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WO2004077062A   [0007]  [0007]  [0007]  [0008]  [0151]  [0151]  [0151]  [0152]  [0152] 
WO2006078161A   [0007]  [0007]  [0009]  [0151]  [0152]  [0152] 
US20030235852A   [0011] 
US20030235852A1   [0210] 
GB9401422W   [0249] 

ACS Chem. Biol.   [0003] 
Chem. Biol.   [0003] 
Prot. Eng.   [0003] 
Chemistry & Biology   [0003] 
Chem. & Biol.   [0003] 
PNAS   [0004]  [0181] 
JACS   [0004]  [0181] 
Nature Biotechnol.   [0004]  [0181] 
PLOS Biology   [0004]  [0181] 
Chem. & Biol.   [0004]  [0181] 
Protein engineering design and selection   [0005] 
Chem Biol   [0006] 
J. Org. Chem   [0007]  [0194] 
ChemBioChem   [0007]  [0007]  [0194] 
Chemical Biology   [0010] 
Cell-penetrating peptides in drug development: enabling intracellular targets   [0116] 
Synthesis of Proteins by Native Chemical Ligation   [0117] 
Subtiligase: a tool for semisynthesis of proteins   [0117] 
Tags for labeling protein N-termini with subtiligase for proteomics   [0117] 
Structure-activity relationship and metabolic stability studies of backbone cyclization and N-methylation of melanocortin peptides   [0155] 
backbone cyclic peptidomimetic melanocortin-4 receptor agonist as a novel orally administered drug lead for treating obesity   [0155] 
J. Mol. Biol.   [0183]  [0195] 
Biochem. Pharmacol.   [0190]  [0202] 
Biochemistry   [0194] 
J. of Molecular Recognition   [0194] 
Phage Display in Biotechnology and Drug Discovery   [0194] 
Bioorganic and Medicinal Chemistry Letters   [0206] 
Medicinal Chemistry   [0206] 
Nature Rev. Drug Discovery   [0206] 
J. of Cardiothoracic and Vascular Anesthesia   [0208] 
Br. J. Anaesth.   [0208] 
Biochemistry   [0208] 
Identification of novel prostate-specific antigen-binding peptides modulating its enzyme activity   [0248] 
Novel peptide inhibitors of human kallikrein 2   [0248] 
A urokinase-type plasminogen activator-inhibiting cyclic peptide with an unusual P2 residue and an extended protease binding surface demonstrates new modalities for enzyme inhibition   [0248] 
A cyclic peptidylic inhibitor of murine urokinase-type plasminogen activator: changing species specificity by substitution of a single residue   [0248] 
Selection of a cyclic nonapeptide inhibitor to alpha-chymotrypsin using a phage display peptide library   [0248] 
Peptide exosite inhibitors of factor VIIa as anticoagulants   [0248]  [0249] 
Novel peptide inhibitors of angiotensin-converting enzyme 2   [0248]  [0249] 
Identification and characterization of peptides that bind human ErbB-2 selected from a bacteriophage display library   [0248] 
New inhibitors of Helicobacter pylori urease holoenzyme selected from phage-displayed peptide libraries   [0248] 
Peptide inhibitor of pancreatic lipase selected by phage display using different elution strategies   [0248] 
A specific peptide inhibitor of the class B metallo-beta-lactamase L-1 from Stenotrophomonas maltophilia identified using phage display   [0248] 
Jr. Phage display selection of a peptide DNase II inhibitor that enhances gene delivery   [0248] 
High-Throughput Screening in Drug Discovery   [0249] 
Hit and lead generation: beyond high-throughput screening   [0249] 
Molecular evolution of proteins on filamentous phage   [0249] 
Guiding the selection of human antibodies from phage display repertoires to a single epitope of an antigen   [0249] 
Engineered antibodies   [0249] 
Highly sensitive in vitro selections for DNA-linked synthetic small molecules with protein binding affinity and specificity   [0249] 
Synthetic compound libraries displayed on the surface of encoded bacteriophage   [0249] 
Encoded combinatorial chemistry   [0249] 
DNA display II. Genetic manipulation of combinatorial chemistry libraries for small-molecule evolution   [0249] 
Selection of optical biosensors from chemisynthetic antibody libraries   [0249] 
Rapid and quantitative cyclization of multiple peptide loops onto synthetic scaffolds for structural mimicry of protein surfaces   [0249] 
The exploration of macrocycles for drug discovery--an underexploited structural class   [0249] 
What can a chemist learn from nature's macrocycles?--a brief, conceptual view   [0249] 
Conformationally restricted cyclic nonapeptides derived from L-cysteine and LL-3-amino-2-piperidino-6-carboxylic acid (LL-acp), a potent b-turn-inducing dipeptide analogue   [0249] 
A stable disulfide-free gene-3-protein of phage fd generated by in vitro evolution   [0249] 
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (150) of an enzymatic reaction   [0249] 
An introduction to organosulfur chemistry   [0249] 
A designed peptide ligase for total synthesis of ribonuclease A with unnatural catalytic residues   [0249] 
Protease inhibitors in the clinic   [0249] 
Targeting proteases: successes, failures and future prospects   [0249] 
Encoded self-assembling chemical libraries   [0249] 
A novel strategy for in vitro selection of peptide-drug conjugates   [0249] 
A general route for post-translational cyclization of mRNA display libraries   [0249] 
Design of cyclic peptides that bind protein surfaces with antibody-like affinity   [0249]