Publication Abstract from PubMed
Nitric oxide (NO) is extremely toxic to Clostridium botulinum, but its molecular targets are unknown. Here, we identify a heme protein sensor (SONO) that displays femtomolar affinity for NO. The crystal structure of the SONO heme domain reveals a previously undescribed fold and a strategically placed tyrosine residue that modulates heme-nitrosyl coordination. Furthermore, the domain architecture of a SONO ortholog cloned from Chlamydomonas reinhardtii indicates that NO signaling through cyclic guanosine monophosphate arose before the origin of multicellular eukaryotes. Our findings have broad implications for understanding bacterial responses to NO, as well as for the activation of mammalian NO-sensitive guanylyl cyclase.
Femtomolar sensitivity of a NO sensor from Clostridium botulinum.,Nioche P, Berka V, Vipond J, Minton N, Tsai AL, Raman CS Science. 2004 Nov 26;306(5701):1550-3. Epub 2004 Oct 7. PMID:15472039[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
