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Structure

Primary Structure:

The primary structure of each monomer of phenylalanine hydroxylase contains 452 residues, weighing around 52kDa.

(Include image of entire amino acid sequence)

Secondary Structure:

PAH contains right-handed alpha helices and antiparallel beta-strands in its secondary structure. There are some amino acids that don't have any secondary structure, and these are found in the loop containing regions. The loop containing regions are residues L42-V45, D59-H69, S70-D75, and H82-V90. (include image of secondary structure)

Tertiary Structure:

The tertiary structure of each monomer of PAH is organized from 2 alpha helices and 4 beta-strands into an alpha-beta sandwich motif (BaBBaB fold). The structural motif of an alpha-beta sandwich motif has the 4 antiparallel beta-strands flanked on one side by the 2 alpha-helices. The tertiary structure of a phenylalanine hydroxylase protein is built from an N-terminal regulatory domain (residues 1-117), a catalytic domain (residues 118-410), and a tetramerization domain (residues 411-452). The catalytic domain includes the binding sites for iron, substrate and cofactor.The binding sites are at residues 285, 290, and 330. (explain what the tetramerization domain is) The ACT domain is in the N-terminal regulatory domain where proposed enzyme binding to an allosteric site (residues 3-11) (explain what the ACT domain is)

Quaternary Structure:

The quaternary structure of PAH is a homotetramer, dimer of dimers. It is a multidomain, homo-oligomeric protein with dihedral (D2) symmetry.

The substrate of phenylalanine hydroxylase is the amino acid L-phenylalanine. The activation of PAH by L-phenylalanine induces a large conformational change, but a slow global conformational change (is it large in magnitude but slow overall?) Full activation of PAH involves the shift and dimerization of the regulatory domains.

PAH is an iron (Fe3+) containing enzyme. The iron binds to 2 histidines at the active site. The cofactors of PAH include 6R-L-erythro-tetrahydrobiopterin (BH4) and oxygen. BH4 is sandwiched between hydrophobic residues and forms several hydrogen bonds with the N-terminal autoregulatory tail. BH4 binding causes a limited conformational change (mostly constrained to the N-terminal tail). PAH lacking this tail is not regulated by either BH4 or L-phenylalanine and is constitutively active. The BH4 binding-site is flanked by the N-terminal (residues 21-32), the active-site lid (130-150), the Fe+2-coordinating residues, the Beta 6-alpha 7 loop (residues 245-251), and F254. Tetrahydrobiopterin induces a negative heterotropic allosteric effect on the enzyme, which is observed as the activation rate is slower for the BH4 holoprotein than compared to the unbound enzyme. Prior to BH4 binding, (PAH unbound state) a polar and salt-bridge interaction network links the three PAH domains.

== Function == PAH is a metabolic enzyme contained in liver cells that catalyzes the hydroxylation reaction of the amino acid L-Phenylalanine to L-Tyrosine. This protein specifically catalyzes the rate-limiting step in the phenylalanine catabolism, which is the para-hydroxylation step of the aromatic side chain. This catalysis is done by hydroxylation of its substrate by incorporation of one oxygen atom into the aromatic ring, and the final reaction includes the reduction of the second oxygen atom to water using electrons supplied by tetrabiopterin (BH4). BH4 functions as a co-substrate that is hydroxylated at each turnover to pterin-4a-carbinolamine (4a-OH-BH4), with consequent dissociation from the enzymes.

The major regulatory mechanisms of PAH include activation of phenylalanine inhibition by BH4, and additional activation by phosphorylation. Substrate activation and positive cooperativity for Phe binding involves all 3 functional domains and all four subunits in the holoenzyme. Phe binds between the regulatory domain and the interacting catalytic domain, near the sequence binding motif. Hypothesized causes of Phe activation mechanism: Homotropic binding of Phe at active site and the regulatory domain is involved in cooperativity through the interactions with the catalytic and oligomerization domains. Phe binds to an allosteric site, besides the active site, on the regulatory domain, inducing large conformational changes. The allosteric. regulation is necessary to maintain Phe below neurotoxic levels. BH4 acts as a negative regulator by blocking Phe activation, however, BH4 binding to a Phe-activated form of PAH results in positive cooperativity. Phosphorylation acts as mediator of Phe activation by decreasing Phe concentration required to activate enzyme phosphorylation at Ser16.

== Function in the body/ Disease == L-Tyrosine is the precursor to neurotransmitters such as epinephrine, dopamine, and serotonin. PAH depletion or mutation leads to excessive accumulation of toxic L-Phe levels (physiological plasmatic levels <120 micromolar) This causes of the autosomal recessive metabolic disorder Phenylketonuria (PKU). PKU is a congenital disorder characterized by excessive amounts of L-Phenylalanine that buildup to neurotoxic amounts leading to cognitive disability and neurological impairment- profound mental retardation, seizures, microcephaly, and delayed development. The severity of mutation indicated the severity of PKU that leaded to increase the accumulation of phenylalanine in the patient blood with toxic effect. PAH secreted from the liver, and a variety of deficiency syndromes causing various levels of hyperphenylalaninemia have been observed in PKU patient. (Shebl 2019) finds, the most severe PKU was a 14-year-old female followed by a 6-month-old male and a 16-year-old male. Tyrosine biosynthesis as liver enzyme associated with melanin-associated physiological processes. Treatments include a lifelong diet avoiding foods containing phenylalanine and supplementation of synthetic formations of the cofactor tetrahydrobiopterin (BH4) PAH mutations result in reduced enzyme activity and stability and some alter its oligomeric state. Mutations spread throughout 3D structure, but most located in catalytic domain. Loss of enzymatic function caused mainly by folding defects leading to decreased stability. PAH proteins found in hepatocytes (liver cells). Found on chromosome 12 with 13 exons.

Relevance

Structural highlights

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