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Mapping of the two intrachain cyclic nucleotide binding sites of adenosine cyclic 3',5'-phosphate dependent protein kinase I.

作者信息

Døskeland S O, Ogreid D, Ekanger R, Sturm P A, Miller J P, Suva R H

出版信息

Biochemistry. 1983 Mar 1;22(5):1094-101. doi: 10.1021/bi00274a016.

DOI:10.1021/bi00274a016
PMID:6301537
Abstract
摘要

相似文献

1
Mapping of the two intrachain cyclic nucleotide binding sites of adenosine cyclic 3',5'-phosphate dependent protein kinase I.
Biochemistry. 1983 Mar 1;22(5):1094-101. doi: 10.1021/bi00274a016.
2
Mapping adenosine cyclic 3',5'-phosphate binding sites on type I and type II adenosine cyclic 3',5'-phosphate dependent protein kinases using ribose ring and cyclic phosphate ring analogues of adenosine cyclic 3',5'-phosphate.
Biochemistry. 1981 Feb 17;20(4):879-87. doi: 10.1021/bi00507a035.
3
Cyclic AMP derivatives as tools for mapping cyclic AMP binding sites of cyclic AMP-dependent protein kinases I and II.环磷酸腺苷衍生物作为绘制环磷酸腺苷依赖性蛋白激酶I和II的环磷酸腺苷结合位点的工具。
Adv Cyclic Nucleotide Res. 1981;14:335-44.
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Probable involvement of both intrachain cAMP binding sites in activation of protein kinase.
J Biol Chem. 1983 Jan 25;258(2):1032-40.
5
1,N6-Etheno-2-aza-adenosine 3', 5'-cyclic phosphate: human erythrocyte membrane binding and activation of membrane protein kinase.1,N6-乙烯基-2-氮杂腺苷3',5'-环磷酸酯:人红细胞膜结合及膜蛋白激酶的激活
J Cyclic Nucleotide Res. 1979;5(2):153-9.
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2-substituted derivatives of adenosine and inosine cyclic 3',5'-phosphate. Synthesis, enzymic activity, and analysis of the structural requirements of the binding locale of the 2-substituent on bovine brain protein kinase.腺苷和肌苷环3',5'-磷酸的2-取代衍生物。牛脑蛋白激酶2-取代基结合位点的结构要求的合成、酶活性及分析
Biochemistry. 1975 Jul 29;14(15):3315-21. doi: 10.1021/bi00686a005.
7
Effect of modification of the 1-, 2-, and 6-positions of 9-beta-D-ribofuranosylpurine cyclic 3',5'-phosphate on the cyclic nucleotide specificity of adenosine cyclic 3',5'-phosphate- and guanosine cyclic 3',5'-phosphate-dependent protein kinases.
Biochem Pharmacol. 1981 Mar 1;30(5):509-15. doi: 10.1016/0006-2952(81)90637-7.
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Investigation of the adenosine 3', 5'-cyclic phosphate binding site of pig brain histone kinase with the aid of some analogues of adenosine 3', 5'-cyclic phosphate.借助3',5'-环磷酸腺苷的一些类似物对猪脑组蛋白激酶的3',5'-环磷酸腺苷结合位点进行研究。
Biochim Biophys Acta. 1975 Apr 19;384(2):413-22. doi: 10.1016/0005-2744(75)90042-x.
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Fluorescent photoaffinity labeling: adenosine 3',5'-cyclic monophosphate receptor sites.荧光光亲和标记:3',5'-环磷酸腺苷受体位点
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1199-203. doi: 10.1073/pnas.75.3.1199.
10
Determination of binding parameters of cyclic AMP and its analogs to cyclic AMP-dependent protein kinase by the fluorescent probe method.用荧光探针法测定环磷酸腺苷及其类似物与环磷酸腺苷依赖性蛋白激酶的结合参数。
Biochim Biophys Acta. 1979 Aug 15;569(2):145-52. doi: 10.1016/0005-2744(79)90049-4.

