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The atomic-resolution structure of human caspase-8, a key activator of apoptosis

Structure (London), 1999-09, Vol.7 (9), p.1135-1143

1999

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Activity of recombinant cysteine-rich domain proteins derived from the membrane-bound MUC17/Muc3 family mucins

Biochimica et biophysica acta, 2010-07, Vol.1800 (7), p.629-638

2010

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Membrane-anchored aspartyl protease with Alzheimer's disease β-secretase activity

Nature (London), 1999-12, Vol.402 (6761), p.533-537

1999

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Employing a superior BACE1 cleavage sequence to probe cellular APP processing

Journal of neurochemistry, 2003-03, Vol.84 (5), p.1006-1017

2003

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Human β-Secretase (BACE) and BACE Inhibitors

Journal of medicinal chemistry, 2003-10, Vol.46 (22), p.4625-4630

2003

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Heterodimer formation is essential for heparanase enzymatic activity

Biochemical and biophysical research communications, 2003-09, Vol.308 (4), p.885-891

2003

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Human intestinal MUC17 mucin augments intestinal cell restitution and enhances healing of experimental colitis

The international journal of biochemistry & cell biology, 2010-06, Vol.42 (6), p.996-1006

2010

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Kinetic and structural characterization of caspase-3 and caspase-8 inhibition by a novel class of irreversible inhibitors

Biochimica et biophysica acta, 2010-09, Vol.1804 (9), p.1817-1831

2010

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Prediction of the tertiary structure and substrate binding site of caspase-8

FEBS letters, 1997-12, Vol.419 (1), p.49-54

1997

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Processing of the Human Heparanase Precursor and Evidence That the Active Enzyme Is a Heterodimer

The Journal of biological chemistry, 1999-10, Vol.274 (42), p.29587-29590

1999

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Evolution of phosphofructokinase-gene duplication and creation of new effector sites

Nature (London), 1984-05, Vol.309 (5967), p.467-469

1984

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Structural and functional properties of a phospholipase A2 purified from an inflammatory exudate

Biochemistry (Easton), 1986-12, Vol.25 (26), p.8381-8385

1986

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Prediction of the tertiary structure of the complement control protein module

Journal of Protein Chemistry, 1997-11, Vol.16 (8), p.765-773

1997

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Mechanism, structure-activity studies, and potential applications of glutathione S-transferase-catalyzed cleavage of sulfonamides

Drug metabolism and disposition, 1999-09, Vol.27 (9), p.992

1999

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Cation binding to the integrin CD11b I domain and activation model assessment

Structure (London), 1998-07, Vol.6 (7), p.923-935

1998

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Effect of Point Mutations on the Kinetics and the Inhibition of Human Immunodeficiency Virus Type 1 Protease: Relationship to Drug Resistance

Biochemistry (Easton), 1995, Vol.34 (4), p.1143-1152

1995

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An efficient method to express and refold a truncated human procaspase-9: A caspase with activity toward Glu-X bonds

Protein expression and purification, 2006-04, Vol.46 (2), p.299-308

2006

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Activated sulfonamides are cleaved by glutathione-S-transferases

Drug metabolism and disposition, 1999-09, Vol.27 (9), p.986

1999

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CXC Chemokines Connective Tissue Activating Peptide-III and Neutrophil Activating Peptide-2 are Heparin/Heparan Sulfate-degrading Enzymes (∗)

The Journal of biological chemistry, 1995-02, Vol.270 (7), p.3268-3277

1995

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Predicting human immunodeficiency virus protease cleavage sites in proteins by a discriminant function method

Proteins, structure, function, and bioinformatics, 1996-01, Vol.24 (1), p.51-72

1996

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[18] Dissection and sequence analysis of phospholipases A2

Methods in Enzymology, 1991, Vol.197, p.201-214

Heinrikson, Robert L.

1991

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Stay the Executioner's Hand

Science (American Association for the Advancement of Science), 2000-04, Vol.288 (5464), p.283-284

2000

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Prediction of the tertiary structure of a caspase-9/inhibitor complex

FEBS letters, 2000-03, Vol.470 (3), p.249-256

2000

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Intrasteric Inhibition of ATP Binding Is Not Required To Prevent Unregulated Autophosphorylation or Signaling by the Insulin Receptor

Molecular and Cellular Biology, 2001-07, Vol.21 (13), p.4197-4207

2001

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A Model of the Complex between Cyclin-Dependent Kinase 5 and the Activation Domain of Neuronal Cdk5 Activator

Biochemical and biophysical research communications, 1999-06, Vol.259 (2), p.420-428

1999

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The atomic-resolution structure of human caspase-8, a key activator of apoptosis

Activity of recombinant cysteine-rich domain proteins derived from the membrane-bound MUC17/Muc3 family mucins

Membrane-anchored aspartyl protease with Alzheimer's disease β-secretase activity

Employing a superior BACE1 cleavage sequence to probe cellular APP processing

Human β-Secretase (BACE) and BACE Inhibitors

Heterodimer formation is essential for heparanase enzymatic activity

Human intestinal MUC17 mucin augments intestinal cell restitution and enhances healing of experimental colitis

Kinetic and structural characterization of caspase-3 and caspase-8 inhibition by a novel class of irreversible inhibitors

Prediction of the tertiary structure and substrate binding site of caspase-8

Processing of the Human Heparanase Precursor and Evidence That the Active Enzyme Is a Heterodimer

Evolution of phosphofructokinase-gene duplication and creation of new effector sites

Structural and functional properties of a phospholipase A2 purified from an inflammatory exudate

Prediction of the tertiary structure of the complement control protein module

Mechanism, structure-activity studies, and potential applications of glutathione S-transferase-catalyzed cleavage of sulfonamides

Cation binding to the integrin CD11b I domain and activation model assessment

Effect of Point Mutations on the Kinetics and the Inhibition of Human Immunodeficiency Virus Type 1 Protease: Relationship to Drug Resistance

An efficient method to express and refold a truncated human procaspase-9: A caspase with activity toward Glu-X bonds

Activated sulfonamides are cleaved by glutathione-S-transferases

CXC Chemokines Connective Tissue Activating Peptide-III and Neutrophil Activating Peptide-2 are Heparin/Heparan Sulfate-degrading Enzymes (∗)

Predicting human immunodeficiency virus protease cleavage sites in proteins by a discriminant function method

[18] Dissection and sequence analysis of phospholipases A2

Stay the Executioner's Hand

Prediction of the tertiary structure of a caspase-9/inhibitor complex

Intrasteric Inhibition of ATP Binding Is Not Required To Prevent Unregulated Autophosphorylation or Signaling by the Insulin Receptor

A Model of the Complex between Cyclin-Dependent Kinase 5 and the Activation Domain of Neuronal Cdk5 Activator

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