https://www.ncbi.nlm.nih.gov/Structure/pdb/5JK6
5JK6: Phenylalanine hydroxylase from dictyostelium - apo form
Phenylalanine-4-hydroxylaseFE (III) IONPIPERAZINE-N,N'-BIS(2-ETHANESULFONIC ACID)
phenylalanine hydroxylasedictyosteliumapoform
https://www.wikidata.org/wiki/Q64004926
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis...
scientific article published on 01 October 1993
phenylalanine hydroxylasemutationalspectrum
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2023.1049816/full
Frontiers | Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns...
Phenylalanine hydroxylase deficiency (PAHD) is autosomal recessive disorder of amino acid metabolism and caused by mutations in the phenylalanine hydroxylase...
mutation analysisphenylalanine hydroxylasefrontiersscreening
https://www.rcsb.org/structure/1TG2
RCSB PDB - 1TG2: Crystal structure of phenylalanine hydroxylase A313T mutant with...
Crystal structure of phenylalanine hydroxylase A313T mutant with 7,8-dihydrobiopterin bound
rcsb pdbcrystal structurephenylalanine hydroxylase
https://www.wikidata.org/wiki/Q68645660
Phenylalanine hydroxylase gene: silent mutation uncovers evolutionary origin of different alleles -...
scientific article published on 01 October 1990
phenylalanine hydroxylasesilent mutationgene
https://www.frontiersin.org/journals/bioengineering-and-biotechnology/articles/10.3389/fbioe.2022.993298/full
Frontiers | Phenylalanine hydroxylase mRNA rescues the phenylketonuria phenotype in mice
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency in functional phenylalanine hydroxylase (PAH), resulting in accumulation of phe...
phenylalanine hydroxylasefrontiersmrnarescuesphenylketonuria
https://pmc.ncbi.nlm.nih.gov/articles/PMC29292/
Mutagenesis of the regulatory domain of phenylalanine hydroxylase - PMC
The regulatory domain of phenylalanine hydroxylase (PAH, EC 1.14.16.1) consists of more than 100 amino acids at the N terminus, the removal of which...
of thephenylalanine hydroxylasemutagenesisregulatorydomain
https://www.ncbi.nlm.nih.gov/Structure/pdb/5JK5
5JK5: Phenylalanine hydroxylase from dictyostelium - BH2 complex
Phenylalanine-4-hydroxylase7,8-DIHYDROBIOPTERINFE (III) IONPIPERAZINE-N,N'-BIS(2-ETHANESULFONIC ACID)
phenylalanine hydroxylasedictyosteliumbh2complex
https://www.wikidata.org/wiki/Q40550881
Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene - Wikidata
scientific article published on September 1, 1992
https://www.rcsb.org/structure/1DMW
RCSB PDB - 1DMW: CRYSTAL STRUCTURE OF DOUBLE TRUNCATED HUMAN PHENYLALANINE HYDROXYLASE WITH BOUND...
CRYSTAL STRUCTURE OF DOUBLE TRUNCATED HUMAN PHENYLALANINE HYDROXYLASE WITH BOUND 7,8-DIHYDRO-L-BIOPTERIN
https://www.wikidata.org/wiki/Q47397629
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with...
scientific article published in May 1987
https://www.ncbi.nlm.nih.gov/protein/1LRM_A
Chain A, Phenylalanine-4-hydroxylase - Protein - NCBI
phenylalanine 4 hydroxylasechainproteinncbi
https://www.ncbi.nlm.nih.gov/protein/1TG2_A
Chain A, Phenylalanine-4-hydroxylase - Protein - NCBI
phenylalanine 4 hydroxylasechainproteinncbi
https://www.ncbi.nlm.nih.gov/protein/1J8U_A
Chain A, PHENYLALANINE-4-HYDROXYLASE - Protein - NCBI
phenylalanine 4 hydroxylasechainproteinncbi
https://www.rcsb.org/structure/1J8U
RCSB PDB - 1J8U: Catalytic Domain of Human Phenylalanine Hydroxylase Fe(II) in Complex with...
Catalytic Domain of Human Phenylalanine Hydroxylase Fe(II) in Complex with Tetrahydrobiopterin