Two nuclear mutations disrupt distinct pathways for targeting proteins to the chloroplast thylakoid.
about
Overlapping functions of components of a bacterial Sec-independent protein export pathwayCRS1 is a novel group II intron splicing factor that was derived from a domain of ancient origin.An organellar maturase associates with multiple group II intronsProtein targeting to the bacterial cytoplasmic membrane.Protein import and routing systems of chloroplasts.Transposon-disruption of a maize nuclear gene, tha1, encoding a chloroplast SecA homologue: in vivo role of cp-SecA in thylakoid protein targeting.Functional reconstitution of bacterial Tat translocation in vitroA thylakoid membrane protein harboring a DnaJ-type zinc finger domain is required for photosystem I accumulation in plantsProkaryotic utilization of the twin-arginine translocation pathway: a genomic survey.Duplication and suppression of chloroplast protein translocation genes in maizeGenome-wide analysis of thylakoid-bound ribosomes in maize reveals principles of cotranslational targeting to the thylakoid membraneGenetics of the biogenesis and dynamics of the photosynthetic machinery in eukaryotes.Evidence for a dynamic and transient pathway through the TAT protein transport machineryThe DCL gene of tomato is required for chloroplast development and palisade cell morphogenesis in leavesA short PPR protein required for the splicing of specific group II introns in angiosperm chloroplasts.MFP1 is a thylakoid-associated, nucleoid-binding protein with a coiled-coil structure.Targeting determinants and proposed evolutionary basis for the Sec and the Delta pH protein transport systems in chloroplast thylakoid membranes.A SecY homologue is required for the elaboration of the chloroplast thylakoid membrane and for normal chloroplast gene expression.The maize tha4 gene functions in sec-independent protein transport in chloroplasts and is related to hcf106, tatA, and tatBIntra-plastid protein trafficking: how plant cells adapted prokaryotic mechanisms to the eukaryotic condition.Component specificity for the thylakoidal Sec and Delta pH-dependent protein transport pathways.A plant-specific RNA-binding domain revealed through analysis of chloroplast group II intron splicing.Mechanistic Aspects of Folded Protein Transport by the Twin Arginine Translocase (Tat).Stable Membrane-Association of mRNAs in Etiolated, Greening and Mature Plastids.Identification of Putative Substrates of SEC2, a Chloroplast Inner Envelope Translocase.TATA-Binding protein-TATA interaction is a key determinant of differential transcription of silkworm constitutive and silk gland-specific tRNA(Ala) genes.Two Chloroplast Proteins Suppress Drought Resistance by Affecting ROS Production in Guard Cells.Thylakoid targeting of Tat passenger proteins shows no delta pH dependence in vivo.Systematic analysis of plant mitochondrial and chloroplast small RNAs suggests organelle-specific mRNA stabilization mechanisms.The Role of Light-Dark Regulation of the Chloroplast ATP Synthase.Arabidopsis mutants lacking the 43- and 54-kilodalton subunits of the chloroplast signal recognition particle have distinct phenotypes.The pentatricopeptide repeat protein PPR5 stabilizes a specific tRNA precursor in maize chloroplasts.A violaxanthin de-epoxidase interacts with a viral suppressor of RNA silencing to inhibit virus amplification.The chloroplast Tat pathway utilizes the transmembrane electric potential as an energy sourceLarge-scale translocation reversal within the thylakoid Tat system in vivo.Pathway specificity for a delta pH-dependent precursor thylakoid lumen protein is governed by a 'Sec-avoidance' motif in the transfer peptide and a 'Sec-incompatible' mature protein.Molecular cloning of the maize gene crp1 reveals similarity between regulators of mitochondrial and chloroplast gene expressionLarge-scale reverse genetics in Arabidopsis: case studies from the Chloroplast 2010 Project.Plastids contain a second sec translocase system with essential functions.Nuclear mutations that block group II RNA splicing in maize chloroplasts reveal several intron classes with distinct requirements for splicing factors.
P2860
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P2860
Two nuclear mutations disrupt distinct pathways for targeting proteins to the chloroplast thylakoid.
description
1995 nî lūn-bûn
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1995年の論文
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1995年学术文章
@wuu
1995年学术文章
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1995年学术文章
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1995年学术文章
@zh-my
1995年学术文章
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1995年學術文章
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1995年學術文章
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1995年學術文章
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name
Two nuclear mutations disrupt ...... to the chloroplast thylakoid.
@en
type
label
Two nuclear mutations disrupt ...... to the chloroplast thylakoid.
@en
prefLabel
Two nuclear mutations disrupt ...... to the chloroplast thylakoid.
@en
P2860
P1433
P1476
Two nuclear mutations disrupt ...... to the chloroplast thylakoid.
@en
P2093
P2860
P304
P407
P577
1995-08-01T00:00:00Z