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Proteomic analysis of wild-type and mutant huntingtin-associated proteins in mouse brains identifies unique interactions and involvement in protein synthesis. 2012 J. Biol. , drives relocalization of protein phosphatase Cdc14 to the cytoplasm during exit from J. Cell , 527– of maize C4 photosynthetic development in a mesophyll cell-defective mutant. 2008 Plant , 1469–, the membrane subunit of protein phosphatase 1{beta}, signals nuclear translocation of the nuclear receptor CAR. 2008 Mol. , 1113-1121.

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一、文献类型与文献载体代码根据gb3469-83《文献类型与文献载体代码》规定,以单字母标识:m——专著(含古籍中的史、志论著)c——论文集n——报纸文章j——期刊文章d——学位论文r——研究报告s——标准p——专利a——专著、论文集中的析出文献z——其他未说明的文献类型电子文献类型以双字母作为标识:db——数据库cp——计算机程序eb——电子公告非纸张型载体电子文献,在参考文献标识中同时标明其载体类型:db/ol——联机网上的数据库db/mt——磁带数据库m/cd——光盘图书cp/dk——磁盘软件j/ol——网上期刊eb/ol——网上电子公告二、参考文献书写格式(参考文献:宋体四号字加黑,顶头)中文≥10篇,英文≥5篇(主要内容用宋体小四号不加黑,中文中标点用全角;英文符号用半角,标注说明如下)(1)杂志:[编号]姓名1,姓名2,姓名3等.文章名称[j].杂志名称,年,卷(期):页码范围.(2)书籍:[编号]姓名1,姓名2,姓名3等.书籍名称(第几版).出版地点:出版社,出版年:起止页码(第一版不标注).(3)学位论文:[编号]姓名.论文名[d].保存地点:保存单位,撰写年,页码范围.(4)会议论文集:[编号]姓名1,姓名2,姓名3等.文章题目名[c].会议名(论文集名),年份,会议地:出版者,页码范围.(5)报纸:[编号]姓名1,姓名2,姓名3等.文章题目名[n].报纸名称,出版年-月-日(版面号).(6)专利:[编号]专利所有者姓名1,姓名2,姓名3等.专利题目名[p].专利国别:专利号,出版日期.(7)电子文献:[编号]姓名1,姓名2,姓名3等.电子文献题名[载体类型].电子文献的出处或可获得地址,发表或更新日期/引用日期.载体类型:联机上网数据库(databaseonline)[db/ol];光盘网数据库(databaseoncd-rom)[db/cd];光盘图书(monographoncd-rom)[m/cd];磁盘软件(computerprogramondisk)[cp/dk];网上期刊(serialonline)[j/ol];网上电子公告(electronicbulletinboardonline)[eb/ol]参考文献:(宋体四号字加黑)(样例)[1]惠晓实,王凯航,陆舟,等.一种基于web技术的网络数据库系统设计[j].计算机应用研究,2000,17(1):84~86.[2]强文久,元章,雯荣.数学分析的基本概念与方法.北京:高等教育出版社,1989:153~167.[3]詹东风.中国漆树酶分离制备及反映功能研究[d].武汉大学博士学位论文,1998:81~89.[4][j].scientificamerican,1994,270(1):78~86.[5]buchbergerb,collinsge,~76.

