跨膜區 的英文怎麼說

中文拼音 [kuàmóqū]
跨膜區 英文
membrane-spanning region
  • 跨 : 動詞1 （抬起一隻腳向前或向左右邁） step; stride 2 （兩腿分在物體的兩邊坐著或立著） bestride; stra...
  • 膜 : 名詞1. [生物學] （像薄皮的組織） membrane 2. （像膜的薄皮） film; thin coating
  • 區 : 區名詞（姓氏） a surname
  1. 2. the sequence of si gene from ibv - lx4 strain was consisted of 1614 bp from initiation codon atg to the possible cleavage site of spike glycoprotein, encoding for a 18 - amino signal - peptide with the n terminus of si protein and a polypeptide of 537 - amino acids. 19 highly conserved, potential glycosylation sites and 17 cysteines residues were characterized with si protein, homology analysis showe that there were gene deletion -

    S1基因：其全序列共1614bp （從起始密碼子atg到s前體蛋白裂解位點） ，編碼537個氨基酸，其氨基端有一編碼18個氨基酸的信號肽序列，第12 13位氨基酸殘基構成了信號肽的切割位點， 14 19位與111 124位氨基酸殘基為s1蛋白的跨膜區域。
  2. The extracellular 100pl ( ecl1 ) and ecl2 was linked by disulfide bond to maintenanced the stability of the protein secondary structure. in recent years, we showed that ccr5 as a co - receptor could interact with hiv - 1 infect ion. ccr5 was paid closed attention to since it was cloned in 1996. the aim is to - obtain the sequence of first extracillular domain of 3 chemokine receptor 5 ( ccr5 ) n - terminal gene fragment with high level expression in e. coli and to prepare its specific antibody f ( ab ' ) ;, and its detected method

    Ccr5具有g蛋白偶聯受體家族（ g - proteincoupledreceptors ， gpcrs ）所特有的7個跨膜區（ transmembrinedomains ， tm ） ，呈螺旋， tm的氨基酸有很高的保守性，膜外第一襻（ extracellularloop1 ， ecl1 ）和ecl2之間有二硫鍵相連，以維持蛋白質二級結構的穩定性。
  3. The full - length cdna of ttom1, 1280 bp in length, encodes a deduced 288 a. a. protein with 7 - pass explasmic domains

    Ttom1全長cdna有1280個堿基對，編碼288個氨基酸，有7個跨膜區，是個典型的跨膜蛋白。
  4. To investigate the secondary structure of this gene, we found it has a transmembrane region near the n - terminus, followed by a proline - rich conserved region, and it has a conserved haemachrome binding region about 60 aa away from carboxyl terminus

    分析氨基酸序列的二級結構發現基因n -端具有跨膜的疏水序列，其後具有富含脯氨酸保守區，在距離羧基端60個氨基酸處具有高度保守的血紅素結合域。
  5. It is divided to extracellular and intracellular part by transmembrane domain. there are 13 n - glycosylation sites, 20 protein kinase c phosphorylation sites, 28 casein kinase ii phosphorylation sites, 4 tyrosine kinase phosphorylation sites and 15 n - myristoylation sites in the extracellular part of bt - r3 protein. an integrin recognition sequences rod lies in intracellular part of bt - r3 protein

    跨膜區域（ tmd ）將它分為胞內和胞外兩個部分，它的胞外有13個潛在的糖基化位點， 20個蛋白激酶c的磷酸化位點， 28個酪蛋白激酶的磷酸化位點， 4個酪氨酸酶的磷酸化位點， 15個豆蔻（十四烷基）酰化位點；它的胞內有1個整合蛋白（ integrin ）識別位點。
  6. Hydrophobicity analysis suggested that the v - h + - atpase subunit c from 5. salsa was a transmembrane protein with four transmembrane domains. earlier experiments indicated the conserve glutamyl residue in the fourth transmembrane domains might participate in the proton translocating across the membranes

    鹽地堿蓬液泡膜h ~ + - atpasec亞基第四個跨膜區存在高度保守的谷氨酸殘基，先前的研究表明此谷氨酸殘基可能與h ~ +跨脂雙層運輸有關。
  7. The single peptide of bt - r3 protein is a a helix which orients from inside to outside, and the transmembrane domain is also a helix which orients from outside to inside

    Bt - r3受體蛋白最前端的信號肽是一個由內向外a螺旋，跨膜區域（ tmd ）是一個由外向內的a螺旋。
  8. Initially, a polyclonal antibodies was used to screen the cdna expression library to isolate pf40 gene from millet. sequence analysis revealed that the pf40 gene contained an open reading frame ( orf ) encoding a protein with 75 % - 35 % sequence identity to the zips ( zinc or iron transporter proteins ) gene family. software analysis of the pf40 gene character showed that pf40 protein had a eight trans - membrane region structure, pf40 protein was also rich in leucine ( 18. 4 % ) and the protein was a hydrophobic protein

    序列分析表明該基因具有一個開放閱讀框（ openreadingframe ， orf ） : genbank中查詢該基因編碼的蛋白與zips （ zincorirontransporterproteins ，離子通道蛋白）基因家族的蛋白有75 - 35的相似性；軟體的分析結果顯示該基因編碼的蛋白為一個有8個跨膜區的跨膜蛋白； pf40蛋白為疏水蛋白，以上的特徵也許是pf40基因發揮作用的基礎。
  9. Hydrophobicity and transmembrane domain analysis show that the protein encoded by orf1 contains five hydrophobic domains and four transmembrane domains. it maybe a transmembrane protein

