Articles - 1q6x mentioned but not cited (5)
- Averaged kick maps: less noise, more signal... and probably less bias. Pražnikar J, Afonine PV, Guncar G, Adams PD, Turk D. Acta Crystallogr D Biol Crystallogr 65 921-931 (2009)
- Choline acetyltransferase structure reveals distribution of mutations that cause motor disorders. Cai Y, Cronin CN, Engel AG, Ohno K, Hersh LB, Rodgers DW. EMBO J 23 2047-2058 (2004)
- An environment-dependent structural switch underlies the regulation of carnitine palmitoyltransferase 1A. Rao JN, Warren GZL, Estolt-Povedano S, Zammit VA, Ulmer TS. J Biol Chem 286 42545-42554 (2011)
- CSmetaPred: a consensus method for prediction of catalytic residues. Choudhary P, Kumar S, Bachhawat AK, Pandit SB. BMC Bioinformatics 18 583 (2017)
- Complex fitness landscape shapes variation in a hyperpolymorphic species. Stolyarova AV, Neretina TV, Zvyagina EA, Fedotova AV, Kondrashov AS, Bazykin GA. Elife 11 e76073 (2022)
Reviews citing this publication (6)
- What have we learned from the congenital myasthenic syndromes. Engel AG, Shen XM, Selcen D, Sine SM. J Mol Neurosci 40 143-153 (2010)
- Congenital myasthenic syndromes. Hantaï D, Richard P, Koenig J, Eymard B. Curr Opin Neurol 17 539-551 (2004)
- Allosteric conformational barcodes direct signaling in the cell. Nussinov R, Ma B, Tsai CJ, Csermely P. Structure 21 1509-1521 (2013)
- Structural insight into function and regulation of carnitine palmitoyltransferase. Rufer AC, Thoma R, Hennig M. Cell Mol Life Sci 66 2489-2501 (2009)
- A model for dynamic regulation of choline acetyltransferase by phosphorylation. Dobransky T, Rylett RJ. J Neurochem 95 305-313 (2005)
- Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes. Barišić N, Chaouch A, Müller JS, Lochmüller H. Eur J Paediatr Neurol 15 189-196 (2011)
Articles citing this publication (27)
- Chemical transmission in the sea anemone Nematostella vectensis: A genomic perspective. Anctil M. Comp Biochem Physiol Part D Genomics Proteomics 4 268-289 (2009)
- Identification of 16 new disease-causing mutations in the CPT2 gene resulting in carnitine palmitoyltransferase II deficiency. Isackson PJ, Bennett MJ, Vladutiu GD. Mol Genet Metab 89 323-331 (2006)
- Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Schara U, Christen HJ, Durmus H, Hietala M, Krabetz K, Rodolico C, Schreiber G, Topaloglu H, Talim B, Voss W, Pihko H, Abicht A, Müller JS, Lochmüller H. Eur J Paediatr Neurol 14 326-333 (2010)
- Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants. Barisic N, Müller JS, Paucic-Kirincic E, Gazdik M, Lah-Tomulic K, Pertl A, Sertic J, Zurak N, Lochmüller H, Abicht A. Eur J Paediatr Neurol 9 7-12 (2005)
- Rat choline acetyltransferase of the peripheral type differs from that of the common type in intracellular translocation. Matsuo A, Bellier JP, Hisano T, Aimi Y, Yasuhara O, Tooyama I, Saito N, Kimura H. Neurochem Int 46 423-433 (2005)
- Functional consequences and structural interpretation of mutations of human choline acetyltransferase. Shen XM, Crawford TO, Brengman J, Acsadi G, Iannaconne S, Karaca E, Khoury C, Mah JK, Edvardson S, Bajzer Z, Rodgers D, Engel AG. Hum Mutat 32 1259-1267 (2011)
- Nuclear choline acetyltransferase activates transcription of a high-affinity choline transporter. Matsuo A, Bellier JP, Nishimura M, Yasuhara O, Saito N, Kimura H. J Biol Chem 286 5836-5845 (2011)
- Therapeutic hypothermia achieves neuroprotection via a decrease in acetylcholine with a concurrent increase in carnitine in the neonatal hypoxia-ischemia. Takenouchi T, Sugiura Y, Morikawa T, Nakanishi T, Nagahata Y, Sugioka T, Honda K, Kubo A, Hishiki T, Matsuura T, Hoshino T, Takahashi T, Suematsu M, Kajimura M. J Cereb Blood Flow Metab 35 794-805 (2015)
- Crystal structure of mouse carnitine octanoyltransferase and molecular determinants of substrate selectivity. Jogl G, Hsiao YS, Tong L. J Biol Chem 280 738-744 (2005)
