4.7 Article

Discovery, Pharmacological Characterisation and NMR Structure of the Novel mu-Conotoxin SxIIIC, a Potent and Irreversible Na-V Channel Inhibitor

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Chemistry, Multidisciplinary

Venomic Interrogation Reveals the Complexity of Conus striolatus Venom

S. W. A. Himaya et al.

AUSTRALIAN JOURNAL OF CHEMISTRY (2020)

Review Neurosciences

Sodium Channels in Human Pain Disorders: Genetics and Pharmacogenomics

Sulayman D. Dib-Hajj et al.

ANNUAL REVIEW OF NEUROSCIENCE, VOL 42 (2019)

Article Multidisciplinary Sciences

Structures of human Nav1.7 channel in complex with auxiliary subunits and animal toxins

Huaizong Shen et al.

SCIENCE (2019)

Article Biochemistry & Molecular Biology

MolProbity: More and better reference data for improved all-atom structure validation

Christopher J. Williams et al.

PROTEIN SCIENCE (2018)

Article Biochemistry & Molecular Biology

Peptide chemistry toolbox - Transforming natural peptides into peptide therapeutics

Milos Erak et al.

BIOORGANIC & MEDICINAL CHEMISTRY (2018)

Article Chemistry, Multidisciplinary

Prediction of disulfide dihedral angles using chemical shifts

David A. Armstrong et al.

CHEMICAL SCIENCE (2018)

Review Pharmacology & Pharmacy

Predicting Structural Details of the Sodium Channel Pore Basing on Animal Toxin Studies

Denis B. Tikhonov et al.

FRONTIERS IN PHARMACOLOGY (2018)

Review Pharmacology & Pharmacy

NaV1.7 as a pain target - From gene to pharmacology

Irina Vetter et al.

PHARMACOLOGY & THERAPEUTICS (2017)

Article Behavioral Sciences

Prey-Capture Strategies of Fish-Hunting Cone Snails: Behavior, Neurobiology and Evolution

Baldomero M. Olivera et al.

BRAIN BEHAVIOR AND EVOLUTION (2015)

Article Biochemistry & Molecular Biology

Combined automated NOE assignment and structure calculation with CYANA

Peter Guentert et al.

JOURNAL OF BIOMOLECULAR NMR (2015)

Article Biochemistry & Molecular Biology

Mammalian Neuronal Sodium Channel Blocker μ-Conotoxin BuIIIB Has a Structured N-Terminus That Influences Potency

Zhihe Kuang et al.

ACS CHEMICAL BIOLOGY (2013)

Article Biochemistry & Molecular Biology

Protein backbone and sidechain torsion angles predicted from NMR chemical shifts using artificial neural networks

Yang Shen et al.

JOURNAL OF BIOMOLECULAR NMR (2013)

Review Neurosciences

The NaV1.7 sodium channel: from molecule to man

Sulayman D. Dib-Hajj et al.

NATURE REVIEWS NEUROSCIENCE (2013)

Article Biochemistry & Molecular Biology

N- and c-terminal extensions of μ-conotoxins increase potency and selectivity for neuronal sodium channels

Christina I. Schroeder et al.

BIOPOLYMERS (2012)

Article Pharmacology & Pharmacy

Mechanism and molecular basis for the sodium channel subtype specificity of μ-conopeptide CnIIIC

Rene Markgraf et al.

BRITISH JOURNAL OF PHARMACOLOGY (2012)

Review Neurosciences

Voltage-gated sodium channels at 60: structure, function and pathophysiology

William A. Catterall

JOURNAL OF PHYSIOLOGY-LONDON (2012)

Review Food Science & Technology

Animal Toxins Can Alter the Function of Nav1.8 and Nav1.9

John Gilchrist et al.

TOXINS (2012)

Article Biochemistry & Molecular Biology

Importance of position 8 in μ-conotoxin KIIIA for voltage-gated sodium channel selectivity

Annelies Van Der Haegen et al.

FEBS JOURNAL (2011)

Article Multidisciplinary Sciences

μ-Conotoxins that differentially block sodium channels NaV1.1 through 1.8 identify those responsible for action potentials in sciatic nerve

Michael J. Wilson et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Pharmacology & Pharmacy

Characterization of endogenous calcium responses in neuronal cell lines

Irina Vetter et al.

BIOCHEMICAL PHARMACOLOGY (2010)

Review Biochemistry & Molecular Biology

The M-superfamily of conotoxins: a review

Reed B. Jacob et al.

CELLULAR AND MOLECULAR LIFE SCIENCES (2010)

Review Neurosciences

NaV1.1 channels and epilepsy

William A. Catterall et al.

JOURNAL OF PHYSIOLOGY-LONDON (2010)

Article Biochemistry & Molecular Biology

Neuronally selective μ-conotoxins from Conus striatus utilize an α-helical motif to target mammalian sodium channels

Christina I. Schroeder et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Chemistry, Multidisciplinary

NMR-Based Mapping of Disulfide Bridges in Cysteine-Rich Peptides: Application to the μ-Conotoxin SxIIIA

Aleksandra Walewska et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)

Article Biochemistry & Molecular Biology

Atomic determinants of state-dependent block of sodium channels by charged local anesthetics and benzocaine

Denis B. Tikhonov et al.

FEBS LETTERS (2006)

Article Biochemistry & Molecular Biology

The CCPN data model for NMR spectroscopy: Development of a software pipeline

WF Vranken et al.

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)

Article Biochemistry & Molecular Biology

RECOORD:: A recalculated coordinate database of 500+proteins from the PDB using restraints from the BioMagResBank

AJ Nederveen et al.

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)

Review Physiology

Conus venoms: A rich source of novel ion channel-targeted peptides

H Terlau et al.

PHYSIOLOGICAL REVIEWS (2004)

Article Biochemistry & Molecular Biology

Clockwise domain arrangement of the sodium channel revealed by μ-conotoxin (GIIIA) docking orientation

RA Li et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2001)

Article Multidisciplinary Sciences

A sodium-channel mutation causes isolated cardiac conduction disease

HL Tan et al.

NATURE (2001)