GroEL dependency affects codon usage--support for a critical role of misfolding in gene evolution.
about
Evolution of molecular error rates and the consequences for evolvability.What distinguishes GroEL substrates from other Escherichia coli proteins?Trm9-Catalyzed tRNA Modifications Regulate Global Protein Expression by Codon-Biased TranslationRNA chaperones buffer deleterious mutations in E. coli.The molecular chaperone DnaK is a source of mutational robustnessCodon usage regulates protein structure and function by affecting translation elongation speed in Drosophila cells.Entrainment to periodic initiation and transition rates in a computational model for gene translationChaperonin activity modulates codon adaptation.A gene's ability to buffer variation is predicted by its fitness contribution and genetic interactions.Genome-scale analysis of translation elongation with a ribosome flow model.Preventing dangerous nonsense: selection for robustness to transcriptional error in human genes.Transition from positive to neutral in mutation fixation along with continuing rising fitness in thermal adaptive evolution.Biophysics of protein evolution and evolutionary protein biophysicsImpact of translational error-induced and error-free misfolding on the rate of protein evolution.Positively charged residues are the major determinants of ribosomal velocityFunctional analysis of archaeal MBF1 by complementation studies in yeastHsp90 promotes kinase evolutionNew universal rules of eukaryotic translation initiation fidelityDeterminants of translation efficiency and accuracy.The effect of chaperonin buffering on protein evolutionComposite effects of gene determinants on the translation speed and density of ribosomes.Chaperones divide yeast proteins into classes of expression level and evolutionary rateEvolutionary layering and the limits to cellular perfection.Flagellated algae protein evolution suggests the prevalence of lineage-specific rules governing evolutionary rates of eukaryotic proteinsSignatures of protein biophysics in coding sequence evolutionEfficient translation initiation dictates codon usage at gene start.High levels of gene expression explain the strong evolutionary constraint of mitochondrial protein-coding genes.Evidence for deep phylogenetic conservation of exonic splice-related constraints: splice-related skews at exonic ends in the brown alga Ectocarpus are common and resemble those seen in humans.Chaperonin-dependent accelerated substitution rates in prokaryotesSynonymous codon changes in the oncogenes of the cottontail rabbit papillomavirus lead to increased oncogenicity and immunogenicity of the virusEvolution of Chaperonin Gene Duplication in Stigonematalean Cyanobacteria (Subsection V)Evolutionary conservation of codon optimality reveals hidden signatures of cotranslational folding.Codon optimality, bias and usage in translation and mRNA decay.Kinetic modelling indicates that fast-translating codons can coordinate cotranslational protein folding by avoiding misfolded intermediates.Cold adaptation of a psychrophilic chaperonin from Psychrobacter sp. and its application for heterologous protein expression
P2860
Q22066264-014E950D-F489-4D7D-998B-D1720DB0F943Q26992040-7C9FE736-7FE4-455B-9B6D-BB2CF27C2A9CQ28551768-33C9D094-A59F-4A78-A307-BC8A66426A05Q30373007-8BBCB69A-C29B-43A6-A465-176AE0FBCA18Q30391567-545DAD13-7355-470A-96C5-A72E3B3BABB1Q30402749-7263E2FA-1E9D-47C4-ADAB-2EC15946BB82Q33572739-A0B69A13-02C4-4CCE-B8FC-08983BEAAFA7Q33668525-0E02AA62-6067-452A-9FC1-87A19850442CQ33847031-1CFAD812-6390-4664-B982-D37BDCD0C08DQ34016175-0BD9285A-124C-45E2-811C-3A67AEC04F38Q34055313-15EA48F1-436A-4FB7-8F64-23CD4C014DA3Q34220343-229552A6-6733-4AC9-88CF-7F635D3DE808Q34311852-A441CB2C-62F7-4E2B-A51C-DFF0FDF8531AQ34344306-58DEB7E5-04A2-48BB-99B5-C22126B22FC5Q34647647-16139CD1-3D95-414B-8E24-46B99427801CQ34708554-1CA740F1-116A-4DB8-AA9A-7B30358D94EEQ34740694-895B8997-9163-4884-9CA7-8B78C083E2EFQ34845179-4EE54AEE-C258-4B03-935F-01C765030182Q35006962-E3A50108-9824-4192-BA25-16248ADDC1D2Q35811177-DD60E9B2-EE8C-4765-B56C-B61603D3CFFCQ35907619-E778B388-D4C0-4559-B505-8EF20C8C9360Q36054030-C90B12FC-D0A9-45C3-8431-21D0EDB14E56Q36414697-30FC0FFA-3F76-4708-ADD9-7083B21802C9Q36905269-A18080E7-6A82-4987-A811-1721D5BD0637Q37731692-16DB72F9-9BDF-4430-A640-B7DA63BFEC1DQ38461794-155B1A08-5C4A-4BBE-A0FC-231BBAAE3170Q38494582-21FF8A83-2926-4561-BC08-AEC78991EB5FQ41903111-C0625A40-781A-44F2-B3E3-4EEF71DBE093Q42069125-69B411E8-97B2-49AB-9AA2-F2DEEE28F599Q42114403-19AFC399-8EDB-43E1-A926-7B61B3C7125CQ42292737-E82DC0DA-D61E-47E9-A65A-ACB97FAC7464Q43178970-104CE5B1-991D-42B9-9AD9-0EA36FD33A70Q47668877-AFB9CDF8-FCFC-4507-9FD1-C71CE2699C4AQ51125807-69EB0077-C3D3-452B-BD3B-85FA64570BEAQ56384751-17F4D72A-FC1D-49FA-84FA-168C75386BBA
P2860
GroEL dependency affects codon usage--support for a critical role of misfolding in gene evolution.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
GroEL dependency affects codon ...... misfolding in gene evolution.
@ast
GroEL dependency affects codon ...... misfolding in gene evolution.
@en
type
label
GroEL dependency affects codon ...... misfolding in gene evolution.
@ast
GroEL dependency affects codon ...... misfolding in gene evolution.
@en
prefLabel
GroEL dependency affects codon ...... misfolding in gene evolution.
@ast
GroEL dependency affects codon ...... misfolding in gene evolution.
@en
P2860
P356
P1476
GroEL dependency affects codon ...... misfolding in gene evolution.
@en
P2860
P356
10.1038/MSB.2009.94
P577
2010-01-19T00:00:00Z