琥珀酰辅酶A合成酶磷酸组氨酸残基和糖原磷酸化酶a磷酸丝氨酸残基的频率依赖性磷-31核磁共振研究。 - Suppr

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超能文献

Frequency-dependent phosphorus-31 nuclear magnetic resonance studies of the phosphohistidine residue to succinyl-CoA synthetase and the phosphoserine residue of glycogen phosphorylase a.

作者信息

Vogel H J, Bridger W A, Sykes B D

出版信息

Biochemistry. 1982 Mar 16;21(6):1126-32. doi: 10.1021/bi00535a003.

DOI:10.1021/bi00535a003

PMID:6803832

Abstract

摘要

相似文献

Frequency-dependent phosphorus-31 nuclear magnetic resonance studies of the phosphohistidine residue to succinyl-CoA synthetase and the phosphoserine residue of glycogen phosphorylase a.琥珀酰辅酶A合成酶磷酸组氨酸残基和糖原磷酸化酶a磷酸丝氨酸残基的频率依赖性磷-31核磁共振研究。

Biochemistry. 1982 Mar 16;21(6):1126-32. doi: 10.1021/bi00535a003.

Phosphorus-31 nuclear magnetic resonance study of the active site phosphohistidine and regulatory phosphoserine residues of rat liver ATP-citrate lyase.大鼠肝脏ATP-柠檬酸裂解酶活性位点磷酸组氨酸和调节性磷酸丝氨酸残基的磷-31核磁共振研究

Biochemistry. 1985 Sep 24;24(20):5527-31. doi: 10.1021/bi00341a037.

An n.m.r. probe of succinyl-coenzyme A synthetase: subunit interactions and the mechanism of action.琥珀酰辅酶A合成酶的核磁共振研究：亚基相互作用及作用机制

Biochem Soc Trans. 1983 Jun;11(3):315-23. doi: 10.1042/bst0110315.

A phosphorus 31 nuclear magnetic resonance study of the intermediates of the Escherichia coli succinyl coenzyme A synthetase reaction. Evidence for substrate synergism and catalytic cooperativity.

J Biol Chem. 1982 May 10;257(9):4834-42.

Evidence for a second histidine at the active site of succinyl-CoA synthetase from Escherichia coli.来自大肠杆菌的琥珀酰辅酶A合成酶活性位点存在第二个组氨酸的证据。

J Biol Chem. 1979 Nov 10;254(21):10925-30.

Affinity labeling of succinyl-CoA synthetase from Escherichia coli by the 2',3'-dialdehyde derivative of adenosine 5'-diphosphate.

Eur J Biochem. 1983 Oct 17;136(1):83-7. doi: 10.1111/j.1432-1033.1983.tb07708.x.

Succinyl coenzyme A synthetase of Escherichia coli. Sequence of a peptide containing the active-site phosphohistidine residue.大肠杆菌的琥珀酰辅酶A合成酶。包含活性位点磷酸组氨酸残基的肽段序列。

Biochemistry. 1972 May 23;11(11):2067-70. doi: 10.1021/bi00761a011.

The direct assay of kinases and acyl-CoA synthetases by HPLC: application to nucleoside diphosphate kinase and succinyl-CoA synthetase.通过高效液相色谱法直接测定激酶和酰基辅酶A合成酶：应用于核苷二磷酸激酶和琥珀酰辅酶A合成酶。

Anal Biochem. 1993 Feb 15;209(1):192-8. doi: 10.1006/abio.1993.1102.

Nonactivated phosphorylase kinase is a phosphoprotein: differentiation of two classes of endogenous phosphoserine residues by phosphorus-31 nuclear magnetic resonance spectroscopy and phosphatase sensitivity.未活化的磷酸化酶激酶是一种磷蛋白：通过磷-31核磁共振光谱法和磷酸酶敏感性区分两类内源性磷酸丝氨酸残基。

Biochemistry. 1984 Jan 3;23(1):112-7. doi: 10.1021/bi00296a018.

Affinity chromatography of acyl-CoA utilizing enzymes on Procion Red-agarose.利用酶对丙酰辅酶A在普施安红琼脂糖上进行亲和层析。

Biochem Biophys Res Commun. 1983 May 16;112(3):1021-6. doi: 10.1016/0006-291x(83)91720-5.

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31P NMR relaxation studies of the activation of the coenzyme phosphate of glycogen phosphorylase. The role of motion of the bound phosphate.糖原磷酸化酶辅酶磷酸激活的³¹P核磁共振弛豫研究。结合态磷酸运动的作用。

Biophys J. 1985 Dec;48(6):1019-26. doi: 10.1016/S0006-3495(85)83864-9.

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