- L-Arginine:glycine
amidinotransferase (AGAT; EC 2.1.4.1) is the
enzyme that
catalyses the
transfer of an
amidino group from L-arginine to glycine. The...
- In enzymology, a scyllo-inosamine-4-phosphate
amidinotransferase (EC 2.1.4.2) is an
enzyme that
catalyzes the
chemical reaction L-arginine +...
- Arginine:glycine
amidinotransferase deficiency or AGAT
deficiency is an
autosomal recessive cerebral creatine deficiency caused by a
deficiency of the...
- In the
first step of the biosynthesis, the
enzyme arginine:glycine
amidinotransferase (AGAT, EC:2.1.4.1)
mediates the
reaction of
glycine and
arginine to...
- two
enzymatic defects of
creatine biosynthesis, arginine:glycine
amidinotransferase deficiency (AGAT deficiency),
caused by
variants in GATM gene and...
-
Glycine amidinotransferase,
mitochondrial is an
enzyme that in
humans is
encoded by the GATM gene. This gene
encodes a
mitochondrial enzyme that belongs...
-
synthase (EC 2.6.1.97, ArcS, TgtA2, MJ1022 (gene), glutamine:preQ0-tRNA
amidinotransferase) is an
enzyme with
systematic name L-glutamine:7-cyano-7-carbaguanine...
-
guanidinoacetate methyltransferase (GAMT)
deficiency and L-arginine:glycine
amidinotransferase (AGAT) deficiency.
Clinical presentation of CTD is
similar to that...
- metE (cobalamin-independent
methionine synthase), GATM (glycine
amidinotransferase), and TYR (tyrosinase),
which are in arginine, methionine, creatinine...
- gene
mutations Dihydrofolate reductase deficiency Arginine:glycine
amidinotransferase deficiency Guanidinoacetate methyltransferase deficiency X-linked...
