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10-30-ramnath
10-30-ramnath

... The vacuolar protein sorting (VPS) pathway of Saccharomyces cerevisiae mediates transport of vacuolar protein precursors from the late Golgi to the lysosomelike vacuole. Sorting of some vacuolar proteins occurs via a prevacuolar endosomal compartment and mutations in a subset of VPS genes (the class ...
Department of Health Information Management
Department of Health Information Management

... • NMR Distance Measurement – Not all proteins are found in solution – This method generally looks at isolated proteins rather than protein complexes – Very time consuming ...
Tertiary Protein Structure
Tertiary Protein Structure

... Some of them are derivative of others. We are hurting on when it comes to understanding membrane proteins. Membrane proteins make up about 30% of the human genome. b. So one class of Globular proteins are the Serine Proteases: I talked all bit about how we can sequence other proteins to them. c. The ...
interrpo_nov16
interrpo_nov16

... • Ways in which we can transfer annotation: ...
GenScript - Protein Services
GenScript - Protein Services

... Please specify your preferred expression format: Secretory expression only (GenScript will only purify the protein from the medium) Protein purification from the cell lysate if very little protein can be obtained from the medium (Extra fee is charged) Expression evaluations on both secretory express ...
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008.
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008.

Cytochrome P450 3A4: The Impossible Protein
Cytochrome P450 3A4: The Impossible Protein

... this situation the drugs will not be oxidized in the same way that they would be if there were only one bound to the protein. This makes it difficult to administer more than one drug at once because of the possible effects that occur due to 3A4. In addition to having this binding property, 3A4 is t ...
coIP就是co-immunoprecipitation,假如有两种蛋白质A,B相互作用
coIP就是co-immunoprecipitation,假如有两种蛋白质A,B相互作用

... technique has become an invaluable tool for the life scientist interested in studying cellular pathways via protein:protein interactions. The pull-down assay is an in vitro method used to determine physical interaction between two or more proteins. Pull-down assays are useful for both confirming the ...
structures
structures

... • List is then analyzed for stretches of amino acids that have a common tendency to form a given secondary structure. • Extend until a region of high probability for either a turn or region with a low probability of both a or b is encountered. • Window is typically <10 ...
GPS-Lipid Manual - CSS-Palm
GPS-Lipid Manual - CSS-Palm

... sorting. The Journal of cell biology, 176, 249-254. Casey, P.J. (1995) Protein lipidation in cell signaling. Science, 268, 221-225. Kurayoshi, M., Yamamoto, H., Izumi, S. and Kikuchi, A. (2007) Post-translational palmitoylation and glycosylation of Wnt-5a are necessary for its signalling. The Bioche ...
Relationship between protein surface and antibody binding
Relationship between protein surface and antibody binding

Cytochrome P450 3A4: The Impossible Protein
Cytochrome P450 3A4: The Impossible Protein

... this situation the drugs will not be oxidized in the same way that they would be if there were only one bound to the protein. This makes it difficult to administer more than one drug at once because of the possible effects that occur due to 3A4. In addition to having this binding property, 3A4 is t ...
Protein Trafficking and Localization
Protein Trafficking and Localization

... CYTOPLASMIC MEMBRANE PROTEINS CONTAIN “SIGNAL SEQUENCE” 15 - 30 HYDROPHOBIC AMINO ACID RESIDUES NEAR THE N-TERMINUS [e.g., GLYCINE, ALANINE, VALINE, LEUCINE, PHENYLALANINE] SIGNAL SEQUENCE ALLOWS PROTEIN TO BIND MEMBRANE AND BE SOLUBLE IN THE PHOSPHOLIPID MATRIX. AND TRANS-MEMBRANE-SPANNING SEQUENCE ...
Protein Purification and Analysis Ion exchange
Protein Purification and Analysis Ion exchange

Senior Scientist, Pre-Formulation Development
Senior Scientist, Pre-Formulation Development

... This Sr. Scientist position will be responsible for leading activities of formulation development. This position will be capable of screening formulation, performing biophysical characterization testing, and designing and executing stability studies to support formulation development. The Sr. Scient ...
Purification of GST::TaABF1 Fusion Protein in Order to Assess its
Purification of GST::TaABF1 Fusion Protein in Order to Assess its

...  N-terminal conserved regions and DNA binding region contain serine residues that can possibly be phosphorylated as a means of regulation  TaABF1 mRNA & protein levels do not increase in presence of ABA → TaABF1 most likely regulated post-translationally  PKABA1 shown to phosphorylate TaABF1  Ta ...
DR6000 for Quantitative Determination of Proteins
DR6000 for Quantitative Determination of Proteins

... Quantitative photometric measurements of proteins The quantitative determination of proteins using photometry is often done on the basis of colour reactions of the functional groups of proteins with the corresponding dye reagents. As with the photometric test for individual parameters, the intensity ...
Sequence Data Analysis: A Bioinformatics Application
Sequence Data Analysis: A Bioinformatics Application

Substrate targeting mechanisms
Substrate targeting mechanisms

... - The ability to select a restricted set of substrates in the cell any one time -15,000+ proteins in the genome - each with many phosphorylatable sites (ser/thr, tyr) ...
ANIONIC EXCHANGE FRACTIONATION
ANIONIC EXCHANGE FRACTIONATION

... Strong anion-exchange (SAX2) protein arrays (Ciphergen Biosystems, Fremont, CA, USA) were used for the analysis of differentially excreted proteins in urine from different patients by SELDI-TOF. 40 µL of the denatured urine samples were diluted in binding buffer (50 mM Tris–HCl, pH 8.5) in the manne ...
Automated Assignment of Backbone NMR Data
Automated Assignment of Backbone NMR Data

... The current iteration of the algorithm assigns data in a three-step process: (1) the protein sequence is searched for short stretches (subsets) containing easily identifiable residues (those with high or low C and C chemical shifts); (2) these subsets are matched with sequentially linked chemical sh ...
Protein phosphorylation remains as a black box in signal
Protein phosphorylation remains as a black box in signal

Topic 6
Topic 6

Immunohistochemistry for Microsatellite Instability Fact Sheet
Immunohistochemistry for Microsatellite Instability Fact Sheet

... Lynch syndrome is a hereditary cancer syndrome associated with a significantly increased lifetime risk for colon, uterine, ovarian, stomach, and other cancers. If identified, patients can receive additional screening and prevention measures to help prevent cancer in the future. ...
Protein Expression and Purification
Protein Expression and Purification

... • Expression levels can vary depending on strain choice ...
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Protein design

This article refers to rational protein design. For the broader engineering of proteins see protein engineering.Protein design is the rational design of new protein molecules to fold to a target protein structure, with the ultimate goal of designing novel function and/or behavior. Proteins can be designed from scratch (de novo design) or by making calculated variations on a known protein structure and its sequence (known as protein redesign). Rational protein design approaches make protein-sequence predictions that will fold to specific structures. These predicted sequences can then be validated experimentally through methods such as peptide synthesis, site-directed mutagenesis, or artificial gene synthesis.Rational protein design dates back to the mid-1970s, although initial protein design approaches were based mostly on sequence composition and did not account for specific interactions between side-chains at the atomic level. Recently, however, improvements in molecular force fields, protein design algorithms, and structural bioinformatics, such as libraries of amino acid conformations, have enabled the development of advanced computational protein design tools. These computational tools can make complex calculations on protein energetics and flexibility, and perform searches over enormous configuration spaces, which would be unfeasible to perform manually. Thanks to the development of computational protein design programs and important successes in the field (e.g., see examples below), rational protein design has become one of the most important tools in protein engineering.
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