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Literature summary for 3.4.22.B75 extracted from

  • Cui, Y.; Yu, H.; Zheng, X.; Peng, R.; Wang, Q.; Zhou, Y.; Wang, R.; Wang, J.; Qu, B.; Shen, N.; Guo, Q.; Liu, X.; Wang, C.
    SENP7 potentiates cGAS activation by relieving SUMO-mediated inhibition of cytosolic DNA sensing (2017), PLoS Pathog., 13, e1006156 .
    View publication on PubMedView publication on EuropePMC

Application

Application Comment Organism
medicine SENP7 is significantly up-regulated in patients with systemic lupus erythematosus Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens Q9BQF6
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Source Tissue

Source Tissue Comment Organism Textmining
THP-1 cell
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Homo sapiens
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(K335, K372, K382)-triSUMOyl-cyclic GMP-AMP synthase + 3 H2O SUMO is conjugated onto the lysine residues 335, 372 and 382. SENP7 reverses this inhibition via catalyzing the deSUMOylation Homo sapiens 3 SUMO + cyclic GMP-AMP synthase
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General Information

General Information Comment Organism
physiological function SENP7 interacted with and potentiated cyclic GMP-AMP synthase cGAS activation. The small ubiquitin-like modifier (SUMO) is conjugated onto the lysine residues 335, 372 and 382 of cGAS, which suppresses its DNA-binding, oligomerization and nucleotidyl-transferase activities. SENP7 reverses this inhibition via catalyzing the cGAS de-SUMOylation. Silencing of SENP7 markedly impaires the IRF3-responsive gene expression induced by cGAS-STING axis Homo sapiens