGCTGGGCTTTTGCTCAAGCGGTCCCGAGGGGGGGCACTTCTATCTGAACAAGAGCTTCTGCTGC TACGGCTACGACCAAGGTTCCAAGTGCTTGGGGTGGAAGTACTGGAGCGATGCGCTCGGTGTCCACGCTGCCGGC GGCAAATGGTTCATCGAATACATCTTTTTCATTCTCTTCTCGGTGACGCTGGCATATTGCGCTGCTGTGCTTGTT CAGGAGTATGCCATGTATGCCAAGCACAGCGGCATCCCGGAGATCAAGACGGTTCTTGGAGGATTCGTCATCCGC AGGTTTCTCGGCACATGGACCCTGGTCACCAAAGCTCTCGGCCTGGTGCTGGCTGTCGGCTCTGGCATGTGGCTT GGAAAGGAGGGGCCACTGGTCCATGTTGCCTGCTGTTGCGCGAGTCTCTTCATTAAGCTCTTCGGCAACATTAGG GACAATGAAGCTCGAAAGCGAGAAGTGCTCTCGGCTGCGGCCGCAGCGGGCATTTCGGTTGCCTTTGGCTCCCCA ATCGGCGGCGTCCTGTTCAGCCTCGAGCAACTCTCGTATTACTTTCCAGACAAAACCATGTGGCAGAGCTTTGTC TGCGCCATGACGGCGGCCGTCGTGCTCCAGGCTTTTGACCCCTTTCGCTCGGGCAAACTTGTCCTCTACCAGACC AAGTACAGCGTAGACTGGCACGGTTTCGAGATTGTCCCTTATGCGCTTCTCGGCATCTTTGGGGGTGTGTACGGT GGCCTGTTTATCAAGGCCAACATGGCTGTTGCGCGATGGAAGACGGCCAGGGCCTGGCTCCCCAGTCCCATTGCC CAGGTCTTGGCCGTGGCCCTGCTGACTGCGCTCATCAACTACCCAAACTCGTATATGAAAGTGCAGTCTTCGGAG CTCGTCTCCAACCTCTTCGCCGACTGCGCGCGCGTCCTCGACGACCAGGTCGGCCTGTGCAAGACGGGTGCGGCG TCTGCCGGCACCATCATTCTCCTGATCCTGGCCGCCGTGCTGGGCTTCCTGCTCGCGACCATCACCTTTGGCCTG CAGATCCCCGCGGGCATCATCCTCCCGTCCATGGCCATCGGCGCCCTGGCCGGGCGCGCCGTGGGCATCATCATG GAGATCTGGGTCAGCAACCACGCCGACTTCTTCGTGTTCTCGTCGTGCGCGCCCGACGCGCCGTGCATCACGCCC GGGACGTACGCCATCATCGGCGCGGCCGCCGCACTCGCGGGCGTCACGCGGATGACGGTGTCCATCGTCGTCATC ACGTTCGAGCTCACCGGGGCGCTCACGTACGTCCTCCCTATCATGGTGGCCGTCATGATCTCCAAGTGGGTCGGC GACGCCTTTTCGCGACGCGGCATCTACGAGTCCTGGATCCATTTCAACGAGTACCCCTTCCTCGACAACAGCGAG GAGATGGTGGTGCCGGACGTGCCCGTCTCGCAGATCATGACGCGCATCGAGGACCTGGTCGTCCTGACCGCCACG GGCCACAGCATCGCCTCGCTCAACGCGATCCTCGAGACGCACCCGTACCGCGGCTTCCCCGTCATCTCGGACCCG CGCGATGCCATCCTACTGGGCTACATCTCGCGCGGCGAGCTGAGCTACAACCTCCGGACGGCGACGCAGCCGCCG CGGTCGCTGGCGCCGGAGACGGAGGCCTTCTTCTCGCACCAGCCGCTGGCGGACCCGCGCTCGACGCTCGACCTG CGCCCCTGGATGGACCAGACGCCGCTGACGCTGCTGTCGCGCACGAGCCTGCACCTCGCCGTCTCGGCCTCCTGA |
| Gene | >Hirsu2|581 ATGAACCGAACCATGTCTAGGGCCATTCAGAGCGACTATGCATTTGCTTCCGCCTCATCGTCTTCCCACTCCCCT CCGGCTAACACGCCGCCCCCTTCCGACGACCGCGACGAGCTCGACTTCCCGGACGACGCCGACGACCAAGAAGAT GGCGATAGCGTCCATGTCCGCCGTTCGGGCGACGATGAAATCCTCGACGACGACCCTACGCGCGACGACATGAGC GTTCCCCTATCCTTCAAGCGAAGGCCGGCTCCCTCGCTGCTCTCCGCGCCGGCCCGCTTCCTCTCCTCCCTTGGC GGCTCGCGATCGCCTCGCCGCGACTTTGCGTCTTCCCAGCCGCGCCGTTCCCCCGGGCTCGCGGGATCCTCCGCC GCGCCGCAAAGAACCGGCCTGAACAGCCTCAACTCAACCGCCAAGGACGCACTGTCGCACGACTGGTATACTGAG GGCCCCGGCCGACGCGTCGGATACGAGGACCTGACGGCCATCGACTGGATCTTCGAATACACGAAGGAACGGCAG