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1 y MptA (MJ0775 gene product), a new class of GTP cyclohydrolase I.
2 he first enzyme in its biosynthetic pathway, GTP cyclohydrolase I.
3 ntameric GFRP associate with one molecule of GTP cyclohydrolase I.
4 nd stimulatory complexes is equal to that of GTP cyclohydrolase I.
5 h of the two outer faces of the torus-shaped GTP cyclohydrolase I.
6 otein (GFRP) mediates feedback inhibition of GTP cyclohydrolase I activity by tetrahydrobiopterin and
7 nase, arginine decarboxylase gene activator, GTP cyclohydrolase I and a repressor of purine biosynthe
8 r in HPS, where activities of the key enzyme GTP-cyclohydrolase I are in the normal range, but total
9 We used a synthetic gene based on mammalian GTP cyclohydrolase I, because this enzyme is predicted t
12 tly increased de novo synthesis for 6BH4 via GTP-cyclohydrolase I concomitant with high levels of 6BH
13 diamino-6-hydroxypyrimidine, an inhibitor of GTP cyclohydrolase I, decreased endothelium-dependent va
16 phenylalanine through complex formation with GTP cyclohydrolase I feedback regulatory protein (GFRP).
17 involved in 6BH4 biosynthesis/recycling and GTP-cyclohydrolase I feedback regulatory protein were ex
19 d a similar situation in Escherichia coli: a GTP cyclohydrolase I (folE) mutant, deficient in pterin
20 um, by targeted transgenic overexpression of GTP-cyclohydrolase I (GCH), prevented hypoxia-induced pu
21 matic l-amino acid decarboxylase (AADC), and GTP cyclohydrolase I (GCH1) transcription; increases str
23 AKR1B1), carbonyl reductase (CBR1 and CBR3), GTP-cyclohydrolase I (GCH1), and 6-pyruvoyltetrahydrobio
27 that the first enzyme of the folate pathway, GTP cyclohydrolase I (GCYH-I), encoded in Escherichia co
28 one and those additionally modified with the GTP cyclohydrolase I gene indicate that BH4 is critical
29 drobiopterin bioavailability by upregulating GTP-cyclohydrolase I gene expression and activity, resul
30 ted with fibro-blasts possessing both TH and GTP cyclohydrolase I genes displayed biochemical restora
32 BH4 levels, in part through the induction of GTP cyclohydrolase I (GTPCH I), the rate-limiting enzyme
37 enzyme in catecholamine (CA) biosynthesis of GTP cyclohydrolase I (GTPCH), rate-limiting enzyme in bi
38 e a selective and direct-acting inhibitor of GTP cyclohydrolase I (GTPCH), the first and rate-limitin
39 s factor alpha (TNF-alpha) without affecting GTP cyclohydrolase I (GTPCH), the rate-limiting enzyme i
42 transfer of human guanosine 5'-triphosphate (GTP) cyclohydrolase I (GTPCH I), the first and rate-limi
43 he key enzyme involved in BH(4) synthesis is GTP-cyclohydrolase I (GTPCH-I), which is stimulated by e
45 sis is controlled by guanosine triphosphate (GTP) cyclohydrolase I (GTPCHI) and its feedback regulato
46 ng human tyrosine hydroxylase (hTH) or human GTP-cyclohydrolase I [GTPCHI, the rate-limiting enzyme f
48 y a single enzyme, as is known to occur with GTP cyclohydrolase I in the Eucarya and Bacteria, but ra
50 al restoration in a rat model of PD and that GTP cyclohydrolase I is sufficient for production of BH4
51 st enzyme in the cofactor synthesis pathway, GTP cyclohydrolase I, is activated by phosphorylation an
55 omato fruit up to 140-fold by overexpressing GTP cyclohydrolase I, the first enzyme of pteridine synt
56 decline by fruit-specific overexpression of GTP cyclohydrolase I, the first enzyme of pteridine synt
57 vitro data demonstrate that NAMDA inhibited GTP cyclohydrolase I, the rate-limiting enzyme for BH4 b
58 h tetracycline-regulated expression of human GTP cyclohydrolase I, the rate-limiting enzyme in BH4 sy
59 ype (X haplotype) in the GCH1 gene, encoding GTP-cyclohydrolase I, the rate-limiting enzyme in biopte
60 cells with Tet-regulated expression of human GTP cyclohydrolase I to regulate intracellular BH4 avail
62 hasone prevented the coordinate induction of GTP cyclohydrolase I with NOS2 after exposure to interle
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