Uroporphyrinogen III Synthase Mutations Related to Congenital Erythropoietic Porphyria Identify a Key Helix for Protein Stability-Reference-Cited by-同舟云学术

Uroporphyrinogen III Synthase Mutations Related to Congenital Erythropoietic Porphyria Identify a Key Helix for Protein Stability

Published:2008-12-19 Issue:2 Volume:48 Page:454-461
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Fortian Arola¹,Castaño David¹,Ortega Gabriel¹,Laín Ana¹,Pons Miquel¹,Millet Oscar¹

Affiliation:

1. Structural Biology Unit, CIC bioGUNE, Bizkaia Technology Park, Building 800, 48160 Derio, Spain, and Institute of Research in Biomedicine, Parc Científic de Barcelona, Josep Samitier 1-5, Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi801731q

Reference40 articles.

1. Structural diversity in metal ion chelation and the structure of uroporphyrinogen III synthase

2. Tetrapyrroles: the pigments of life

3. Comparative Density Functional Study of Models for the Reaction Mechanism of Uroporphyrinogen III Synthase

4. Congenital erythropoietic porphyria: advances in pathogenesis and treatment

5. Human Gene Mutation Database: towards a comprehensive central mutation database

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