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Structure of the TatC core of the twin-arginine protein transport system

Nature (London), 2012-12, Vol.492 (7428), p.210-214

2012

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Characterization of the interaction between the influenza A virus polymerase subunit PB1 and the host nuclear import factor Ran-binding protein 5

Journal of general virology, 2011-08, Vol.92 (Pt 8), p.1859-1869

2011

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Engineered botulinum neurotoxin B with improved efficacy for targeting human receptors

Nature communications, 2017-07, Vol.8 (1), p.53-53, Article 53

2017

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Crystal Structure of the Catalytic Domain of a Botulinum Neurotoxin Homologue from Enterococcus faecium: Potential Insights into Substrate Recognition

International journal of molecular sciences, 2023-08, Vol.24 (16), p.12721

2023

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Variations in the Botulinum Neurotoxin Binding Domain and the Potential for Novel Therapeutics

Toxins, 2018-10, Vol.10 (10), p.421

2018

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Crystal Structures of the Clostridium botulinum Neurotoxin A6 Cell Binding Domain Alone and in Complex with GD1a Reveal Significant Conformational Flexibility

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9620

2022

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Structural Features of Clostridium botulinum Neurotoxin Subtype A2 Cell Binding Domain

Toxins, 2022-05, Vol.14 (5), p.356

2022

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Crystal Structures of Botulinum Neurotoxin Subtypes A4 and A5 Cell Binding Domains in Complex with Receptor Ganglioside

Toxins, 2022-02, Vol.14 (2), p.129

2022

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Augmentation of VAMP-catalytic activity of botulinum neurotoxin serotype B does not result in increased potency in physiological systems

PloS one, 2017-10, Vol.12 (10), p.e0185628

2017

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Structural basis for nuclear import complex dissociation by RanGTP

Nature, 2005-06, Vol.435 (7042), p.693-696

2005

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High‐resolution crystal structures of the botulinum neurotoxin binding domains from subtypes A5 and A6

FEBS open bio, 2020-08, Vol.10 (8), p.1474-1481

2020

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New Modified Recombinant Botulinum Neurotoxin Type F with Enhanced Potency

Toxins, 2021-11, Vol.13 (12), p.834

2021

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Crystal structure of botulinum neurotoxin subtype A3 cell binding domain in complex with GD1a co‐receptor ganglioside

FEBS open bio, 2020-03, Vol.10 (3), p.298-305

2020

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High resolution crystal structures of the receptor-binding domain of Clostridium botulinum neurotoxin serotypes A and FA

PeerJ (San Francisco, CA), 2018-03, Vol.6, p.e4552-e4552, Article e4552

2018

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Crystal Structure of the Catalytic Domain of a Botulinum Neurotoxin Homologue from IEnterococcus faecium/I: Potential Insights into Substrate Recognition

International journal of molecular sciences, 2023-08, Vol.24 (16)

2023

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High resolution crystal structures of Clostridium botulinum neurotoxin A3 and A4 binding domains

Journal of structural biology, 2018-05, Vol.202 (2), p.113-117

2018

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Structural Basis for the High-affinity Binding of Nucleoporin Nup1p to the Saccharomyces cerevisiae Importin-β Homologue, Kap95p

Journal of molecular biology, 2005-06, Vol.349 (3), p.515-525

2005

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Chimeras of anthrax toxin and botulinum neurotoxin as novel analgesic proteins

Toxicon (Oxford), 2018-12, Vol.156, p.S118-S118

2018

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Botulinum neurotoxin B engineered for increased receptor affinity has improved clinical potential

Toxicon (Oxford), 2018-12, Vol.156, p.S27-S28

2018

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Augmentation of the catalytic activity of Botulinum neurotoxin type B does not result in increased potency in physiologic systems

Toxicon (Oxford), 2016-12, Vol.123, p.S26-S26

2016

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Rational modification of botulinum neurotoxin by directed scanning mutagenesis

Toxicon (Oxford), 2016-12, Vol.123, p.S55-S55

2016

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Engineered botulinum neurotoxin B with improved binding to human receptors has enhanced efficacy in preclinical models

Science advances, 2019-01, Vol.5 (1), p.eaau7196

2019

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Structure of the TatC core of the twin-arginine protein transport system

Nature (London), 2012-12, Vol.492 (7428), p.210

2012

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A High-Throughput Screening System for Arabidopsis Transcription Factors and Its Application to Med25-Dependent Transcriptional Regulation

Molecular plant, 2011-05, Vol.4 (3), p.546-555

2011

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Structure of the TatC core of the twin-arginine protein transport system

Characterization of the interaction between the influenza A virus polymerase subunit PB1 and the host nuclear import factor Ran-binding protein 5

Engineered botulinum neurotoxin B with improved efficacy for targeting human receptors

Crystal Structure of the Catalytic Domain of a Botulinum Neurotoxin Homologue from Enterococcus faecium: Potential Insights into Substrate Recognition

Variations in the Botulinum Neurotoxin Binding Domain and the Potential for Novel Therapeutics

Crystal Structures of the Clostridium botulinum Neurotoxin A6 Cell Binding Domain Alone and in Complex with GD1a Reveal Significant Conformational Flexibility

Structural Features of Clostridium botulinum Neurotoxin Subtype A2 Cell Binding Domain

Crystal Structures of Botulinum Neurotoxin Subtypes A4 and A5 Cell Binding Domains in Complex with Receptor Ganglioside

Augmentation of VAMP-catalytic activity of botulinum neurotoxin serotype B does not result in increased potency in physiological systems

Structural basis for nuclear import complex dissociation by RanGTP

High‐resolution crystal structures of the botulinum neurotoxin binding domains from subtypes A5 and A6

New Modified Recombinant Botulinum Neurotoxin Type F with Enhanced Potency

Crystal structure of botulinum neurotoxin subtype A3 cell binding domain in complex with GD1a co‐receptor ganglioside

High resolution crystal structures of the receptor-binding domain of Clostridium botulinum neurotoxin serotypes A and FA

Crystal Structure of the Catalytic Domain of a Botulinum Neurotoxin Homologue from IEnterococcus faecium/I: Potential Insights into Substrate Recognition

High resolution crystal structures of Clostridium botulinum neurotoxin A3 and A4 binding domains

Anthrax toxins regulate pain signaling and can deliver molecular cargoes into ANTXR2 + DRG sensory neurons

Structural Basis for the High-affinity Binding of Nucleoporin Nup1p to the Saccharomyces cerevisiae Importin-β Homologue, Kap95p

Chimeras of anthrax toxin and botulinum neurotoxin as novel analgesic proteins

Botulinum neurotoxin B engineered for increased receptor affinity has improved clinical potential

Augmentation of the catalytic activity of Botulinum neurotoxin type B does not result in increased potency in physiologic systems

Rational modification of botulinum neurotoxin by directed scanning mutagenesis

Engineered botulinum neurotoxin B with improved binding to human receptors has enhanced efficacy in preclinical models

Structure of the TatC core of the twin-arginine protein transport system

A High-Throughput Screening System for Arabidopsis Transcription Factors and Its Application to Med25-Dependent Transcriptional Regulation

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