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Proteins regulatory

However, before going further, the regulatory and cytoskeletal muscle proteins will be concisely described with reference to Table I. [Pg.3]

The major regulatory proteins located on an actin filament are troponin and tropomyosin, each occupying 5% of the total myofibrillar proteins. Both proteins confer calcium sensitivity on the ATP-actin-myosin interactions (see Section II). There are minor regulatory proteins that modify the fine structures of myosin and actin filaments and also of Z lines. [Pg.3]

Starr and Offer (1971) examined the SDS—gel electrophoresis patterns of conventional myosin preparations and pointed out the presence of several unknown protein bands other than myosin heavy and light chains. As a result, C (135 kDa), F (121 kDa), and H (74 kDa) proteins have been isolated and shown to be myosin-associated proteins. The C protein, discovered by Offer et al. (1973), is localized to seven regularly spaced stripes in each half of the A bands of rabbit psoas muscle (Craig and Offer, 1976), and studies using monoclonal antibodies have shown [Pg.3]

During the preparation of C protein. Offer et al. (1973) obtained F protein (121 kDa) as a by-product. Miyahara et al. (1980) characterized F protein and showed its binding to myosin. The H protein (74 kDa) has been purified and its specific location closer to the M line than to the C-protein zone has been shown by Yamamoto (1984). The I protein (50 kDa), which inhibits the ATPase activity of myosin, is localized in the edge regions of the A band, but is easily translocated to near the Z lines in aged myofibrils (Ohashi and Maruyama, 1985). The structural roles of F, H, and I proteins have not yet been clarified. [Pg.4]

Paratropomyosin (34 kDa x 2), discovered by Takahashi etal. (1985), is a protein very similar to tropomyosin, but is located at the A-I junction region and translocated to the I-band region to release myosin and actin binding in postmortem myofibrils. [Pg.4]


Transactivation. Protein synthesis is initiated or inhibited by the action of the activated GR on DNA. The use of glucocorticoids leads to antiinflammatory effects by first controlling gene expression, which subsequentiy leads to the synthesis and/or suppression of inflammation regulatory proteins. [Pg.98]

Pig. 3. Representation of promoter sites on the pro-enkephalin gene. The numbers represent the distance in nucleotides from the pro-enkephalin initiation codon the arrow indicates the direction of transcription. The TATA promoter box occurs immediately before the pro-enkephalin initiation site the AP-2 site, which binds immediate-early gene products, is 70 nucleotides upstream, and the CRE site, which binds a regulatory protein involved in cAMP induction of mRNA synthesis, is 107 nucleotides upstream from the initiation codon. The expanded section shows that the CRE site actually consists of two elements, ENKCRE-1 and ENKCRE-2, which separately confer cAMP sensitivity to pro-enkephalin mRNA synthesis. [Pg.446]

Most sequence-specific regulatory proteins bind to their DNA targets by presenting an a helix or a pair of antiparallel p strands to the major groove of DNA. Recognition of the TATA box by TBP is therefore exceptional it utilizes a concave pleated sheet protein surface that interacts with the minor groove of DNA. Since the minor groove has very few sequence-specific... [Pg.156]

Neer, E.J., et al. The ancient regulatory-protein family of WD-repeat proteins. Nature 371 297-300, 1994. [Pg.280]

Regulatory proteins Insulin Somatotropin Thyrotropin lac repressor NEl (nuclear factor 1) Catabolite activator protein (CAP) API... [Pg.121]

In addition to the major proteins of striated muscle (myosin, actin, tropomyosin, and the troponins), numerous other proteins play important roles in the maintenance of muscle structure and the regulation of muscle contraction. Myosin and actin together account for 65% of the total muscle protein, and tropomyosin and the troponins each contribute an additional 5% (Table 17.1). The other regulatory and structural proteins thus comprise approximately 25% of the myofibrillar protein. The regulatory proteins can be classified as either myosin-associated proteins or actin-associated proteins. [Pg.546]

