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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/08/13 23:42:03」(JST)
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- 1. 腸球菌における抗菌薬耐性の機構 mechanisms of antibiotic resistance in enterococci
English Journal
- Identification of genes involved in rice seed priming in the early imbibition stage.
- Cheng J1, Wang L1, Zeng P1, He Y1, Zhou R1, Zhang H1, Wang Z1.
- Plant biology (Stuttgart, Germany).Plant Biol (Stuttg).2016 Feb 2. doi: 10.1111/plb.12438. [Epub ahead of print]
- Phase II of seed imbibition is a critical process during seed priming. To identify genes involved in rice seed priming, the altered proteins between the dry and imbibed (24 h) seeds were compared using a two-dimensional gel electrophoresis system in this stuy. Ten significantly changed proteins (fol
- PMID 26833720
- Structural insights into the synthesis of FMN in prokaryotic organisms.
- Herguedas B1, Lans I1, Sebastián M1, Hermoso JA2, Martínez-Júlvez M1, Medina M1.
- Acta crystallographica. Section D, Biological crystallography.Acta Crystallogr D Biol Crystallogr.2015 Dec 1;71(Pt 12):2526-42. doi: 10.1107/S1399004715019641. Epub 2015 Nov 27.
- Riboflavin kinases (RFKs) catalyse the phosphorylation of riboflavin to produce FMN. In most bacteria this activity is catalysed by the C-terminal module of a bifunctional enzyme, FAD synthetase (FADS), which also catalyses the transformation of FMN into FAD through its N-terminal FMN adenylyltransf
- PMID 26627660
- Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literature.
- Hedergott A1, Volk AE2,3, Herkenrath P4, Thiele H5, Fricke J6, Altmüller J5,7, Nürnberg P5,8,9, Kubisch C2,3, Neugebauer A6.
- Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie.Graefes Arch Clin Exp Ophthalmol.2015 Dec;253(12):2239-46. doi: 10.1007/s00417-015-3174-0. Epub 2015 Oct 13.
- BACKGROUND: Leber congenital amaurosis (LCA) is a severe retinal dystrophy, typically manifesting in the first year of life. Mutations in more than 18 genes have been reported to date. In recent studies, biallelic mutations in NMNAT1 encoding nicotinamide mononucleotide adenylyltransferase 1 have be
- PMID 26464178
Japanese Journal
- Protection of vincristine-induced neuropathy by WldS expression and the independence of the activity of Nmnat1
- Watanabe Masashi,Tsukiyama Tadasuke,Hatakeyama Shigetsugu
- Neuroscience Letters 411(3), 228-232, 2007-01-16
- … The slow Wallerian degeneration protein (WldS), a fusion protein containing amino-terminal E4B and full-length nicotinamide mononucleotide adenylyltransferase 1 (Nmnat1), delays axon degeneration caused by physical damages, toxins and genetic mutations which result in patients being diagnosed with neurodegenerative diseases. …
- NAID 120000969949
- A nicotinamide mononucleotide adenylyltransferase with unique adenylyl group donor specificity from a hyperthermophilic archaeon, Pyrococcus horikoshii OT-3
- Sakuraba H,Kanai K,Goda S,Kawarabayasi Y,Ohshima T
- JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC 23(2-6), 273-279, 2003
- NAID 120004253652
Related Links
- Definition of Adenylyltransferase with photos and pictures, translations, sample usage, and additional links for more information. ... ¹ Source: wiktionary.com Adenylyltransferase Pictures Click the following link to bring up a new ...
- For Reference Purpose Only! NMNAT2 (Nicotinamide mononucleotide adenylyltransferase 2) Product Data Sheet For Research Use Only, Not for use in diagnostic procedures Cat#: CY-E1252-2 1 Version#: 120420 NMNAT2
Related Pictures
★リンクテーブル★
| リンク元 | 「アデニル酸転移酵素」 |
| 拡張検索 | 「nicotinamide-nucleotide adenylyltransferase」「sulfate adenylyltransferase」「glucose-1-phosphate adenylyltransferase」「polynucleotide adenylyltransferase」 |
「アデニル酸転移酵素」
「nicotinamide-nucleotide adenylyltransferase」
ニコチンアミドヌクレオチドアデニル基転移酵素、ニコチンアミドヌクレオチドアデニリルトランスフェラーゼ
「sulfate adenylyltransferase」
硫酸アデニルトランスフェラーゼ、硫酸アデニリルトランスフェラーゼ