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Publications by J Ureña
SH2 Domains Exhibit High-Affinity Binding to Tyrosine-Phosphorylated Peptides Yet Also Exhibit Rapid Dissociation and Exchange.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Related publications
Binding Affinities of Tyrosine-Phosphorylated Peptides to the COOH-terminal SH2 and NH-terminal Phosphotyrosine Binding Domains of SHC
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Synthetic Antimicrobial Peptides Exhibit Two Different Binding Mechanisms to the Lipopolysaccharides Isolated fromPseudomonas aeruginosaandKlebsiella Pneumoniae
International Journal of Medicinal Chemistry
Biochemistry
Drug Discovery
Molecular Medicine
Redundant Group a Streptococcus Signaling Peptides Exhibit Unique Activation Potentials
Journal of Bacteriology
Microbiology
Molecular Biology
The C-Terminal SH2 Domain of P85 Accounts for the High Affinity and Specificity of the Binding of Phosphatidylinositol 3-Kinase to Phosphorylated Platelet-Derived Growth Factor Beta Receptor.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Dissociation of Apolipoprotein E Oligomers to Monomer Is Required for High-Affinity Binding to Phospholipid Vesicles
Biochemistry
Biochemistry
Delineation of a T-Cell Activation Motif Required for Binding of Protein Tyrosine Kinases Containing Tandem SH2 Domains.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Interactions Between SH2 Domains and Tyrosine-Phosphorylated Platelet-Derived Growth Factor Beta-Receptor Sequences: Analysis of Kinetic Parameters by a Novel Biosensor-Based Approach.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
The Human Exhibit
CMAJ
Medicine
Hydrocarbon Constrained Peptides – Understanding Preorganisation and Binding Affinity
Chemical Science
Chemistry
