Sandbox GGC1

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== Structural highlights ==
== Structural highlights ==
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The SAM domains need to form an octamer for SARM1 to be able to cleave NAD+. Five <scene name='75/752263/Important_hydrophobic_residues/2'>Amino Acids</scene> were found to be important for this to occur: Leu 442, Ile 461, Leu 514, Leu 531, and Val 533. These amino acids are found in <scene name='75/752263/Area_of_interest/1'>each of the eight domains</scene> that make up the octamer. <scene name='75/752263/Close_up_hydrophobic_residues/2'>If these amino acids</scene> were changed to arginine or aspartate, then NAD+ would no longer be able to be cleaved. <scene name='75/752263/Important_hydrophobic_residues/2'>ImportantAminoAcids</scene> <scene name='75/752263/Area_of_interest/1'>each of the eight domains</scene> <scene name='75/752263/Close_up_hydrophobic_residues/2'>CloseUpOfAminoAcids</scene>
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The SAM domains need to form an octamer for SARM1 to be able to cleave NAD+. Five <scene name='75/752263/Important_hydrophobic_residues/2'>Amino Acids</scene> were found to be important for this to occur: Leu 442, Ile 461, Leu 514, Leu 531, and Val 533. These amino acids are found in <scene name='75/752263/Area_of_interest/1'>each of the eight domains</scene> that make up the octamer. <scene name='75/752263/Close_up_hydrophobic_residues/2'>If these amino acids</scene> were changed to arginine or aspartate, then NAD+ would no longer be able to be cleaved.
== Relevance ==
== Relevance ==
If the five amino acids in the SAM domains that help form the octamer are changed to arginine or asparagine, then it may be possible to inhibit the function of SARM1 and thus stop or slow down neuropathies.
If the five amino acids in the SAM domains that help form the octamer are changed to arginine or asparagine, then it may be possible to inhibit the function of SARM1 and thus stop or slow down neuropathies.

Revision as of 17:20, 20 November 2019

Crystal structure of the tandem SAM domains from human SARM1

PDB ID 6O0S

Drag the structure with the mouse to rotate

References

1. Horsefield, S., Burdett, H., Zhang, X., Manik, M. K., Shi, Y., Chen, J., … Kobe, B. (2019). NAD cleavage activity by animal and plant TIR domains in cell death pathways. Science, 365(6455), 793–799. doi: 10.1126/science.aax1911

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