Amino acids week 7(mine new)
... Amino Acids • Naturally occurring amino acids are all α amino acids. • This means that both the carboxyl and the amino functional groups are on the SAME carbon atom. • This leads to the general formula on the next slide. • These compounds are BIFUNCTIONAL since both functional groups act independen ...
... Amino Acids • Naturally occurring amino acids are all α amino acids. • This means that both the carboxyl and the amino functional groups are on the SAME carbon atom. • This leads to the general formula on the next slide. • These compounds are BIFUNCTIONAL since both functional groups act independen ...
Towards the molecular mechanism of biomolecules in water treated by atmospheric plasma jet in He/O2 gas mixture
... To pinpoint the modified amino acids and therefore the exact location of the oxidation, a tryptic digestion on the protein samples was performed. The three peptide digestion mixtures were analysed by LC-MSMS (LTQOrbitrap Velos, Thermo). The preliminary data analysis was performed with the PEAKS 6.0 ...
... To pinpoint the modified amino acids and therefore the exact location of the oxidation, a tryptic digestion on the protein samples was performed. The three peptide digestion mixtures were analysed by LC-MSMS (LTQOrbitrap Velos, Thermo). The preliminary data analysis was performed with the PEAKS 6.0 ...
carboxylic acid
... • remove the e and add oic acid after the basic name • number the chain starting with the C in COOH being 1 • as in alkanes, prefix with alkyl substituents • side chain positions are numbered relative to Carbon atom number 1 ...
... • remove the e and add oic acid after the basic name • number the chain starting with the C in COOH being 1 • as in alkanes, prefix with alkyl substituents • side chain positions are numbered relative to Carbon atom number 1 ...
Synthetic Biology and its Regulation in the EU
... EU. This legislation regulates activities by which organisms are genetically modified and by which the resulting genetically modified organisms (GMOs) are used in any other way, including marketing the GMOs or their products. Synthetic biology has developed its own language. For example, the recipie ...
... EU. This legislation regulates activities by which organisms are genetically modified and by which the resulting genetically modified organisms (GMOs) are used in any other way, including marketing the GMOs or their products. Synthetic biology has developed its own language. For example, the recipie ...
Cha. 3 Cell structure
... Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing ea ...
... Please note that due to differing operating systems, some animations will not appear until the presentation is viewed in Presentation Mode (Slide Show view). You may see blank slides in the “Normal” or “Slide Sorter” views. All animations will appear after viewing in Presentation Mode and playing ea ...
propy: a tool to generate various modes of
... features for proteins and peptides covered by the current version of propy is summarized in Table 1. These features can be divided into five groups, each of which has been independently predicting protein- and peptide-related problems by using machine-learning methods. The first group includes three ...
... features for proteins and peptides covered by the current version of propy is summarized in Table 1. These features can be divided into five groups, each of which has been independently predicting protein- and peptide-related problems by using machine-learning methods. The first group includes three ...
Whitten, Davis, and Peck, General Chemistry, 6th Edition
... Hornback’s Organic Chemistry, Second Edition The table below matches sections from the book with recommended CER labs. Click on the experiment title to view a PDF of each lab. Go to www.CERLabs.com to search the complete CER database and to learn more about customizing your lab manual through CER. T ...
... Hornback’s Organic Chemistry, Second Edition The table below matches sections from the book with recommended CER labs. Click on the experiment title to view a PDF of each lab. Go to www.CERLabs.com to search the complete CER database and to learn more about customizing your lab manual through CER. T ...
Pierce Trypsin Protease, MS Grade
... Products are warranted to operate or perform substantially in conformance with published Product specifications in effect at the time of sale, as set forth in the Product documentation, specifications and/or accompanying package inserts (“Documentation”). No claim of suitability for use in applicati ...
... Products are warranted to operate or perform substantially in conformance with published Product specifications in effect at the time of sale, as set forth in the Product documentation, specifications and/or accompanying package inserts (“Documentation”). No claim of suitability for use in applicati ...
ppt2 DNA Transcription and Translation
... brings amino acids to the ribosomes; found in cytoplasm 3. rRNA “ribosomal” part of the ribosome; this is where proteins are made ...
... brings amino acids to the ribosomes; found in cytoplasm 3. rRNA “ribosomal” part of the ribosome; this is where proteins are made ...
Exam Name___________________________________
... 29) What are the major organic products when 1 equivalent of acetic formic anhydride reacts with 1 equivalent of methanol? ...
... 29) What are the major organic products when 1 equivalent of acetic formic anhydride reacts with 1 equivalent of methanol? ...
