Proline metabolism and microenvironmental stress

JM Phang, WEI Liu, O Zabirnyk - Annual review of nutrition, 2010 - annualreviews.org
Proline, the only proteinogenic secondary amino acid, is metabolized by its own family of
enzymes responding to metabolic stress and participating in metabolic signaling. Collagen …

The metabolism of proline, a stress substrate, modulates carcinogenic pathways

JM Phang, SP Donald, J Pandhare, Y Liu - Amino acids, 2008 - Springer
The resurgence of interest in tumor metabolism has led investigators to emphasize the
metabolism of proline as a “stress substrate” and to suggest this pathway as a potential anti …

[图书][B] Amino acids: biochemistry and nutrition

G Wu - 2021 - taylorfrancis.com
Following its predecessor, the second edition of Amino Acids: Biochemistry and Nutrition
presents exhaustive coverage of amino acids in the nutrition, metabolism and health of …

Prolidase-dependent regulation of collagen biosynthesis

A Surazynski, W Miltyk, J Palka, JM Phang - Amino acids, 2008 - Springer
Abstract Prolidase [EC. 3.4. 13.9] is a cytosolic imidodipeptidase, which specifically splits
imidodipeptides with C-terminal proline or hydroxyproline. The enzyme plays an important …

Clinical genetics of prolidase deficiency: an updated review

M Spodenkiewicz, M Spodenkiewicz, M Cleary… - Biology, 2020 - mdpi.com
Prolidase is a ubiquitous enzyme that plays a major role in the metabolism of proline-rich
proteins. Prolidase deficiency is a rare autosomal recessive inborn metabolic and …

[HTML][HTML] Proline metabolism and cancer

JM Phang, W Liu - Frontiers in bioscience (Landmark edition), 2012 - ncbi.nlm.nih.gov
Proline plays a special role in cancer metabolism. Proline oxidase (POX), aka proline
dehydrogenase (PRODH), is among a few genes induced rapidly and robustly by P53, the …

Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins

N Alrumayyan, D Slauenwhite, SM McAlpine… - Allergy, Asthma & …, 2022 - Springer
Background Prolidase deficiency (PD) is an autosomal recessive inborn multisystemic
disease caused by mutations in the PEPD gene encoding the enzyme prolidase D, leading …

Prolidase–a protein with many faces

P Wilk, E Wątor, MS Weiss - Biochimie, 2021 - Elsevier
Prolidase is a metal-dependent peptidase specialized in the cleavage of dipeptides
containing proline or hydroxyproline on their C-termini. Prolidase homologues are found in …

Prolidase stimulates proliferation and migration through activation of the PI3K/Akt/mTOR signaling pathway in human keratinocytes

M Misiura, W Baszanowska, I Ościłowska… - International Journal of …, 2020 - mdpi.com
Recent reports have indicated prolidase (PEPD) as a ligand of the epidermal growth factor
receptor (EGFR). Since this receptor is involved in the promotion of cell proliferation, growth …

Correlated mutations: a hallmark of phenotypic amino acid substitutions

A Kowarsch, A Fuchs, D Frishman… - PLoS computational …, 2010 - journals.plos.org
Point mutations resulting in the substitution of a single amino acid can cause severe
functional consequences, but can also be completely harmless. Understanding what …