Effect of the temperature-sensitive mutation hsp90G17OD on the activity of the c-src regulatory kinase Csk and on the maturation of c-srcK295M at the semirestrictive.

Slides:



Advertisements
Similar presentations
Human embryonic stem cells Human induced pluripotent stem cells Yamanaka S. et al. Cell 2007 Thomson J. et al. Science 2007.
Advertisements

Skin temperature, tactile processing, and vividness of the illusion Moseley G L et al. PNAS 2008;105: ©2008 by National Academy of Sciences.
Productive Replication of Ebola Virus Is Regulated by the c-Abl1 Tyrosine Kinase by Mayra García, Arik Cooper, Wei Shi, William Bornmann, Ricardo Carrion,
Comparison (θ) of the mean dinucleotide variability distribution for (A) genes with MAE vs. Comparison (θ) of the mean dinucleotide variability distribution.
Comparison (R) of the mean observed to expected dinucleotide distribution for (A) genes with MAE vs. Comparison (R) of the mean observed to expected dinucleotide.
(A) Schematic illustration of the experimental design for the analysis of the RNase activity of MARF1 in oocytes by mutating the conserved D272 residue.
تحليل الحساسية Sensitive Analysis.
Balancing selection characterizes both MAE genes and cell type-specific genes (expressed in either nsc or asl but not in both). Balancing selection characterizes.
Identification and characterization of a xap5 mutant in Chlamydomonas.
(A) Heat map showing expression changes during in vitro differentiation of nscs to astrocytes. (A) Heat map showing expression changes during in vitro.
Expression of α5β1-integrin enhances EboV GP-mediated infection of GD25 cells. Expression of α5β1-integrin enhances EboV GP-mediated infection of GD25.
The mechanisms that regulate systemic resilience in humans and animals
FAM49B controls T cell activation by regulating cytoskeleton remodeling. FAM49B controls T cell activation by regulating cytoskeleton remodeling. (A) J.FAM49B.
Schematic representation of possible effects of different factors on systemic resilience. Schematic representation of possible effects of different factors.
The evolution of WCI for biological specificity makes organisms more evolvable. The evolution of WCI for biological specificity makes organisms more evolvable.
DHEA(S) and Allo induced the phosphorylation of PKC in serum-deprived PC12 cells. DHEA(S) and Allo induced the phosphorylation of PKC in serum-deprived.
Volume 100, Issue 1, Pages (January 2000)
PGAM5 dephosphorylates ASK1.
REV-ERBα agonists reduce protein O-GlcNAcylation.
Interaction of xFRS2 with the Src family kinase Laloo.
WCI evolve as organisms become more complex.
Reduced cell motility and expression of phosphorylated FAK in a fibroblast cell line of an individual with T3257I mutation. Reduced cell motility and expression.
GPR124 promotes cell migration.
Despite a relatively small amount of PI3Kβ being associated with activated PDGFRs, it generates a more substantial proportion of the PIP3 that accumulates.
Phosphatase activity of PGAM5 is required for activation of ASK1.
PGAM5 associates with and activates ASK1.
Summary of fusion event frequency for wild-type (wt) and Cav1
Themis acts to increase phosphorylation of Shp1.
PPARγ is SUMOylated at K107 in WAT
In vitro analysis of K107R white adipocytes.
Phosphatase activity associated with Themis and Shp1 in response to different affinity peptide ligands. Phosphatase activity associated with Themis and.
Extracellular GABA level is decreased by genetic deletion of Best1 or MAOB but increased by overexpression of MAOB. (A) Schematic illustration for microdialysis.
Themis interacts with Shp2 when Shp1 is genetically deleted.
Phosphatase activity associated with Shp1 is reduced in Themis−/− thymocytes. Phosphatase activity associated with Shp1 is reduced in Themis−/− thymocytes.
Light-activated RPS6 phosphorylation depends on auxin but not photosynthesis or exogenous glucose. Light-activated RPS6 phosphorylation depends on auxin.
Supplement Figure 3 SYF cells
Characterizing the Killer Colorectal Carcinomas
Detection rate for EGFR mutations in cfDNA.
