Schematic representation of p53 molecule

Slides:



Advertisements
Similar presentations
Metabolism of ganglioside GM2 in GM2 activator-deficient fibroblasts
Advertisements

Progression model of the two types of endometrial carcinoma
A: Population frequency histogram of urinary debrisoquine/4-hydroxydebrisoquine ratios after debrisoquine administration to 258 individuals in a healthy.
Genomic organization of the human cathepsin K gene
Simplified view of the cellular RNA and protein quality surveillance or control systems. Stop-codon introductions as well as splice-site variations, resulting.
Simplified view of the cellular RNA and protein quality surveillance or control systems. Stop-codon introductions as well as splice-site variations, resulting.
More detailed view of the process shown in Fig
A, Diagnosis of clinical severity (mild, moderate, severe) of hemophilia is based on in vitro coagulant activity as shown. B, Distribution of severe and.
Spectrum of different types of human gene mutations logged in Human Gene Mutation Database as of September 13, 1998 ( Source: The.
Physical map of a human chromosome
Advantages of isolated liver transplantation before kidney failure over combined liver-kidney transplantation afterwards. Oxalate excretion: Black line.
Patterns of genetic change in neuroblastomas
Morphologic appearance of EH skin. Shown is a semithin section (0
Distribution of diagnoses among the nearly 115,000 cases of lymphoid malignancy diagnosed in There are 5400 cases of acute lymphoid leukemia (ALL),
Distribution of diagnoses among the nearly 115,000 cases of lymphoid malignancy diagnosed in There are 5400 cases of acute lymphoid leukemia (ALL),
IX; formation of sphingolipids, sphingosine is synthesised from L-serine and palmitoyl-CoA. Source: Serine deficiency disorders, The Online Metabolic and.
Proposed model for the structure of ABC1 within the plasma membrane (modified from reference202 ). The two symmetric halves consisting of six membrane-spanning.
Illustration of the origin of tubular cysts
Structure of the A-subunit gene and identified mutations
The lymphocyte markers that distinguish the various stages of B-cell differentiation are shown. Markers that are expressed on the cell surface are indicated.
Schematic representation of the DTDST protein
The PKD1 and PKD2 gene products are integral transmembrane proteins
Prototypical eukaryotic gene
A section of the cerebellum stained with Sevier-Munger preparation from the brain of a 10-year-old SCA1 patient with 82 CAG repeats who died after 6 years.
Effect of chenodeoxycholic acid feeding on the bilirubin levels of a 10-year-old boy with 3β-hydroxy-Δ5-oxidoreductase/isomerase deficiency. (From Setchell.
Aggregation-mediated passive sorting of secretory and membrane proteins during the biogenesis of a secretory granule in the TGN. (1) The luminal contents.
Urinary excretion (mg/h) of tryptophan derivatives following administration of oral L-tryptophan (about 70 mg per kilogram body weight) administered to.
Schematic drawing of the human X chromosome and physical map the Xp interval carrying the ND gene. A 640-kb yeast artificial chromosome (YAC) clone was.
Free energy folding landscape for a hypothetical protein
Representation of Southern blot analysis revealing an expanding triplet repeat mutation in a myotonic dystrophy family. A grandmother and mother with the.
Model depicting the cycling of REP
Relation between the fractional catabolic rate (FCR) for plasma LDL and the number of LDL receptors on fibroblasts in patients with FH. The values for.
Two children with LPI. The pictures were taken at the time of diagnosis. A, Child 12 years old. B, Child 6 years old. Note the prominent abdomen, hypotrophic.
Evolution of the ubiquitous α-, β-, and γ-crystallins and their structure. Details are described in the text. The α-crystallins are related to heat-shock.
Mechanism of NO synthesis
A comparison of normal cardiac anatomy (A) and the pathology of hypertrophic cardiomyopathy (B). Hypertrophic cardiomyopathy causes cardiomegaly (570 g;
Amino acid sequence and tentative structure for human prepro factor IX
Structure and mutation spectrum of BRCA1
Orofacial dyskinesia in a patient with Huntington's disease
OCTN2 mRNA in fibroblasts from normal controls and patients with primary carnitine deficiency. PolyA RNA isolated from fibroblasts of normal controls or.
Mechanism of NO synthesis
Insulin secretion rates during graded intravenous glucose infusions administered to 6 MODY-2 subjects with glucokinase (GCK) mutations and 6 control subjects.
Photosensitive skin lesions on the face of a child with C4 deficiency
Expression of mutant human P5C dehydrogenase alleles in yeast
Karyotype of glioblastoma
Recovery of E1 activity in E1 variants carrying type IA MSUD mutations as a function of increasing TMAO concentrations. Y368C-α (▪), F364C-α (•), and Y393N-α.
Hydrolysis of membrane-associated ceramide by acid ceramidase in the presence of saposins and bis(monoacylglycero)phosphate (BMP) in the acidic lysosomal.
Crystal structure of cdk2, cyclin A-cdk2, and cyclin A-cdk2-p27 complexes. A, The structure of monomeric cdk2. The T-loop is indicated in yellow, and the.
MRI contrast-enhancement and progression of X-ALD
Key structural elements of p53 DNA binding
Interactions between complementary SNAREs may determine the specificity of vesicle targeting to an acceptor membrane. SNAREs are integral membrane proteins.
Electrophoregram profiles showing the 35delG mutation of CX26 (GJB2) in an individual with recessively inherited hearing loss, and in his heterozygous.
YAC and BAC cloning systems
Corneal opacity in a heterozygote observed by slit-lamp microscopy
Models of Fibrin Generation
FISH of glioblastoma. This interphase nucleus from a glioblastoma contains three chromosome 7 centromere signals (dark) and one centromere 10 signal (light).
A model of the protein C activation complex
Progression model of the two types of endometrial carcinoma
Young female with OCA1B. The hair was white at birth
Overview of the TGF-β signaling pathway
Structural features of the p53 gene and its encoded protein
The effects of apo E alleles on various lipoprotein parameters
Hepatic glucose production as a function of fasting plasma glucose levels. These studies involved the same individuals who were studied in Fig
Basic algorithm for cancer risk assessment that employs gene testing.
Schematic working model of the hepatic microsomal glucose-6-phosphatase system. ER = endoplasmic reticulum. This model is not meant to represent the actual.
Detection of XIST RNA in interphase cells from a normal male, a normal female, and a 49,XXXXX female by RNA fluorescence in situ hybridization. Male.
Structure and mutation spectrum of BRCA2
Composite megalosaccharide proposed for blood group substance
Complete chemical structures of the neutral glycosphingolipids that accumulate in Fabry disease. A, Globotriaosylceramide, the major accumulated substrate.
Structure of red cell glycophorins. A
Presentation transcript:

