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1 Information theory as a model of genomic sequences Chengpeng
1 Information theory as a model of genomic sequences Chengpeng

... Shannon and Weaver (1949) developed their theory of information in order to understand the transmission of electronic signals and model the communication system. Gatlin (1972) first described its extension to biology. Information theory is an obvious tool to use in looking for patterns in DNA and pr ...
1 Biochemistry 462a – Enzyme Mechanisms Reading
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Chymotrypsin
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2009/05/21 Lecture
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Peroxisome Proliferator-Activated Receptors (PPARs)
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ppt - Chair of Computational Biology
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... Structural differences between cis and trans isomers Structural differences between the cis and trans Itk SH2 domain provide a basis for conformer-specific binding to the Itk SH3 domain. a, A backbone ribbon representation of the Itk cis SH2 domain with the Itk polyproline peptide (KPLPPTP shown in ...
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Slide 1 - Elsevier
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... Figure 3-26 Genomic mechanism of activation by steroids. The interaction of steroids with different genes in a target cell may direct the synthesis of structural proteins such as cytoskeletal elements or receptors as well as enzymes. These enzymes may produce a variety of effects within the cell. T ...
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... filters to optimize detection levels and background. The optical systems use two scanning monochromators so the user can determine optimal excitation and emission settings, resulting in assay performance similar to that of dedicated single-mode readers. ...
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Erlanson et al. PNAS - UCSF Macromolecular Structure Group

... binding compounds would improve the success rate, but screening at high concentrations is generally impractical because of compound insolubility and assay artifacts. Moreover, the screening process does not target specific sites for drug design, only those sites for which a high-throughput assay is ...
Full Text
Full Text

... The helices are reasonably well packed without gross spaces between them when studied as a space-filling model (Figure 1B). The crossing of the helices in a left-handed fourhelical bundle produces a funnel shaped cavity within the core of the four-helix bundle. This cavity has access to the outside ...
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Ligand binding assay

Ligand Binding Assays (LBA) is an assay, or an analytic procedure, whose procedure or method relies on the binding of ligand molecules to receptors, antibodies or other macromolecules. A detection method is used to determine the presence and extent of the ligand-receptor complexes formed, and this is usually determined electrochemically or through a fluourescence method. This type of analytic test can be used to test for the presence of target molecules in a sample that are known to bind to the receptor.There are numerous types of ligand binding assays, both radioactive and non-radioactive. As such, ligand binding assays are a superset of radiobinding assays, which are the conceptual inverse of radioimmunoassays (RIA). Some newer types are called ""mix-and-measure"" assays because they do not require separation of bound ligands.Ligand binding assays are used primarily in pharmacology for various demands. Specifically, despite the human body’s endogenous receptors, hormones, and other neurotransmitters, pharmacologists utilize assays in order to create drugs that are selective, or mimic, the endogenously found cellular components. On the other hand, such techniques are also available to create receptor antagonists in order to prevent further cascades. Such advances provide researchers with the ability not only to quantify hormones and hormone receptors, but also to contribute important pharmacological information in drug development and treatment plans.
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