PMC Links for Protein (Select 109148542) - PMC

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Items: 15

Select item 64511231.

The G3-U70-independent tRNA recognition by human mitochondrial alanyl-tRNA synthetase

Qi-Yu Zeng, Gui-Xin Peng, Guang Li, Jing-Bo Zhou, Wen-Qiang Zheng, Mei-Qin Xue, En-Duo Wang, Xiao-Long Zhou

Nucleic Acids Res. 2019 Apr 8; 47(6): 3072–3085. Published online 2019 Feb 14. doi: 10.1093/nar/gkz078

PMCID:: PMC6451123

Abstract Article PDF–3.5M

Select item 62407302.

Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities

Marian A J Weterman, Molly Kuo, Susan B Kenter, Sara Gordillo, Dyah W Karjosukarso, Ryuichi Takase, Marieke Bronk, Stephanie Oprescu, Fred van Ruissen, Ron J W Witteveen, Henriette M E Bienfait, Martijn Breuning, Camiel Verhamme, Ya-Ming Hou, Marianne de Visser, Anthony Antonellis, Frank Baas

Hum Mol Genet. 2018 Dec 1; 27(23): 4036–4050. Published online 2018 Aug 14. doi: 10.1093/hmg/ddy290

PMCID:: PMC6240730

Abstract Article PDF–20M

Select item 51671783.

Two crystal structures reveal design for repurposing the C-Ala domain of human AlaRS

Litao Sun, Youngzee Song, David Blocquel, Xiang-Lei Yang, Paul Schimmel

Proc Natl Acad Sci U S A. 2016 Dec 13; 113(50): 14300–14305. Published online 2016 Nov 28. doi: 10.1073/pnas.1617316113

PMCID:: PMC5167178

Abstract Article PDF–1.3M

Select item 418214.

Wide cross-species aminoacyl-tRNA synthetase replacement in vivo: yeast cytoplasmic alanine enzyme replaced by human polymyositis serum antigen.

T L Ripmaster, K Shiba, P Schimmel

Proc Natl Acad Sci U S A. 1995 May 23; 92(11): 4932–4936. doi: 10.1073/pnas.92.11.4932

PMCID:: PMC41821

Summary Page Browse PDF–1.9M

Select item 68806225.

RU486 Metabolite Inhibits CCN1/Cyr61 Secretion by MDA-MB-231-Endothelial Adhesion

Suhong Yu, Cuicui Yan, Wenjing Wu, Sudan He, Min Liu, Jian Liu, Xingtian Yang, Ji Ma, Yusheng Lu, Lee Jia

Front Pharmacol. 2019; 10: 1296. Published online 2019 Nov 20. doi: 10.3389/fphar.2019.01296

PMCID:: PMC6880622

Abstract Article PDF–6.3M

Select item 68804946.

An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

Christina Sundal, Susana Carmona, Maria Yhr, Odd Almström, Maria Ljungberg, John Hardy, Carola Hedberg-Oldfors, Åsa Fred, José Brás, Anders Oldfors, Oluf Andersen, Rita Guerreiro

Acta Neuropathol Commun. 2019; 7: 188. Published online 2019 Nov 27. doi: 10.1186/s40478-019-0843-y

PMCID:: PMC6880494

Abstract Article PDF–1.5M

Select item 62099797.

Lysine Acetylation Regulates Alanyl-tRNA Synthetase Activity in Escherichia coli

Takuya Umehara, Saori Kosono, Dieter Söll, Koji Tamura

Genes (Basel) 2018 Oct; 9(10): 473. Published online 2018 Sep 28. doi: 10.3390/genes9100473

PMCID:: PMC6209979

Abstract Article PDF–2.7M

Select item 56083758.

A single Danio rerio hars gene encodes both cytoplasmic and mitochondrial histidyl-tRNA synthetases

Ashley L. Waldron, Sara Helms Cahan, Christopher S. Franklyn, Alicia M. Ebert

PLoS One. 2017; 12(9): e0185317. Published online 2017 Sep 21. doi: 10.1371/journal.pone.0185317

Correction in:: PLoS One. 2018; 13(1): e0190757.

PMCID:: PMC5608375

Abstract Article PDF–6.1M

Select item 55993419.

Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathy

Tojo Nakayama, Jiang Wu, Patricia Galvin-Parton, Jody Weiss, Mary R. Andriola, R. Sean Hill, Dylan Vaughan, Malak El-Quessny, Brenda J. Barry, Jennifer N. Partlow, A. James Barkovich, Jiqiang Ling, Ganeshwaran H. Mochida

Hum Mutat. Author manuscript; available in PMC 2018 Oct 1.

Published in final edited form as: Hum Mutat. 2017 Oct; 38(10): 1348–1354. Published online 2017 Jun 23. doi: 10.1002/humu.23250

PMCID:: PMC5599341

Abstract Article PDF–276K

Select item 496698210.

The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas

Jaimee Reck, Alexandria M. Schauer, Kristyn VanderWaal Mills, Raqual Bower, Douglas Tritschler, Catherine A. Perrone, Mary E. Porter

Mol Biol Cell. 2016 Aug 1; 27(15): 2404–2422. doi: 10.1091/mbc.E16-03-0191

PMCID:: PMC4966982

Abstract Article PDF–1.5M

Select item 493055811.

Proteomic profiling of cellular steatosis with concomitant oxidative stress in vitro

Khalida Ann Lockman, Varanand Htun, Rohit Sinha, Philipp Treskes, Leonard J. Nelson, Sarah F. Martin, Sophie M. Rogers, Thierry Le Bihan, Peter C. Hayes, John N. Plevris

Lipids Health Dis. 2016; 15: 114. Published online 2016 Jul 2. doi: 10.1186/s12944-016-0283-7

PMCID:: PMC4930558

Abstract Article PDF–781K

Select item 324069312.

A Recurrent Loss-of-Function Alanyl-tRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N)

Heather M. McLaughlin, Reiko Sakaguchi, William Giblin, NIH Intramural Sequencing Center, Thomas E. Wilson, Leslie Biesecker, James R. Lupski, Kevin Talbot, Jeffery M. Vance, Stephan Züchner, Yi-Chung Lee, Marina Kennerson, Ya-Ming Hou, Garth Nicholson, Anthony Antonellis

Hum Mutat. Author manuscript; available in PMC 2013 Jan 1.

Published in final edited form as: Hum Mutat. 2012 Jan; 33(1): 244–253. Published online 2011 Nov 9. doi: 10.1002/humu.21635

Correction in:: volume 35 on page 512

PMCID:: PMC3240693

Abstract Article PDF–527K

Select item 313675113.

Granzyme B cleavage of autoantigens in autoimmunity

Erika Darrah, Antony Rosen

Cell Death Differ. Author manuscript; available in PMC 2011 Jul 15.

Published in final edited form as: Cell Death Differ. 2010 Apr; 17(4): 624–632. Published online 2010 Jan 15. doi: 10.1038/cdd.2009.197

PMCID:: PMC3136751

Abstract Article PDF–793K

Select item 280175014.

A Major Determinant for Binding and Aminoacylation of tRNA^Ala in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease

Philippe Latour, Christel Thauvin-Robinet, Chantal Baudelet-Méry, Pierre Soichot, Veronica Cusin, Laurence Faivre, Marie-Claire Locatelli, Martine Mayençon, Annie Sarcey, Emmanuel Broussolle, William Camu, Albert David, Robert Rousson

Am J Hum Genet. 2010 Jan 8; 86(1): 77–82. doi: 10.1016/j.ajhg.2009.12.005