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Protein batches from downstream processing studies can be cost-effective tools for fast and specific protein quantification assays

Analytical biochemistry, 2005-10, Vol.345 (1), p.167-169

Sarubbi, Edoardo

2005

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Acyl Ureas as Human Liver Glycogen Phosphorylase Inhibitors for the Treatment of Type 2 Diabetes

Journal of medicinal chemistry, 2005-10, Vol.48 (20), p.6178-6193

2005

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SAR and X-ray. A New Approach Combining Fragment-Based Screening and Rational Drug Design: Application to the Discovery of Nanomolar Inhibitors of Src SH2

Journal of medicinal chemistry, 2002-06, Vol.45 (12), p.2379-2387

2002

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Characterization of the spoT gene of Escherichia coli

The Journal of biological chemistry, 1989-09, Vol.264 (25), p.15074-15082

1989

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Protein Sequences Encoded by the relA and the spoT Genes of Escherichia coli Are Interrelated

The Journal of biological chemistry, 1989-06, Vol.264 (16), p.9122-9125

1989

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Evaluation of phenylboronate agarose for industrial-scale purification of erythropoietin from mammalian cell cultures

Journal of biotechnology, 2003-03, Vol.101 (3), p.275-287

2003

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A new cytokine-receptor binding mode revealed by the crystal structure of the IL-1 receptor with an antagonist

Nature (London), 1997-03, Vol.386 (6621), p.194-200

1997

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Requirements for specific binding of low affinity inhibitor fragments to the SH2 domain of (pp60)Src are identical to those for high affinity binding of full length inhibitors

Journal of medicinal chemistry, 2003-11, Vol.46 (24), p.5184-5195

2003

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GE20372 Factor A and B: New HIV-1 Protease Inhibitors, Produced by Streptomyces sp. ATCC 55925

The Journal of Antibiotics, 1995/04/25, Vol.48(4), pp.332-334

1995

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Antibiotics GE23077, Novel Inhibitors of Bacterial RNA Polymerase: I. Taxonomy, Isolation and Characterization

The Journal of Antibiotics, 2004/03/25, Vol.57(3), pp.210-217

2004

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Particle concentration fluorescence as an alternative to radioactivity for cytokine receptor binding assays

Journal of immunological methods, 1996-11, Vol.198 (2), p.113-118

Sarubbi, Edoardo

1996

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Mode of action of the microbial metabolite GE23077, a novel potent and selective inhibitor of bacterial RNA polymerase

European journal of biochemistry, 2004-08, Vol.271 (15), p.3146-3154

2004

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GE20372 Factor A and B. New HIV-l Protease Inhibitors, Produced by Strcptomyccs sp. ATCC 55925

Journal of antibiotics, 1995, Vol.48 (4), p.332-334

1995

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ISOLATION OF α-MAPI FROM FERMENTATION BROTHS DURING A SCREENING PROGRAM FOR HIV-1 PROTEASE INHIBITORS

The Journal of Antibiotics, 1991/09/25, Vol.44(9), pp.1019-1022

1991

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Principles Governing the Binding of a Class of Non-Peptidic Inhibitors to the SH2 Domain of src Studied by X-ray Analysis

Journal of medicinal chemistry, 2002-07, Vol.45 (14), p.2915-2922

2002

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High-affinity Src-SH2 ligands which do not activate Tyr(527)-phosphorylated Src in an experimental in vivo system

Biochemical and biophysical research communications, 2002-10, Vol.298 (2), p.185-192

2002

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Endogenous Glutathione-Binding Proteins of Insect Cell Lines: Characterization and Removal from Glutathione S-Transferase (GST) Fusion Proteins

Protein expression and purification, 2000-06, Vol.19 (1), p.197-201

2000

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Discovery of Thioazepinone Ligands for Src SH2: From Non-specific to Specific Binding

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (16), p.2127-2131

2001

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Epitope mapping of the anti-urokinase monoclonal antibody 5B4 by isolated domains of urokinase

Thrombosis and haemostasis, 1989-11, Vol.62 (3), p.934

1989

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Human IL-1 receptor antagonist from Escherichia coli: Large-scale microbial growth and protein purification

