EFTu provides an internal kinetic standard for translational accuracy.
about
GTP hydrolysis controls stringent selection of the AUG start codon during translation initiation in Saccharomyces cerevisiaeAlterations in ribosomal protein RPS28 can diversely affect translational accuracy in Saccharomyces cerevisiae.Functional association of essential splicing factor(s) with PRP19 in a protein complex.Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily.Snt309p, a component of the Prp19p-associated complex that interacts with Prp19p and associates with the spliceosome simultaneously with or immediately after dissociation of U4 in the same manner as Prp19p.Translational misreading: a tRNA modification counteracts a +2 ribosomal frameshiftTowards engineering proteins by site-directed incorporation in vivo of non-natural amino acids.Identification of Streptomyces coelicolor proteins that are differentially expressed in the presence of plant material.How translational accuracy influences reading frame maintenanceDifferent fates of the chloroplast tufA gene following its transfer to the nucleus in green algae.The yeast omnipotent suppressor SUP46 encodes a ribosomal protein which is a functional and structural homolog of the Escherichia coli S4 ram protein.Sequence analysis and expression of the two genes for elongation factor 1 alpha from the dimorphic yeast Candida albicans.A comprehensive analysis of translational missense errors in the yeast Saccharomyces cerevisiae.Programmed +1 translational frameshifting in the yeast Saccharomyces cerevisiae results from disruption of translational error correction.The frequency of translational misreading errors in E. coli is largely determined by tRNA competition.Editing of errors in selection of amino acids for protein synthesisAn mRNA sequence derived from the yeast EST3 gene stimulates programmed +1 translational frameshifting.Testing constraints on rRNA bases that make nonsequence-specific contacts with the codon-anticodon complex in the ribosomal A site.Saturation mutagenesis of a +1 programmed frameshift-inducing mRNA sequence derived from a yeast retrotransposon.Evidence for functional interaction between elongation factor Tu and 16S ribosomal RNA.Septin ring assembly involves cycles of GTP loading and hydrolysis by Cdc42p.Elongation factor EF-1 alpha gene dosage alters translational fidelity in Saccharomyces cerevisiae.Sequence and functional similarity between a yeast ribosomal protein and the Escherichia coli S5 ram proteinErrors and alternatives in reading the universal genetic code.Accuracy modulating mutations of the ribosomal protein S4-S5 interface do not necessarily destabilize the rps4-rps5 protein-protein interaction.Fidelity at the molecular level: lessons from protein synthesis.Translational accuracy during exponential, postdiauxic, and stationary growth phases in Saccharomyces cerevisiae.Interactions between tRNA identity nucleotides and their recognition sites in glutaminyl-tRNA synthetase determine the cognate amino acid affinity of the enzyme.Components of fitness become effectively neutral in equilibrium populations.Structural aspects of translation termination on the ribosome.Positions 13 and 914 in Escherichia coli 16S ribosomal RNA are involved in the control of translational accuracyA mutation in the 530 loop of Escherichia coli 16S ribosomal RNA causes resistance to streptomycinStop making sense: or Regulation at the level of termination in eukaryotic protein synthesis.Direct detection of viable bacteria, molds, and yeasts by reverse transcriptase PCR in contaminated milk samples after heat treatmentQuantitative analysis of in vivo ribosomal events at UGA and UAG stop codonsSingle-base mutations at position 2661 of Escherichia coli 23S rRNA increase efficiency of translational proofreading.Pulling the ribosome out of frame by +1 at a programmed frameshift site by cognate binding of aminoacyl-tRNA.Kinetic timing: a novel mechanism that improves the accuracy of GTPase timers in endosome fusion and other biological processes.Codon-dependent conformational change of elongation factor Tu preceding GTP hydrolysis on the ribosome.Elongation factor Tu, a GTPase triggered by codon recognition on the ribosome: mechanism and GTP consumption.
