Complete genome structure of the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1.
Absence of the PsbZ subunit prevents association of PsbK and Ycf12 with the PSII complex in the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1.
Architecture of the photosynthetic oxygen-evolving center.
Crystal structure of monomeric photosystem II from Thermosynechococcus elongatus at 3.6 A resolution.
Cyanobacterial photosystem II at 2.9-A resolution and the role of quinones, lipids, channels and chloride.
Room temperature femtosecond X-ray diffraction of photosystem II microcrystals.
Serial time-resolved crystallography of photosystem II using a femtosecond X-ray laser.
Simultaneous femtosecond X-ray spectroscopy and diffraction of photosystem II at room temperature.
Structural basis of cyanobacterial photosystem II inhibition by the herbicide terbutryn.
Taking snapshots of photosynthetic water oxidation using femtosecond X-ray diffraction and spectroscopy.
Targeted disruption of psbX and biochemical characterization of photosystem II complex in the thermophilic cyanobacterium Synechococcus elongatus.
Ycf12 is a core subunit in the photosystem II complex.
The cyanobacterial cytochrome b6f subunit PetP adopts an SH3 fold in solution.
Structures of lipoyl synthase reveal a compact active site for controlling sequential sulfur insertion reactions.
Heterologous expression and initial characterization of recombinant RbcX protein from Thermosynechococcus elongatus BP-1 and the role of RbcX in RuBisCO assembly.
Rubisco Accumulation Factor 1 from Thermosynechococcus elongatus participates in the final stages of ribulose-1,5-bisphosphate carboxylase/oxygenase assembly in Escherichia coli cells and in vitro.
Crystal structure of CyanoQ from the thermophilic cyanobacterium Thermosynechococcus elongatus and detection in isolated photosystem II complexes.
Redox-coupled proton pumping drives carbon concentration in the photosynthetic complex I.
Loss of quaternary structure is associated with rapid sequence divergence in the OSBS family.
Photosystem I at 4-A resolution represents the first structural model of a joint photosynthetic reaction centre and core antenna system.
Photosystem I, an improved model of the stromal subunits PsaC, PsaD, and PsaE.
Three-dimensional structure of cyanobacterial photosystem I at 2.5 A resolution.
Structural basis of light-induced redox regulation in the Calvin-Benson cycle in cyanobacteria.
Functional analysis of psbV and a novel c-type cytochrome gene psbV2 of the thermophilic cyanobacterium Thermosynechococcus elongatus strain BP-1.
Structural and EPR characterization of the soluble form of cytochrome c-550 and of the psbV2 gene product from the cyanobacterium Thermosynechococcus elongatus.
Towards complete cofactor arrangement in the 3.0 A resolution structure of photosystem II.
Co-crystal Structure of Thermosynechococcus elongatus Sucrose Phosphate Synthase With UDP and Sucrose-6-Phosphate Provides Insight Into Its Mechanism of Action Involving an Oxocarbenium Ion and the Glycosidic Bond.
Remarkable stability of the proton translocating F1FO-ATP synthase from the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1.
Ycf48 involved in the biogenesis of the oxygen-evolving photosystem II complex is a seven-bladed beta-propeller protein.
Isolation, subunit composition and interaction of the NDH-1 complexes from Thermosynechococcus elongatus BP-1.
Cyanobacterial photosystem II at 3.2 A resolution -- the plastoquinone binding pockets.
The antenna system of photosystem II from Thermosynechococcus elongatus at 3.2 A resolution.
Structure of CyanoP at 2.8 A: implications for the evolution and function of the PsbP subunit of photosystem II .
Roles of PsbI and PsbM in photosystem II dimer formation and stability studied by deletion mutagenesis and X-ray crystallography.
PSII-Tc protein plays an important role in dimerization of photosystem II.
An alternative plant-like cyanobacterial ferredoxin with unprecedented structural and functional properties.
Localization of two phylloquinones, QK and QK', in an improved electron density map of photosystem I at 4-A resolution.
Reversed-phase HPLC determination of chlorophyll a' and phylloquinone in photosystem I of oxygenic photosynthetic organisms.
Structure of a cyanobacterial BLUF protein, Tll0078, containing a novel FAD-binding blue light sensor domain.
Structural adaptations of photosynthetic complex I enable ferredoxin-dependent electron transfer.
Structural basis for electron transport mechanism of complex I-like photosynthetic NAD(P)H dehydrogenase.
Structural insights into NDH-1 mediated cyclic electron transfer.
Structure of the complex I-like molecule NDH of oxygenic photosynthesis.
Structure of the complex I-like molecule NDH ofoxygenic photosynthesis.
Cyanobacterial non-mevalonate pathway: (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase interacts with ferredoxin in Thermosynechococcus elongatus BP-1.
Crystal structure of the C-terminal clock-oscillator domain of the cyanobacterial KaiA protein.