- Crystal structures of murine carnitine acetyltransferase in ternary complexes with its substrates. Hsiao YS, Jogl G, Tong L. J Biol Chem 281 28480-28487 (2006)
- Hyaluronic acid-based hydrogel enhances neuronal survival in spinal cord slice cultures from postnatal mice. Schizas N, Rojas R, Kootala S, Andersson B, Pettersson J, Hilborn J, Hailer NP. J Biomater Appl 28 825-836 (2014)
- Protein kinase C isoforms differentially phosphorylate human choline acetyltransferase regulating its catalytic activity. Dobransky T, Doherty-Kirby A, Kim AR, Brewer D, Lajoie G, Rylett RJ. J Biol Chem 279 52059-52068 (2004)
- Saccharomyces cerevisiae Atf1p is an alcohol acetyltransferase and a thioesterase in vitro. Nancolas B, Bull ID, Stenner R, Dufour V, Curnow P. Yeast 34 239-251 (2017)
- Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations. Arredondo J, Lara M, Gospe SM, Mazia CG, Vaccarezza M, Garcia-Erro M, Bowe CM, Chang CH, Mezei MM, Maselli RA. Hum Mutat 36 881-893 (2015)
- Crystal structure of homoserine O-acetyltransferase from Leptospira interrogans. Wang M, Liu L, Wang Y, Wei Z, Zhang P, Li Y, Jiang X, Xu H, Gong W. Biochem Biophys Res Commun 363 1050-1056 (2007)
- Development of the caudal nerve cord, motoneurons, and muscle innervation in the appendicularian urochordate Oikopleura dioica. Søviknes AM, Chourrout D, Glover JC. J Comp Neurol 503 224-243 (2007)
- Identification of a mutation in the CHAT gene of Old Danish Pointing Dogs affected with congenital myasthenic syndrome. Proschowsky HF, Flagstad A, Cirera S, Joergensen CB, Fredholm M. J Hered 98 539-543 (2007)
- Nuclear 82-kDa choline acetyltransferase decreases amyloidogenic APP metabolism in neurons from APP/PS1 transgenic mice. Albers S, Inthathirath F, Gill SK, Winick-Ng W, Jaworski E, Wong DY, Gros R, Rylett RJ. Neurobiol Dis 69 32-42 (2014)
- The production of antibodies that distinguish rat choline acetyltransferase from its splice variant product of a peripheral type. Kimura S, Bellier JP, Matsuo A, Tooyama I, Kimura H. Neurochem Int 50 251-255 (2007)
- Illumination with 630 nm Red Light Reduces Oxidative Stress and Restores Memory by Photo-Activating Catalase and Formaldehyde Dehydrogenase in SAMP8 Mice. Zhang J, Yue X, Luo H, Jiang W, Mei Y, Ai L, Gao G, Wu Y, Yang H, An J, Ding S, Yang X, Sun B, Luo W, He R, Jia J, Lyu J, Tong Z. Antioxid Redox Signal 30 1432-1449 (2019)
- First visualization of cholinergic cells and fibers by immunohistochemistry for choline acetyltransferase of the common type in the optic lobe and peduncle complex of Octopus vulgaris. D'Este L, Kimura S, Casini A, Matsuo A, Bellier JP, Kimura H, Renda TG. J Comp Neurol 509 566-579 (2008)
- Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic kadazandusun family. Tan JS, Ambang T, Ahmad-Annuar A, Rajahram GS, Wong KT, Goh KJ. Muscle Nerve 53 822-826 (2016)
- Two methods for large-scale purification of recombinant human choline acetyltransferase. Kim AR, Doherty-Kirby A, Lajoie G, Rylett RJ, Shilton BH. Protein Expr Purif 40 107-117 (2005)
- CHAT gene polymorphism rs3810950 is associated with the risk of Alzheimer's disease in the Czech population. Hálová A, Janoutová J, Ewerlingová L, Janout V, Bonczek O, Zeman T, Gerguri T, Balcar VJ, Šerý O. J Biomed Sci 25 41 (2018)
- Mutation of a serine near the catalytic site of the choline acetyltransferase a gene almost completely abolishes motility of the zebrafish embryo. Joshi S, Virdi S, Etard C, Geisler R, Strähle U. PLoS One 13 e0207747 (2018)
- Toxicological Study and Genetic Basis of BTEX Susceptibility in Drosophila melanogaster. Adebambo TH, Fox DT, Otitoloju AA. Front Genet 11 594179 (2020)
- Analysis of Caenorhabditis elegans acetylcholine synthesis mutants reveals a temperature-sensitive requirement for cholinergic neuromuscular function. Duerr JS, McManus JR, Crowell JA, Rand JB. Genetics 218 iyab078 (2021)