Dihydropteroate synthase

From WikiMD's Medical Encyclopedia

Revision as of 17:22, 22 May 2024 by Prab (talk | contribs) (CSV import)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

THFsynthesispathway.png

Dihydropteroate synthase (DHPS) is an enzyme that plays a crucial role in the folate biosynthesis pathway. It catalyzes the formation of dihydropteroate from para-aminobenzoic acid (PABA) and dihydropterin pyrophosphate (DHPP). This reaction is essential for the production of tetrahydrofolate, a cofactor involved in the synthesis of nucleotides and amino acids.

Function[edit]

DHPS is responsible for the condensation of PABA with DHPP to form dihydropteroate, which is subsequently converted into dihydrofolate and then into tetrahydrofolate. Tetrahydrofolate is vital for the transfer of one-carbon units in various metabolic processes, including the synthesis of purines, thymidylate, and certain amino acids.

Mechanism[edit]

The enzyme operates through a mechanism that involves the nucleophilic attack of the amino group of PABA on the pyrophosphate group of DHPP. This reaction results in the formation of dihydropteroate and the release of pyrophosphate.

Inhibition and Antibiotic Resistance[edit]

DHPS is a target for sulfonamide antibiotics, which are structural analogs of PABA. These antibiotics competitively inhibit the enzyme, thereby blocking folate synthesis and bacterial growth. However, resistance to sulfonamides can occur through mutations in the DHPS gene, which reduce the binding affinity of the antibiotic to the enzyme.

Clinical Significance[edit]

Mutations in the DHPS gene can lead to resistance against sulfonamide antibiotics, posing a challenge in the treatment of bacterial infections. Understanding the structure and function of DHPS is crucial for the development of new antibiotics and the management of antibiotic resistance.

Structure[edit]

The structure of DHPS typically consists of a core domain that binds to DHPP and a flexible loop that interacts with PABA. The enzyme is usually found as a homodimer, with each subunit contributing to the active site.

Research and Development[edit]

Ongoing research aims to elucidate the detailed structure of DHPS and its interaction with inhibitors. This knowledge is essential for designing new drugs that can overcome resistance mechanisms.

See also[edit]

References[edit]


Stub icon
   This article is a enzyme-related stub. You can help WikiMD by expanding it!



Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes


Ad. Transform your life with W8MD's

GLP-1 weight loss injections special from $29.99

W8MD weight loss doctors team
W8MD weight loss doctors team

W8MD Medical Weight Loss, Sleep and Medspa offers physician-supervised medical weight loss programs: NYC medical weight loss Philadelphia medical weight loss

Affordable GLP-1 Weight Loss ShotsAffordable GLP-1 Weight Loss Shots

Budget GLP-1 injections NYC (insurance & self-pay options) Popular treatments:

✔ Most insurances accepted for visits ✔ Prior authorization support when eligible

Start your physician weight loss NYC journey today:

📍 NYC: Brooklyn weight loss center 📍 Philadelphia: Philadelphia weight loss center

📞 Call: 718-946-5500 (NYC) | 215-676-2334 (Philadelphia)

Tags: Affordable GLP1 weight loss NYC, Wegovy NYC, Zepbound NYC, Philadelphia medical weight loss


Advertise on WikiMD


WikiMD Medical Encyclopedia

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.