「r rna」の共起表現(1語左で並び替え)

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共起表現

「r rna」の共起表現一覧(1語左で並び替え)

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In enzymology, a	rRNA (adenine-N6-)-methyltransferase (EC 2.1.1.48)
In enzymology, a	rRNA (adenosine-2'-O-)-methyltransferase (EC 2.1.1.6
not predicted to guide to 2'O-methylation of a	rRNA or snRNA.
es of this enzyme are S-adenosyl methionine and	rRNA, whereas its two products are S-adenosylhomocys
Overall, 50S is generally monolithic and	rRNA structure is stabilized by proteins.
D is found in tRNA and	rRNA molecules as a nucleoside; the corresponding nu
es of this enzyme are S-adenosyl methionine and	rRNA, whereas its two products are S-adenosylhomocys
catalyze their own excision from mRNA, tRNA and	rRNA precursors in a wide range of organisms.
ition to these, mitochondrial and chloroplastic	rRNA are also amplified.
oteins preferentially bind to its complementary	rRNA if it is present, rather than mRNA.
It will decrease	rRNA and other genes transcription but will increase
ure found upstream of genes predicted to encode	rRNA methyltransferases, possibly for 23S rRNA.
y, thermophily and monophyly from environmental	rRNA sequences".
roliferation and it may also be a regulator for	rRNA transcription.
are usually reserved for sections that code for	rRNA, whereas endolytic cleavage corresponds to tRNA
This binding causes a reduction in	rRNA transcription.
ght be more proteins or transcripts involved in	rRNA than previously and/or that some snoRNAs have d
Targets of (p)ppGpp include	rRNA operons, of which there are seven in Escherichi
c regions of rDNA (for small- and large-subunit	rRNA), variation among individual rDNA repeats can s
The RNA molecules (	rRNA and tRNA) played an important role in the catal
m primers which amplify all RNA which is mostly	rRNA, miRNA microarray ligate an oligonucleotide to
For this reason many thousands of	rRNA sequences are known and stored in specialized d
ecause it a) is (due to the high copy number of	rRNA genes) easy to amplify even from small quantiti
A reduced amount of	rRNA means that ribosomal proteins (r-proteins) will
e software package for phylogenetic analysis of	rRNA and other biological sequences.
Trees based on	rRNA show the Hartmannellidae as usually defined are
Read from 5' to 3', this polycistronic	rRNA precursor transcript contains the 5' external t
In the nucleus it is involved in precursor	rRNA processing, where it cleaves the internal trans
ose methylation of the large 28S ribosomal RNA (	rRNA) subunit on residue G4198 .
he 2'O-ribose methylation of 18S ribosomal RNA (	rRNA) residue C517.
s as a methylation guide for 18S ribosomal RNA (	rRNA) in plants .
he 2'O-ribose methylation of 18S ribosomal RNA (	rRNA) at residue A99 3
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) at residue C3848.. Its is related to mouse sno
function in the modification of ribosomal RNA (	rRNA) and transfer RNA (tRNA).
ts at a specific site in the 28S ribosomal RNA (	rRNA) genes of most insect genomes In order to inser
ins and single-strand RNA called ribosomal RNA (	rRNA).
seudouridylation of U4938 of 28S ribosomal RNA (	rRNA).
pseudouridylation of U119 of 18S ribosomal RNA (	rRNA).
uide the 2'-O-methylation of 28S ribosomal RNA (	rRNA) residue A-2634 .
seudouridylation of U4393 of 28S ribosomal RNA (	rRNA).
seudouridylation of U1692 of 18S ribosomal RNA (	rRNA).
seudouridylation of U1664 of 28S ribosomal RNA (	rRNA).
seudouridylation of U3801 of 28S ribosomal RNA (	rRNA).
seudouridylation of U4643 of 28S ribosomal RNA (	rRNA).
pseudouridylation of U649 of 18S ribosomal RNA (	rRNA).
pseudouridylation of U55 of 5.8S ribosomal RNA (	rRNA).
seudouridylation of U1004 of 18S ribosomal RNA (	rRNA).
pseudouridylation of U36 of 18S ribosomal RNA (	rRNA).
he 2'O-ribose methylation of 18S ribosomal RNA (	rRNA) at residue G436.
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) residue C4506 .
he 2'O-ribose methylation of 18S ribosomal RNA (	rRNA) residue G601.
) is a 959 nt long mitochondrial ribosomal RNA (	rRNA).
de 2'O-ribose methylation of 28s ribosomal RNA (	rRNA) at position U3797.
residues U4373 and U4427 of 28S ribosomal RNA (	rRNA) .
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) at residue G3923.
guide 2'O-ribose methylation of ribosomal RNA (	rRNA) 28S at residue C3866.
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) residue A3764 .
n of 2'-O-ribose residues in 28S ribosomal RNA (	rRNA).
by any ribosomal proteins but by ribosomal RNA (	rRNA), a ribozyme.
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) residue A4493 .
he 2'O-ribose methylation of 28S ribosomal RNA (	rRNA) residue G4020.
e 2'-O-ribose methylation of 28s ribosomal RNA (	rRNA) at residue A4531.
he 2'O-ribose methylation of 18S ribosomal RNA (	rRNA) reside A590.
'O-ribose methylation of the 28S ribosomal RNA (	rRNA) at residue A3697 .
However, the GC content of ribosomal RNA (	rRNA) and transfer RNA (tRNA) genes in hyperthermoph
RNA situated between structural ribosomal RNAs (	rRNA) on a common precursor transcript.
transcriptional modification of ribosomal RNAs (	rRNA) and in some cases of small nuclear RNAs (sRNAs
tures proteins, including RNases, and separates	rRNA from ribosomes, while phenol, isopropanol and w
/ACA snoRNA to the correct region of its target	rRNA.
attractive hypothesis in view of the fact that	rRNA methyltransferases can bind RNA, and therefore
r, in one case it is far (3 kilobases) from the	rRNA methyltransferase gene.
ue specific) and the lack of complementarity to	rRNA and SnRNA.
The large 50S ribosomal subunit contains two	rRNA species (the 5S and 23S rRNAs).
ed identification methods are mainly based upon	rRNA derived phylogenetic conclusions.
Lemuridae has been dated to 26.1 ±3.3 mya while	rRNA sequences of mtDNA place the split at 24.9 ±3.6

共起表現

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「r rna」の共起表現一覧(1語左で並び替え)