Zhou-shen Zhao

ORCID: 0009-0004-7083-2360
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About
Contact & Profiles
Research Areas
  • Protein Kinase Regulation and GTPase Signaling
  • Microtubule and mitosis dynamics
  • Cellular Mechanics and Interactions
  • Protein Structure and Dynamics
  • Glycosylation and Glycoproteins Research
  • Immune Response and Inflammation
  • Plant Taxonomy and Phylogenetics
  • Enzyme Structure and Function
  • Oral microbiology and periodontitis research
  • Topic Modeling
  • Neurofibromatosis and Schwannoma Cases
  • Receptor Mechanisms and Signaling
  • Skin and Cellular Biology Research
  • RNA Research and Splicing
  • Mediterranean and Iberian flora and fauna
  • Biotin and Related Studies
  • Artificial Intelligence in Healthcare
  • Monoclonal and Polyclonal Antibodies Research
  • Advanced Proteomics Techniques and Applications
  • Ubiquitin and proteasome pathways
  • Cell Adhesion Molecules Research
  • Machine Learning in Healthcare
  • Caveolin-1 and cellular processes
  • Cellular transport and secretion

Institute of Molecular and Cell Biology
1998-2005

The p21-activated kinase PAK is targeted to focal complexes (FCs) through interactions with the SH3 domains of PAK-interacting exchange factor PIX and Nck. a Rac GTP that also binds G-protein-coupled receptor kinase-interacting protein known as GIT1. Overexpression GIT1 in fibroblasts or epithelial cells causes loss paxillin from FCs stimulates cell motility. This due direct interaction C-terminal 125-residue domain paxillin, under regulation PIX. In its activated state, can promote FC...

10.1128/mcb.20.17.6354-6363.2000 article EN Molecular and Cellular Biology 2000-09-01

ABSTRACTαPAK in a constitutively active form can exert morphological effects (E. Manser, H.-Y. Huang, T.-H. Loo, X.-Q. Chen, J.-M. Dong, T. Leung, and L. Lim, Mol. Cell. Biol. 17:1129–1143, 1997) resembling those of Cdc42G12V. PAK family kinases, conserved from yeasts to humans, are directly activated by Cdc42 or Rac1 through interaction with N-terminal motif (corresponding residues 71 137 αPAK). αPAK mutants substitutions this that resulted severely reduced binding be recruited normally...

10.1128/mcb.18.4.2153 article EN Molecular and Cellular Biology 1998-04-01

The kinase PAK binds tightly to the SH3 domain of its partner PIX via a central proline-rich sequence.A different N-terminal sequence allows ␣PAK bind an adaptor Nck.The Nck SH3[2] interacts equally with 18-mer PAK-derived peptide and full-length ␣PAK.Detailed analysis this binding by saturation substitution related targets be accurately identified from characteristics alone.All proteins, including PAK, NIK, synaptojanin, PRK2, WIP, possess motif PXXPXRXXS; in case serine phosphorylation at...

10.1128/mcb.20.11.3906-3917.2000 article EN Molecular and Cellular Biology 2000-06-01

PIX is a Rho-family guanine nucleotide exchange factor that binds PAK. We previously described two isoforms of differ in their N termini. Here, we report the identification new splice variant βPIX, designated β2PIX, dominant species brain and lacks region ∼120 residues with predicted coiled-coil structure at C terminus β1PIX. Instead, β2PIX contains serine-rich terminus. To determine whether these variants cellular function, studied effect expressing proteins HeLa cells. found plays key role...

10.1242/jcs.114.23.4239 article EN Journal of Cell Science 2001-12-01

AbstractA variety of techniques can be used to find protein partners, including immunoprecipitation, affinity chromatography, blot overlays, and yeast twohybrid screening. Of these, the overlay protocol sodium dodecyl sulfate (SDS)-acrylamide-gel-separated proteins provides perhaps most direct assessment target binding, since one simultaneously screen multiple cell types or tissue extracts, infer size-and in some cases relative affinity-of binding proteins. Combined use with other such as...

10.1385/1-59259-281-3:087 article EN Humana Press eBooks 2003-11-15
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