A citation-based method for searching scientific literature

Steffen Augustin, Florian Gerdes, Sukyeong Lee, Francis T F Tsai, Thomas Langer, Takashi Tatsuta. Mol Cell 2009
Times Cited: 74







List of co-cited articles
828 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


AAA+ proteins: have engine, will work.
Phyllis I Hanson, Sidney W Whiteheart. Nat Rev Mol Cell Biol 2005
803
41

Rebuilt AAA + motors reveal operating principles for ATP-fuelled machines.
Andreas Martin, Tania A Baker, Robert T Sauer. Nature 2005
273
37

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.
Mark Nolden, Sarah Ehses, Mirko Koppen, Andrea Bernacchia, Elena I Rugarli, Thomas Langer. Cell 2005
276
31

Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.
Mirko Koppen, Metodi D Metodiev, Giorgio Casari, Elena I Rugarli, Thomas Langer. Mol Cell Biol 2007
133
31

Evolutionary relationships and structural mechanisms of AAA+ proteins.
Jan P Erzberger, James M Berger. Annu Rev Biophys Biomol Struct 2006
516
29

Pore loops of the AAA+ ClpX machine grip substrates to drive translocation and unfolding.
Andreas Martin, Tania A Baker, Robert T Sauer. Nat Struct Mol Biol 2008
192
28

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.
G Casari, M De Fusco, S Ciarmatori, M Zeviani, M Mora, P Fernandez, G De Michele, A Filla, S Cocozza, R Marconi,[...]. Cell 1998
600
27

m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria.
Takashi Tatsuta, Steffen Augustin, Mark Nolden, Björn Friedrichs, Thomas Langer. EMBO J 2007
86
25

Evolutionary history and higher order classification of AAA+ ATPases.
Lakshminarayan M Iyer, Detlef D Leipe, Eugene V Koonin, L Aravind. J Struct Biol 2004
556
25

Structures of asymmetric ClpX hexamers reveal nucleotide-dependent motions in a AAA+ protein-unfolding machine.
Steven E Glynn, Andreas Martin, Andrew R Nager, Tania A Baker, Robert T Sauer. Cell 2009
197
25

Structure of the whole cytosolic region of ATP-dependent protease FtsH.
Ryoji Suno, Hajime Niwa, Daisuke Tsuchiya, Xiaodong Zhang, Masasuke Yoshida, Kosuke Morikawa. Mol Cell 2006
102
24


Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.
Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali,[...]. Nat Genet 2010
210
24


Loops in the central channel of ClpA chaperone mediate protein binding, unfolding, and translocation.
Jörg Hinnerwisch, Wayne A Fenton, Krystyna J Furtak, George W Farr, Arthur L Horwich. Cell 2005
189
21

Mechanism of DNA translocation in a replicative hexameric helicase.
Eric J Enemark, Leemor Joshua-Tor. Nature 2006
380
21

Membrane protein degradation by AAA proteases in mitochondria: extraction of substrates from either membrane surface.
K Leonhard, B Guiard, G Pellecchia, A Tzagoloff, W Neupert, T Langer. Mol Cell 2000
142
20

Asymmetric interactions of ATP with the AAA+ ClpX6 unfoldase: allosteric control of a protein machine.
Greg L Hersch, Randall E Burton, Daniel N Bolon, Tania A Baker, Robert T Sauer. Cell 2005
131
20


AAA+ proteases: ATP-fueled machines of protein destruction.
Robert T Sauer, Tania A Baker. Annu Rev Biochem 2011
467
20

Structure and function of the AAA+ nucleotide binding pocket.
Petra Wendler, Susanne Ciniawsky, Malte Kock, Sebastian Kube. Biochim Biophys Acta 2012
179
20

The crystal structure of apo-FtsH reveals domain movements necessary for substrate unfolding and translocation.
Christoph Bieniossek, Barbara Niederhauser, Ulrich M Baumann. Proc Natl Acad Sci U S A 2009
60
23

Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration.
Francesca Maltecca, Raffaella Magnoni, Federica Cerri, Gregory A Cox, Angelo Quattrini, Giorgio Casari. J Neurosci 2009
76
17

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia.
Luigia Atorino, Laura Silvestri, Mirko Koppen, Laura Cassina, Andrea Ballabio, Roberto Marconi, Thomas Langer, Giorgio Casari. J Cell Biol 2003
191
17

