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Amino acid sequence elucidation of human acrosin-trypsin inhibitor (HUSI-II) reveals that Kazal-type proteinase inhibitors are structurally related to β-subunits of glycoprotein hormones

机译：人类丙烯醛-胰蛋白酶抑制剂（HUSI-II）的氨基酸序列分析表明，Kazal型蛋白酶抑制剂与糖蛋白激素的β亚基在结构上相关

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Fink Edwin; Hehlein-Fink Christa; Eulitz Manfred;
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年度 1990
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1. Amino acid sequence elucidation of human acrosin‐trypsin inhibitor (HUSI‐II) reveals that Kazal‐type proteinase inhibitors are structurally related to β‐subunits of glycoprotein hormones [J] . Eulitz Manfred, Fink Edwin, Hehlein-Fink Christa FEBS Letters . 1990,第1a2期

机译：对人类丙烯醛-胰蛋白酶抑制剂（HUSI-II）的氨基酸序列分析表明，Kazal型蛋白酶抑制剂与糖蛋白激素的β-亚基在结构上相关
2. Amino acid sequence elucidation of human acrosin‐trypsin inhibitor (HUSI‐II) reveals that Kazal‐type proteinase inhibitors are structurally related to β‐subunits of glycoprotein hormones [J] . Eulitz Manfred, Fink Edwin, Hehlein-Fink Christa FEBS Letters . 1990,第1a2期

机译：对人类丙烯醛-胰蛋白酶抑制剂（HUSI-II）的氨基酸序列分析表明，Kazal型蛋白酶抑制剂与糖蛋白激素的β-亚基在结构上相关
3. Structurally unique recombinant Kazal-type proteinase inhibitor retains activity when terminally extended and glycosylated [J] . Kludkiewicz B, Kodrik D, Grzelak K, Protein Expression and Purification . 2005,第2期

机译：结构独特的重组Kazal型蛋白酶抑制剂在末端扩展和糖基化时保留活性
4. A NEW FAMILY OF SERINE PROTEINASE INHIBITORS: PURIFICATION, AMINO ACID SEQUENCE, TOPOLOGY OF DISULFIDE BRIDGES AND CHEMICAL SYNTHESIS OF INHIBITORS ISOLATED FROM Mirabilis jalapa AND Spinacia oleracea SEEDS [C] . Joanna Kowalska, Anna Wilimowska-Pelc, Izabela Lorenc-Kubis the European Peptide Symposium . 2007

机译：一种新的丝氨酸蛋白酶抑制剂系列：纯化，氨基酸序列，二硫化物桥的拓扑，抑制剂的化学合成从Mirabilis jalapa和Spinacia Oleracea种子中分离出来
5. Part one. Synthesis of phosphorus-containing amino acid analogues derived from trans-4-hydroxyproline and the study of their bioactivity in the glutamate excitatory neurotransmitter system. Part two. Synthesis, structural modifications and in vitro pharmacology of quinoline-2,4-dicarboxylic acids as proposed inhibitors of the glutamate vesicular transporter. [D] . Carrigan, Christina Nicole. 2000

机译：第一部分。反式-4-羟基脯氨酸衍生的含磷氨基酸类似物的合成及其在谷氨酸兴奋性神经递质系统中的生物活性的研究。第二部分。喹啉-2,4-二羧酸作为谷氨酸囊泡转运蛋白的抑制剂的合成，结构修饰和体外药理作用。
6. Molecular basis for defective secretion of the Z variant of human alpha-1-proteinase inhibitor: secretion of variants having altered potential for salt bridge formation between amino acids 290 and 342. [O] . A A McCracken, K B Kruse, J L Brown 1989

机译：人α-1-蛋白酶抑制剂Z变体分泌缺陷的分子基础：分泌具有改变的氨基酸290和342之间盐桥潜力的变体。
7. Amino acid sequence elucidation of human acrosin-trypsin inhibitor (HUSI-II) reveals that Kazal-type proteinase inhibitors are structurally related to β-subunits of glycoprotein hormones [O] . Fink Edwin, Hehlein-Fink Christa, Eulitz Manfred 1990

机译：人类顶体蛋白酶 - 胰蛋白酶抑制剂（HUsI-II）的氨基酸序列分析表明，Kazal型蛋白酶抑制剂在结构上与糖蛋白激素的β-亚基相关。

Amino acid sequence elucidation of human acrosin-trypsin inhibitor (HUSI-II) reveals that Kazal-type proteinase inhibitors are structurally related to β-subunits of glycoprotein hormones

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