Monomethyl-sulfatase
Monomethyl-sulfatase (also known as MMS) is an enzyme that plays a crucial role in the metabolism of sulfates in the human body. It is involved in the breakdown of sulfate esters, which are compounds that contain a sulfate group attached to another molecule.
Function[edit | edit source]
Monomethyl-sulfatase catalyzes the hydrolysis of sulfate esters, a process that involves the addition of a water molecule to break the bond between the sulfate group and the rest of the molecule. This reaction is important for the metabolism of various substances in the body, including hormones, neurotransmitters, and drugs.
Structure[edit | edit source]
The structure of monomethyl-sulfatase is complex and not fully understood. However, it is known to be a protein that contains several amino acids and a cofactor, which is a non-protein chemical compound that is required for the protein's biological activity.
Clinical significance[edit | edit source]
Deficiencies in monomethyl-sulfatase can lead to a variety of health problems. For example, a lack of this enzyme can result in the accumulation of sulfate esters in the body, which can cause toxicity. This can lead to symptoms such as nausea, vomiting, and diarrhea. In severe cases, it can even lead to organ failure.
Research[edit | edit source]
Research into monomethyl-sulfatase is ongoing, with scientists seeking to better understand its structure and function, as well as its role in human health and disease. This research could potentially lead to new treatments for conditions caused by deficiencies in this enzyme.
See also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD