「Ribosome」の共起表現一覧(1語右で並び替え)
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| linked by peptide bonds (put together by the | ribosome, according to the genetic code as stored in D |
| A | ribosome also has 3 binding sites called A, P, and E. |
| ent to genes encoding protein subunits of the | ribosome, although they are not necessarily in the sam |
| in the functionally essential regions of the | ribosome and spliceosome. |
| 451 and A2452 residues in the 23S rRNA of the | ribosome and inhibits peptide bond formation. |
| Upon translation, the NatA binds to the | ribosome and then "stretches" to the front end of the |
| tion, nuclear and mitochondrial splicing, and | ribosome and spliceosome assembly. |
| rotein are not high, they are occupied in the | ribosome, and are not available in significant quantit |
| molecular structure of the 30S subunit of the | ribosome and its complexes with several antibiotics. |
| tion, nuclear and mitochondrial splicing, and | ribosome and spliceosome assembly. |
| ers, proteins, biological membranes, viruses, | ribosome and macromolecules. |
| raction of a protein that forms a part of the | ribosome, and to make sure that the concentration is n |
| ponent of the large subunit of the eukaryotic | ribosome and so plays an important role in protein tra |
| he frameshift signal is thought to impede the | ribosome and cause slippage in the 5' direction, this |
| n of S6 Ribosomal protein (a component of the | ribosome) and other components of the translational ma |
| ability to bind at two sites at the bacterial | ribosome as well as having a structural modification t |
| ird region of interactions with the bacterial | ribosome, as compared with two binding sites for other |
| he 5S RNA transcript until it is required for | ribosome assembly. |
| e translocation of the tRNA and mRNA down the | ribosome at the end of each round of polypeptide elong |
| e translocation of the tRNA and mRNA down the | ribosome at the end of each round of polypeptide elong |
| ly defined as the point, sequence, at which a | ribosome begins to translate a sequence of RNA into am |
| The alpha operon | ribosome binding site in bacteria is surrounded by thi |
| subtilis groE promoter, lac operator and gsiB | ribosome binding site. |
| In prokaryotes, the 5' UTR usually contains a | ribosome binding site (RBS), also known as the Shine D |
| hock proteins by presenting a more accessible | ribosome binding site. |
| he discovered the RNA sequence necessary for | ribosome binding and the initiation of protein synthes |
| nd causes the stem loop to open, exposing the | ribosome binding site. |
| and a possible mechanism for sequestering the | ribosome binding site, it was proposed that the sucA R |
| At high temperatures (45°C+), the | ribosome binding site of cIII mRNA is occluded, preven |
| -CBL to 5' UTRs in relevant genes, preventing | ribosome binding and translation of those genes. |
| edicted Shine-Dalgarno sequences (involved in | ribosome binding) of the downstream sucA genes. |
| The 3' end of the 16S rRNA (in a | ribosome) binds to a sequence on the 5' end of mRNA ca |
| Ribosome biogenesis is the process of making ribosomes | |
| It modulates IF2 binding to the | ribosome by increasing its affinity. |
| tRNA to fully occupy the E site (and exit the | ribosome complex), and the mRNA to shift three nucleot |
| The | ribosome continues to translate the remaining codons o |
| ng the resulting protein library to rounds of | ribosome display, the affinity can be directed towards |
| RNA (tRNA) molecule enters the A site of the | ribosome, due to the shortage of amino acid required b |
| the first part of the protein that exits the | ribosome during protein biosynthesis. |
| rmational switch in the pseudoknot region and | ribosome entrapment. |
| s family represents the Picornavirus internal | ribosome entry site (IRES). |
| This family represents the internal | ribosome entry site (IRES) of the aphthoviruses. |
| This family represents the internal | ribosome entry site (IRES) of the Hepatitis A virus. |
| The N-myc internal | ribosome entry site (IRES) is an RNA element found in |
| This internal | ribosome entry site (IRES) allows cap independent tran |
| It is thought that FGF-1 internal | ribosome entry site (IRES) activity is strictly contro |
| 216 nucleotide long 5' UTR contains internal | ribosome entry site activity. |
| arcoma-associated herpesvirus (KSHV) internal | ribosome entry site (IRES) present in the vCyclin gene |
| The HIF-1α internal | ribosome entry site (IRES) allows translation to be ma |
| The HIF-1α internal | ribosome entry site (IRES) is an RNA element present i |
| ed by the heat shock response due to internal | ribosome entry site (IRES)-dependent translation. |
| The BiP internal | ribosome entry site (IRES) is an RNA element present i |
| The bag-1 internal | ribosome entry site (IRES) is a cis-acting element loc |
| The c-myc internal | ribosome entry site (IRES) is an RNA element present i |
| The APC internal | ribosome entry site (IRES) is an RNA element which is |
| The connexin-32 internal | ribosome entry site (IRES) is an RNA element present i |
| revents splicing of an intron that contains a | ribosome entry site necessary for efficient expression |
| The Cripavirus internal | ribosome entry site (IRES) is an RNA element required |
