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== Structural highlights ==
== Structural highlights ==
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Il-12 is a heterodimer, meaning it has two polypeptide chains that differ in their composition and number of amino acids. Those polypeptide chains have carbohydrates attached meaning that il-12 is also a glycoprotein. It has two disulfide linked subunits p35 and '''p40 (1F42)'''. <ref>DOI10.1093/emboj/19.14.3530</ref> The p35 subunit is similar in structure to other class 1 cytokines. The p40 subunit is similar to hematopoietic cytokines. Hematopoietic cytokines make hematopoietic cells turn into different blood cells. P35 is unstable without p40 and can not be secreted but p40 can function without p35. <ref>DOI10.1093/emboj/19.14.3530</ref> P35 has a long chain four helix bundle that binds to a soluble alpha chain receptor subunit which is p40.<ref>DOI10.1093/emboj/19.14.3530</ref> There is an '''arginine residue (I didn’t know if there was a way to highlight the arginine residue in the pocket)''' that projects from the p35 into a pocket in p40. That pocket could be a spot for an inhibitor to bind so Il-12 cannot form. When p35 and p40 combine they form il-12 which is also known as p70. When looking at the disulfide bond between p35 and p40 they found the it is not necessary to form and secrete il-12 but it makes sure there is stabilization between these subunits. <ref>DOI10.1093/emboj/19.14.3530</ref>
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Il-12 is a heterodimer, meaning it has two polypeptide chains that differ in their composition and number of amino acids. Those polypeptide chains have carbohydrates attached meaning that il-12 is also a glycoprotein. It has two disulfide linked subunits p35 and '''p40 (1F42)'''. <ref name="charged">DOI10.1093/emboj/19.14.3530</ref> The p35 subunit is similar in structure to other class 1 cytokines. The p40 subunit is similar to hematopoietic cytokines. Hematopoietic cytokines make hematopoietic cells turn into different blood cells. P35 is unstable without p40 and can not be secreted but p40 can function without p35. <ref>DOI10.1093/emboj/19.14.3530</ref> P35 has a long chain four helix bundle that binds to a soluble alpha chain receptor subunit which is p40.<ref>DOI10.1093/emboj/19.14.3530</ref> There is an '''arginine residue (I didn’t know if there was a way to highlight the arginine residue in the pocket)''' that projects from the p35 into a pocket in p40. That pocket could be a spot for an inhibitor to bind so Il-12 cannot form. When p35 and p40 combine they form il-12 which is also known as p70. When looking at the disulfide bond between p35 and p40 they found the it is not necessary to form and secrete il-12 but it makes sure there is stabilization between these subunits. <ref>DOI10.1093/emboj/19.14.3530</ref>
== Function ==
== Function ==

Revision as of 23:52, 28 April 2020

Interleukin-12

Caption for this structure

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References

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
  3. Lasek W, Zagozdzon R, Jakobisiak M. Interleukin 12: still a promising candidate for tumor immunotherapy? Cancer Immunol Immunother. 2014 May;63(5):419-35. doi: 10.1007/s00262-014-1523-1., Epub 2014 Feb 11. PMID:24514955 doi:http://dx.doi.org/10.1007/s00262-014-1523-1
  4. . PMID:216315890657
  5. . PMID:216315890657
  6. . PMID:216315890657
  7. . PMID:216315890657

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