Interactions between complementary SNAREs may determine the specificity of vesicle targeting to an acceptor membrane. SNAREs are integral membrane proteins.

Slides:



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

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.
Model for regulation of the Ras p21 product and for the GTPase-activating protein (GAP) as a downstream effector and regulator of ras activity. Ras is.
Physical map of a human chromosome
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),
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
The lymphocyte markers that distinguish the various stages of B-cell differentiation are shown. Markers that are expressed on the cell surface are indicated.
Pathways for the incorporation of polypeptides into mitochondria. A
Schematic representation of the DTDST protein
Radiographic appearance of intracranial meningioma in NF2
The PKD1 and PKD2 gene products are integral transmembrane proteins
Crystal structure of human short/branched chain acyl-CoA dehydrogenase (PDB file 2JIF). A homotetramer with bound butyryl-Co as substrate is represented.
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.
A hypothetical model of the central apoptotic pathway
Free energy folding landscape for a hypothetical protein
Model depicting the cycling of REP
Factors that regulate the activity of GTP-binding proteins of the ras superfamily. In the active GTP-containing state (represented by a triangle) the protein.
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.
Model accounting for the mechanisms linking epipodophyllotoxin therapy, MLL fusion proteins, cell cycle progression, and the relaxation of cell cycle checkpoints,
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.
RhoGEFs activate a Rho protein GTPase by catalyzing the exchange of GDP for GTP. A variety of stimuli lead to the activation of Rho protein family members.
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;
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
Photosensitive skin lesions on the face of a child with C4 deficiency
Expression of mutant human P5C dehydrogenase alleles in yeast
Karyotype of glioblastoma
The renin-angiotensin-aldosterone system
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.
Liver cell ultrastructure of girl M. S
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
Role of molecular chaperones in the importation of polypeptides into the mitochondrial matrix. Recently synthesized cytoplasmic polypeptides are kept in.
Key structural elements of p53 DNA binding
Electrophoregram profiles showing the 35delG mutation of CX26 (GJB2) in an individual with recessively inherited hearing loss, and in his heterozygous.
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
Model of the function of the protein C anticoagulant pathway
Young female with OCA1B. The hair was white at birth
Overview of the TGF-β signaling pathway
Schematic representation of p53 molecule
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.
The PBDs can be caused by defects in peroxisomal matrix protein import or peroxisome membrane synthesis. Immunofluorescence microscopy shows that human.
The mammalian unfolded protein response pathway
Presentation transcript:

Interactions between complementary SNAREs may determine the specificity of vesicle targeting to an acceptor membrane. SNAREs are integral membrane proteins that, in general, appear to be inserted in the membrane through their C-terminal ends and have most of their mass exposed on the cytoplasmic surface of the membrane. Complementary SNAREs are thought to be present in both the transport vesicles (v-SNARE), which acquire them during vesicle formation in the donor membrane, and in the acceptor membranes (t-SNARE), to which the vesicles are targeted.349 SNAP proteins bound to SNAREs are capable of binding NSF in the presence of ATP. In this scheme, SNAREs are presumed to be bivalent, having one site that binds to a SNAP and another that is specific for a complementary SNARE. Vesicle docking would then involve an NSF-mediated interaction between SNAPs bound to a v-SNARE and to a t-SNARE, as well as the direct specific interaction between the SNAREs themselves. The sequence of events that follows and leads to membrane fusion is not known. A rab protein may also be involved in the targeting and/or triggering of membrane fusion, but at this time the functional relationship between rab proteins and SNAREs is obscure. Nevertheless, hydrolysis of ATP (in NSF) and GTP (in a rab protein) are likely to follow the interaction between complementary SNAREs. Source: The Biogenesis of Membranes and Organelles, 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/ch16fg28.png&sec=62648215&BookID=971&ChapterSecID=62647964&imagename= Accessed: December 23, 2017 Copyright © 2017 McGraw-Hill Education. All rights reserved