Complex RNA maturation in chloroplasts. The psbB operon from spinach.
Cryo-EM structure of the spinach cytochrome b6f complex at 3.6A resolution.
Full subunit coverage liquid chromatography electrospray ionization mass spectrometry (LCMS+) of an oligomeric membrane protein: cytochrome b(6)f complex from spinach and the cyanobacterium Mastigocladus laminosus.
High-resolution cryo-EM structures of plant cytochrome b6f at work.
Sequence homology and structural similarity between cytochrome b of mitochondrial complex III and the chloroplast b6-f complex: position of the cytochrome b hemes in the membrane.
The gene for the Mr 10,000 phosphoprotein associated with photosystem II is part of the psbB operon of the spinach plastid chromosome.
The plastid chromosome of spinach (Spinacia oleracea): complete nucleotide sequence and gene organization.
Cryo-EM structure of the large subunit of the spinach chloroplast ribosome.
Cryo-EM study of the spinach chloroplast ribosome reveals the structural and functional roles of plastid-specific ribosomal proteins.
Purification and characterization of seven chloroplast ribosomal proteins: evidence that organelle ribosomal protein genes are functional and that NH2-terminal processing occurs via multiple pathways in chloroplasts.
The complete structure of the chloroplast 70S ribosome in complex with translation factor pY.
The plastid ribosomal proteins. Identification of all the proteins in the 50S subunit of an organelle ribosome (chloroplast).
Cotranscription of the S10- and spc-like operons in spinach chloroplasts and identification of three of their gene products.
The plastid ribosomal proteins. Identification of all the proteins in the 30S subunit of an organelle ribosome (chloroplast).
Overexpression of spinach non-symbiotic hemoglobin in Arabidopsis resulted in decreased NO content and lowered nitrate and other abiotic stresses tolerance.
A model for the photosystem II reaction center core including the structure of the primary donor P680.
Electrospray-ionization mass spectrometry of intact intrinsic membrane proteins.
Nucleotide sequence of the clustered genes for the 44kd chlorophyll a apoprotein and the '32kd'-like protein of the photosystem II reaction center in the spinach plastid chromosome.
Structure of the spinach chloroplast genes for the D2 and 44 kd reaction-centre proteins of photosystem II and for tRNASer (UGA).
Tandem mass spectrometry reveals that three photosystem II proteins of spinach chloroplasts contain N-acetyl-O-phosphothreonine at their NH2 termini.
Enolase from Trypanosoma brucei, from the amitochondriate protist Mastigamoeba balamuthi, and from the chloroplast and cytosol of Euglena gracilis: pieces in the evolutionary puzzle of the eukaryotic glycolytic pathway.
Junctions of the large single copy region and the inverted repeats in Spinacia oleracea and Nicotiana debneyi chloroplast DNA: sequence of the genes for tRNAHis and the ribosomal proteins S19 and L2.
A common structural basis for the inhibition of ribulose 1,5-bisphosphate carboxylase by 4-carboxyarabinitol 1,5-bisphosphate and xylulose 1,5-bisphosphate.
Calcium supports loop closure but not catalysis in Rubisco.
Crystallographic analysis of ribulose 1,5-bisphosphate carboxylase from spinach at 2.4-A resolution. Subunit interactions and active site.
Identification of Interactions between Abscisic Acid and Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase.
Large structures at high resolution: the 1.6-A crystal structure of spinach ribulose-1,5-bisphosphate carboxylase/oxygenase complexed with 2-carboxyarabinitol bisphosphate.
Post-translational modifications in the large subunit of ribulose bisphosphate carboxylase/oxygenase.
Reaction-intermediate analogue binding by ribulose bisphosphate carboxylase/oxygenase causes specific changes in proteolytic sensitivity: the amino-terminal residue of the large subunit is acetylated proline.
Reexamination of the three-dimensional structure of the small subunit of RuBisCo from higher plants.
Sequences of two active-site peptides from spinach ribulosebisphosphate carboxylase/oxygenase.
Structure of a product complex of spinach ribulose-1,5-bisphosphate carboxylase/oxygenase.
The structure of the complex between rubisco and its natural substrate ribulose 1,5-bisphosphate.
The structure of the gene for the large subunit of ribulose 1,5-bisphosphate carboxylase from spinach chloroplast DNA.
Reversed-phase HPLC determination of chlorophyll a' and phylloquinone in photosystem I of oxygenic photosynthetic organisms.
Three-dimensional structure of higher plant photosystem I determined by electron crystallography.
Eubacterial origin of nuclear genes for chloroplast and cytosolic glucose-6-phosphate isomerase from spinach: sampling eubacterial gene diversity in eukaryotic chromosomes through symbiosis.
Kinetic properties of bifunctional 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase from spinach leaves.
N-terminal sequencing of photosystem II low-molecular-mass proteins. 5 and 4.1 kDa components of the O2-evolving core complex from higher plants.
Purification and partial sequence of the Mr 10,000 phosphoprotein from spinach thylakoids.
A gene cluster in the spinach and pea chloroplast genomes encoding one CF1 and three CF0 subunits of the H+-ATP synthase complex and the ribosomal protein S2.
