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UDP-N-acetylglucosamine:lysosomal enzyme precursor N-acetylglucosamine-1-phosphotransferase. Partial purification and characterization of the rat liver Golgi enzyme.

作者信息

Waheed A, Hasilik A, von Figura K

出版信息

J Biol Chem. 1982 Oct 25;257(20):12322-31.

PMID:6288715
Abstract
摘要

相似文献

1
UDP-N-acetylglucosamine:lysosomal enzyme precursor N-acetylglucosamine-1-phosphotransferase. Partial purification and characterization of the rat liver Golgi enzyme.UDP-N-乙酰葡糖胺:溶酶体酶前体N-乙酰葡糖胺-1-磷酸转移酶。大鼠肝脏高尔基体酶的部分纯化及特性鉴定
J Biol Chem. 1982 Oct 25;257(20):12322-31.
2
UDP-N-acetylglucosamine: lysosomal enzyme N-acetylglucosamine-1-phosphotransferase.
Methods Enzymol. 1984;107:163-72. doi: 10.1016/0076-6879(84)07010-5.
3
Enzymatic transfer of galactosyl phosphate from UDP-galactose to UDP-N-acetylglucosamine.将磷酸半乳糖从尿苷二磷酸半乳糖酶促转移至尿苷二磷酸-N-乙酰葡糖胺。
FEBS Lett. 1983 Jan 10;151(1):15-8. doi: 10.1016/0014-5793(83)80332-9.
4
Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in I-cell fibroblasts.在UDP-N-乙酰葡糖胺存在的情况下溶酶体酶的酶促磷酸化。I型细胞成纤维细胞中缺乏该活性。
Biochem Biophys Res Commun. 1981 Feb 12;98(3):761-7. doi: 10.1016/0006-291x(81)91177-3.
5
Synthesis of phosphorylated recognition marker in lysosomal enzymes is located in the cis part of Golgi apparatus.溶酶体酶中磷酸化识别标记的合成位于高尔基体的顺面部分。
J Biol Chem. 1982 May 25;257(10):5323-5.
6
Translocation of UDP-N-acetylglucosamine into vesicles derived from rat liver rough endoplasmic reticulum and Golgi apparatus.UDP-N-乙酰葡糖胺转运至源自大鼠肝脏粗面内质网和高尔基体的囊泡中。
J Biol Chem. 1985 Apr 25;260(8):4671-8.
7
Subfractionation of rat liver Golgi apparatus: separation of enzyme activities involved in the biosynthesis of the phosphomannosyl recognition marker in lysosomal enzymes.大鼠肝脏高尔基体的亚分级分离:溶酶体酶中磷酸甘露糖识别标记生物合成相关酶活性的分离
Proc Natl Acad Sci U S A. 1983 Jul;80(13):3938-42. doi: 10.1073/pnas.80.13.3938.
8
Incorporation of N-acetylglucosamine from UDP-N-acetylglucosamine into proteins and lipid intermediates in microsomal and Golgi membranes from rat liver.将来自UDP-N-乙酰葡糖胺的N-乙酰葡糖胺掺入大鼠肝脏微粒体和高尔基体膜中的蛋白质和脂质中间体。
Biochim Biophys Acta. 1978 Sep 11;512(1):123-35. doi: 10.1016/0005-2736(78)90223-7.
9
Formation of N-acetylglucosamine 6-phosphate from UDP-N-acetylglucosamine in rat tissues.大鼠组织中由UDP-N-乙酰葡糖胺形成N-乙酰葡糖胺6-磷酸。
Sci Rep Res Inst Tohoku Univ Med. 1974 Jul;21(1-2):1-9.
10
Pool levels of UDP N-acetylglucosamine and UDP N-acetylglucosamine-enolpyruvate in Escherichia coli and correlation with peptidoglycan synthesis.大肠杆菌中UDP-N-乙酰葡糖胺和UDP-N-乙酰葡糖胺-烯醇丙酮酸的总体水平及其与肽聚糖合成的相关性。
J Bacteriol. 1983 Jun;154(3):1284-90. doi: 10.1128/jb.154.3.1284-1290.1983.

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Structural and Functional Insights into the Stealth Protein CpsY of .结构与功能分析揭示 中隐匿蛋白 CpsY 的奥秘
Biomolecules. 2023 Nov 3;13(11):1611. doi: 10.3390/biom13111611.
2
Structures of the mannose-6-phosphate pathway enzyme, GlcNAc-1-phosphotransferase.甘露糖-6-磷酸途径酶,GlcNAc-1-磷酸转移酶的结构。
Proc Natl Acad Sci U S A. 2022 Aug 16;119(33):e2203518119. doi: 10.1073/pnas.2203518119. Epub 2022 Aug 8.
3
Quantitative Proteome Analysis of Mouse Liver Lysosomes Provides Evidence for Mannose 6-phosphate-independent Targeting Mechanisms of Acid Hydrolases in Mucolipidosis II.
小鼠肝脏溶酶体的定量蛋白质组分析为黏脂贮积症II中酸性水解酶的非甘露糖6-磷酸靶向机制提供了证据。
Mol Cell Proteomics. 2017 Mar;16(3):438-450. doi: 10.1074/mcp.M116.063636. Epub 2017 Jan 6.
4
TGN exit of the cation-independent mannose 6-phosphate receptor does not require acid hydrolase binding.不依赖阳离子的甘露糖6-磷酸受体从反式高尔基体网络的输出不需要酸性水解酶结合。
Cell Logist. 2014 Jul 3;4(3):e954441. doi: 10.4161/21592780.2014.954441. eCollection 2014 Jul-Sep.
5
High resolution crystal structure of human β-glucuronidase reveals structural basis of lysosome targeting.人β-葡萄糖醛酸苷酶的高分辨率晶体结构揭示了溶酶体靶向的结构基础。
PLoS One. 2013 Nov 19;8(11):e79687. doi: 10.1371/journal.pone.0079687. eCollection 2013.
6
N-/O-glycosylation analysis of human FVIIa produced in the milk of transgenic rabbits.对转基因兔乳汁中产生的人活化凝血因子VII进行N-糖基化和O-糖基化分析。
Glycobiology. 2013 Dec;23(12):1531-46. doi: 10.1093/glycob/cwt085. Epub 2013 Oct 2.
7
Strategies for carbohydrate recognition by the mannose 6-phosphate receptors.甘露糖6-磷酸受体识别碳水化合物的策略。
Glycobiology. 2008 Sep;18(9):664-78. doi: 10.1093/glycob/cwn061. Epub 2008 Jul 11.
8
Mannose 6-phosphate receptor targeting and its applications in human diseases.甘露糖6-磷酸受体靶向作用及其在人类疾病中的应用。
Curr Med Chem. 2007;14(28):2945-53. doi: 10.2174/092986707782794005.
9
Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha / beta -subunits precursor gene.黏脂贮积症II型(I型细胞病)和黏脂贮积症IIIA型(典型的假胡尔勒多营养不良症)是由N-乙酰葡糖胺磷酸转移酶α/β亚基前体基因突变引起的。
Am J Hum Genet. 2006 Mar;78(3):451-63. doi: 10.1086/500849. Epub 2006 Jan 24.
10
Four monoclonal antibodies inhibit the recognition of arylsulphatase A by the lysosomal enzyme phosphotransferase.四种单克隆抗体可抑制溶酶体酶磷酸转移酶对芳基硫酸酯酶A的识别。
Biochem J. 1994 Jan 1;297 ( Pt 1)(Pt 1):123-30. doi: 10.1042/bj2970123.