    經疏水性和跨膜區分析， orf1編碼的蛋白含有5個疏水區、 4個跨膜區，應為跨膜蛋白。
  10. Hydrophobicity analysis of the noeb showed that it is a transmembrane protein and includes four transmembrane regions at n - terminal., consisting of three primary helixs and one secondary helix

    疏水性分析發現， noeb是一個跨膜蛋白，在n末端有4個跨膜區，其中包含3個初級螺旋和1個次級螺旋。
  11. The cdna of hn gene from b95 strain, shares a high identity between 88 % and 95. 1 % with that of reported hn genes. the amino acid residues predicted, shares an identity between 92. 1 % and 96. 1 % with that of other strains

    1 ，氨基酸的差異主要集中在n端18 75位。該范圍內包括hn蛋白胞質區、跨膜區和細胞外區。這些變異對hn蛋白生物活性的影響還有待進一步研究。
  12. Hydrophobicity analysis predicted a 36 - residue hydrophobic signal peptide for secretion in the n - terminus, and no transmembrane region was present, suggesting it might be a type of secretory protein. some generic and atipical n - glycosylation sites were present in clsp, suggesting that the protein might represent a glycoprotein. the clsp protein contained one cub ( clr / cls, an embryonic sea urchin protein uegf, and bone morphogenetic protein i ) domain from 39th to 164th ammo acids, which is known to be involved in protein - protein or protein - substrate interaction, and a trypsin - like serine protease domain positioned from 244th to 483rd amino acids

    Clsp分子具有補體樣絲氨酸蛋白酶的多種結構特徵，包括36個氨基酸組成的疏水信號膚，一個cub （ clr / cls ， anembryonicseaurehinproteinuegf ， andbonemorphogeneticproteinl ）結構域和一個胰酶樣絲氨酸蛋白酶結構域（ t汀psin一likeserineproteasedomain ）和幾個保守的糖基化位點等，沒有發現有跨膜區的存在。
  13. The cdna of subunit b was 1470 nucleotides long coding for 489 amino acids with a conservative atp binding site " 324 - sgsit - 328 " and a predicted molecular mass of 54. 29 kda. amino acid sequence alignment analysis suggested that the v - h + - atpase b subunit of s. salsa had high homology with other reported v - h + - atpase subunit b. the h + - atpase subunit h from s. salsa was a hydrophilic protein with 465 amino acids and a predicted molecular mass of 52. 8 kda, which was encoded by a cdna with 1398 nucleotides in orf. blast analysis indicated that the h + - atpase subunit h from s. salsa had a high amino acid sequence identity with those coming from plants, but had relatively low sequence identity with those coming from other species

    鹽地堿蓬液泡膜h ~ + - atpaseb亞基是由1470個核苷酸編碼的長達489個氨基酸的多肽，分子量約54 . 29kda ，存在保守的atp結合序列「 324 - sgsit - 328 」 ，與其他物種來源的v - h ~ + - atpaseb亞基具有較高的氨基酸序列相似性； h亞基為親水多肽，開放閱讀框長達1398 - bp ，編碼465個氨基酸殘基，分子量約52 . 8kda ，與植物來源的液泡膜h ~ + - atpaseh亞基具有較高的氨基酸序列相似性，而與其他物種來源的v - h ~ + - atpaseh亞基同源性較低； c亞基開放閱讀框為495 - bp ，編碼164個氨基酸殘基，分子量約16 . 6kda ，為一跨膜多肽，存在四個可能的跨膜區。
  14. The thesis has two parts, one is the prediction the other is the confirmation. in the first part all proteins of mtb h37rv were scaned in use of two bio - software ( signal ? and tmhmm ) to analyse signal peptide and trans - menbrane helix, and discovered 182 proteins are possible secreted proteins

    預測部分利用了兩個生物學軟體（ signalp 、 tmhmm ）對結核桿菌全蛋白質組做信號肽分析和跨膜區分析，通過數據整理找到182個蛋白可能是分泌性蛋白，再經blastp對ncbi已收錄的蛋白質庫中所有序列進行相似性比對分析，發現這182個蛋白中有12個為結核桿菌所特有。
  15. Comparison between the transmembrane action potentials recorded from central ischemic zone and ischemisc border zone of rabbit s left ventrocular muscle in situ

    在體兔心左室肌缺血中心區與邊緣區跨膜電位的比較
  16. Blast in genbank indicated that it is novel gene named par - 1. the characteristics of the protein coded by this gene were analyzed by bioinformatics. the result showed that this protein was instable, p1 9. 65, located in bacterial inner membrane, and composed of alpha helix, extrended strand and random coil. there was a srong transmembrance domain and contained some conserved sites such as protein dinase c phosphorylation

    通過網際網路數據庫及生物信息學分析工具進行初步分析表明：該基因編碼的蛋白是一種等電點為9 . 65的不穩定蛋白，定位於細胞內膜；由螺旋、延伸帶、和隨機捲曲三種形式組成，具有蛋白激酶c磷酸化位點等多個位點，並具有一個強跨膜疏水區。
分享友人
分享到 Line

分享到臉書