Biochemical and molecular characterization of senescence-related cysteine protease-cystatin complex from spinach leaf.
Isolation and characterization of monomeric and dimeric CP47-reaction center photosystem II complexes.
L protein, encoded by psbL, restores normal functioning of the primary quinone acceptor, QA, in isolated D1/D2/CP47/Cytb-559/I photosystem II reaction center core complex.
Tissue- and stage-specific modulation of RNA editing of the psbF and psbL transcript from spinach plastids -- a new regulatory mechanism?
Expression of the rpl23, rpl2 and rps19 genes in spinach chloroplasts.
Spinach plastid genes coding for initiation factor IF-1, ribosomal protein S11 and RNA polymerase alpha-subunit.
Cloning of a nitrate reductase inactivator (NRI) cDNA from Spinacia oleracea L. and expression of mRNA and protein of NRI in cultured spinach cells.
Inactivation of chloroplast H(+)-ATPase by modification of Lys beta 359, Lys alpha 176 and Lys alpha 266.
The structure of the chloroplast F1-ATPase at 3.2 A resolution.
Purification and characterization of chloroplast dehydroascorbate reductase from spinach leaves.
Spinach chloroplast rpoBC genes encode three subunits of the chloroplast RNA polymerase.
Structure and expression of spinach leaf cDNA encoding ribulosebisphosphate carboxylase/oxygenase activase.
Evidence for a post-translational modification, aspartyl aldehyde, in a photosynthetic membrane protein.
Nucleotide sequence of the gene for the P680 chlorophyll alpha apoprotein of the photosystem II reaction center from spinach.
Posttranslational modifications in the CP43 subunit of photosystem II.
A missing link in cupredoxins: crystal structure of cucumber stellacyanin at 1.6-A resolution.
Cloning, expression, and spectroscopic characterization of Cucumis sativus stellacyanin in its nonglycosylated form.
Crystal structure of plantacyanin, a basic blue cupredoxin from spinach.
Uclacyanins, stellacyanins, and plantacyanins are distinct subfamilies of phytocyanins: plant-specific mononuclear blue copper proteins.
A cDNA clone encoding a spinach 70-kilodalton heat-shock cognate.
Rapid evolution of RNA editing sites in a small non-essential plastid gene.
Coordinate and non-coordinate expression of the stress 70 family and other molecular chaperones at high and low temperature in spinach and tomato.
A new photosystem II reaction center component (4.8 kDa protein) encoded by chloroplast genome.
Purification and partial amino acid sequence of the chloroplast cytochrome b-559.
Polypeptide composition of higher plant photosystem I complex. Identification of psaI, psaJ and psaK gene products.
COOH-terminal residues of D1 and the 44 kDa CPa-2 at spinach photosystem II core complex.
Nucleotide sequence of the gene for the M-r 32,000 thylakoid membrane protein from Spinacia oleracea and Nicotiana debneyi predicts a totally conserved primary translation product of M-r 38,950.
Crystallization of the c14-rotor of the chloroplast ATP synthase reveals that it contains pigments.
The role of RNA editing in conservation of start codons in chloroplast genomes.
Nucleotide sequences of cDNA clones encoding the entire precursor polypeptide for subunit VI and of the plastome-encoded gene for subunit VII of the photosystem I reaction center from spinach.
The protein responsible for center A/B in spinach photosystem I: isolation with iron-sulfur cluster(s) and complete sequence analysis.
Structures of the genes for the beta and epsilon subunits of spinach chloroplast ATPase indicate a dicistronic mRNA and an overlapping translation stop/start signal.
CPD photolyase gene from Spinacia oleracea: repair of UV-damaged DNA and expression in plant organs.
Over-expression and refolding of beta-subunit from the chloroplast ATP synthase.
Photolabeling of the phosphate binding site of chloroplast coupling factor 1 with [32P]azidonitrophenyl phosphate.
Differential regulation of RNA levels of gibberellin dioxygenases by photoperiod in spinach.
Characterization of a large inversion in the spinach chloroplast genome relative to Marchantia: a possible transposon-mediated origin.
Large unidentified open reading frame in plastid DNA (ORF2280) is expressed in chloroplasts.
Structural characterization of two aquaporins isolated from native spinach leaf plasma membranes.
Molecular characterization of nucleus-localized RNA-binding proteins from higher plants.
Erythromycin and 5S rRNA binding properties of the spinach chloroplast ribosomal protein CL22.
Functional analysis of B and C class floral organ genes in spinach demonstrates their role in sexual dimorphism.
Microsequencing and cDNA cloning of the Calvin cycle/OPPP enzyme ribose-5-phosphate isomerase (EC 5.3.1.6) from spinach chloroplasts.
Mercury increases water permeability of a plant aquaporin through a non-cysteine-related mechanism.
Structural and functional analysis of SoPIP2;1 mutants adds insight into plant aquaporin gating.
Structural basis for pH gating of plant aquaporins.
Structural mechanism of plant aquaporin gating.
The major integral proteins of spinach leaf plasma membranes are putative aquaporins and are phosphorylated in response to Ca2+ and apoplastic water potential.