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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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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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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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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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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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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 covalent and tertiary structure of bovine liver rhodanese

Nature (London), 1978-05, Vol.273 (5658), p.124-129

1978

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Structural alterations in the peptide backbone of beta-amyloid core protein may account for its deposition and stability in Alzheimer's disease

The Journal of biological chemistry, 1993-02, Vol.268 (5), p.3072-3083

1993

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Substrate analog inhibition and active site titration of purified recombinant HIV-1 protease

Biochemistry (Easton), 1990-01, Vol.29 (1), p.264-269

1990

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Zinc inhibition of renin and the protease from human immunodeficiency virus type 1

Biochemistry (Easton), 1991-09, Vol.30 (36), p.8717-8721

1991

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Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity

Journal of medicinal chemistry, 1991-08, Vol.34 (8), p.2344-2356

1991

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An active FK506-binding domain of 17,000 daltons is isolated following limited proteolysis of chicken thymus HSP56

Biochemistry (Easton), 1993-11, Vol.32 (47), p.12571-12576

1993

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Dissociative inhibition of dimeric enzymes. Kinetic characterization of the inhibition of HIV-1 protease by its COOH-terminal tetrapeptide

The Journal of biological chemistry, 1991-08, Vol.266 (24), p.15591-15594

1991

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Sequence analysis and expression of the cDNA for the phenol-sulfating form of human liver phenol sulfotransferase

Molecular pharmacology, 1993-01, Vol.43 (1), p.70-77

1993

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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

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

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

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

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

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

The covalent and tertiary structure of bovine liver rhodanese

Structural alterations in the peptide backbone of beta-amyloid core protein may account for its deposition and stability in Alzheimer's disease

Substrate analog inhibition and active site titration of purified recombinant HIV-1 protease

Zinc inhibition of renin and the protease from human immunodeficiency virus type 1

Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity

An active FK506-binding domain of 17,000 daltons is isolated following limited proteolysis of chicken thymus HSP56

Dissociative inhibition of dimeric enzymes. Kinetic characterization of the inhibition of HIV-1 protease by its COOH-terminal tetrapeptide

Sequence analysis and expression of the cDNA for the phenol-sulfating form of human liver phenol sulfotransferase

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