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Tetraspanin CD63 Bridges Autophagic and Endosomal Processes To Regulate Exosomal Secretion and Intracellular Signaling of Epstein-Barr Virus LMP1
Intrinsic disorder within AKAP79 fine-tunes anchored phosphatase activity toward substrates and drug sensitivity.
Hox proteins Ubx and AbdA collaborate with the transcription pausing factor M1BP to regulate gene transcription.
dock-and-coalesce mechanism for the association of a WASP disordered region with the Cdc42 GTPase.
Zika-Virus-Encoded NS2A Disrupts Mammalian Cortical Neurogenesis by Degrading Adherens Junction Proteins.
Mapping the contact surfaces in the Lamin A:AIMP3 complex by hydrogen/deuterium exchange FT-ICR mass spectrometry.
Structure of Simian Immunodeficiency Virus Envelope Spikes Bound with CD4 and Monoclonal Antibody 36D5.
Rate Constants and Mechanisms of Protein-Ligand Binding.
Protein folding, binding, and droplet formation in cell-like conditions.
Mechanism of ribosome rescue by ArfA and RF2.
Oxytocin receptor binding sites in the periphery of the neonatal mouse.
Biochemical and biophysical investigations of the interaction between human glucokinase and pro-apoptotic BAD.
Structural Heterogeneity in Pre-40S Ribosomes.
Regulated large-scale nucleosome density patterns and precise nucleosome positioning correlate with V(D)J recombination.
Semiclosed Conformations of the Ligand-Binding Domains of NMDA Receptors during Stationary Gating.
Prediction of homoprotein and heteroprotein complexes by protein docking and template-based modeling
Allosteric activation of SENP1 by SUMO1 β-grasp domain involves a dock-and-coalesce mechanism.
Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture.
Enhanced troponin I binding explains the functional changes produced by the hypertrophic cardiomyopathy mutation A8V of cardiac troponin C.
DNA Interactions Probed by Hydrogen-Deuterium Exchange (HDX) Fourier Transform Ion Cyclotron Resonance Mass Spectrometry Confirm External Binding Sites on the Minichromosomal Maintenance (MCM) Helicase.
DEAD-box Protein Rok1 Orchestrates 40S and 60S Ribosome Assembly by Promoting the Release of Rrp5 from Pre-40S Ribosomes to Allow for 60S Maturation.
Protein Allostery and Conformational Dynamics.
Mechanism and rate constants of the Cdc42 GTPase binding with intrinsically disordered effectors.
Non-Stem-Loop CRISPR RNA Is Processed by Dual Binding Cas6.
LARP6 Meets Collagen mRNA
Bipartite recognition of target RNAs activates DNA cleavage by the Type III-B CRISPR-Cas system.
Structure of an E. coli integral membrane sulfurtransferase and its structural transition upon SCN(-) binding defined by EPR-based hybrid method.
Mcm10 coordinates the timely assembly and activation of the replication fork helicase.
ORF33 and ORF38 of Kaposi's Sarcoma-Associated Herpesvirus Interact and Are Required for Optimal Production of Infectious Progeny Viruses.
Conserved mechanism for coordinating replication fork helicase assembly with phosphorylation of the helicase.
Dpb11 protein helps control assembly of the Cdc45·Mcm2-7·GINS replication fork helicase.
14-3-3τ promotes surface expression of Cav2.2 (α1B) Ca2+ channels.
Myelin basic protein induces neuron-specific toxicity by directly damaging the neuronal plasma membrane.
potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome.
Characterization of binding of LARP6 to the 5' stem-loop of collagen mRNAs
Serine-threonine kinase receptor-associated protein (STRAP) regulates translation of type I collagen mRNAs.
Novel E3 ubiquitin ligases that regulate histone protein levels in the budding yeast Saccharomyces cerevisiae.
transcription factor YY1 is a novel substrate for Aurora B kinase at G2/M transition of the cell cycle.
Essential roles of CKIdelta and CKIepsilon in the mammalian circadian clock.
Rhythmic PER abundance defines a critical nodal point for negative feedback within the circadian clock mechanism.
Histone levels are regulated by phosphorylation and ubiquitylation-dependent proteolysis.
DNA damage checkpoints inhibit mitotic exit by two different mechanisms.