1 - 1 |
AAA plus proteins Lupas AN, Martin J, Zwickl P |
2 - 11 |
Classification of AAA+ proteins Ammelburg M, Frickey T, Lupas AN |
12 - 28 |
Going through the motions: The ATPase cycle of p97 Pye VE, Dreveny I, Briggs LC, Sands C, Beuron F, Zhang XD, Freemont PS |
29 - 40 |
Diverse functions with a common regulator: Ubiquitin takes command of an AAA ATPase Ye YH |
41 - 49 |
A conserved role of Caenorhabditis elegans CDC-48 in ER-associated protein degradation Mouysset J, Kahler C, Hoppe T |
50 - 61 |
Cdc48 is required for the stability of Cut1/separase in mitotic anaphase Ikai N, Yanagida M |
62 - 71 |
The Arabidopsis thaliana AAA protein CDC48A interacts in vivo with the somatic embryogenesis receptor-like kinase 1 receptor at the plasma membrane Aker J, Borst JW, Karlova R, de Vries S |
72 - 83 |
Proteasomes and their associated ATPases: A destructive combination Smith DM, Benaroudj N, Goldberg A |
84 - 92 |
Functional and structural characterization of the Methanosarcina mazei proteasome and PAN complexes Medalia N, Sharon M, Martinez-Arias R, Mihalache O, Robinson CV, Medalia O, Zwickl P |
93 - 100 |
Mutational analysis of the functional motifs in the ATPase domain of Caenorhabditis elegans fidgetin homologue FIGL-1: Firm evidence for an intersubunit catalysis mechanism of ATP hydrolysis by AAA ATPases Yakushiji Y, Nishikori S, Yamanaka K, Ogura T |
101 - 108 |
Substrate specific consequences of central pore mutations in the i-AAA protease Yme1 on substrate engagement Graef M, Langer T |
109 - 114 |
Characterization of mutants of the Escherichia coli AAA protease, FtsH, carrying a mutation in the central pore region Okuno T, Yamanaka K, Ogura T |
115 - 119 |
Flavodoxin, a new fluorescent substrate for monitoring proteolytic activity of FtsH lacking a robust unfolding activity Okuno T, Yamanaka K, Ogura T |
120 - 129 |
Characterization of a new AAA plus protein from archaea Summer H, Bruderer R, Weber-Ban E |
130 - 138 |
Characterization of AMA, a new AAA protein from Archaeoglobus and methanogenic archaea Djuranovic S, Rockel B, Lupas AN, Martin J |
139 - 148 |
The molecular chaperone Hsp 104 - A molecular machine for protein disaggregation Bosl B, Grimminger V, Walter S |
149 - 164 |
Structure and function of Hsp78, the mitochondrial C1pB homolog Leidhold C, von Janowsky B, Becker D, Bender T, Voos W |
165 - 174 |
Crystal structure at 1.9 angstrom of E-coli ClpP with a peptide covalently bound at the active site Szyk A, Maurizi MR |
175 - 181 |
Autoinhibitory and other autoregulatory elements within the dynein motor domain Vallee RB, Hook P |
182 - 189 |
Head-head coordination is required for the processive motion of cytoplasmic dynein, an AAA(+) molecular motor Shima T, Imamula K, Kon T, Ohkura R, Sutoh K |
190 - 199 |
Structures and organisation of AAA plus enhancer binding proteins in transcriptional activation Schumacher J, Joly N, Rappas M, Zhang XD, Buck M |
200 - 209 |
MoxR AAA+ ATPases: A novel family of molecular chaperones? Snider J, Houry WA |
210 - 219 |
Structural studies of the archaeal MCM complex in different functional states Costa A, Pape T, van Heel M, Brick P, Patwardhan A, Onesti S |
220 - 229 |
An isolated Hda-clamp complex is functional in the regulatory inactivation of DnaA and DNA replication Kawakami H, Su'etsugu M, Katayama T |
230 - 243 |
Modeling AAA+ ring complexes from monomeric structures Diemand AV, Lupas AN |