殘基 的英文怎麼說

中文拼音 [cánjī]
殘基 英文
[生物化學] residue
  • 殘 : Ⅰ形容詞1 （不完整; 殘缺） incomplete; deficient 2 （剩餘的; 將盡的） remnant; remaining 3 （兇惡...
  1. 2 gene and had conservative amino acids of catalase

    2基因具有45的同源性，具有過氧化氫酶的保守氨基酸殘基。
  2. Its action site is located on the postsynaptic membrane and the biological activity of hwtx - i is located in the fifth p - turn containing lys25 and lys 27. to - conotoxin mviia is a neurotoxin belonging to one of n - type ca2 + channels inhibitors, purified from the venom of the conus marine snails, contains 25 amino acid residues with three disulfide binds. it adopts the pattern of ick and its linkage of the disulfide binds and space conformation are highly similar to hwtx - i

    -芋螺毒素mviia （ - conotoxinmviia ）是從芋螺屬（ conus ）海底蝸牛毒液中分離提純的一種活性多肽，屬于n -型ca ~ （ 2 + ）通道阻斷劑中一種，含25個氨基酸殘基，三對二硫鍵，其二硫鍵連接方式、分子的空間構象與hwtx -很相似，採取ick結構模體。
  3. Two spider silk protein genes ( avfl and avf2 ) screened from the library are characterized in a lot of repetitive motifs, a high guanosines or cytidines content, a strong preference for adenosine or thymidine in the third position of a codon and rich residues of glycines or alanines in the proteins translated

    試驗結果，該文庫容量為4 . 9 10 ~ 6 。從文庫中篩選到avf1和avf2蛛絲蛋白新基因，具有典型重復序列多， g c含量高，密碼子第三個堿基偏愛使用a t及編碼蛋白中含有大量gly和ala殘基等特點。
  4. Whole mount in situ hybridization showed that amphihmgb transcripts were present ubiquitously in the early embryos from zygote to neurula, but they decreased gradually in mesoderm and endoderm and neural tube with development, and became restricted to epidermal cells in the hatched larva. it appear s that hmgb plays a role in the mitosis and differentiation of embryonic cells. another amphioxus cdna, amphiubf80, encoding ubiquitin / ribosomal fused protein s27a, was isolated from the gut cdna library of b. belcheri tsingtauense

    S004cdna序列編碼一個156個氨基酸殘基組成的蛋白質，與人的泛素蛋白ubf80具有較高的氨基酸序列同源性（ 145 / 156同源） ，且該蛋白具有泛素蛋白ubf80所共有的兩個結構域，即由72個氨基酸組成的泛素介導的蛋白降解結構域和由48個氨基酸組成的核糖體蛋白s27a結構域。
  5. This time, using cdna of zmcdc5 as template, we amplify a sequence by means of pcr technology. and then, using restrict endoenzyme and ligase, we conjunct the 0. 8kb length dna sequence in a expression vector, pet - 30a. after induction, expression and purification, we obtained a 35. 4kda truncated fusing zmcdc5 protein which contains 267aa ( 647 to 914aa in zmcdc5 ). with the purified protein, we got its antibody and testified the antibody by means of western blotting and dot blotting

    本實驗是以zmcdc5的cdna為模板，使用pcr獲得基因片段，再通過酶切連接，將得到的0 . 8kb的基因片段構建於pet - 30a表達載體上，經過誘導表達和純化，獲得zmcdc5的融合蛋白，其中包括了zmcdc5925個氨基酸中647 914共267個氨基酸殘基
  6. 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。
  7. The helix makes a complete turn every 3. 6 residues.

    每個36個殘基，螺旋正好轉一圈。
  8. The relationship between protein secondary structureand messenger rna secondary structure

    多肽鏈二級結構的氫鍵定義及氨基酸殘基間的氫鍵分佈
  9. The sequence of hntx - v had been determined by 491 sequencer : nh2 - eclgfgkgcnpsdqccksanlvcsrkhrwckyei - cooh, in which there were 35 amino acid residues and six cys. the toxin could block neuromuscular transmission in an isolated mouse phrenic nerve diaphragm preparation. hntx - v is a natural mutant of hntx - iv, for there is only one different residue ( ala20ser )

    Hntx -經491測序儀測得其氨基酸組成為： nh2 - eclgfgkgcnpsdqccksanlvcsrkhrwckyei - cooh ，含35個氨基酸殘基， 6個半胱氨酸全部參與了二硫鍵的形成，該毒素對小鼠膈神經-膈肌標本有阻遏作用。
  10. Can link with tyr, thus results in prion ' s aggregation with the extension of the reaction chain

    可與正常tyr殘基發生交聯反應，隨著反應鏈的延伸，最終導致prion的聚集沉澱。
  11. Ricin is a heterodimeric rip comprised of a and b chains joined through a disulfide bond

    A鏈（ rta ）是活性鏈，分子量約32kd ，第十位殘基asn連接一條寡糖鏈。
  12. In this study, we at first aimed at obtaining the gene encoding the specific ige antibody related proteins by immunoscreening the schistosoma juponi cum adult worm cdna library with the pooled high - titer ige antisera from the individuals living in the schistosome epidemic regions