P2860
Q27935355-B2C6A54A-B862-4468-84D0-8AC2B27A421CQ27936038-0130316C-251C-40B1-ADF2-727E8201BE0AQ27939025-7A3AB148-A273-4CCD-8D48-E7BC0BDD9A90Q27939653-75CCD8DA-50D1-4D11-A706-43B88A8DD5B5Q27939803-4D9EF8BA-B5C1-4E48-B440-1E594F7EF21DQ28349567-C2BA3AB3-08F1-4D92-9614-2D0EE060ED85Q30418501-F9553389-B789-4646-ACDC-E61412748BCCQ33186615-9CC7A44B-FC14-455A-B529-EAAC11B3A8B1Q33540905-668A7E9C-2B03-4BEE-BC12-13D545C5147CQ33685290-27FC79D8-64BE-4780-87C9-DD648C0F4A1DQ33959932-50C578A3-79D9-45B7-A225-2D099D1AC43DQ33978504-DD586D71-778E-41D8-A3EE-B602D8E30650Q34075919-F133ED28-4E76-47D0-816F-8E8A87EE9E4CQ35133679-C4AEF9C5-5CAB-4FC8-A64B-13E4BABF3CBEQ35230528-ADB4A19F-D3C2-4580-8EF1-A7329BCE5ADEQ35403101-6163A091-9422-41F6-BD50-24467FCD90FFQ35697496-EB394D0C-24E9-4273-A231-E348333ACD0AQ35902017-32340597-EC5B-40F6-ADE3-0B28D8217382Q36088349-94FD70B2-BADD-468F-A22B-F47493092C9CQ36103824-B37D2D10-5A58-4FB5-9BF6-818C2DFCB712Q36381135-F343A947-C15D-45E6-9B8A-FEA7E26438C2Q36763127-2D0B4950-994F-4479-AD2F-4570EC498F06Q36774937-981F308D-A624-47BB-91D6-34F40EDBF452Q37055639-676A6E87-120B-4E3B-873A-9F7A2107372AQ37200656-D5355472-40F3-48EA-A3BD-77CE9C1525CDQ37400330-43C0CBAE-9B50-49F8-8D7F-20EBFD9765C3Q37421805-395AEF3F-B0EB-4166-9B1B-F349031A78C5Q37477522-BFDA096B-D444-45D1-BBAD-800619CE036DQ37715405-4AF6AD94-361B-45B1-B5C5-FCEC3C8F4EE6Q37893830-B1AC4EEE-6851-4DFB-9BF4-FB1553690C7EQ38310915-EE4FFD3E-5455-4F39-947A-07102BE6E9B4Q38346257-83D77E87-7C1E-49D5-84B7-254BB48D868AQ39514050-90C1F884-6856-4F85-9A08-3F149B2047BBQ39561506-8D50643A-DC1D-456C-B5C6-E09DA7B662E8Q39723925-D9630255-B4EC-4752-8729-606D7663532BQ39940128-5A236F1D-A34F-4062-BA48-EF917EB897A4Q40021492-DEC22966-DED8-4803-8F3E-9F545D758892Q40740814-F76C8C62-4F78-41DA-838B-C41FA769352EQ40806950-85CFCFDA-79B1-4C53-8A57-02FA0014769CQ41043888-46A9CA0F-9958-4974-BD57-1113567AA0C3
P2860
EFTu provides an internal kinetic standard for translational accuracy.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
EFTu provides an internal kinetic standard for translational accuracy.
@en
EFTu provides an internal kinetic standard for translational accuracy.
@nl
type
label
EFTu provides an internal kinetic standard for translational accuracy.
@en
EFTu provides an internal kinetic standard for translational accuracy.
@nl
prefLabel
EFTu provides an internal kinetic standard for translational accuracy.
@en
EFTu provides an internal kinetic standard for translational accuracy.
@nl
P1476
EFTu provides an internal kinetic standard for translational accuracy.
@en
P2093
Thompson RC
P356
10.1016/0968-0004(88)90047-3
P577
1988-03-01T00:00:00Z