Results 71 to 80 of about 2,983 (148)
Cyclic ADP-ribose (cADPR) is an intracellular calcium mobilizer generated from NAD(+) by the ADP-ribosyl cyclases CD38 and BST-1. cADPR, both exogenously added and paracrinally produced by a CD38(+) feeder layer, has recently been demonstrated to ...
ZOCCHI, ELENA +12 more
core +1 more source
Partitioning reaction mechanism of bCD38.
The nicotinamide-ribosyl bond of NAD+ is cleaved via a dissociative process with a late transition state, leading to a ribooxocarbenium ion reaction intermediate stabilized by the side-chain of invariant Glu218.
Esther Kellenberger (170384) +7 more
core +1 more source
Locally released oxytocin (OT) activates OT receptors (2.1:OXY:1:OT:) in neighboring neurons in the hypothalamus and their terminals in the posterior pituitary, resulting in further OT release, best known in autoregulation occurring during labor or milk ...
Amina, Sarwat +4 more
core
Regulation of adenylyl cyclase from Blastocladiella emersonii by guanine nucleotides
GTPγS stimulates adenylyl cyclase in particulate fractions of Blastocladiella emersonii zoospores. Cholera toxin catalyses the ADP-ribosylation of a membrane protein of a molecular weight (46,000) similar to that of the α subunit of Gs found in ...
Terenzi, Hernán +3 more
core +1 more source
Cyclic ADP-ribose (cADPR) is a novel Ca 2+ -mobilizing second messenger in mammalian cells including cardiomyocytes. It is unknown whether myocardial ischemia and reperfusion affect the metabolism of cADPR in the myocardium.
Garrett J Gross +6 more
core
Emerging chemical strategies for CD38 inhibition: restoring NAD<sup>+</sup> metabolism and disease control. [PDF]
Zhang Z, Ansari AJ, Fayne ER, Zhang Y.
europepmc +1 more source
NAD<sup>+</sup> metabolism at the host-virus interface. [PDF]
Jhandai P, Vaddadi K, Liu L.
europepmc +1 more source
In prior reports (Moss, J., Manganiello, V. C., and Vaughan, M. (1976) Proc. Natl. Acd Sci. U. S. A. 73, 4424-4427), it was demonstrated that choleragen preparations possessed NAD glycohydrolase activity. Tait and Van Heyningen ((1978) Biochem. J.
Lin, MC, Moss, J, Stanley, SJ
core
Pathological Mechanisms in Sjögren's Disease Likely Involve the ADP-Ribosyl Cyclase Family Members: CD38 and CD157. [PDF]
Rosecka M +6 more
europepmc +1 more source
Antibacterial ADP-ribosyl cyclase toxins inhibit bacterial growth by rapidly depleting NAD(P). [PDF]
Colautti J, Kim Y, Whitney JC.
europepmc +1 more source

