Citations for
1AARS1, METTL21C
Methyltransferase-like 21C (METTL21C) methylates alanine tRNA synthetase at Lys-943 in muscle tissue
Zoabi M, Zhang L, Li TM, Elias JE, Carlson SM, Gozani O.
J Biol Chem. Aug 14;295(33):11822-11832. doi: 10.1074/jbc.RA120.014505. Epub 2020 Jul 1. 2020
2AARS1, EIEPN
Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect.
Simons C, Griffin LB, Helman G, Golas G, Pizzino A, Bloom M, Murphy JL, Crawford J, Evans SH, Topper S, Whitehead MT, Schreiber JM, Chapman KA, Tifft C, Lu KB, Gamper H, Shigematsu M, Taft RJ, Antonellis A, Hou YM, Vanderver A.
Am J Hum Genet 96(4):675-81. doi: 10.1016/j.ajhg.2015.02.012. Epub 2015 Mar 26. 2015
3AARS1
Deficiencies in tRNA synthetase editing activity cause cardioproteinopathy.
Liu Y, Satz JS, Vo MN, Nangle LA, Schimmel P, Ackerman SL.
Proc Natl Acad Sci U S A 111(49):17570-5. doi: 10.1073/pnas.1420196111. Epub 2014 Nov 24. 2014
4AARS1, CMT2N
A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).
McLaughlin HM, Sakaguchi R, Giblin W; NISC Comparative Sequencing Program, Wilson TE, Biesecker L, Lupski JR, Talbot K, Vance JM, Züchner S, Lee YC, Kennerson M, Hou YM, Nicholson G, Antonellis A.
Hum Mutat 33(1):244-53. doi: 10.1002/humu.21635. Epub 2011 Nov 9. 2012
5AARS1, DICTM3
Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy.
Zhao Z, Hashiguchi A, Hu J, Sakiyama Y, Okamoto Y, Tokunaga S, Zhu L, Shen H, Takashima H.
Neurology 78(21):1644-9. doi: 10.1212/WNL.0b013e3182574f8f. Epub 2012 May 9. 2012
6AARS1, DICTM3
An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations.
Stum M, McLaughlin HM, Kleinbrink EL, Miers KE, Ackerman SL, Seburn KL, Antonellis A, Burgess RW.
Mol Cell Neurosci 46(2):432-43. doi: 10.1016/j.mcn.2010.11.006. Epub 2010 Nov 27. 2011
7AARS1, CMT2N, DICMT3
A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal charcot-marie-tooth disease.
Latour P, Thauvin-Robinet C, Baudelet-Méry C, Soichot P, Cusin V, Faivre L, Locatelli MC, Mayençon M, Sarcey A, Broussolle E, Camu W, David A, Rousson R.
Am J Hum Genet 86(1):77-82. Epub 2009 Dec 31.PMID: 20045102 2010
8AARS1
The structure of alanyl-tRNA synthetase with editing domain.
Sokabe M, Ose T, Nakamura A, Tokunaga K, Nureki O, Yao M, Tanaka I.
Proc Natl Acad Sci U S A 106(27):11028-33. doi: 10.1073/pnas.0904645106. Epub 2009 Jun 19. 2009
9AARS1, EEF1A2
An aminoacyl-tRNA synthetase:elongation factor complex for substrate channeling in archaeal translation.
Hausmann CD, Praetorius-Ibba M, Ibba M.
Nucleic Acids Res 35(18):6094-102. Epub 2007 Sep 1. 2007
10AARS1
An unusual pattern of protein expression and localization of yeast alanyl-tRNA synthetase isoforms.
Huang HY, Tang HL, Chao HY, Yeh LS, Wang CC.
Mol Microbiol 60(1):189-98. 2006
11AARS1
Alanyl-tRNA synthetase crystal structure and design for acceptor-stem recognition.
Swairjo MA, Otero FJ, Yang XL, Lovato MA, Skene RJ, McRee DE, Ribas de Pouplana L, Schimmel P.
Mol Cell 13(6):829-41. 2004
12AARS1, EEF1A1, EEF1D, EPRS, LARS
Interaction network of human aminoacyl-tRNA synthetases and subunits of elongation factor 1 complex.
Sang Lee J, Gyu Park S, Park H, Seol W, Lee S, Kim S.
Biochem Biophys Res Commun 291(1):158-64. 2002
13AARS1, GARS, GART
Localization of two human autoantigen genes by PCR screening and in situ hybridization - glycyl-tRNA synthetase locates to 7p15 and alanyl-tRNA synthetase locates to 16q22.
Nichols RC, et al.
Genomics 30 : 131-132. 1995