Chapter 21: Carboxylic acid Derivatives I. Introduction
... 1) Name the related carboxylic acid. 2) Replace the “-oic acid” (for IUPAC names) or the “-ic acid” suffix (for common names) with “-amide”. 3) If the are alkyl groups on the nitrogen, put the name of each alkyl group in front with an “N-” prefix (for example: N-ethyl). Examples: ...
... 1) Name the related carboxylic acid. 2) Replace the “-oic acid” (for IUPAC names) or the “-ic acid” suffix (for common names) with “-amide”. 3) If the are alkyl groups on the nitrogen, put the name of each alkyl group in front with an “N-” prefix (for example: N-ethyl). Examples: ...
CHAPTER 12
... C10. It can recognize 5–GGU–3, 5–GGC–3, and 5–GGA–3. All of these specify glycine. C12. All tRNA molecules have some basic features in common. They all have a cloverleaf structure with three stemloop structures. The second stem-loop contains the anticodon sequence that recognizes the codon seq ...
... C10. It can recognize 5–GGU–3, 5–GGC–3, and 5–GGA–3. All of these specify glycine. C12. All tRNA molecules have some basic features in common. They all have a cloverleaf structure with three stemloop structures. The second stem-loop contains the anticodon sequence that recognizes the codon seq ...
Chapter 12
... Disulfide bond A covalent bond between two sulfur atoms of two different amino acids in a protein molecule. Salt bridge An attraction between a negatively charged side chain and a positively charged side chain in a protein molecule. Triglyceride A compound with three hydrocarbon groups attached to a ...
... Disulfide bond A covalent bond between two sulfur atoms of two different amino acids in a protein molecule. Salt bridge An attraction between a negatively charged side chain and a positively charged side chain in a protein molecule. Triglyceride A compound with three hydrocarbon groups attached to a ...
Should I Worry About MRSA?
... What makes the MRSA different from other staph infections is that it has built up an immunity to the antibiotics doctors usually use to treat staph infections. (Methicillin is a type of antibiotic, which is why the strain is called "methicillin-resistant.") ...
... What makes the MRSA different from other staph infections is that it has built up an immunity to the antibiotics doctors usually use to treat staph infections. (Methicillin is a type of antibiotic, which is why the strain is called "methicillin-resistant.") ...
Acidic and Basic Character of Carboxylic Acids
... The inductive effect of electron-withdrawing groups close to the carboxy group causes an increase in acidity. Three electron-withdrawing groups on the -carbon sometimes results in acidity near that of some inorganic acids. ...
... The inductive effect of electron-withdrawing groups close to the carboxy group causes an increase in acidity. Three electron-withdrawing groups on the -carbon sometimes results in acidity near that of some inorganic acids. ...
TV RajanBabu Chemistry, 730 Autumn 1997
... Constitution, configuration and conformation Specifying stereochemistry - CIP notation, Fischer convention Chirality as a property of matter Enantiomeric relationships Enantiomeric excess (ee), optical activity - how to determine it Origin of chirality - asymmetric carbon atom, asymmetric heteroatom ...
... Constitution, configuration and conformation Specifying stereochemistry - CIP notation, Fischer convention Chirality as a property of matter Enantiomeric relationships Enantiomeric excess (ee), optical activity - how to determine it Origin of chirality - asymmetric carbon atom, asymmetric heteroatom ...
Bottromycin
Bottromycin is a macrocyclic peptide with antibiotic activity. It was first discovered in 1957 as a natural product isolated from Streptomyces bottropensis. It has been shown to inhibit methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE) among other Gram-positive bacteria and mycoplasma. Bottromycin is structurally distinct from both vancomycin, a glycopeptide antibiotic, and methicillin, a beta-lactam antibiotic.Bottromycin binds to the A site of the ribosome and blocks the binding of aminoacyl-tRNA, therefore inhibiting bacterial protein synthesis. Although bottromycin exhibits antibacterial activity in vitro, it has not yet been developed as a clinical antibiotic, potentially due to its poor stability in blood plasma. To increase its stability in vivo, some bottromycin derivatives have been explored.The structure of bottromycin contains a macrocyclic amidine as well as a thiazole ring. The absolute stereochemistry at several chiral centers has been determined as of 2009. In 2012, a three-dimensional solution structure of bottromycin was published. The solution structure revealed that several methyl groups are on the same face of the structure.Bottromycin falls within the ribosomally synthesized and post-translationally modified peptide class of natural product.