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1989 2
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17 results

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Prolidase - A protein with many faces.
Wilk P, Wątor E, Weiss MS. Wilk P, et al. Biochimie. 2021 Apr;183:3-12. doi: 10.1016/j.biochi.2020.09.017. Epub 2020 Oct 10. Biochimie. 2021. PMID: 33045291 Review.
Prolidase homologues are found in all kingdoms of life. The importance of prolidase in human health is underlined by a rare hereditary syndrome referred to as Prolidase Deficiency. A growing number of studies highlight the importance of prolidase …
Prolidase homologues are found in all kingdoms of life. The importance of prolidase in human health is underlined by a rare he …
Prolidase function in proline metabolism and its medical and biotechnological applications.
Kitchener RL, Grunden AM. Kitchener RL, et al. J Appl Microbiol. 2012 Aug;113(2):233-47. doi: 10.1111/j.1365-2672.2012.05310.x. Epub 2012 May 10. J Appl Microbiol. 2012. PMID: 22512465 Free article. Review.
Prolidase is a multifunctional enzyme that possesses the unique ability to degrade imidodipeptides in which a proline or hydroxyproline residue is located at the C-terminal end. ...Collagen comprises nearly one-third of the total protein in the body, and it is essential in …
Prolidase is a multifunctional enzyme that possesses the unique ability to degrade imidodipeptides in which a proline or hydroxyproli …
[Pulmonary phenotypes of inborn errors of metabolism].
Mauhin W, Brassier A, London J, Subran B, Zeggane A, Besset Q, Jammal C, Montardi C, Mellot C, Strauss C, Borie R, Lidove O. Mauhin W, et al. Rev Mal Respir. 2022 Nov;39(9):758-777. doi: 10.1016/j.rmr.2022.09.002. Epub 2022 Oct 10. Rev Mal Respir. 2022. PMID: 36229356 Review. French.
In this review, we focus on different metabolic diseases with respiratory symptoms in adults: lysosomal glycosphingolipidoses such as acid sphingomyelinase deficiency (Niemann-Pick types A and B disease), Gaucher, Fabry, Pompe diseases and mucopolysaccharidoses in general. …
In this review, we focus on different metabolic diseases with respiratory symptoms in adults: lysosomal glycosphingolipidoses such as acid s …
Biotechnological applications of recombinant microbial prolidases.
Theriot CM, Tove SR, Grunden AM. Theriot CM, et al. Adv Appl Microbiol. 2009;68:99-132. doi: 10.1016/S0065-2164(09)01203-9. Adv Appl Microbiol. 2009. PMID: 19426854 Review.
Prolidase is a metallopeptidase that is ubiquitous in nature and has been isolated from mammals, bacteria and archaea. ...Prolidases are also employed in the cheese-ripening process to improve cheese taste and texture. In humans, prolidase deficiency (PD) is …
Prolidase is a metallopeptidase that is ubiquitous in nature and has been isolated from mammals, bacteria and archaea. ...Prolidases …
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations.
Lupi A, Tenni R, Rossi A, Cetta G, Forlino A. Lupi A, et al. Amino Acids. 2008 Nov;35(4):739-52. doi: 10.1007/s00726-008-0055-4. Epub 2008 Mar 14. Amino Acids. 2008. PMID: 18340504 Review.
Recombinant human prolidase was produced in prokaryotic and eukaryotic hosts with biochemical properties similar to the endogenous enzyme and represents a valid tool both to better understand the structure and biological function of the enzyme and to develop an enzyme repl …
Recombinant human prolidase was produced in prokaryotic and eukaryotic hosts with biochemical properties similar to the endogenous en …
Prolidase deficiency: a case report and literature review.
Milligan A, Graham-Brown RA, Burns DA, Anderson I. Milligan A, et al. Br J Dermatol. 1989 Sep;121(3):405-9. doi: 10.1111/j.1365-2133.1989.tb01437.x. Br J Dermatol. 1989. PMID: 2679858 Review.
We describe a patient in whom chronic leg ulceration was due to prolidase deficiency. The clinical features of this condition are described and we discuss the metabolic abnormality and the treatment regimes which have been employed. We also report the further findin …
We describe a patient in whom chronic leg ulceration was due to prolidase deficiency. The clinical features of this condition …
Current Understanding of the Emerging Role of Prolidase in Cellular Metabolism.
Misiura M, Miltyk W. Misiura M, et al. Int J Mol Sci. 2020 Aug 17;21(16):5906. doi: 10.3390/ijms21165906. Int J Mol Sci. 2020. PMID: 32824561 Free PMC article. Review.
Prolidase [EC 3.4.13.9], known as PEPD, cleaves di- and tripeptides containing carboxyl-terminal proline or hydroxyproline. ...PEPD also participates in the maturation of the interferon alpha/beta receptor by regulating its expression. In addition to the biological effects …
Prolidase [EC 3.4.13.9], known as PEPD, cleaves di- and tripeptides containing carboxyl-terminal proline or hydroxyproline. ...PEPD a …
Leg ulcers secondary to prolidase deficiency.
Trent JT, Kirsner RS. Trent JT, et al. Adv Skin Wound Care. 2004 Nov-Dec;17(9):468-72. doi: 10.1097/00129334-200411000-00011. Adv Skin Wound Care. 2004. PMID: 15632738 Review. No abstract available.
Rare diseases that mimic Systemic Lupus Erythematosus (Lupus mimickers).
Chasset F, Richez C, Martin T, Belot A, Korganow AS, Arnaud L. Chasset F, et al. Joint Bone Spine. 2019 Mar;86(2):165-171. doi: 10.1016/j.jbspin.2018.10.007. Epub 2018 Oct 26. Joint Bone Spine. 2019. PMID: 30837156 Review.
Some of these "SLE mimickers" are very common, such as rosacea which can be mistaken for the butterfly rash, while others such as Kikuchi disease, type-1 interferonopathies, Castleman's disease, prolidase deficiency, angioimmunoblastic T-cell lymphoma, Evans' syndro …
Some of these "SLE mimickers" are very common, such as rosacea which can be mistaken for the butterfly rash, while others such as Kikuchi di …
Prolidase deficiency and the biochemical assays used in its diagnosis.
Kurien BT, Patel NC, Porter AC, D'Souza A, Miller D, Matsumoto H, Wang H, Scofield RH. Kurien BT, et al. Anal Biochem. 2006 Feb 15;349(2):165-75. doi: 10.1016/j.ab.2005.10.018. Epub 2005 Oct 27. Anal Biochem. 2006. PMID: 16298326 Review. No abstract available.
17 results