Structure of the mitochondrial inner membrane AAA+ protease YME1 gives insight into substrate processing.
Cristina Puchades, Anthony J Rampello, Mia Shin, Christopher J Giuliano, R Luke Wiseman, Steven E Glynn, Gabriel C Lander. Science 2017
107
17

The mitochondrial protease AFG3L2 is essential for axonal development.
Francesca Maltecca, Asadollah Aghaie, David G Schroeder, Laura Cassina, Benjamin A Taylor, Sandra J Phillips, Mariachiara Malaguti, Stefano Previtali, Jean-Louis Guénet, Angelo Quattrini,[...]. J Neurosci 2008
78
16


Autocatalytic processing of m-AAA protease subunits in mitochondria.
Mirko Koppen, Florian Bonn, Sarah Ehses, Thomas Langer. Mol Biol Cell 2009
37
32

Conserved pore residues in the AAA protease FtsH are important for proteolysis and its coupling to ATP hydrolysis.
Tomoko Yamada-Inagawa, Takashi Okuno, Kiyonobu Karata, Kunitoshi Yamanaka, Teru Ogura. J Biol Chem 2003
104
16


The molecular architecture of the metalloprotease FtsH.
Christoph Bieniossek, Thomas Schalch, Mario Bumann, Markus Meister, Reto Meier, Ulrich Baumann. Proc Natl Acad Sci U S A 2006
110
16

Thermotolerance requires refolding of aggregated proteins by substrate translocation through the central pore of ClpB.
Jimena Weibezahn, Peter Tessarz, Christian Schlieker, Regina Zahn, Zeljka Maglica, Sukyeong Lee, Hanswalter Zentgraf, Eilika U Weber-Ban, David A Dougan, Francis T F Tsai,[...]. Cell 2004
352
16

Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease.
Sukyeong Lee, Steffen Augustin, Takashi Tatsuta, Florian Gerdes, Thomas Langer, Francis T F Tsai. J Biol Chem 2011
43
27

Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.
Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F Cherukuri, Jamie K Teer, Nancy F Hansen, Pedro Cruz, James C Mullikin For The Nisc Comparative Sequencing Program, Robert W Blakesley,[...]. PLoS Genet 2011
137
16

Chaperone-like activity of the AAA domain of the yeast Yme1 AAA protease.
K Leonhard, A Stiegler, W Neupert, T Langer. Nature 1999
162
14

Central pore residues mediate the p97/VCP activity required for ERAD.
Byron DeLaBarre, John C Christianson, Ron R Kopito, Axel T Brunger. Mol Cell 2006
166
14


Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.
Florian Bonn, Takashi Tatsuta, Carmelina Petrungaro, Jan Riemer, Thomas Langer. EMBO J 2011
54
20

UCSF Chimera--a visualization system for exploratory research and analysis.
Eric F Pettersen, Thomas D Goddard, Conrad C Huang, Gregory S Couch, Daniel M Greenblatt, Elaine C Meng, Thomas E Ferrin. J Comput Chem 2004
14

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.
Fatima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Valentina Valsecchi, Giorgia Dina, Vania Broccoli, Alberto Auricchio, Fiorella Piemonte, Giulia Tozzi, Laura Gaeta,[...]. J Clin Invest 2004
206
13


SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.
Claudia Cagnoli, Caterina Mariotti, Franco Taroni, Marco Seri, Alessandro Brussino, Chiara Michielotto, Marina Grisoli, Daniela Di Bella, Nicola Migone, Cinzia Gellera,[...]. Brain 2006
82
13


Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1.
Sarah Ehses, Ines Raschke, Giuseppe Mancuso, Andrea Bernacchia, Stefan Geimer, Daniel Tondera, Jean-Claude Martinou, Benedikt Westermann, Elena I Rugarli, Thomas Langer. J Cell Biol 2009
372
13


Crystal structures of the HslVU peptidase-ATPase complex reveal an ATP-dependent proteolysis mechanism.
J Wang, J J Song, M C Franklin, S Kamtekar, Y J Im, S H Rho, I S Seong, C S Lee, C H Chung, S H Eom. Structure 2001
203
13



ATP-dependent proteases of bacteria: recognition logic and operating principles.
Tania A Baker, Robert T Sauer. Trends Biochem Sci 2006
198
12



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.