- toxoflavin.
Several GTP
cyclohydrolases exist,
which sometimes synthesize different products for
different purposes: GTP
cyclohydrolase I, part of the tetrahydrobiopterin...
- GTP
cyclohydrolase I (GTPCH) (EC 3.5.4.16) is a
member of the GTP
cyclohydrolase family of enzymes.
GTPCH is part of the
folate and
biopterin biosynthesis...
-
Autosomal dominant GTP
cyclohydrolase I
deficiency (AD-GTPCHD) is a
disease caused by
dysfunction of GTP
cyclohydrolase I, an
enzyme that
plays an important...
- and 2NTM.
Graupner M, Xu H,
White RH (March 2002). "New
class of IMP
cyclohydrolases in
Methanococcus jannaschii". J. Bacteriol. 184 (5): 1471–3. doi:10...
- and ribA (GTP
cyclohydrolase II) all
reside in the lux operon. RibB is
sometimes found as a
bifunctional enzyme with GTP
cyclohydrolase II that catalyses...
-
Methylenetetrahydrofolate dehydrogenase,
cyclohydrolase and
formyltetrahydrofolate synthetase 1 (MTHFD1) is a gene
located in
humans on
chromosome 14 that...
- In enzymology, a phosphoribosyl-AMP
cyclohydrolase (EC 3.5.4.19) is an
enzyme that
catalyzes the
chemical reaction 1-(5-phosphoribosyl)-AMP + H2O ⇌ {\displaystyle...
- In enzymology, a
methenyltetrahydromethanopterin cyclohydrolase (EC 3.5.4.27) is an
enzyme that
catalyzes the
chemical reaction 5,10-methenyl-5,6,7...
- 5-aminoimidazole-4-carboxamide
ribonucleotide formyltransferase EC 3.5.4.10 - IMP
cyclohydrolase GRCh38:
Ensembl release 89: ENSG00000138363 – Ensembl, May 2017 GRCm38:...
-
Autosomal dominant GTP
cyclohydrolase I
deficiency (autosomal
dominant Segawa syndrome)
Autosomal recessive GTP
cyclohydrolase I
deficiency Tyrosine hydroxylase...