Immunofluorescece analysis of c-src and v-src distribution in wild-type yeast cells. Immunofluorescece analysis of c-src and v-src distribution in wild-type.
Distinct TF motifs are associated with decreased or increased H3K27 acetylation peaks in hypothyroidism. Distinct TF motifs are associated with decreased.
Effect of agonists on receptor mobility.
ICSBP stimulates GAS reporter activity in JAK/STAT-pathway-deficient cells. 2fTGH, U3A, U4A, and γ1A cells were cotransfected with the WT GAS reporter.
Volume 134, Issue 2, Pages (July 2008)
Lymphocyte lineage trees produced by long-term live cell microscopy.
ONC201 activates the ATF4 pathway through the eIF2α kinases HRI and PKR. ONC201 activates the ATF4 pathway through the eIF2α kinases HRI and PKR. (A) Western.
NsiR4 expression is mediated through an NtcA-activated promoter.
Coutilization of glucose–xylose mixtures by batch fermentations.
CKL family is involved in the circadian clock.
Figure 1 Examination of MuSK antibody levels and B-cell subsetsFlow cytometric analysis (n = 13) using standardized Human Immunology Project Consortium.
Individual ice sheet contributions to SLR for 2100 L (A) and H (B) temperature scenarios, assuming dependences between the ice sheets in terms of the processes.
Figure 2 DNM1 mutations inhibit transferrin uptake Inhibition of transferrin internalization in mammalian cell lines. DNM1 mutations inhibit transferrin.
Multiple sequence alignment of STAT6 and other STAT proteins produced by ClusterW and ESpript (espript.ibcp.fr/ESPript/ESPript/). Multiple sequence alignment.
Activation of PKR by the PBM decoy peptide.
The saturation scan database for Ubv.2.1 (A) and Ubv.21.4 (B).
Pi and FGF2 differentially activate the FGFR1-FRS2α-ERK pathway.
Ectopic overexpression of WOR3 drives switching to the opaque cell type. Ectopic overexpression of WOR3 drives switching to the opaque cell type. (A) Visualization.
Accumulation of asialoglycoproteins, agalactoglycoproteins, and Man-terminated N-glycans during blood protein aging. Accumulation of asialoglycoproteins,
Mediation model of study 4.
VacA does not induce phosphorylation of Src in RPTPα constitutive-knockdown AZ-521 cells. VacA does not induce phosphorylation of Src in RPTPα constitutive-knockdown.
Distinct requirements for Kita and Mitfa.
TNAP and IAP t1/2s and N-glycan remodeling following zanamivir treatment. TNAP and IAP t1/2s and N-glycan remodeling following zanamivir treatment. (A.
Conceptual model of airflow-mediated mucus clearance from airways.
Correlation between Ti→jS(r) and Ti→jM(r) for pair of locations (gray dots) separated by a distance of (A) r=1 km, (B) r=5 km, (C) r=20 km, (D) r=50 km,
Degradation of the COPI proteins Ret1 and Sec21 by the AID system.
Vps36 interacts with Smo in the absence of Hh
Summary of the new mechanistic findings of the present study.
Histogram of channel events observed in Cx43-TM (gray) and Cx43-WT-expressing cells. Histogram of channel events observed in Cx43-TM (gray) and Cx43-WT-expressing.
Receptor tyrosine kinase (RTK) responds to external stimuli including extracellular matrix components and chemokines and subsequently activates phosphoinositide.
PKM2 is tyrosine phosphorylated and inhibited by FGFR1 in cancer cells with oncogenic or overexpressed FGFR1. PKM2 is tyrosine phosphorylated and inhibited.
Inhibition of BCR-mediated signaling by ARQ 531.
Presentation transcript:

Effect of the temperature-sensitive mutation hsp90G17OD on the activity of the c-src regulatory kinase Csk and on the maturation of c-srcK295M at the semirestrictive temperature. Effect of the temperature-sensitive mutation hsp90G17OD on the activity of the c-src regulatory kinase Csk and on the maturation of c-srcK295M at the semirestrictive temperature. (A) Csk produced at 32°C: accumulation of c-srcK295M and Csk and Csk-mediated tyrosine phosphorylation of c-srcK295M in wild-type (WT) and G170D (TS) cells. (B) Csk and c-srcK295M produced at 32°C: accumulation of c-srcK295M and Csk and Csk-mediated tyrosine phosphorylation of c-srcK295M in wild-type (WT) and G170D (TS) cells. Yang Xu et al. PNAS 1999;96:1:109-114 ©1999 by National Academy of Sciences