CGGCAGCGAGTGCTGTCCTCCAGTGCAACTGGAATCCTTGGCTATGCACAGCGGCTTCTGGACGCCAGCCAGATC TGGGTCGTCTTGATCCTGACCGGTCTTCTCGTCGGTGTCATAGCTGCGGGCATCGACATAACTACCGACTGGCTG GCCGATCTGAAGCTGGGCTTTTGCTCAAGCGGTCCCGAGGGGGGGCACTTCTATCTGAACAAGAGCTTCTGCTGC TACGGCTACGACCAAGGTTCCAAGTGCTTGGGGTGGAAGTACTGGAGCGATGCGCTCGGTGTCCACGCTGCCGGC GGCAAATGGTTCATCGAATACATCTTTTTCATTCTCTTCTCGGTACGCAGTCGCTTCGCGAACCCGTGGGAACCC GTCGTCTTGTGCTGACAAGTGCGGTAAGGTGACGCTGGCATATTGCGCTGCTGTGCTTGTTCAGGAGTATGCCAT GTATGCCAAGCACAGCGGCATCCCGGAGATCAAGACGGTTCTTGGAGGATTCGTCATCCGCAGGTTTCTCGGCAC ATGGACCCTGGTCACCAAAGCTCTCGGCCTGGTGAGACTTCTCTCACCCCTCCCATACGAGCTCCATGAAGCCGT GACTGAACATGGCGAGCAGGTGCTGGCTGTCGGCTCTGGCATGTGGCTTGGAAAGGAGGGGCCACTGGTCCATGT TGCCTGCTGTTGCGCGAGTCTCTTCATTAAGCTCTTCGGCAACATTAGGGACAATGAAGGTGGGAAAGCTGTAGA CCCGGCGCTCCGGGGGCTGGCGGCTGATTCACGGCAGCTCGAAAGCGAGAAGTGCTCTCGGCTGCGGCCGCAGCG GGCATTTCGGTTGCCTTTGGCTCCCCAATCGGCGGCGTCCTGTTCAGCCTCGAGGTATCGATGTCGTCTTCTTGT CGTCTGCCGGTCGACTTGCGTATTCTTGGCTGCTGACTCTGCCCCAGCAACTCTCGTATTACTTTCCAGACAAAA CCATGTGGCAGAGCTTTGTCTGCGCCATGACGGCGGCCGTCGTGCTCCAGGCTTTTGACCCCTTTCGCTCGGGCA AACTTGTCCTCTACCAGACCAAGTACAGCGTAGACTGGCACGGTTTCGAGATTGTCCCTTATGCGCTTCTCGGCA TCTTTGGGGTCCGTTCCCTCCAAGTGTGCCCTTGGTTATTTGTCAATGGTGGACGAATACTGATGCGCATCGCAG GGTGTGTACGGTGGCCTGTTTATCAAGGCCAACATGGCTGTTGCGCGATGGAAGACGGCCAGGGCCTGGCTCCCC AGTCCCATTGCCCAGGTCTTGGCCGTGGCCCTGCTGACTGCGCTCATCAACTACCCAAACTCGTATATGAAAGTG CAGTCTTCGGAGCTCGTCTCCAACCTCTTCGCCGACTGCGCGCGCGTCCTCGACGACCAGGTCGGCCTGTGCAAG ACGGGTGCGGCGTCTGCCGGCACCATCATTCTCCTGATCCTGGCCGCCGTGCTGGGCTTCCTGCTCGCGACCATC ACCTTTGGCCTGCAGATCCCCGCGGGCATCATCCTCCCGTCCATGGCCATCGGCGCCCTGGCCGGGCGCGCCGTG GGCATCATCATGGAGATCTGGGTCAGCAACCACGCCGACTTCTTCGTGTTCTCGTCGTGCGCGCCCGACGCGCCG TGCATCACGCCCGGGACGTACGCCATCATCGGCGCGGCCGCCGCACTCGCGGGCGTCACGCGGATGACGGTGTCC ATCGTCGTCATCACGTTCGAGCTCACCGGGGCGCTCACGTACGTCCTCCCTATCATGGTGGCCGTCATGATCTCC AAGTGGGTCGGCGACGCCTTTTCGCGACGCGGCATCTACGAGTCCTGGATCCATTTCAACGAGTACCCCTTCCTC GACAACAGCGAGGAGATGGTGGTGCCGGACGTGCCCGTCTCGCAGATCATGACGCGCATCGAGGACCTGGTCGTC CTGACCGCCACGGGCCACAGCATCGCCTCGCTCAACGCGATCCTCGAGACGCACCCGTACCGCGGCTTCCCCGTC ATCTCGGACCCGCGCGATGCCATCCTACTGGGCTACATCTCGCGCGGCGAGCTGAGCTACAACCTCCGGACGGCG ACGCAGCCGCCGCGGTCGCTGGCGCCGGAGACGGAGGCCTTCTTCTCGCACCAGCCGCTGGCGGACCCGCGCTCG ACGCTCGACCTGCGCCCCTGGATGGACCAGACGCCGCTGACGCTGCTGTCGCGCACGAGCCTGCACCTCGCCGTC TCGTACTTCCAGAAGCTCGGCCTGCGCTACGTCCTCTTCAGCGACCGCGGCGCCCTTCAGGGCCTCCTGA |