Hb Hope αC2Aβ2（H14）甘氨酸-天冬氨酸的异常功能特性：一种具有降低的二磷酸甘油酸（DPG）效应的低氧亲和力血红蛋白。 - Suppr

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超能文献

Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect.

作者信息

Thillet J, Caburi J, Brun B, Cohen-Solal M, Garel M C, Minh M N, Rosa J

出版信息

FEBS Lett. 1974 Oct 1;47(1):47-52. doi: 10.1016/0014-5793(74)80423-0.

DOI:10.1016/0014-5793(74)80423-0

PMID:4426396

Abstract

摘要

相似文献

Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect.Hb Hope αC2Aβ2（H14）甘氨酸-天冬氨酸的异常功能特性：一种具有降低的二磷酸甘油酸（DPG）效应的低氧亲和力血红蛋白。

FEBS Lett. 1974 Oct 1;47(1):47-52. doi: 10.1016/0014-5793(74)80423-0.

Hemoglobin Chesapeake (92 alpha, arginine--leucine). Precise measurements and analyses of oxygen equilibrium.血红蛋白切萨皮克（92α，精氨酸 - 亮氨酸）。氧平衡的精确测量与分析。

J Biol Chem. 1974 Dec 10;249(23):7607-12.

A method for isolation of abnormal haemoglobins with high oxygen affinity due to a frozen quaternary r-structure: application to Hb Creteil alpha 2 A beta 2 (F5) 89 ASN.一种用于分离因冻结的四级R结构而具有高氧亲和力的异常血红蛋白的方法：应用于血红蛋白克雷泰伊α2Aβ2（F5）89天冬酰胺。

FEBS Lett. 1974 Jul 1;43(1):93-6. doi: 10.1016/0014-5793(74)81113-0.

Hemoglobin E: its oxygen affinity in relation with the ionic environment.

FEBS Lett. 1974 Apr 15;41(1):147-50. doi: 10.1016/0014-5793(74)80975-0.

Functional properties of hemoglobin Kempsey.肯普西血红蛋白的功能特性。

J Biol Chem. 1974 Dec 10;249(23):7402-9.

Hb Helsinki: a variant with a high oxygen affinity and a substitution at a 2,3-DPG binding site (beta82[EF6] Lys replaced by Met).赫尔辛基血红蛋白：一种具有高氧亲和力且在2,3 - 二磷酸甘油酸（2,3 - DPG）结合位点存在取代（β82[EF6]赖氨酸被甲硫氨酸取代）的变体。

Acta Haematol. 1976;56(5):257-75. doi: 10.1159/000207947.

The alkaline Bohr effect of human hemoglobin.人类血红蛋白的碱性波尔效应。

Ann N Y Acad Sci. 1974 Nov 29;241(0):465-71. doi: 10.1111/j.1749-6632.1974.tb21903.x.

The hemoglobin of the crossopterygian fish, Latimeria chalumnae (Smith). Subunit structure and oxygen equilibria.

Arch Biochem Biophys. 1974 Aug;163(2):728-34. doi: 10.1016/0003-9861(74)90534-7.

Functional studies of two new abnormal hemoglobins with their mutation located at intersubunit contacts: Hb Hotel Dieu beta99 (G1) Asp replaced by Gly and Hb Pitie Salpetriere beta34 (B16) Val replaced by Phe.两种新的异常血红蛋白的功能研究，其突变位于亚基间接触点：迪厄医院血红蛋白β99（G1）天冬氨酸被甘氨酸取代，皮提耶尔 - 萨尔佩特里埃医院血红蛋白β34（B16）缬氨酸被苯丙氨酸取代。

Biochim Biophys Acta. 1981 Sep 29;670(2):260-4. doi: 10.1016/0005-2795(81)90018-0.

Hemoglobin Syracuse (alpha2beta2-143(H21)His leads to Pro), a new high-affinity variant detected by special electrophoretic methods. Observations on the auto-oxidation of normal and variant hemoglobins.血红蛋白锡拉丘兹（α2β2-143（H21）组氨酸突变为脯氨酸），一种通过特殊电泳方法检测到的新型高亲和力变体。关于正常和变体血红蛋白自动氧化的观察。

J Clin Invest. 1975 Mar;55(3):469-77. doi: 10.1172/JCI107953.

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J Diabetes Sci Technol. 2021 Jul;15(4):974-975. doi: 10.1177/19322968211008521. Epub 2021 May 10.

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BMC Evol Biol. 2010 Jul 16;10:214. doi: 10.1186/1471-2148-10-214.

Probing the energetics of proteins through structural perturbation: sites of regulatory energy in human hemoglobin.

Proc Natl Acad Sci U S A. 1982 Mar;79(6):1849-53. doi: 10.1073/pnas.79.6.1849.

High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.老挝血红蛋白疾病的高遗传多态性。由相关地中海贫血综合征导致的复杂表型。

Hum Genet. 1979 Sep;50(3):327-36. doi: 10.1007/BF00399399.

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