RNA Type | tRNA |
---|---|
SOTerm | None |
Original Source | LC530715.1 |
Secondary Structure | (((((((..((((.........)))).(((((.......)))))....(((((.....)))))))))))).... |
Sequence (UNICHARACTER ENCODING) | GUUUAUGUѢLCUUACCUCCUCAAAGCAAPACACUGAA*APGUUUAGA?GGGCUCACAUCACCCCAUAAACACCA |
Sequence (SHORT NAMES ENCODING) | GUUUAUGUpm1Apm2GCUUACCUCCUCAAAGCAApYACACUGAApms2i6AApYGUUUAGApm5CGGGCUCACAUCACCCCAUAAACACCA |
Sequence (MODOMICS CODE ENCODING) | GUUUAUGU2000001551A2000002551GCUUACCUCCUCAAAGCAA2000009551UACACUGAA2002161551AA2000009551UGUUUAGA2000005551CGGGCUCACAUCACCCCAUAAACACCA |
Consensus Secondary Structure | .(((((((..((((......[....)))).(((((.......)))))........................(((((..]....)))))))))))).... |
Alignment with Modification | -GUUUAUGUѢLCUUACCUCCUCA--AAGCAAPACACUGAA*APGUUUAGA?--------------------GGGCUCACAU--CACCCCAUAAACACCA |
Method Classification | Score |
---|---|
Multiple direct experimental evidence | 1 |
Direct experimental evidence | 2 |
Inferred based on indirect experimental evidence | 3 |
Predicted computationally | 4 |
Evidence not yet annotated (Unknown) | 5 |
Irrelevant | 6 |
Position in the alignment | 9 | 10 | 28 | 37 | 39 |
---|---|---|---|---|---|
Position in the sequence | 10 | 11 | 32 | 41 | 43 |
Modification positions | pm1A | pm2G | pY | pms2i6A | pY |
Source | 32859890 | 32859890 | 32859890 | 32859890 | 32859890 |
Position in the alignment | 9 | 10 | 28 | 37 | 39 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Position in the sequence | 10 | 11 | 32 | 41 | 43 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Source: 32859890 | N | G+ | G+ | G+ | G+ | G+ | G+ | G+ | N | N | G+ | G+ | G+ | G+ | N | N | N | N | N | N | ms2t6A | N | N | N | N | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | N | G+ | G+ | G+ | G+ | G+ | N | N | N | N | N | N | N | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | N | G+ | G+ | G+ | G+ | G+ | N | N | m1Y | N | N | N | N | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | cmnm5Um | N | N | N | N |
Level of Experimental Reliability | 2 | 2 | 2 | 2 | 2 | 2 | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None |
Level of Experimental Evidence | 2 | 2 | 2 | 2 | 2 | 2 | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None | None |