Regulatory proteins Major Tropomyosin 33 X 2 5 I band Binds to actin and... [Pg.547]

Substrate RuBP binds much more tightly to the inactive E form of rubisco (An = 20 nM) than to the active ECM form (A, for RuBP = 20 ixM). Thus, RuBP is also a potent inhibitor of rubisco activity. Release of RuBP from the active site of rubisco is mediated by rubisco activase. Rubisco activase is a regulatory protein it binds to A-form rubisco and, in an ATP-dependent reaction, promotes the release of RuBP. Rubisco then becomes activated by carbamylation and Mg binding. Rubisco activase itself is activated in an indirect manner by light. Thus, light is the ultimate activator of rubisco. [Pg.732]

It is now apparent that bacteria have developed resistance to heavy metals and the detoxifying process is initiated and controlled by metallo-regulatory proteins which are able selectively to recognize metal ions. MerR is a small DNA-binding protein which displays a remarkable sensitivity to Hg +. The metal apparently binds to S atoms of cysteine and this has been a major incentive to recent work on Hg-S chemistry. [Pg.1226]

Group II assays consist of those monitoring cellular second messengers. Thus, activation of receptors to cause Gs-protein activation of adenylate cyclase will lead to elevation of cytosolic or extracellularly secreted cyclic AMP. This second messenger phosphorylates numerous cyclic AMP-dependent protein kinases, which go on to phosphorylate metabolic enzymes and transport and regulatory proteins (see Chapter 2). Cyclic AMP can be detected either radiometrically or with fluorescent probe technology. [Pg.83]

Adenylyl Cyclases. Figure 4 Regulation of adenylyl cyclases by G-proteins. Abbreviations Hs, Hj, Rs, and Rj denote hormones and receptors that lead to stimulation or inhibition, respectively, of adenylyl cyclases, Ca and Ci are active and inactive configurations of adenylyl cyclase, Fo forskolin binding site, Gs and Gj are GTP-dependent regulatory proteins comprising their respective as, and (3y subunits. [Pg.32]

In higher organisms, calpain superfamily contains 16 independent genes that modulate cellular function. Out of them, 14 are Ca2+-dependent cysteine proteases. The other two encode smaller regulatory proteins that... [Pg.311]

Caspases. Figure 2 Caspase activating complexes. Schematic representation of all described long prodomain caspase activation complexes. Each complex contains essentially three functionally different building blocks a sensor/platform, an adaptor and an effector in the form of a particular caspase. Some instigating ligands, possible outcomes and regulatory proteins are indicated. [Pg.330]

A model called histone code theory includes more aspects of chromatin regulation which have been identified. The histone code theory predicts that histone acetylation and other posttranslational histone modifications serve as binding sites for regulatory proteins which mediate processes like gene transcription upon recruitment (see Fig. 2b) [3]. In this context histone modifications can be understood as... [Pg.592]

S-acylated proteins include many GTP-binding regulatory proteins (G proteins), including most a subunits of heterotrimeric G-proteins and also many members of the Ras superfamily of monomeric G proteins, a number of G protein-coupled receptors, several nonreceptor tyrosine kinases, and a number of other signaling molecules, -acylation is posttranslational and reversible, a property that allows the cell to control... [Pg.691]

Ras activates a number of pathways among them is the mitogen-activated protein (MAP) kinases, which transmit signals downstream to other protein kinases and gene regulatory proteins... [Pg.1060]

Both the thick and thin filaments contain other proteins. For example, the thick filament contains titin (molecular weight about 3,000,000) and the thin filament contains nebulin (although not in cardiac muscle), and the regulatory proteins troponin (molecular weight about 33,000) and tropomyosin (molecular weight about 70,000). Nebulin and titin are thought to be ruler proteins, that is, they determine the overall length of the thin and the thick filament, respectively. The... [Pg.208]


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