Results 41 - 60 of 187 are showing below:
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ID | Location | Perfect MFE.* | RefSeq Acc. | strand | Start Position | R_P_ratio# | P value |
Predicted miRNA align pattern | |||||||
14625 | 3' | -60.2 | NC_003521.1 | + | 149179 | 0.66 | 0.850956 |
Target: 5'- cUCGGCGCGC--GUCGCCa-C-CGGCGg -3' miRNA: 3'- -GGUCGCGCGacUAGUGGgcGaGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 116869 | 0.66 | 0.850956 |
Target: 5'- aCCuGCGCGCgcagugGcgCGgCUGCggCGGCGc -3' miRNA: 3'- -GGuCGCGCGa-----CuaGUgGGCGa-GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 196416 | 0.66 | 0.850956 |
Target: 5'- gCAGCGgcacagacaguCGCUG-UCGCCCgGgUCGGCc -3' miRNA: 3'- gGUCGC-----------GCGACuAGUGGG-CgAGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 181467 | 0.66 | 0.850956 |
Target: 5'- cCCAGUcgGCGCaGAcgGCCCaucccaGCUCGGUGa -3' miRNA: 3'- -GGUCG--CGCGaCUagUGGG------CGAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 110678 | 0.66 | 0.835825 |
Target: 5'- gCCAGCGCGUcGGUgGCCUcgaGCUUgaggucgaaGGCGc -3' miRNA: 3'- -GGUCGCGCGaCUAgUGGG---CGAG---------CCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 92444 | 0.66 | 0.834276 |
Target: 5'- cCCAGCcuccccgcacccCGCUcGGcUUGCCCGCUCGGgGg -3' miRNA: 3'- -GGUCGc-----------GCGA-CU-AGUGGGCGAGCCgC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 127227 | 0.66 | 0.833499 |
Target: 5'- gCUGGCGCGgUGGUCcuccacgaagagcgGCUCG-UCGGCGu -3' miRNA: 3'- -GGUCGCGCgACUAG--------------UGGGCgAGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 145724 | 0.66 | 0.828013 |
Target: 5'- -aAGCGCGCg---CGgCCGCUCaaGGCGc -3' miRNA: 3'- ggUCGCGCGacuaGUgGGCGAG--CCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 216828 | 0.67 | 0.795267 |
Target: 5'- -uGGCGCGCaggaGGUCgcaGCCCGCggCGGaCGa -3' miRNA: 3'- ggUCGCGCGa---CUAG---UGGGCGa-GCC-GC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 44593 | 0.67 | 0.795267 |
Target: 5'- gUCAGCGCGC-GA-CACCUGCagCuGCGa -3' miRNA: 3'- -GGUCGCGCGaCUaGUGGGCGa-GcCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 109575 | 0.67 | 0.803665 |
Target: 5'- gCUAGCauGCGCgUGAagugCGCCaGCUCGGCc -3' miRNA: 3'- -GGUCG--CGCG-ACUa---GUGGgCGAGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 163009 | 0.67 | 0.795267 |
Target: 5'- -gAGCGCGCUGcUCACCaugaucuGCgagaaCGGCa -3' miRNA: 3'- ggUCGCGCGACuAGUGGg------CGa----GCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 150679 | 0.67 | 0.802831 |
Target: 5'- gCGGCGCcgcugcuGCUGGgugCugCUGCgccggCGGCGa -3' miRNA: 3'- gGUCGCG-------CGACUa--GugGGCGa----GCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 69187 | 0.67 | 0.78674 |
Target: 5'- gCGGcCGCGCUaGAcaUACCCGacgUCGGCGg -3' miRNA: 3'- gGUC-GCGCGA-CUa-GUGGGCg--AGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 42962 | 0.67 | 0.78674 |
Target: 5'- cCCAGCgaGCGCg----ACCCGC-CGGCGc -3' miRNA: 3'- -GGUCG--CGCGacuagUGGGCGaGCCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 137043 | 0.67 | 0.77809 |
Target: 5'- aCCGGCG-GCUGAccUCAggcaCCGCcCGGCc -3' miRNA: 3'- -GGUCGCgCGACU--AGUg---GGCGaGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 129232 | 0.67 | 0.77809 |
Target: 5'- uCCGGCGcCGCUG---GCCaCGCgCGGCa -3' miRNA: 3'- -GGUCGC-GCGACuagUGG-GCGaGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 138398 | 0.67 | 0.820045 |
Target: 5'- gCGGCGCGUcugGAUCGCCgUGUggaccagccucuUCGGCu -3' miRNA: 3'- gGUCGCGCGa--CUAGUGG-GCG------------AGCCGc -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 43566 | 0.67 | 0.811926 |
Target: 5'- gCCGGCGcCGC--GUCAagcaCCGCUCcucgGGCGg -3' miRNA: 3'- -GGUCGC-GCGacUAGUg---GGCGAG----CCGC- -5' |
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14625 | 3' | -60.2 | NC_003521.1 | + | 63092 | 0.67 | 0.820045 |
Target: 5'- gCCGGCGCGCUGccCGCCCuC-CaGCa -3' miRNA: 3'- -GGUCGCGCGACuaGUGGGcGaGcCGc -5' |
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Note:
When operating RNAhybrid, the pipeline first calculates the perfect minimum free energy (Perfect mfe *) of a putative miRNA when the entire putative miRNA binds to a perfectly complementary target site, then it calculates the minimum free energy of RNA duplex (mfe of the miRNA/mRNA duplex), abbreviated as Rd_mfe. An alignment for which the Rd_mfe to its correspondent Perfect mfe ratio (R_P_ratio #) is more than 66% is regarded as a positive alignment as described by Krek et al. (21). The P_value is calculated by RNAhybrid.
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