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Enzymatic activity of circular sortase A under denaturing conditions: An advanced tool for protein ligation

Biochemical engineering journal, 2014-01, Vol.82, p.200-209

2014

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1H, 13C and 15N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

Biomolecular NMR assignments, 2011-10, Vol.5 (2), p.135-138

2011

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Inhibition of Ubiquitin/Proteasome-Dependent Protein Degradation by the Gly-Ala Repeat Domain of the Epstein-Barr Virus Nuclear Antigen 1

Proceedings of the National Academy of Sciences - PNAS, 1997-11, Vol.94 (23), p.12616-12621

1997

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Site-specific labelling with a metal chelator for protein-structure refinement

Journal of biomolecular NMR, 2004-07, Vol.29 (3), p.351-361

2004

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Molecular cloning, expression, and purification of pig interleukin-5

Immunogenetics (New York), 2000-01, Vol.51 (1), p.59-64

2000

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Functional p53 Chimeras Containing the Epstein-Barr Virus Gly-Ala Repeat are Protected from Mdm2- and HPV-E6-Induced Proteolysis

Proceedings of the National Academy of Sciences - PNAS, 2002-02, Vol.99 (3), p.1532-1537

2002

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Solution Structure of the R3H Domain from Human Sμbp-2

Journal of molecular biology, 2003-02, Vol.326 (1), p.217-223

2003

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super(1)H, super(13)C and super(15)N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

Biomolecular NMR assignments, 2011-10, Vol.5 (2), p.135-138

2011

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cis-Inhibition of proteasomal degradation by viral repeats: impact of length and amino acid composition

FEBS letters, 2001-06, Vol.499 (1), p.137-142

2001

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Inhibition of ubiquitin-dependent proteolysis by a synthetic glycine–alanine repeat peptide that mimics an inhibitory viral sequence

FEBS letters, 2002-07, Vol.522 (1), p.93-98

2002

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sup 1^H, ^sup 13^C and ^sup 15^N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

Biomolecular NMR assignments, 2011-10, Vol.5 (2), p.135

2011

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Solution structure of the R3H domain from human Smubp-2

Journal of molecular biology, 2003-02, Vol.326 (1), p.217-223

2003

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A minimal glycine-alanine repeat prevents the interaction of ubiquitinated I kappaB alpha with the proteasome: a new mechanism for selective inhibition of proteolysis

Nature medicine, 1998-08, Vol.4 (8), p.939-944

1998

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Random coil conformation of a Gly/Ala-rich insert in IkappaB alpha excludes structural stabilization as the mechanism for protection against proteasomal degradation

FEBS letters, 1998-12, Vol.440 (3), p.365-369

1998

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Assessing nanobody interaction with SARS-CoV-2 Nsp9

PloS one, 2024-05, Vol.19 (5), p.e0303839

2024

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Discovery and structure–activity relationship studies of irreversible benzisothiazolinone-based inhibitors against Staphylococcus aureus sortase A transpeptidase

Bioorganic & medicinal chemistry, 2014-11, Vol.22 (21), p.5988-6003

2014

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Sorting out the Superbugs: Potential of Sortase A Inhibitors among Other Antimicrobial Strategies to Tackle the Problem of Antibiotic Resistance

Antibiotics (Basel), 2021-02, Vol.10 (2), p.164

2021

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Pyrrolomycins as antimicrobial agents. Microwave-assisted organic synthesis and insights into their antimicrobial mechanism of action

Bioorganic & medicinal chemistry, 2019-03, Vol.27 (5), p.721-728

2019

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Discovery of a New Class of Sortase A Transpeptidase Inhibitors to Tackle Gram-Positive Pathogens: 2-(2-Phenylhydrazinylidene)alkanoic Acids and Related Derivatives

Molecules (Basel, Switzerland), 2016-02, Vol.21 (2), p.241-241

2016

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Targeting Bacterial Sortase A with Covalent Inhibitors: 27 New Starting Points for Structure-Based Hit-to-Lead Optimization

ACS infectious diseases, 2020-02, Vol.6 (2), p.186-194

2020

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Selenopheno[3,2-c]- and [2,3-c]coumarins: Synthesis, cytotoxicity, angiogenesis inhibition, and antioxidant properties

