Home

Tyrosinerelated

Tyrosine-related is a term used to describe topics connected to the amino acid tyrosine and its metabolic, biochemical, and clinical contexts. Tyrosine is a nonessential amino acid in humans, synthesized from phenylalanine by the enzyme phenylalanine hydroxylase, and incorporated into proteins. It serves as a precursor for several important molecules, including catecholamines (dopamine, norepinephrine, and epinephrine), thyroid hormones (thyroxine T4 and triiodothyronine T3), and melanin through various enzymatic pathways.

Key enzymes and pathways associated with tyrosine include phenylalanine hydroxylase, tyrosine hydroxylase, and tyrosinase. Tyrosinase catalyzes

Medical relevance includes disorders of tyrosine metabolism, such as tyrosinemias, caused by defects in enzymes like

the
oxidation
of
tyrosine
in
melanin
synthesis,
a
process
foundational
to
pigment
formation
in
skin,
hair,
and
eyes.
In
cellular
signaling,
tyrosine
residues
can
undergo
post-translational
modification
by
phosphorylation,
a
central
mechanism
in
receptor
and
non-receptor
tyrosine
kinase
signaling
pathways
that
regulate
growth,
differentiation,
and
metabolism.
Tyrosine
can
also
participate
in
tyrosine
phosphorylation–dependent
signaling
and
in
protein
tyrosination,
a
reversible
modification
impacting
cytoskeletal
dynamics.
fumarylacetoacetate
hydrolase.
Tyrosinemia
type
I
is
the
most
severe
form,
requiring
medical
management
that
may
include
dietary
restrictions
and
specific
drugs.
Phenylketonuria
can
affect
tyrosine
availability
because
phenylalanine
accumulates
when
its
conversion
to
tyrosine
is
impaired.
Diet,
diagnostics,
and
treatment
strategies
in
these
conditions
illustrate
the
practical
importance
of
tyrosine-related
biology.