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[1] Thoroson J S, Hoster T J, Jiang J, et al. Nature′s carbohydrate chemists: the enzymatic glycosylation of bioactive bacterial metabolites [J]. Curr Org Chem,2001,5(2):139[2] Weymouth?Wilson A C. The role of carbohydrates in biologically active natural products [J]. Nat Prod Rep,1997,14(2):99[3] Losey H C, Peczuh M W, Chen Z, et al. Tandem action of glycosyltransferases in the maturation of vancomycin and teicoplanin aglycones: novel glycopeptides [J]. Biochemistry,2001,40(15):4745[4] Cudic P, Kranz J K, Behenna D C, et al. Complexation of peptidoglycan intermediates by the lipoglycodepsipeptide antibiotic ramoplanin: minimal structural requirements for intermolecular complexation and fibril formation [J]. Proc Natl Acad Sci,2002,99(11):7384[5] Gellert M, O′Dea M H, Itoh T, et al. Novobiocin and coumermycin inhibit DNA supercoiling catalyzed by DNA gyrase [J]. Proc Natl Acad Sci,1976,73(12):4474[6] Sosio M, Stinchi S, Beltrametti F, et al. The gene cluster for the biosynthesis of the glycopeptide antibiotic A40926 by nonomuraea species [J]. Chem Biol,2003,10(6):541[7] Quiros L M, Aguirrezabalaga I, Olano C, et al. Two glycosyltransferases and a glycosidase are involved in oleandomycin modification during its biosynthesis by Streptomyces antibioticus [J]. Mol Microbiol,1998,28(6):1177[8] Gourmelen A, Blondelet?Rouault M H, Pernodet J L. Characterization of a glycosyl transferase inactivating macrolides, encoded by gimA from Streptomyces ambofaciens [J]. Antimicrob Agents Chemother,1998,42(10):2612[9] 代焕琴. 安丝菌素生物合成的后修饰研究[D]. 中国科学院博士学位论文,2006:40[10] Walsh C T, Losey H C, Freel C L. Antibiotic glycosyltransferases [J]. Biochem Soc Trans,2003,31(Pt3):487[11] Lu C, Bai L, Shen Y. A novel amide N?glycoside of ansamitocins from Actinosynnema pretiosum [J]. J Antibiot,2004,57(5):348[12] Hoffmeister D, Ichinose K, Bechthold A. Two sequence elements of glycosyltransferases involved in urdamycin biosynthesis are responsible for substrate specificity and enzymatic activity [J]. Chem Biol,2001,8(16):557[13] Mulichak A M, Losey H C, Walsh C T, et al. Structure of the UDP?glucosyltransferase GtfB that modifies the heptapeptide aglycone in the biosynthesis of vancomycin group antibiotics [J]. Structure,2001,9(7):547[14] Sanchez C, ButovichI A, Brana A F, et al. The biosynthetic gene cluster for the antitumor rebeccamycin: characterization and generation of indolocarbazole derivatives [J]. Chem Biol,2002,9(4):519[15] Otten S L, Liu X, Ferguson J, et al. Cloning and characterization of the Streptomyces peucetius dnrQS genes encoding a daunosamine biosynthesis enzyme and a glycosyltransferase involved in daunorubicin biosynthesis [J]. J Bacteriol,1995,177(22):6688[16] Zhao Y, Ahlert J, Xue Y, et al. Engineering a methy?mycin/pikromycin?calicheamicin hybrid: construction of two new macrolides carrying a designed sugar moiety [J]. J Am Chem Soc,1999,121(42):9881[17] Hoffmeister D, Ichinose K, Domann S, et al. The NDP?sugar co?substrate concentration and the enzyme expression level influence the substrate specificity of glycosyltransferases: cloning and characterization of deoxysugar biosynthetic genes of the urdamycin biosynthetic gene cluster [J]. Chem Biol,2000,7(11):821[18] Walsh C, Freel C L, Losey H C. Antibiotic glycosyltransferases: antibiotic maturation and prospects for reprogramming [J]. J Med Chem,2003,46(16):3425[19] Blanco G, Patallo E P, Brana A F, et al. Identification of a sugar flexible glycosyltransferase from Streptomyces olivaceus: the producer of the antitumor polyketide elloramycin [J]. Chem Biol,2001,8(3):253[20] Dürr C, Hoffmeister D, Wohlert S E, et al. The glycosyltransferase UrdGT2 establishes both C? and O?glycosidic bonds [J]. Angewandte,2004,43(22):2962[21] Freel C L, Anderson J W, Kahne D, et al. Initial characterization of novobiocic acid noviosyl transferase activity of NovM in biosynthesis of the antibiotic novobiocin [J]. Biochemistry,2002,42(14):4179[22] Mendez C, Salas J A. Altering the glycosylation pattern of bioactive compounds [J]. Trends Biotechnol,2001,19(11):449[23] He X, M Liu, H W. Formation of unusual sugars: mechanistic studies and biosynthetic applications [J]. Annu Rev Biochem,2002,71:701[24] Oberthur M, Leimkuhler C, Kruger R G, et al. A systematic investigation of the synthetic utility of glycopeptide glycosyltransferases [J]. J Am Chem Soc,2005,127(30):10747[25] Wohlert S E, Blanco G, Lombo F, et al. Novel hybrid tetracenomycins through combinatorial biosynthesis using a glycosyltransferase encoded by elm genes in cosmid 16F4 and which shows a broad sugar substrate specificity [J]. J Am Chem Soc,1998,120(41):10596[26] Salas J A, Mendez C. Biosynthesis pathways for deoxysugars in antibiotic?producing actinomycetes: isolation, characterization and generation of novel glycosylated derivatives [J]. J Mol Microbiol Biotechnol,2005,9(2):77[27] Sanchez C, Zhu L, Brana A F, et al. Combinatorial biosynthesis of antitumor indolocarbazole compounds [J]. Proc Natl Acad Sci,2005,102(2):461[28] Salas A P, Zhu L, Sanchez C, et al. Deciphering the late steps in the biosynthesis of the anti?tumour indolocarbazole staurosporine: sugar donor substrate flexibility of the StaG glycosyltransferase [J]. Mol Microbiol,2005,58(1):17[29] Doumith M, Legrand R, Lang C, et al. Interspecies complementation in Saccharopolyspora erythraea: elucidation of the function of oleP1, oleG1 and oleG2 from the oleandomycin biosynthetic gene cluster of Streptomyces antibioticus and generation of new ery

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