1 / 17

Glycerol 3-phosphate Cytidylyltransferase

Glycerol 3-phosphate Cytidylyltransferase . Ashley Mericle. Sequence. Overall Structure . Structure. 5 parallel β sheets α -helices pack next to the sheets Form α / β supersecondary structure 3 10 helices connect the β sheets . Function.

lev
Download Presentation

Glycerol 3-phosphate Cytidylyltransferase

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Glycerol 3-phosphate Cytidylyltransferase Ashley Mericle

  2. Sequence

  3. Overall Structure

  4. Structure • 5 parallel β sheets • α-helices pack next to the sheets • Form α/βsupersecondary structure • 310 helices connect the β sheets

  5. Function • Teichoic acids are major componenets of the cell walls of most Gram-positive bacteria. The genes concerned with the synthesis of poly(glycerol phosphate) are organized into two operons. The gene of the tagDEFoperon, tagD,encodes glycerol-3-phosphate cytidylyltransferase. • It catalyzes the transfer of the cytidyl group of CTP to glycerol phosphate.

  6. Teichoic Acid Production Pathway

  7. Overall Reaction Glycerol 3-phosphate Cytidine 5’-triphosphate (CTP) Cytidinediphosphoglycerol (CDP-glycerol) Vmax: 55.1 ± 8.3 μmol/min/mg Km: 1.4 ± 0.1

  8. Important Amino Acids • Lysine 44 • Lysine 46

  9. Dimer Interface • Arginine 63 is buried • From one of the conserved sequences • Tryptophan 15 • Leucine12 and Leucine 13 • hydrophobic

  10. Interface Amino Acids • Leucine 12 • Leucine 13 • Tryptophan 15

  11. Helical Wheels of Interface Helices

  12. Active Site • Residues that interact with CTP do not extend across the dimer interface. • This suggests each chain possesses its own active site • There is the possibility for interaction between them due to the conserved residues • The active site is shaped like a bowl and is open to solvent at its top.

  13. Active Site

  14. Sequence Alignment

  15. Conserved Residues • GX(Y/F)DXXHXGH • RTXGISTT • RYVDEVI • The first two conserved sequences comprise one side of the active site bowl.

  16. Medical Relevance • Some bacteria, which are normally found in the mouth, digestive tract, urinary tract, and upper airways of the respiratory system can cause endocarditis. If the bacteria get in the bloodstream, it can get to the heart and cause inflammation in the heart lining. • It is thought that if the reaction involving GCT can be stopped, then the production of infected heart lining can be stopped.

  17. References • Pattridge KA, Weber CH, Friesen JA, Sanker S, Kent C, Ludwig ML. (2003) J Biol Chem. 278, 51863-51871 • Weber CH, Park YS, Sanker S, Kent C, Ludwig ML. (1999) Structure Fold Des. 7, 1113-1124.

More Related