Asp263 missense variants perturb the active site of human phosphoglucomutase 1 (PGM1)

Những quyển sách tương tự

• Compromised Catalysis and Potential Folding Defects in in Vitro Studies of Missense Mutants Associated with Hereditary Phosphoglucomutase 1 Deficiency
  Bằng: Lee, Yingying, et al.
  Được phát hành: (2014)
• Induced structural disorder as a molecular mechanism for enzyme dysfunction in phosphoglucomutase 1 deficiency
  Bằng: Stiers, Kyle M., et al.
  Được phát hành: (2016)
• A hotspot for disease-associated variants of human PGM1 is associated with impaired ligand binding and loop dynamics
  Bằng: Stiers, Kyle M., et al.
  Được phát hành: (2018)
• Sequence-structure relationships, expression profiles, and disease-associated mutations in the paralogs of phosphoglucomutase 1
  Bằng: Muenks, Andrew G., et al.
  Được phát hành: (2017)
• The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombination.
  Bằng: March, R E, et al.
  Được phát hành: (1993)