Biochemical characterization of motif VI mutants—R592A and H594A

Slides:



Advertisements
Similar presentations
‘Immunosequencing’ of heparan sulfate from human cell lines and rat kidney: the (GlcNS6S-IdoA2S) 3 motif, recognized by antibody NS4F5, is located towards.
Advertisements

Circulating FGF21 proteolytic processing mediated by fibroblast activation protein by Eugene Y. Zhen, Zhaoyan Jin, Bradley L. Ackermann, Melissa K. Thomas,
Selective inhibition of BCL10-induced NF-κB activation by Tat–Peptide VIII HEK-293 cells were transiently co-transfected with an expression vector encoding.
Interaction of Stau1 with ribosomal protein P0 (A) Schematic representation of Stau1, showing its dRBDs I–IV (boxes) and PP1 interaction domain (circle),
Adam W. Van Wynsberghe, Qiang Cui  Structure 
Phosphorylation of serine 73 targets SREBP-1c for ubiquitination and proteasomal degradation Phosphorylation of serine 73 targets SREBP-1c for ubiquitination.
Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll pigments Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll.
Reaction co-ordinate for an uncatalysed compared with enzyme-catalysed reaction Reaction co-ordinate for an uncatalysed compared with enzyme-catalysed.
SP1 was a downstream target of miR-150-3p
The crystal structure of rhodopsin.
Amide bonds in a polypeptide
Insulin regulates the expression and intra-membrane proteolysis of the recombinant HA-pSREBP-1c-Flag protein in McA-RH7777 cells Insulin regulates the.
Autophagy defects in NPC1 disease and the bypass mechanism of autophagosome maturation for restoring autophagic flux Autophagy defects in NPC1 disease.
Nucleophilic substitution at a carbonyl group
Keto–enol tautomerism
WZ4003, a specific NUAK1 and NUAK2 inhibitor (A) Chemical structure of the NUAK1/NUAK2 inhibitor WZ4003. WZ4003, a specific NUAK1 and NUAK2 inhibitor (A)
Reversible addition at a carbonyl group
Models of amino acid-dependent mTORC1 regulation
mTORC1 signalling links cellular growth with autophagy
Differentiation-induced changes in Tfam mRNA stability (A) The nt sequence corresponding to the 3′-UTR of mouse Tfam is illustrated. Differentiation-induced.
Σ and π bonds σ and π bonds In these images, atomic orbitals and bonds are depicted as line drawings indicating shape and as isosurfaces, regions of space.
Purification of budding yeast cohesin and its loader.
Volume 16, Issue 2, Pages (February 2008)
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.
Amino acid-dependent regulation of autophagy by mTORC1
Effects of 8-week insulin or Voglibose treatment
Selected mechanisms of colistin resistance
Biochemical characterization of the protein phosphatases Saci-PP2A.
Biochemical characterization of the protein phosphatases Saci-PTP.
GSK-3 phosphorylates nSREBP-1c and nSREBP-1a proteins in vitro
Changes in transcript abundance of the TR-ACS gene family in white clover roots over 24 h in response to Pi supply Changes in transcript abundance of the.
XIST regulated miR-29c by directly targetting in TMZ-resistant glioma cells XIST regulated miR-29c by directly targetting in TMZ-resistant glioma cells.
Effects of XIST on glioma cell proliferation and chemoresistance to TMZ Effects of XIST on glioma cell proliferation and chemoresistance to TMZ (A) siRNA-NC/siRNA-XIST.
Involvement of PI3K activation in TCR/CD3-dependent HIF-1α protein expression. Involvement of PI3K activation in TCR/CD3-dependent HIF-1α protein expression.
Overexpression of miR-340 inhibited osteoclast differentiation
Rapamycin inhibits TCR/CD3 engagement-dependent HIF-1α protein expression. Rapamycin inhibits TCR/CD3 engagement-dependent HIF-1α protein expression. Human.
Morphological studies in the hippocampus of sut mice (A) Low-power images of the hippocampus from WT and sut mice. Morphological studies in the hippocampus.
Proposed model of signalling pathways involved in RBC shrinkage and vesiculation Inhibition of the depicted kinases induces shrinkage and vesiculation.
Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.
