Selenocistein
Selenocistein (Se-Cys) je aminokiselina koja je prisutna u više enzima (na primer: glutationske peroksidaze, tetrajodotironin 5' dejodinaze, tioredoksin reduktaze, format dehidrogenaze, glicin reduktaze, i pojedine hidrogenaze).
Selenocistein[1] | |||
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IUPAC ime |
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Drugi nazivi | L-Selenocistein; 3-Selanil-L-alanin; Selen cistein | ||
Identifikacija | |||
CAS registarski broj | 10236-58-5 | ||
PubChem[2][3] | 25076 | ||
ChemSpider[4] | 23436 | ||
DrugBank | DB02345 | ||
KEGG[5] | |||
ChEBI | 16633 | ||
ChEMBL[6] | CHEMBL109962 | ||
Jmol-3D slike | Slika 1 | ||
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Svojstva | |||
Molekulska formula | C3H7NO2Se | ||
Molarna masa | 168.05 g mol−1 | ||
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |||
Infobox references |
Nomenklatura
urediIUPAC/IUBMB su zvanično preporučili simbole Sec i U za selenocistein.[7]
Struktura
urediSelenocistein je strukturno sličan sa cisteinom. Jedan atom selena zauzima mesto sumpora, formirajući selenol grupu. Proteini koji sadrže jedan ili više selenocisteinskih ostataka se nazivaju selenoproteinima.
Biologija
urediSelenocistein ima nižu pKa vrednost (5.47) i viši redukcioni potencijal od cisteina. Te osobine ga čine veoma podobnim za proteine koji učestvuju u antioksidantskim aktivnostima.[8]
Reference
uredi- ↑ Susan Budavari, ur. (2001). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th izd.). Merck Publishing. ISBN 0-911910-13-1.
- ↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.
- ↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
- ↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.
- ↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594.
- ↑ IUPAC-IUBMB Joint Commission on Biochemical Nomenclature (JCBN) and Nomenclature Committee of IUBMB (NC-IUBMB) (1999). „Newsletter 1999” (reprint, with permission). European Journal of Biochemistry 264 (2): 607–609. DOI:10.1046/j.1432-1327.1999.news99.x.
- ↑ BJ. Byun and YK. Kang (2011). „Conformational preferences and pK(a) value of selenocysteine residue.”. Biopolymers 95 (5): 345–53. DOI:10.1002/bip.21581. PMID 21213257.
Literatura
uredi- F. Zinoni, A. Birkmann, T. C. Stadtman and A. Bock (1986). „Nucleotide sequence and expression of the selenocysteine-containing polypeptide of formate dehydrogenase (formate-hydrogen-lyase-linked) from Escherichia coli”. PNAS 83 (13): 4650–4654. DOI:10.1073/pnas.83.13.4650. PMC 323799. PMID 2941757.
- F. Zinoni, A. Birkmann, W. Leinfelder and A. Bock (1987). „Cotranslational insertion of selenocysteine into formate dehydrogenase from Escherichia coli directed by a UGA codon”. PNAS 84 (10): 3156–3160. DOI:10.1073/pnas.84.10.3156. PMC 304827. PMID 3033637.
- Boyce E. Cone, Rafael Martin Del Rio, Joe Nathan Davis, and Thressa C. Stadtman (1976). „Chemical characterization of the selenoprotein component of clostridial glycine reductase: identification of selenocysteine as the organoselenium moiety”. PNAS 73 (8): 2659–63. DOI:10.1073/pnas.73.8.2659. PMC 430707. PMID 1066676.