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Amino acid sequence of an Escherichia coli ADPglucose synthetase allosteric mutant as deduced from the DNA sequence of the glg C gene.从glg C基因的DNA序列推导的大肠杆菌ADP葡萄糖合成酶变构突变体的氨基酸序列。
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Biosynthesis of bacterial glycogen: primary structure of Salmonella typhimurium ADPglucose synthetase as deduced from the nucleotide sequence of the glgC gene.细菌糖原的生物合成:从glgC基因的核苷酸序列推导鼠伤寒沙门氏菌ADP葡萄糖合成酶的一级结构。
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Cloning and expression of the Escherichia coli glgC gene from a mutant containing an ADPglucose pyrophosphorylase with altered allosteric properties.来自一株含有变构性质改变的ADP葡萄糖焦磷酸化酶的突变体的大肠杆菌glgC基因的克隆与表达。
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Cloning of the ADPglucose pyrophosphorylase (glgC) and glycogen synthase (glgA) structural genes from Salmonella typhimurium LT2.鼠伤寒沙门氏菌LT2的ADP葡萄糖焦磷酸化酶(glgC)和糖原合酶(glgA)结构基因的克隆
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Genetic and transgenic perturbations of carbon reserve production in Arabidopsis seeds reveal metabolic interactions of biochemical pathways.拟南芥种子中碳储备产物的遗传和转基因扰动揭示了生化途径的代谢相互作用。
Planta. 2006 Dec;225(1):153-64. doi: 10.1007/s00425-006-0337-6. Epub 2006 Jul 29.
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Isolation and expression analysis of cDNA clones encoding a small and a large subunit of ADP-glucose pyrophosphorylase from sugar beet.甜菜中编码ADP - 葡萄糖焦磷酸化酶小亚基和大亚基的cDNA克隆的分离与表达分析
Plant Mol Biol. 1995 Jan;27(1):191-7. doi: 10.1007/BF00019190.
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Molecular cloning and characterization of novel isoforms of potato ADP-glucose pyrophosphorylase.马铃薯 ADP - 葡萄糖焦磷酸化酶新亚型的分子克隆与特性分析
Mol Gen Genet. 1995 Mar 10;246(5):538-48. doi: 10.1007/BF00298960.
4
Functions of the gene products of Escherichia coli.大肠杆菌基因产物的功能。
Microbiol Rev. 1993 Dec;57(4):862-952. doi: 10.1128/mr.57.4.862-952.1993.
5
Comparison of the primary sequences of two potato tuber ADP-glucose pyrophosphorylase subunits.两种马铃薯块茎ADP-葡萄糖焦磷酸化酶亚基一级序列的比较。
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本文引用的文献

1
Biosynthesis of bacterial glycogen. Primary structure of Escherichia coli ADP-glucose synthetase as deduced from the nucleotide sequence of the glg C gene.细菌糖原的生物合成。根据glg C基因的核苷酸序列推导的大肠杆菌ADP - 葡萄糖合成酶的一级结构。
J Biol Chem. 1983 Apr 25;258(8):5084-8.
2
Sequencing end-labeled DNA with base-specific chemical cleavages.通过碱基特异性化学切割对末端标记的DNA进行测序。
Methods Enzymol. 1980;65(1):499-560. doi: 10.1016/s0076-6879(80)65059-9.
3
Covalent modification of the inhibitor-binding site(s) of Escherichia coli ADP-glucose synthetase. Isolation and structural characterization of 8-azido-AMP-incorporated peptides.
J Biol Chem. 1986 Nov 25;261(33):15402-9.
4
Cloning and expression of the Escherichia coli glgC gene from a mutant containing an ADPglucose pyrophosphorylase with altered allosteric properties.来自一株含有变构性质改变的ADP葡萄糖焦磷酸化酶的突变体的大肠杆菌glgC基因的克隆与表达。
J Bacteriol. 1986 Jul;167(1):82-8. doi: 10.1128/jb.167.1.82-88.1986.
5
Biosynthesis of bacterial glycogen. Isolation and characterization of the pyridoxal-P allosteric activator site and the ADP-glucose-protected pyridoxal-P binding site of Escherichia coli B ADP-glucose synthase.细菌糖原的生物合成。大肠杆菌B ADP-葡萄糖合酶的磷酸吡哆醛变构激活位点及ADP-葡萄糖保护的磷酸吡哆醛结合位点的分离与鉴定。
J Biol Chem. 1978 Nov 10;253(21):7638-45.

Amino acid sequence of an Escherichia coli ADPglucose synthetase allosteric mutant as deduced from the DNA sequence of the glg C gene.

作者信息

Lee Y M, Kumar A, Preiss J

机构信息

Department of Biochemistry, Michigan State University, E. Lansing 48824.

出版信息

Nucleic Acids Res. 1987 Dec 23;15(24):10603. doi: 10.1093/nar/15.24.10603.

DOI:10.1093/nar/15.24.10603
PMID:2827128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC339983/
Abstract
摘要