| The FGF-1 internal | ribosome entry site (IRES) is an RNA element present i |
| The heat shock protein 70 (Hsp70) internal | ribosome entry site (IRES) is an RNA element that allo |
| The c-sis internal | ribosome entry site (IRES) is a RNA element found in t |
| is family are uncapped and encode an internal | ribosome entry site. |
| rnative method of translation via an internal | ribosome entry site where ribosomes are recruited to t |
| lternative method of translation via internal | ribosome entry where ribosomes are recruited to the IR |
| ily represents an Epstein-Barr virus internal | ribosome entry site (IRES) which is found in the U lea |
| The internal | ribosome entry site contains three modules that can in |
| olon for oxidative energy generation, and the | ribosome for protein sythesis. |
| Eubacterial 70S | Ribosome from Thermus thermophilus. |
| lving the genetic code, protein synthesis and | ribosome function that led to the Nobel Prize in Physi |
| the cytoplasm with the transcription of many | ribosome gene operons. |
| The later dissociation of EF-Tu from the | ribosome, however, requires that the GTP first be hydr |
| se initiation factors must associate with the | ribosome in stoichiometric proportions, while Rli1p is |
| ogous to EF-Tu + tRNA, EF-G also binds to the | ribosome in its GTP-bound state. |
| determined the atomic structure of the whole | ribosome in complex with its tRNA and mRNA ligands. |
| antibody Fab fragment fused with bouganin, an | ribosome inactivating protein from the plant Bougainvi |
| oxidase and lactoferrin from several species, | ribosome inactivating protein and its complex with a n |
| The mature mRNA may then be translated by the | ribosome into protein. |
| Consequently she showed that the | ribosome is a ribozyme that places its substrates in s |
| nonsense codon are not displaced because the | ribosome is released from the transcript before reachi |
| These genes encodes the | ribosome modulation factor protein, which affects the |
| This | ribosome modulation is a part of the stringent respons |
| pothesis is bolstered by the observation that | ribosome modulation factor binds ribosomal RNA, and ma |
| ms when the cell has an excess of leucine and | ribosome movement over the leader transcript is not im |
| unterpart is 60S, is the large subunit of 70S | ribosome of prokaryotes. |
| nteractions between separate RNA units in the | ribosome or spliceosome. |
| Also, if the oncoming | ribosome pauses because of a knot in the RNA, then the |
| ier to mRNA translocation so therefore causes | ribosome pausing. |
| in translocation, EF-G, working together with | Ribosome Recycling Factor promotes ribosome recycling |
| circular formation, creating a cycle of rapid | ribosome recycling, and utilization of ribosomes. |
| (2555) induces a conformational change in the | ribosome, resulting in movement of U2541 (2506), U2620 |
| Proposed a molecular mechanism of the | ribosome role in protein synthesis (1968). |
| ernative use of initiation codons due to weak | ribosome scanning mechanisms. |
| here initiation from the 5' cap structure and | ribosome scanning is reduced. |
| Ribosome shunting is a mechanism of translation initia | |
| entrations of the relevant amino acid is low, | ribosome stalling leads to an alternate structure that |
| In eukaryotic cells, the 60S (28S component) | ribosome subunit contains the peptidyl transferase com |
| In Bacteria, the 50S (23S component) | ribosome subunit contains the peptidyl transferase com |
| over ribozymes in nature (the other being the | ribosome), the discovery of which earned Sidney Altman |
| For example, the functional part of the | ribosome, the molecular machine that translates RNA in |
| nd discovered within the otherwise asymmetric | ribosome, the universal symmetrical region that provid |
| The growing protein exits the | ribosome through the polypeptide exit tunnel in the la |
| at a site on the 50S subunit of the bacterial | ribosome through an interaction that differs from othe |
| wo tRNA molecules and mRNA in relation to the | ribosome) thus blocking translational elongation. |
| ch acts as a special recognition site for the | ribosome to allow a tRNA-ribosome complex to form duri |
| EF-Tu requires GTP in order for the | ribosome to bind it, necessary for recruiting an amino |
| This sequence helps recruit the | ribosome to the mRNA to initiate protein synthesis by |
| ety incorporate itself into the A site of the | Ribosome to disruptits flow and "release" the protein |
| The tmRNP binds to the A-site, allowing the | ribosome to switch templates from the broken message o |
| s a deficiency of the charged leucyl tRNA the | ribosome translating the leader peptide stalls and the |
| Its function is thought to be in 5.8S rRNA | ribosome translocation. |
| ory that there is a multistage ratchet in the | ribosome which tests the match several times before in |
| well as the primary enzymatic function of the | ribosome, which forms peptide links between adjacent a |
| h halts translation of the polypeptide by the | ribosome while it attaches the ribosome to the SRP rec |
| trans-Translation stages A through F. A | ribosome with its RNA binding sites, designated E, P, |
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