Raz Zarivach

Characterization of Escherichia coli null mutants for glutaredoxin 2.

Protein structure: experimental and theoretical aspects.

The RNA helicase DbpA exhibits a markedly different conformation in the ADP-bound state when compared with the ATP- or RNA-bound states.

Initiation and inhibition of protein biosynthesis studies at high resolution.

On the interaction of colicin E3 with the ribosome.

Antibiotics targeting ribosomes: crystallographic studies.

Structural basis of the ribosomal machinery for peptide bond formation, translocation, and nascent chain progression.

The conserved Glu-60 residue in Thermoanaerobacter brockii alcohol dehydrogenase is not essential for catalysis.

Structural basis for the antibiotic activity of ketolides and azalides.

Prediction of the structure of the complex between the 30S ribosomal subunit and colicin E3 via weighted-geometric docking.

Genetic analysis of familial colorectal cancer in Israeli Arabs.

On peptide bond formation, translocation, nascent protein progression and the regulatory properties of ribosomes. Derived on 20 October 2002 at the 28th FEBS Meeting in Istanbul.

Structural insight into the antibiotic action of telithromycin against resistant mutants.

Ribosomal crystallography: peptide bond formation and its inhibition.

Ribosomal crystallography: a flexible nucleotide anchoring tRNA translocation, facilitates peptide-bond formation, chirality discrimination and antibiotics synergism.

23S rRNA base pair 2057-2611 determines ketolide susceptibility and fitness cost of the macrolide resistance mutation 2058A-->G.

Reproducible growth of well diffracting ribosomal crystals.

Early encounters of a nascent membrane protein: specificity and timing of contacts inside and outside the ribosome.

Symmetry at the active site of the ribosome: structural and functional implications.

Structural analysis of a prototypical ATPase from the type III secretion system.

Structural analysis of the essential self-cleaving type III secretion proteins EscU and SpaS.

Crystal structure of the talin integrin binding domain 2.

Crystallization and preliminary crystallographic analysis of the Magnetospirillum magneticum AMB-1 and M. gryphiswaldense MSR-1 magnetosome-associated proteins MamA.

Metalloprotease type III effectors that specifically cleave JNK and NF-κB.

Self-recognition mechanism of MamA, a magnetosome-associated TPR-containing protein, promotes complex assembly.

The cation diffusion facilitator proteins MamB and MamM of Magnetospirillum gryphiswaldense have distinct and complex functions, and are involved in magnetite biomineralization and magnetosome membrane assembly.

The molecular basis for the broad substrate specificity of human sulfotransferase 1A1.

Structural and functional discussion of the tetra-trico-peptide repeat, a protein interaction module.

Association of the chromosome replication initiator DnaA with the Escherichia coli inner membrane in vivo: quantity and mode of binding.

Crystallization and preliminary crystallographic analysis of the C-terminal domain of MamM, a magnetosome-associated protein from Magnetospirillum gryphiswaldense MSR-1.

Inter-phylum structural conservation of the magnetosome-associated TPR-containing protein, MamA.

Characterization of the N-terminal domain of BteA: a Bordetella type III secreted cytotoxic effector.

RNA-DNA differences in human mitochondria restore ancestral form of 16S ribosomal RNA.

A high-resolution structure that provides insight into coiled-coil thiodepsipeptide dynamic chemistry.

Aerobic iron-based cross-dehydrogenative coupling enables efficient diversity-oriented synthesis of coumestrol-based selective estrogen receptor modulators.

BtcA, A class IA type III chaperone, interacts with the BteA N-terminal domain through a globular/non-globular mechanism.

Structure prediction of magnetosome-associated proteins.

Cation diffusion facilitators transport initiation and regulation is mediated by cation induced conformational changes of the cytoplasmic domain.

Bacterial magnetosome biomineralization--a novel platform to study molecular mechanisms of human CDF-related Type-II diabetes.

ZnT-1 extrudes zinc from mammalian cells functioning as a Zn(2+)/H(+) exchanger.

Crystal structure of the magnetobacterial protein MtxA C-terminal domain reveals a new sequence-structure relationship.

MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria.

From invagination to navigation: The story of magnetosome-associated proteins in magnetotactic bacteria.

Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons.

Structure-function studies of the magnetite-biomineralizing magnetosome-associated protein MamC.

Engineering of Methylation State Specific 3xMBT Domain Using ELISA Screening.

Genetic manipulation of iron biomineralization enhances MR relaxivity in a ferritin-M6A chimeric complex.

Structural Basis for p53 Lys120-Acetylation-Dependent DNA-Binding Mode.

Ribosomal Antibiotics: Contemporary Challenges.

An Extended Loop of the Pup Ligase, PafA, Mediates Interaction with Protein Targets.

Disease-Homologous Mutation in the Cation Diffusion Facilitator Protein MamM Causes Single-Domain Structural Loss and Signifies Its Importance.

Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates.

A Look into the Biochemistry of Magnetosome Biosynthesis in Magnetotactic Bacteria.

Zinc transport and the inhibition of the L-type calcium channel are two separable functions of ZnT-1.

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome.