Schematic representation of p53 molecule Schematic representation of p53 molecule. The p53 protein consists of 393 amino acids with functional domains, evolutionarily conserved domains, and regions designated as mutational hotspots. Functional domains include the transactivation region (amino acids 20–42; diagonal striped block), sequence-specific DNA-binding region (amino acids 100–293), nuclear localization sequence (amino acids 316–325; vertical striped block), and oligomerization region (amino acids 319–360; horizontal striped block). Cellular or oncoviral proteins bind to specific areas of the p53 protein. Evolutionarily conserved domains (amino acids 17–29, 97–292, and 324–352; black areas) were determined using the MACAW program. Seven mutational hotspot regions within the large conserved domain are identified: amino acids 130–142, 151–164, 171–181, 193–200, 213–223, 234–258, and 270–286; checkered blocks). Functional domains and protein binding sites (gray bars underneath) were compiled from references. Vertical lines above the schematic, missense mutations; lines below schematic, nonmissense mutations. Source: Hepatocellular Carcinoma, The Online Metabolic and Molecular Bases of Inherited Disease Citation: Valle D, Beaudet AL, Vogelstein B, Kinzler KW, Antonarakis SE, Ballabio A, Gibson K, Mitchell G. The Online Metabolic and Molecular Bases of Inherited Disease; 2014 Available at: https://ommbid.mhmedical.com/DownloadImage.aspx?image=/data/books/971/ch59fg2.png&sec=62669663&BookID=971&ChapterSecID=62669651&imagename=&gboscontainerID=0 Accessed: December 30, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved