恶性疟原虫脂肪酰辅酶A合成酶家族（PfACS）及其在受感染红细胞中的差异阶段特异性表达。 - Suppr

The Plasmodium falciparum fatty acyl-CoA synthetase family (PfACS) and differential stage-specific expression in infected erythrocytes.

作者信息

Matesanz Fuencisla, Téllez María del-Mar, Alcina Antonio

机构信息

Department of Immunology and Cellular Biology, Instituto de Parasitología y Biomedicina López Neyra, CSIC, C/Ventanilla 11, Granada 18001, Spain.

出版信息

Mol Biochem Parasitol. 2003 Jan;126(1):109-12. doi: 10.1016/s0166-6851(02)00242-6.

DOI:10.1016/s0166-6851(02)00242-6

PMID:12554091

Abstract

摘要

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The Plasmodium falciparum fatty acyl-CoA synthetase family (PfACS) and differential stage-specific expression in infected erythrocytes.恶性疟原虫脂肪酰辅酶A合成酶家族（PfACS）及其在受感染红细胞中的差异阶段特异性表达。

Mol Biochem Parasitol. 2003 Jan;126(1):109-12. doi: 10.1016/s0166-6851(02)00242-6.

The cloning and expression of Pfacs1, a Plasmodium falciparum fatty acyl coenzyme A synthetase-1 targeted to the host erythrocyte cytoplasm.恶性疟原虫脂肪酸辅酶A合成酶-1（Pfacs1）的克隆与表达，该酶定位于宿主红细胞细胞质。

J Mol Biol. 1999 Aug 6;291(1):59-70. doi: 10.1006/jmbi.1999.2964.

The C-terminal domain of the Plasmodium falciparum acyl-CoA synthetases PfACS1 and PfACS3 functions as ligand for ankyrin.恶性疟原虫酰基辅酶A合成酶PfACS1和PfACS3的C末端结构域作为锚蛋白的配体发挥作用。

Mol Biochem Parasitol. 2003 Jul;129(2):191-8. doi: 10.1016/s0166-6851(03)00123-3.

Duplication, gene conversion, and genetic diversity in the species-specific acyl-CoA synthetase gene family of Plasmodium falciparum.恶性疟原虫物种特异性酰基辅酶A合成酶基因家族中的重复、基因转换和遗传多样性。

Mol Biochem Parasitol. 2006 Nov;150(1):10-24. doi: 10.1016/j.molbiopara.2006.06.004. Epub 2006 Jul 10.

Correlation of the efficiency of fatty acid derivatives in suppressing Plasmodium falciparum growth in culture with their inhibitory effect on acyl-CoA synthetase activity.

Mol Biochem Parasitol. 1988 Feb;28(1):39-42. doi: 10.1016/0166-6851(88)90177-6.

Affinity labeling fatty acyl-CoA synthetase with 9-p-azidophenoxy nonanoic acid and the identification of the fatty acid-binding site.用9-对叠氮苯氧基壬酸对脂肪酰辅酶A合成酶进行亲和标记及脂肪酸结合位点的鉴定

J Biol Chem. 2000 Dec 8;275(49):38547-53. doi: 10.1074/jbc.M006413200.

Multiple erythroid isoforms of human long-chain acyl-CoA synthetases are produced by switch of the fatty acid gate domains.人类长链脂酰辅酶A合成酶的多种红系同工型是通过脂肪酸门控结构域的切换产生的。

BMC Mol Biol. 2006 Jul 11;7:21. doi: 10.1186/1471-2199-7-21.

Human very long-chain acyl-CoA synthetase and two human homologs: initial characterization and relationship to fatty acid transport protein.人类超长链酰基辅酶A合成酶及两种人类同源物：初步表征及其与脂肪酸转运蛋白的关系。

Prostaglandins Leukot Essent Fatty Acids. 1999 May-Jun;60(5-6):323-8. doi: 10.1016/s0952-3278(99)80007-6.

Mouse fatty acid transport protein 4 (FATP4): characterization of the gene and functional assessment as a very long chain acyl-CoA synthetase.小鼠脂肪酸转运蛋白4（FATP4）：基因特征及作为极长链酰基辅酶A合成酶的功能评估

Gene. 2001 May 30;270(1-2):31-40. doi: 10.1016/s0378-1119(01)00489-9.

The human liver-specific homolog of very long-chain acyl-CoA synthetase is cholate:CoA ligase.超长链酰基辅酶A合成酶的人肝脏特异性同源物是胆酸盐：辅酶A连接酶。

J Biol Chem. 2000 May 26;275(21):15605-8. doi: 10.1074/jbc.C000015200.

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Nature. 2022 Feb;602(7895):106-111. doi: 10.1038/s41586-021-04288-3. Epub 2021 Dec 9.

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Differential Gene Expression and Protein Localization of Cryptosporidium parvum Fatty Acyl-CoA Synthetase Isoforms.微小隐孢子虫脂肪酰辅酶A合成酶同工型的差异基因表达与蛋白质定位

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The Plasmodium falciparum fatty acyl-CoA synthetase family (PfACS) and differential stage-specific expression in infected erythrocytes.

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