Journal of biotechnology, 1998-10, Vol.64 (2), p.187-196

1998

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The differential glycosylation of human pro-urokinase from various recombinant mammalian cell lines does not affect activity and binding to PAI-1

Thrombosis and haemostasis, 1989-11, Vol.62 (3), p.927

1989

Volltextzugriff (PDF)

An elongation factor Tu (EF‐Tu) resistant to the EF‐Tu inhibitor GE2270 in the producing organism Planobispora rosea

Molecular microbiology, 1996-10, Vol.22 (1), p.43-51

1996

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Peptide aldehydes as inhibitors of HIV protease

FEBS letters, 1993-03, Vol.319 (3), p.253-256

1993

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Src homology-2 domain binding assays by scintillation proximity and surface plasmon resonance

Journal of molecular recognition, 2001-07, Vol.14 (4), p.254-260

2001

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Natural kirromycin resistance of elongation factor Tu from the kirrothricin producer Streptomyces cinnamoneus

Microbiology (Society for General Microbiology), 1997-02, Vol.143 ( Pt 2), p.617

1997

Volltextzugriff (PDF)

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Protein batches from downstream processing studies can be cost-effective tools for fast and specific protein quantification assays

Acyl Ureas as Human Liver Glycogen Phosphorylase Inhibitors for the Treatment of Type 2 Diabetes

SAR and X-ray. A New Approach Combining Fragment-Based Screening and Rational Drug Design: Application to the Discovery of Nanomolar Inhibitors of Src SH2

Characterization of the spoT gene of Escherichia coli

Protein Sequences Encoded by the relA and the spoT Genes of Escherichia coli Are Interrelated

Evaluation of phenylboronate agarose for industrial-scale purification of erythropoietin from mammalian cell cultures

A new cytokine-receptor binding mode revealed by the crystal structure of the IL-1 receptor with an antagonist

Requirements for specific binding of low affinity inhibitor fragments to the SH2 domain of (pp60)Src are identical to those for high affinity binding of full length inhibitors

GE20372 Factor A and B: New HIV-1 Protease Inhibitors, Produced by Streptomyces sp. ATCC 55925

Antibiotics GE23077, Novel Inhibitors of Bacterial RNA Polymerase: I. Taxonomy, Isolation and Characterization

Particle concentration fluorescence as an alternative to radioactivity for cytokine receptor binding assays

Mode of action of the microbial metabolite GE23077, a novel potent and selective inhibitor of bacterial RNA polymerase

GE20372 Factor A and B. New HIV-l Protease Inhibitors, Produced by Strcptomyccs sp. ATCC 55925

ISOLATION OF α-MAPI FROM FERMENTATION BROTHS DURING A SCREENING PROGRAM FOR HIV-1 PROTEASE INHIBITORS

Principles Governing the Binding of a Class of Non-Peptidic Inhibitors to the SH2 Domain of src Studied by X-ray Analysis

High-affinity Src-SH2 ligands which do not activate Tyr(527)-phosphorylated Src in an experimental in vivo system

Endogenous Glutathione-Binding Proteins of Insect Cell Lines: Characterization and Removal from Glutathione S-Transferase (GST) Fusion Proteins

Discovery of Thioazepinone Ligands for Src SH2: From Non-specific to Specific Binding

Epitope mapping of the anti-urokinase monoclonal antibody 5B4 by isolated domains of urokinase

Human IL-1 receptor antagonist from Escherichia coli: Large-scale microbial growth and protein purification

The differential glycosylation of human pro-urokinase from various recombinant mammalian cell lines does not affect activity and binding to PAI-1

An elongation factor Tu (EF‐Tu) resistant to the EF‐Tu inhibitor GE2270 in the producing organism Planobispora rosea

Peptide aldehydes as inhibitors of HIV protease

Src homology-2 domain binding assays by scintillation proximity and surface plasmon resonance

Natural kirromycin resistance of elongation factor Tu from the kirrothricin producer Streptomyces cinnamoneus

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