Literature DB >> 1029019

Studies on a patient with iminopeptiduria. I. Identification of urinary iminopeptides.

H Kodama, S Umemura, M Shimomura, S Mizuhara, J Arata, Y Yamamoto, A Yasutake, N Izumiya.   

Abstract

A patient suffering from recurrent ulcers on the legs was found to excrete large amounts of iminodipeptides in the urine. Among the iminodipeptides excreted, Glu-Hyp, Asp-Pro, Glu-Pro, Leu-Hyp, Gly-Pro, Thr-Pro, Ser-Pro, Ala-Pro, Val-Pro, Ile-Pro, Leu-Pro, and Phe-Pro were identified and their quantities estimated. Some of the iminopeptides had to be synthesized for purposes of identification.

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Year:  1976        PMID： 1029019

Source DB:  PubMed          Journal:  Physiol Chem Phys        ISSN： 0031-9325


  6 in total

1.  Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiency.

Authors:  P M Royce; D M Danks
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

2.  Screening method for prolidase deficiency.

Authors:  F Endo; I Matsuda
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Prolidase activity dysregulation and its correlation with oxidative-antioxidative status in chronic obstructive pulmonary disease.

Authors:  Mehmet Gencer; Nurten Aksoy; E Canan Dagli; Elmas Uzer; Sahin Aksoy; Sahbettin Selek; Hakim Celik; Hale Cakir
Journal:  J Clin Lab Anal       Date:  2011       Impact factor: 2.352

4.  Biochemical studies on prolidase in sera from control, patients with prolidase deficiency and their mother.

Authors:  T Ohhashi; T Ohno; J Arata; H Kodama
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

5.  Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria).

Authors:  I Lombeck; U Wendel; J Versieck; L van Ballenberghe; H J Bremer; R Duran; S Wadman
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

6.  Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases.

Authors:  Francis Rossignol; Marvid S Duarte Moreno; Carlos R Ferreira; Manuel Schiff; Jean-François Benoist; Manfred Boehm; Emmanuelle Bourrat; Aline Cano; Brigitte Chabrol; Claudine Cosson; José Luís Dapena Díaz; Arthur D'Harlingue; David Dimmock; Alexandra F Freeman; María Tallón García; Cheryl Garganta; Tobias Goerge; Sara S Halbach; Jan de Laffolie; Christina T Lam; Ludovic Martin; Esmeralda Martins; Andrea Meinhardt; Isabelle Melki; Amanda K Ombrello; Noémie Pérez; Dulce Quelhas; Anna Scott; Anne M Slavotinek; Ana Rita Soares; Sarah L Stein; Kira Süßmuth; Jenny Thies
Journal:  Genet Med       Date:  2021-05-26       Impact factor: 8.822
  6 in total

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