guanosine

The systematic name of this enzyme class is guanosine aminohydrolase.

For example, treatment with 7-methylguanosine gives guanosine.

Inosines are recognised as guanosine by the cells translational machinery.

It is an ester of phosphoric acid with the nucleoside guanosine.

These are examples of modified adenosine or guanosine.

One such alteration is decreased affinity for Cyclic guanosine monophosphate.

This enzyme is also called guanosine aminase.

Molybdopterins, in turn, are synthesized from guanosine triphosphate (see synthetic route at right).

It acts by inhibiting the enzyme cyclic guanosine monophosphate phosphodiesterase.

This drug is the only approved antiretroviral that is active as a guanosine analogue in vivo.

Carbovir is a related guanosine analogue that had poor oral bioavailability and thus was withdrawn from clinical development.

It has a highly conserved guanosine as the first and an adenosine as the last loop residue.

The biosynthesis of molybdopterin begins with guanosine triphosphate.

The enzyme catalyses the methylation of guanosine.

The guanine nucleoside is called guanosine.

ABC is an analog of guanosine (a purine).

Didanosine (ddI) is a nucleoside analogue of guanosine.

This guanosine is methylated on the 7 position directly after capping in vivo by a methyl transferase.

It has also been reported that phosphoramidites activated with 1H-tetrazole react, to a small extent, with the O position of guanosine.

This gene encodes tuberin, a guanosine triphosphatase-activating protein.

Ribavirin's carboxamide group can make the native nucleoside drug resemble adenosine or guanosine, depending on its rotation.

Other names in common use include guanosine triphosphate cyclohydrolase II, and GTP-8-formylhydrolase.

Abacavir, also called ABC, has the trade name Ziagen, is an analog of guanosine.

Sensitivity to light is modulated by changes in intracellular calcium ions and cyclic guanosine monophosphate.

The α subunit can bind with guanosine diphosphate, GDP.