NMR structure of the KaiC-interacting C-terminal domain of KaiA, a circadian clock protein: implications for KaiA-KaiC interaction.
Structure of the C-terminal domain of the clock protein KaiA in complex with a KaiC-derived peptide: implications for KaiC regulation.
The 1.6 A resolution structure of Fe-superoxide dismutase from the thermophilic cyanobacterium Thermosynechococcus elongatus.
The unique nucleotide specificity of the sucrose synthase from Thermosynechococcus elongatus.
Absence of the psbH gene product destabilizes the Photosystem II complex and prevents association of the Photosystem II-X protein in the thermophilic cyanobacterium Thermosynechococcus elongatus BP-1.
Structural and biochemical characterization of Gun4 suggests a mechanism for its role in chlorophyll biosynthesis.
Solution structure of ferredoxin from the thermophilic cyanobacterium Synechococcus elongatus and its thermostability.
Structure of Synechococcus elongatus [Fe2S2] ferredoxin in solution.
ATP-induced hexameric ring structure of the cyanobacterial circadian clock protein KaiC.
Core and rod structures of a thermophilic cyanobacterial light-harvesting phycobilisome.
Crystal structure and redox properties of a novel cyanobacterial heme protein with a His/Cys heme axial ligation and a Per-Arnt-Sim (PAS)-like domain.
A dodecameric CcmK2 structure suggests beta-carboxysomal shell facets have a double-layered organization.
Omp85 from the thermophilic cyanobacterium Thermosynechococcus elongatus differs from proteobacterial Omp85 in structure and domain composition.
Interactions and structural variability of beta-carboxysomal shell protein CcmL.
Structural basis of the day-night transition in a bacterial circadian clock.
Crystal structures of cyanobacterial light-dependent protochlorophyllide oxidoreductase.
Structural basis for enzymatic photocatalysis in chlorophyll biosynthesis.
Acta Crystallogr. F Struct. Biol. Commun.
Structure of the RuBisCO chaperone RbcX from the thermophilic cyanobacterium Thermosynechococcus elongatus.
Structural insights into cyanobacterial photosystem II intermediates associated with Psb28 and Tsl0063.
Structural insights into photosystem II assembly.
Immunocytochemical localization of IdiA, a protein expressed under iron or manganese limitation in the mesophilic cyanobacterium Synechococcus PCC 6301 and the thermophilic cyanobacterium Synechococcus elongatus.
A third metal is required for catalytic activity of the signal-transducing protein phosphatase M tPphA.
Structural analysis of the PP2C phosphatase tPphA from Thermosynechococcus elongatus: a flexible flap subdomain controls access to the catalytic site.
Crystal structure of the Psb27 assembly factor at 1.6 A: implications for binding to Photosystem II.
Functional characterization of monomeric photosystem II core preparations from Thermosynechococcus elongatus with or without the Psb27 protein.
Psb27, a cyanobacterial lipoprotein, is involved in the repair cycle of photosystem II.
Crystal structure of a non-discriminating glutamyl-tRNA synthetase.
Two new high-resolution crystal structures of carboxysome pentamer proteins reveal high structural conservation of CcmL orthologs among distantly related cyanobacterial species.
The asymmetric IscA homodimer with an exposed [2Fe-2S] cluster suggests the structural basis of the Fe-S cluster biosynthetic scaffold.
Solution structure of the NDH-1 complex subunit CupS from Thermosynechococcus elongatus.
A novel inert crystal delivery medium for serial femtosecond crystallography.
Refined structure of c-phycocyanin from the cyanobacterium Synechococcus vulcanus at 1.6 A: insights into the role of solvent molecules in thermal stability and co-factor structure.
Serial femtosecond crystallography of soluble proteins in lipidic cubic phase.
Serial millisecond crystallography of membrane and soluble protein microcrystals using synchrotron radiation.
The 1.45 A three-dimensional structure of C-phycocyanin from the thermophilic cyanobacterium Synechococcus elongatus.
Thermosynechococcus elongatus DpsA binds Zn(II) at a unique three histidine-containing ferroxidase center and utilizes O2 as iron oxidant with very high efficiency, unlike the typical Dps proteins.
Crystal structure of photosystem II from Synechococcus elongatus at 3.8 A resolution.
Oligomeric states in sodium ion-dependent regulation of cyanobacterial histidine kinase-2.
Structural basis of the oxidative activation of the carboxysomal gamma-carbonic anhydrase, CcmM.
The small RbcS-like domains of the beta-carboxysome structural protein CcmM bind RubisCO at a site distinct from that binding the RbcS subunit.
The complete purification and characterization of three forms of ferredoxin-NADP(+) oxidoreductase from a thermophilic cyanobacterium Synechococcus elongatus.
Antioxidant Dps protein from the thermophilic cyanobacterium Thermosynechococcus elongatus.