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Fischer convention for assigning the enantiomers of glyceraldehyde

Fischer convention for assigning the enantiomers of glyceraldehyde. Configuration of L-glyceraldehyde and L- a -amino acids. The structural formula of L-glyceraldehyde. Greek lettering scheme used to identify the atoms in the glutamyl and lysyl sidechains.

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Fischer convention for assigning the enantiomers of glyceraldehyde

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  1. Fischer convention for assigning the enantiomers of glyceraldehyde

  2. Configuration of L-glyceraldehyde and L-a-amino acids

  3. The structural formula of L-glyceraldehyde

  4. Greek lettering scheme used to identify the atoms in the glutamyl and lysyl sidechains

  5. Structure of cystine: redox chemistry

  6. Titration curve of glycine

  7. Amino acid analysis via HPLC

  8. Condensation of two a-amino acids to form a dipeptide

  9. Structure of the tetrapeptide, Ala-Tyr-Asp-Gly

  10. Titration curves of ribonuclease A at 25 °C

  11. Views of ethanol: prochirality

  12. Uncommon amino acids that are components of certain proteins

  13. Biologically produced derivatives of “standard” amino acids and amino acids that are not components of proteins

  14. END

  15. Enantiomers of fluorochlorobromomethane

  16. General structural formula for a-amino acids

  17. Zwitterionic form of the a-amino acids that occur at physiological pH values

  18. The structural formula of L-alanine

  19. “CORN crib” mnemonic for the “handedness” of L-amino acids

  20. Fischer projections of L-threonine stereoisomers

  21. Newman projections of the stereoisomers of threonine and isoleucine derived from proteins

  22. Schematic diagram of a polarimeter

  23. Structure of phenylalanine: ball-and-stick representation

  24. Structure of phenylalanine: space-filling representation

  25. Views of acetaldehyde: re and si faces

  26. The three stereoisomers of cystine

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