Comptes rendus. Chimie, 2015-04, Vol.18 (4), p.399-409

2015

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A new class of phenylhydrazinylidene derivatives as inhibitors of Staphylococcus aureus biofilm formation

Medicinal chemistry research, 2016-05, Vol.25 (5), p.870-878

2016

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Synthesis and study of new 5-substituted 1-acetyl-4-phenyl-3-pyrrolin-2-ones as potential antitumor agents

Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2018-05, Vol.54 (5), p.514-519

2018

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Crystal structure of c5321: a protective antigen present in uropathogenic Escherichia coli strains displaying an SLR fold

BMC structural biology, 2013-10, Vol.13 (1), p.19-19, Article 19

2013

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Synthesis, structure and biological activity of new 6,6-dimethyl-2-oxo-4-{2-[5-organylsilyl(germyl)]furan(thiophen)-2-yl}vinyl-5,6-dihydro-2H-pyran-3-carbonitriles

Applied organometallic chemistry, 2015-11, Vol.29 (11), p.756-763

2015

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Enzymatic activity of circular sortase A under denaturing conditions: An advanced tool for protein ligation

1H, 13C and 15N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

Inhibition of Ubiquitin/Proteasome-Dependent Protein Degradation by the Gly-Ala Repeat Domain of the Epstein-Barr Virus Nuclear Antigen 1

Site-specific labelling with a metal chelator for protein-structure refinement

Molecular cloning, expression, and purification of pig interleukin-5

Functional p53 Chimeras Containing the Epstein-Barr Virus Gly-Ala Repeat are Protected from Mdm2- and HPV-E6-Induced Proteolysis

Solution Structure of the R3H Domain from Human Sμbp-2

super(1)H, super(13)C and super(15)N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

cis-Inhibition of proteasomal degradation by viral repeats: impact of length and amino acid composition

Inhibition of ubiquitin-dependent proteolysis by a synthetic glycine–alanine repeat peptide that mimics an inhibitory viral sequence

sup 1^H, ^sup 13^C and ^sup 15^N assignment of the GNA1946 outer membrane lipoprotein from Neisseria meningitidis

Solution structure of the R3H domain from human Smubp-2

A minimal glycine-alanine repeat prevents the interaction of ubiquitinated I kappaB alpha with the proteasome: a new mechanism for selective inhibition of proteolysis

Random coil conformation of a Gly/Ala-rich insert in IkappaB alpha excludes structural stabilization as the mechanism for protection against proteasomal degradation

Assessing nanobody interaction with SARS-CoV-2 Nsp9

Discovery and structure–activity relationship studies of irreversible benzisothiazolinone-based inhibitors against Staphylococcus aureus sortase A transpeptidase

Sorting out the Superbugs: Potential of Sortase A Inhibitors among Other Antimicrobial Strategies to Tackle the Problem of Antibiotic Resistance

Pyrrolomycins as antimicrobial agents. Microwave-assisted organic synthesis and insights into their antimicrobial mechanism of action

Discovery of a New Class of Sortase A Transpeptidase Inhibitors to Tackle Gram-Positive Pathogens: 2-(2-Phenylhydrazinylidene)alkanoic Acids and Related Derivatives

Targeting Bacterial Sortase A with Covalent Inhibitors: 27 New Starting Points for Structure-Based Hit-to-Lead Optimization

Selenopheno[3,2-c]- and [2,3-c]coumarins: Synthesis, cytotoxicity, angiogenesis inhibition, and antioxidant properties

A new class of phenylhydrazinylidene derivatives as inhibitors of Staphylococcus aureus biofilm formation

Synthesis and study of new 5-substituted 1-acetyl-4-phenyl-3-pyrrolin-2-ones as potential antitumor agents

Crystal structure of c5321: a protective antigen present in uropathogenic Escherichia coli strains displaying an SLR fold

Synthesis, structure and biological activity of new 6,6-dimethyl-2-oxo-4-{2-[5-organylsilyl(germyl)]furan(thiophen)-2-yl}vinyl-5,6-dihydro-2H-pyran-3-carbonitriles

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