A novel ATP-dependent conformation in p97 N–D1 fragment revealed by crystal structures of disease-related mutants

Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings

(2010) Kishore R. Kumar et al.   NEUROMUSCULAR DISORDERS

Purification, crystallization and preliminary X-ray diffraction analysis of disease-related mutants of p97

(2009) Wai-Kwan Tang et al.   Acta Crystallographica Section F-Structural Biology and Crystallization Communications

Hereditary Inclusion Body Myopathy-Linked p97/VCP Mutations in the NH2 Domain and the D1 Ring Modulate p97/VCP ATPase Activity and D2 Ring Conformation

(2009) D. Halawani et al.   MOLECULAR AND CELLULAR BIOLOGY

A novel mutation in the VCP gene (G157R) in a german family with inclusion-body myopathy with paget disease of bone and frontotemporal dementia

(2009) Atbin Djamshidian et al.   MUSCLE & NERVE

UBX domain proteins: major regulators of the AAA ATPase Cdc48/p97

(2008) C. Schuberth et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

The use of blue native PAGE in the evaluation of membrane protein aggregation states for crystallization

(2008) Jichun Ma et al.   JOURNAL OF APPLIED CRYSTALLOGRAPHY

Analysis of Nucleotide Binding to P97 Reveals the Properties of a Tandem AAA Hexameric ATPase

(2008) Louise C. Briggs et al.   JOURNAL OF BIOLOGICAL CHEMISTRY