Pages that link to "Q55324033"

The following pages link to Matthew J. Smith (Q55324033):

Displaying 23 items.

• FF domains of CA150 bind transcription and splicing factors through multiple weak interactions (Q24563484) (← links)
• Conformational states of syntaxin-1 govern the necessity of N-peptide binding in exocytosis of PC12 cells and Caenorhabditis elegans (Q27305052) (← links)
• Structural studies of FF domains of the transcription factor CA150 provide insights into the organization of FF domain tandem arrays (Q27657224) (← links)
• The PTB domain of ShcA couples receptor activation to the cytoskeletal regulator IQGAP1 (Q28505266) (← links)
• Analysis of a Shc family adaptor protein, ShcD/Shc4, that associates with muscle-specific kinase (Q28507045) (← links)
• Interaction domains of Sos1/Grb2 are finely tuned for cooperative control of embryonic stem cell fate (Q28584946) (← links)
• Screening for PTB domain binding partners and ligand specificity using proteome-derived NPXY peptide arrays (Q33257954) (← links)
• Oncogenic and RASopathy-associated K-RAS mutations relieve membrane-dependent occlusion of the effector-binding site (Q35669207) (← links)
• NMR-based functional profiling of RASopathies and oncogenic RAS mutations. (Q36712670) (← links)
• Inhibition of RAS function through targeting an allosteric regulatory site. (Q37540897) (← links)
• Real-time NMR monitoring of biological activities in complex physiological environments (Q38366398) (← links)
• Probing the GTPase cycle with real-time NMR: GAP and GEF activities in cell extracts (Q38458035) (← links)
• Biochemical Classification of Disease-associated Mutants of RAS-like Protein Expressed in Many Tissues (RIT1). (Q38768357) (← links)
• Subcellular receptor redistribution and enhanced microspike formation by a Ret receptor preferentially recruiting Dok. (Q40000616) (← links)
• Engineering the recruitment of phosphotyrosine binding domain-containing adaptor proteins reveals distinct roles for RET receptor-mediated cell survival. (Q40254769) (← links)
• Integrated RAS signaling defined by parallel NMR detection of effectors and regulators. (Q41792391) (← links)
• Evolution of AF6-RAS association and its implications in mixed-lineage leukemia. (Q42646002) (← links)
• Real-time NMR study of three small GTPases reveals that fluorescent 2'(3')-O-(N-methylanthraniloyl)-tagged nucleotides alter hydrolysis and exchange kinetics. (Q42918070) (← links)
• A comparative CEST NMR study of slow conformational dynamics of small GTPases complexed with GTP and GTP analogues (Q45050798) (← links)
• Matthew Smith (Q71688539) (← links)
• Conformational resolution of nucleotide cycling and effector interactions for multiple small GTPases determined in parallel (Q92020882) (← links)
• Structure of the DOCK2-ELMO1 complex provides insights into regulation of the auto-inhibited state (Q97529790) (← links)
• RASSF effectors couple diverse RAS subfamily GTPases to the Hippo pathway (Q100533230) (← links)