引用本文的文献

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-modified cAMP derivatives that activate protein kinase A also act as full agonists of murine HCN2 channels.修饰后的环腺苷酸衍生物能激活蛋白激酶 A,也能作为鼠 HCN2 通道的完全激动剂。
J Biol Chem. 2019 Nov 22;294(47):17978-17987. doi: 10.1074/jbc.RA119.010246. Epub 2019 Oct 15.
2
The gene product of a Trypanosoma equiperdum ortholog of the cAMP-dependent protein kinase regulatory subunit is a monomeric protein that is not capable of binding cyclic nucleotides.克氏锥虫环腺苷酸依赖蛋白激酶调节亚基同源基因的产物是一种单体蛋白,不能结合环核苷酸。
Biochimie. 2018 Mar;146:166-180. doi: 10.1016/j.biochi.2017.12.010. Epub 2017 Dec 27.
3
Switching Cyclic Nucleotide-Selective Activation of Cyclic Adenosine Monophosphate-Dependent Protein Kinase Holoenzyme Reveals Distinct Roles of Tandem Cyclic Nucleotide-Binding Domains.
切换环磷酸腺苷依赖性蛋白激酶全酶的环核苷酸选择性激活揭示串联环核苷酸结合结构域的不同作用。
ACS Chem Biol. 2017 Dec 15;12(12):3057-3066. doi: 10.1021/acschembio.7b00732. Epub 2017 Nov 21.
4
Mutations of PKA cyclic nucleotide-binding domains reveal novel aspects of cyclic nucleotide selectivity.蛋白激酶A环核苷酸结合结构域的突变揭示了环核苷酸选择性的新方面。
Biochem J. 2017 Jul 6;474(14):2389-2403. doi: 10.1042/BCJ20160969.
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Resonant mirror biosensor analysis of type Ialpha cAMP-dependent protein kinase B domain--cyclic nucleotide interactions.Iα型环磷酸腺苷依赖性蛋白激酶B结构域与环核苷酸相互作用的共振镜生物传感器分析
Protein Sci. 2000 Dec;9(12):2446-56. doi: 10.1110/ps.9.12.2446.
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Isoleucine 368 is involved in low-affinity binding of N6-modified cAMP analogues to site B of the regulatory subunit of cAMP-dependent protein kinase I.异亮氨酸368参与N6修饰的环磷酸腺苷(cAMP)类似物与环磷酸腺苷依赖性蛋白激酶I调节亚基位点B的低亲和力结合。
Biochem J. 1996 May 15;316 ( Pt 1)(Pt 1):337-43. doi: 10.1042/bj3160337.
7
Regulation of calcium-activated nonselective cation channel activity by cyclic nucleotides in the rat insulinoma cell line, CRI-G1.
J Membr Biol. 1995 Jun;145(3):267-78. doi: 10.1007/BF00232718.
8
Selective modulation of protein kinase isozymes by the site-selective analog 8-chloroadenosine 3',5'-cyclic monophosphate provides a biological means for control of human colon cancer cell growth.
Proc Natl Acad Sci U S A. 1988 Sep;85(17):6319-22. doi: 10.1073/pnas.85.17.6319.
9
Insulin inhibition of hepatic cAMP-dependent protein kinase: decreased affinity of protein kinase for cAMP and possible differential regulation of intrachain sites 1 and 2.胰岛素对肝脏环磷酸腺苷(cAMP)依赖性蛋白激酶的抑制作用:蛋白激酶对cAMP的亲和力降低以及链内位点1和位点2可能存在的差异调节。
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2218-22. doi: 10.1073/pnas.84.8.2218.
10
cAMP analogs promote survival and neurite outgrowth in cultures of rat sympathetic and sensory neurons independently of nerve growth factor.环磷酸腺苷(cAMP)类似物可促进大鼠交感神经元和感觉神经元培养物的存活及神经突生长,且与神经生长因子无关。
Proc Natl Acad Sci U S A. 1988 Feb;85(4):1257-61. doi: 10.1073/pnas.85.4.1257.