Pages that link to "Q77560849"

The following pages link to Protein-tyrosine phosphatases: structure, mechanism, and inhibitor discovery (Q77560849):

Displaying 43 items.

• Residue 259 is a key determinant of substrate specificity of protein-tyrosine phosphatases 1B and alpha (Q22253482) (← links)
• Site-specific incorporation of a phosphotyrosine mimetic reveals a role for tyrosine phosphorylation of SHP-2 in cell signaling (Q24291843) (← links)
• The role of the C-terminal domain of protein tyrosine phosphatase-1B in phosphatase activity and substrate binding (Q24321328) (← links)
• Kinetic and structural analysis of a bacterial protein tyrosine phosphatase-like myo-inositol polyphosphatase (Q24648772) (← links)
• Cellular biochemistry methods for investigating protein tyrosine phosphatases (Q26826916) (← links)
• 2-(oxalylamino)-benzoic acid is a general, competitive inhibitor of protein-tyrosine phosphatases (Q27621646) (← links)
• Crystal structure of the Yersinia protein-tyrosine phosphatase YopH complexed with a specific small molecule inhibitor (Q27641444) (← links)
• Discovery and SAR of novel, potent and selective protein tyrosine phosphatase 1B inhibitors (Q27641940) (← links)
• High-Resolution Structure of the Yersinia pestis Protein Tyrosine Phosphatase YopH in Complex with a Phosphotyrosyl Mimetic-Containing Hexapeptide (Q27642518) (← links)
• Protein tyrosine phosphatase (PC12, Br7,S1) family: expression characterization in the adult human and mouse (Q28137874) (← links)
• Conservative tryptophan mutants of the protein tyrosine phosphatase YopH exhibit impaired WPD-loop function and crystallize with divanadate esters in their active sites (Q28829658) (← links)
• Cdc25 as a potential target of anticancer agents. (Q30326904) (← links)
• Inactivation and unfolding of protein tyrosine phosphatase from Thermus thermophilus HB27 during urea and guanidine hydrochloride denaturation. (Q30367174) (← links)
• Improved mapping of protein binding sites (Q30844880) (← links)
• Aurintricarboxylic acid blocks in vitro and in vivo activity of YopH, an essential virulent factor of Yersinia pestis, the agent of plague. (Q31151176) (← links)
• Cooperation of Mtmr8 with PI3K regulates actin filament modeling and muscle development in zebrafish (Q33422870) (← links)
• Determination of the Substrate Specificity of Protein-tyrosine Phosphatase TULA-2 and Identification of Syk as a TULA-2 Substrate (Q33645197) (← links)
• Phosphoryltyrosyl mimetics in the design of peptide-based signal transduction inhibitors (Q34263558) (← links)
• Protein tyrosine phosphatases: prospects for therapeutics (Q34318066) (← links)
• Pulling strings below the surface: hormone receptor signaling through inhibition of protein tyrosine phosphatases (Q34381500) (← links)
• Phosphatases in cell-matrix adhesion and migration (Q35542014) (← links)
• Arylstibonic acids are potent and isoform-selective inhibitors of Cdc25a and Cdc25b phosphatases (Q36074853) (← links)
• Cell Transformation by PTP1B Truncated Mutants Found in Human Colon and Thyroid Tumors (Q36195241) (← links)
• Knowledge-based characterization of similarity relationships in the human protein-tyrosine phosphatase family for rational inhibitor design (Q37610132) (← links)
• Pseudophosphatases: methods of analysis and physiological functions (Q38142438) (← links)
• Characterization of SHP-1 protein tyrosine phosphatase transcripts, protein isoforms and phosphatase activity in epithelial cancer cells (Q39085208) (← links)
• Protein Tyrosine Phosphatases in Systemic Sclerosis: Potential Pathogenic Players and Therapeutic Targets. (Q39233347) (← links)
• Tripeptide inhibitors of Yersinia protein-tyrosine phosphatase (Q41466295) (← links)
• Peptidic α-Ketocarboxylic Acids and Sulfonamides as Inhibitors of Protein Tyrosine Phosphatases (Q41467626) (← links)
• alpha-Ketocarboxylic acid-based inhibitors of protein tyrosine phosphatases (Q41475464) (← links)
• The novel protein PTPIP51 exhibits tissue- and cell-specific expression (Q42472048) (← links)
• Design, synthesis and inhibition activity of novel cyclic peptides against protein tyrosine phosphatase A from Mycobacterium tuberculosis (Q42836502) (← links)
• Phospho-Azatyrosine, a less effective protein-tyrosine phosphatase substrate than phosphotyrosine (Q43630101) (← links)
• Probing the molecular basis for potent and selective protein-tyrosine phosphatase 1B inhibition (Q44112967) (← links)
• Structure-based design and discovery of novel inhibitors of protein tyrosine phosphatases (Q44378329) (← links)
• Enzyme kinetic characterization of protein tyrosine phosphatases (Q44451344) (← links)
• Formylchromone derivatives as a novel class of protein tyrosine phosphatase 1B inhibitors (Q44508056) (← links)
• Mechanism of insulin sensitization by BMOV (bis maltolato oxo vanadium); unliganded vanadium (VO4) as the active component (Q44530727) (← links)
• Structure-based prediction of free energy changes of binding of PTP1B inhibitors (Q44711412) (← links)
• Recent advances in electrophilic fluorination (Q59664611) (← links)
• Examination of novel non-phosphorus-containing phosphotyrosyl mimetics against protein-tyrosine phosphatase-1B and demonstration of differential affinities toward Grb2 SH2 domains (Q73895550) (← links)
• Identification of novel, less toxic PTP-LAR inhibitors using in silico strategies: pharmacophore modeling, SADMET-based virtual screening and docking (Q83979002) (← links)
• Rubrofusarin as a Dual Protein Tyrosine Phosphate 1B and Human Monoamine Oxidase-A Inhibitor: An in Vitro and in Silico Study (Q92948135) (← links)