Fig. 4. SMXL6 is degraded in response to SL treatment.
Comparison of fluorescence spectra of cells expressing the FL-IFN-γR2/EBFP and FL-IFN-γR2/GFP chains in the presence and absence of the IFN-γR1 chain and.
SYK activity is required for anti-IgM–induced CD86 expression.
Model of Shp2-Ras-Sprouty2 signaling in lens and lacrimal gland development. Model of Shp2-Ras-Sprouty2 signaling in lens and lacrimal gland development.
Enrichment of 3-aa motifs upon addition of Ery.
MiR-431-5p directly targets RAF1 and is negatively correlated to RAF1 expression (A) The predicted binding sites of miR-431-5p and RAF1 3′-UTR, and mutant.
FBXL19-AS1 acts as a sponge of miR-431-5p in lung cancer (A) The predicted binding sites of FBXL19-AS1 and miR-431-5p, and the mutant sites in mutant-type.
TSC1 knockdown enhances hypoxia-mediated lymphocyte death via mTORC1 activation TSC1 knockdown enhances hypoxia-mediated lymphocyte death via mTORC1 activation.
Kinetics of BDNF-induced Erk, Akt and PLCγ activation in the presence of 15 mM NaCl or 15 mM KCl. Representative western blots (A) and quantitative plots.
Pharmacological analysis of four mutant receptors compared with wild-type GLP-1R: Lys-288–Ala4.64, Asn-300–AlaECL2, Trp-306–Ala5.36 or Arg-310–Ala5.40.
Thermostability of A2AR–SMALP and DDM-solubilized A2AR from P
Liver transfection efficiency of pDNA-P79-98
NIPD for trisomy 21 NIPD for trisomy 21 (A) Foetal cell-free DNA (cfDNA) from the foetal circulation crosses the placenta into the maternal circulation,
Schematic map of the X and Y chromosomes
Hypoxia decreases lipogenesis via mTORC1 signalling in lymphocytes
PKM2 is tyrosine phosphorylated and inhibited by FGFR1 in cancer cells with oncogenic or overexpressed FGFR1. PKM2 is tyrosine phosphorylated and inhibited.
Hyperoxidation of ERp57 is intensified by removal of regulatory disulfide bonds in Ero1β (A–C) Where indicated, expression of Ero1β variants was induced.
Allele-specific PCR by positioning the variant at the 3′ end of one primer Allele-specific PCR by positioning the variant at the 3′ end of one primer (A)
DNA methylation status is heritable but requires maintenance
The electron transport chain
Chromatin status is influenced by DNA methylation and histone acetylation Chromatin status is influenced by DNA methylation and histone acetylation In.
RAS activation RAS activation (A) RAS is bound to GDP in the inactive state. Signal transduction can lead to the activation of RAS, via a GEF (GDP/GTP.
E. coli RtcB efficiently mediate HAC1/XBP1 splicing in yeast
FBXL19-AS1 knockdown inhibits proliferation, migration and invasion, and reduces the expression levels of angiogenesis related proteins in lung cancer.
Fertilisation outcomes
CF symptoms depend on residual CFTR activity
Analysis of CF31 RXR-α binding.
Comparison of mean Gensini scores (GS) and atherosclerotic scores (AS) according to the C282Y mutation in patients with single, double, and triple vessel.
Hcy decreases VEGFR1/2 and Angs (Ang1, Ang2) gene transcription
Oncogenic mutations Oncogenic mutations Examples of oncogene activating mutations are depicted. (A) Gene amplification leading to increased expression.
The cytotoxicity of Bacillus subtilis or surfactin in IPEC-J2 cells.
Presentation transcript:

Biochemical characterization of motif VI mutants—R592A and H594A Biochemical characterization of motif VI mutants—R592A and H594A (A) Clustal W analysis of motif VI in SWI2/SNF2 proteins [41]. (B) Comparison of ATPase activity of R592A and H594A with wild-type ADAAD. (C) Comparison of the CD spectra of R592A with wild-type ADAAD in the absence of ligands. (D) Comparison of the CD spectra of R592A with wild-type ADAAD in the presence of ligands. (E) Comparison of kinetic data of H594A with the wild-type protein. (F) Comparison of the CD spectra of H594A with wild-type ADAAD in the absence of ligands. (G) Comparison of CD spectra of H594A with wild-type ADAAD in the presence of ligands. Ritu Bansal et al. Biosci. Rep. 2018;38:BSR20180568 ©2018 by Portland Press Ltd