User:Thomas McNamara/Sandbox 1

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==Immunoglobulin G (mAB231)==
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==Immunoglobulin G==
<Structure load='1IGT' size='350' frame='true' align='right' caption='Immunoglobulin G' scene='Insert optional scene name here' />
<Structure load='1IGT' size='350' frame='true' align='right' caption='Immunoglobulin G' scene='Insert optional scene name here' />
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Immunoglobulin G proteins, more commonly referred to as antibodies, make up a large family of secreted proteins that are potent regulators of the immune system. Furthermore, Immunoglobulin G proteins are the most common type of antibodies present in the serum, and utilize their two identical, but very unique, binding sites to recognize pathogens. It is these binding sites that differ in amino acid sequence between each Immunoglobulin G protein in a particular organism, giving each antibody a different binding target -- ultimately giving the immune system a large class of weapons that can bind to and recognize almost any foreign pathogen.
This is a default text for your page '''Thomas McNamara/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs./Users/Tom/Desktop/AntibodyStrucMovie.mov
This is a default text for your page '''Thomas McNamara/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs./Users/Tom/Desktop/AntibodyStrucMovie.mov

Revision as of 21:55, 16 December 2018

Contents

Immunoglobulin G

Immunoglobulin G

Drag the structure with the mouse to rotate


Immunoglobulin G proteins, more commonly referred to as antibodies, make up a large family of secreted proteins that are potent regulators of the immune system. Furthermore, Immunoglobulin G proteins are the most common type of antibodies present in the serum, and utilize their two identical, but very unique, binding sites to recognize pathogens. It is these binding sites that differ in amino acid sequence between each Immunoglobulin G protein in a particular organism, giving each antibody a different binding target -- ultimately giving the immune system a large class of weapons that can bind to and recognize almost any foreign pathogen.

This is a default text for your page Thomas McNamara/Sandbox 1. Click above on edit this page to modify. Be careful with the < and > signs./Users/Tom/Desktop/AntibodyStrucMovie.mov You may include any references to papers as in: the use of JSmol in Proteopedia [1] or to the article describing Jmol [2] to the rescue.

Function

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Disease

Relevance

Structural highlights

This is a sample scene created with SAT to by Group, and another to make of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

</StructureSection>

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

Proteopedia Page Contributors and Editors (what is this?)

Thomas McNamara

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