Highly Efficient Flavin-Adenine Dinucleotide Glucose Dehydrogenase Fused to a Minimal Cytochrome C Domain.

A quantitative assessment of the membrane-integral sub-proteome of a bacterial magnetic organelle.

Transition metal binding selectivity in proteins and its correlation with the phylogenomic classification of the cation diffusion facilitator protein family.

The dual role of MamB in magnetosome membrane assembly and magnetite biomineralization.

The importance of the helical structure of a MamC-derived magnetite-interacting peptide for its function in magnetite formation.

Human CCL5 trimer: expression, purification and initial crystallographic studies.

CPAP3 proteins in the mineralized cuticle of a decapod crustacean.

Directed evolution of SIRT6 for improved deacylation and glucose homeostasis maintenance.

The 3-D structure of VNG0258H/RosR - A haloarchaeal DNA-binding protein in its ionic shell.

The FtsZ-like protein FtsZm of Magnetospirillum gryphiswaldense likely interacts with its generic homolog and is required for biomineralization under nitrate deprivation.

Understanding the Biomineralization Role of Magnetite-Interacting Components (MICs) From Magnetotactic Bacteria.

Molecular cross-talk in a unique parasitoid manipulation strategy.

CAP2 mutation leads to impaired actin dynamics and associates with supraventricular tachycardia and dilated cardiomyopathy.

Zinc transporter 10 (ZnT10)-dependent extrusion of cellular Mn is driven by an active Ca-coupled exchange.

Metal binding to the dynamic cytoplasmic domain of the cation diffusion facilitator (CDF) protein MamM induces a 'locked-in' configuration.

The plus-tip tracking and microtubule stabilizing activities of Javelin-like regulate microtubule organization and cell polarity.

A novel endogenous selection marker for the diatom Phaeodactylum tricornutum based on a unique mutation in phytoene desaturase 1.

Unexpected implications of STAT3 acetylation revealed by genetic encoding of acetyl-lysine.

Specificity of protein-DNA interactions in hypersaline environment: structural studies on complexes of Halobacterium salinarum oxidative stress-dependent protein hsRosR.

Structure and membrane-targeting of a Bordetella pertussis effector N-terminal domain.

The interdimeric interface controls function and stability of Ureaplasma urealiticum methionine S-adenosyltransferase.

Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase.

The Role of the Small Export Apparatus Protein, SctS, in the Activity of the Type III Secretion System.

Integrative Model to Coordinate the Oligomerization and Aggregation Mechanisms of CCL5.

From conservation to structure, studies of magnetosome associated cation diffusion facilitators (CDF) proteins in Proteobacteria.

A common genetic variant in zinc transporter ZnT2 (Thr288Ser) is present in women with low milk volume and alters lysosome function and cell energetics.

A gain of function mutation in SlNRC4a enhances basal immunity resulting in broad-spectrum disease resistance.

The metal binding site composition of the cation diffusion facilitator protein MamM cytoplasmic domain impacts its metal responsivity.

The cation diffusion facilitator protein MamM's cytoplasmic domain exhibits metal-type dependent binding modes and discriminates against Mn.

Folding of an Intrinsically Disordered Iron-Binding Peptide in Response to Sedimentation Revealed by Cryo-EM.

Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity.

Distinct features of the Leishmania cap-binding protein LeishIF4E2 revealed by CRISPR-Cas9 mediated hemizygous deletion.

Tyr-Asp inhibition of glyceraldehyde 3-phosphate dehydrogenase affects plant redox metabolism.

Flexible microtubule anchoring modulates the bi-directional motility of the kinesin-5 Cin8.

SAMase of Bacteriophage T3 Inactivates Escherichia coli's Methionine -Adenosyltransferase by Forming Heteropolymers.

Metal transport mechanism of the cation diffusion facilitator (CDF) protein family - a structural perspective on human CDF (ZnT)-related diseases.

Distinct Regions of the Haloferax volcanii Dolichol Phosphate-Mannose Synthase AglD Mediate the Assembly and Subsequent Processing of the Lipid-Linked Mannose.

Current view of iron biomineralization in magnetotactic bacteria.

Magnetite-binding proteins from the magnetotactic bacterium BW-1.

Loss-of-function mutants are associated with gut dysbiosis and alterations in intestinal gene expression in preterm infants.

Revisiting the Role of -Tubulin in Development: is not an Essential Gene, and its Novel Allele has a Tissue-Specific Dominant-Negative Impact.

Evolution of homo-oligomerization of methionine S-adenosyltransferases is replete with structure-function constrains.

PSMC1 variant causes a novel neurological syndrome.

High-Resolution Cryo-Electron Microscopy Reveals the Unique Striated Hollow Structure of Photocatalytic Macrocyclic Polydiacetylene Nanotubes.

Asgard ESCRT-III and VPS4 reveal conserved chromatin binding properties of the ESCRT machinery.

A Missense Variation in Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans.

Limb girdle muscular disease caused by mutation and statin myopathy treatable with mevalonolactone.

Novel Susceptibility Genes Drive Familial Non-Medullary Thyroid Cancer in a Large Consanguineous Kindred.