    J測定。 jnij序結果顯示，該插入片段為1200hp ，第一開讀框長507hp ，編碼169個氨基酸殘基，理論分子量為19 3kdi 。
  13. Using molecular imprinting method, the 1, 3 - dimethylxanthine theophylline, tho molecular recognition membranes, containing an segments as membrane formation sites and aa segments as functional sites, were prepared by the phase inversion technique. here, tho was selected as a template molecule. the hydrogen bonding between aa segments and the tho templates was measured by ft - ir and nmr. the tho templates can be removed from the membrane through washing with acetic acid aqueous solution. the permeation of tho through the membranes is far more than that of 1, 3, 7 - trimethylxanthine caffeine, caf, which demonstrated the function of tho molecular recognition of the membrane. the results also show that the increase of the tho templates concentration in the cast solution caused an increase of tho amounts taken into the copolymer membrane

    Ft - ir及nmr測試結果表明：制備的高分子膜中， tho模板分子和膜中的丙烯酸功能殘基存在著氫鍵鍵合作用。大量的極性醋酸水溶液可抽出膜中的模板分子。 tho溶液和與模板分子具有相似結構的1 ， 3 ， 7 -三甲基黃嘌呤咖啡因， caf溶液的基質透過實驗結果：進入膜結構中tho分子的量遠大於caf分子，這表明制備的高分子膜具有tho分子識別功能。
  14. These changes were relevant to the concentration, the hydrophilic or hydrophobic nature and the length of arm spacers of crosslinker

    親水性edc對psll的蛋白質中tyr和trp殘基所處微環境的影響較小；而親脂性dcc 、 hmdi
  15. In this paper, the relationship between cyanide - resistant respiration and expression of alternative oxidase ( aox ) using polyantibodies prepared by synthetic polypeptide in mung bean seedling, as well as the effects of vernalization on cyanide - resistant respiration and expression of aox in winter wheat were studied respectively. in the first part, twelve peptides, including eight conservative amino acid residues in the amino acid sequence of hydrophilic s helix of aox. were synthesized by solid - phase method

    第一部分，我們按照交替氧化酶（ alternativeoxidase ， aox ）位於線粒體內膜外側親水區s螺旋的氨基酸序列，用固相法合成由12個氨基酸殘基組成的多肽，將此多肽與-牛胰凝乳蛋白酶原a相連，用作半抗原，免疫家兔制備人工合成12肽的抗體。
  16. The residues capable of forming amphipathic a - helice structure in the first conserved domain are identical to those of ap2, while the structure in the second conserved domain lacks 9 amino acids as compared to that of ap2

    螺旋的氨基酸殘基與apz的完全相同，而另一個區域中形成。螺旋g ：氦基酸歿基與apz相比少9個氨基酸。
  17. Surprisingly, in both of archaebacteria and chloroplast, ftsz is the main component in the process of division but it is n ' t effective in mitochodria division, instead is a dynamin protein

    此外ftsz還是一種400個殘基的保守蛋白， ftsz與真核tubulin在結構、功能和進化上有一定的相似性及同源性，都具gtpase結構域，屬于g蛋白家族。
  18. The three isoforms have a common carboxy - terminal domain of 188 amino acids, and this region is highly homologous to the reticulon protein family

    在nogo分子的c -末端，有兩個跨膜片段，被66個氨基酸殘基組成的環狀結構（ nogo - 66 ）所分隔。
  19. The a - transglucosidase was selectively modified by pcmb, me, edc, clac, acetyl acetone and nbs, and changes in the activities of the enzyme have been detected. the reaction of a - transglucosidase with pcmb, me, edc and clac resulted in a strong inhibition of the enzyme activities which decreased with the increase of modifier concentration. the acetyl acetone and nbs were found without inhibition effect

    酚丙酮、小涅代唬拍酷亞胺剛b引等化學修飾劑對a葡萄糖轉苦酶的幾種氨基酸殘基進行選擇修飾，並測定其酶活力變化，結果表明： pcmb 、 me 、 edc 、 ciac能顯著抑制酶的活性，活力的下降與修飾劑的濃度有關，乙酚丙酮、 nbs白巾飾對酶的奪製作用不明顯。
  20. Badh cdna ( 1901bp ) included a 66 bp 5 " utr, a 329 bp 3 " utr and a 1506 bp orf encoding a 501 - ammo - acid polypeptide which showed 88 % sequence identity to badh from spinach, sugar beet and atriplex hortensis respectively. the deduced amino acid sequence included a decapeptide sequence " vtlelggksp ", which is highly conserved among general aldehyde dehydrogenases ( aldh ), and a cysteine residue

    Badhcdna全長1901bp ， 5端非編碼區66bp ， 3端非編碼區329bp ，含有2個可能的加polya信號： aataa ，開放閱讀框架1506bp ，編碼一個由501個氨基酸構成的多肽，與菠菜、甜菜、山菠菜badh的氨基酸序列同源性均為88 ，其中有醛脫氫酶的保守序列vtlelggksp和半胱氨酸殘基。
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