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Cysteine

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Names IUPAC nameCysteineSystematic IUPAC name2-Amino-3-sulfanylpropanoic acidOther names 2-Amino-3-sulfhydrylpropanoic acid2-Amino-3-mercaptopropanoic acidIdentifiers CAS Number52-90-452-89-1 (hydrochloride)921-01-7 D-cysteine3D model (JSmol)Interactive imageZwitterion: Interactive imageAbbreviations Cys, C ChEBICHEBI:15356ChEMBLChEMBL54943ChemSpider574 (Racemic)5653 (L-form)ECHA InfoCard100.000.145EC Number200-158-2E numberE920 (glazing agents, ...)IUPHAR/BPS4782KEGGD00026PubChemCID5862UNIIK848JZ4886A9U1687S1S (hy…

CystineCystineNames IUPAC name3,3'-Disulfanediylbis(2-ammoniopropanoate)Identifiers CAS Number56-89-33D model (JSmol)Interactive imageChEBICHEBI:35492ChEMBLChEMBL366563ChemSpider575ECHA InfoCard100.000.270IUPHAR/BPS5413KEGGC01420PubChemCID67678UNII48TCX9A1VTCompTox Dashboard(EPA)DTXSID2046418InChIInChI=1S/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)Key: LEVWYRKDKASIDU-UHFFFAOYSA-NInChI=1/C6H12N2O4S2/c7-3(5(9)10)1-13-14-2-4(8)6(11)12/h3-4H,1-2,7-8H2,(H,9,10)(H,11,12)Key: LEVWYRKDKASIDU-UHFFFAOYAASMILESC(C(C(=O)O)N)SSCC(C(=O)O)NProperties Chemical formulaC6H12N2O4S2Molar mass240.29 g·mol Hazards Safety data sheet (SDS) External MSDSExcept where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).Nverify ( ?)Proteinogenic amino acidProteinogenic amino acidProteinogenic amino acids are amino acids that are incorporated biosynthetically into proteins during translation from RNA. The word "proteinogenic" means "protein creating". Throughout known life, there are 22 genetically encoded (proteinogenic) amino acids, 20 in the standard genetic code and an additional 2 (selenocysteine and pyrrolysine) that can be incorporated by special translation mechanisms.ThiolThiolIn organic chemistry, a thiol (; from Ancient Greek θεῖον (theion) 'sulfur') or thiol derivative is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group.DisulfideIn chemistry, a disulfide (or disulphide in British English) is a compound containing a R−S−S−R′ functional group or the S22− anion. In inorganic chemistry, the anion appears in the common mineral pyrite but is otherwise rare. Compounds of the form R−S−S−H are usually called persulfides instead. Disulfide bridges also appear as a common post-translational modification in proteins.ProteinProteinBiomolecule consisting of chains of amino acid residuesA representation of the 3D structure of the protein myoglobin showing turquoise α-helices. This protein was the first to have its structure solved by X-ray crystallography. Toward the right-center among the coils, a prosthetic group called a heme group (shown in gray) with a bound oxygen molecule (red).Proteins are large biomolecules and macromolecules that comprise one or more long chains of amino acidresidues.E numberE numberE numbers, short for Europe numbers, are codes for substances used as food additives, including those found naturally in many foods, such as vitamin C, for use within the European Union (EU) and European Free Trade Association (EFTA). Commonly found on food labels, their safety assessment and approval are the responsibility of the European Food Safety Authority (EFSA).Chemical formulaChemical formulaA chemical formula is any of several kinds of notation for expressing the composition and structure of a chemical compound. Chemical formulas use element symbols for the atoms of each chemical element in a compound. There are several conventional types of chemical formula that present different levels of detail.NucleophileNucleophileIn chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are Lewis bases. Nucleophilic describes the affinity of a nucleophile to bond with positively charged atomic nuclei.Ancient GreekAncient GreekAncient Greek (Ἑλληνική, Hellēnikḗ [hellɛːnikɛ̌ː]) includes the forms of the Greek language used in ancient Greece and the ancient world from around 1500 BC to 300 BC. It is often roughly divided into the following periods: Mycenaean Greek (c. 1400 – c. 1200 BC), Dark Ages (c. 1200 – c. 800 BC), the Archaic or Homeric period (c. 800 – c. 500 BC), and the Classical period (c. 500 – c. 300 BC).LifeLifeLife is the capacity in matter, formed of one or more units called cells, for processes such as cell signaling, homeostasis, metabolism, cell growth, adaptation, response to stimuli, and reproduction. All life eventually reaches a state of death. Many philosophical definitions of living systems have been proposed, such as self-organizing systems.EnzymeEnzymeLarge biological molecule that acts as a catalystThe enzyme glucosidase converts the sugar maltose into two glucose sugars. Active site residues in red, maltose substrate in black, and NADcofactor in yellow. (PDB: 1OBB​)An enzyme is a biological macromolecule, usually a protein, that acts as a biological catalyst, accelerating chemical reactions without being consumed in the process.

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