terminal sequence 中文意思是什麼
terminal sequence
解釋
末端排列-
Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosphatidylinositol ( gpi ). gpi - anchored proteins are synthesized on membrane - bound ribosomes. upon translocation of the pro - protein across the endoplasmic reticulum membrane, gpi : protein transamidase ( gp1t ) recognize and removes the carboxy terminal gpi signal sequence and attaches a gpi molecule to the newly exposed carboxy terminal amino acid
Gpi化前體蛋白在依附於膜的核糖體上合成，當其易位穿過內質網（ er ）膜后，被gpi ：蛋白質轉酰胺基酶（ gpit ）識別， gpit在移走其羧基端gpi信號序列的同時將gpi分子連接至新生成的氨基酸位點上。 -
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。 -
The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins
將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。 -
The ir sequence of mxmybl is most homologous with that of atmyb ( 86. 9 % ) and somewhat homologous with that of stmyb 1 ( 77. 0 % ) ; there is very low homology among n - and c - terminal regions outside of the ir regions of all of the mybs ; the protein mxmybl contains a proline - rich region as well as a serine - rich region near the c - terminus, such structure motifs are implicated in transcriptional activation
9 ，與馬鈴薯stmyb的ir序列的同源性達77 0 ，所有這些nnrb蛋白除了瓜區具有較高的同源性外，其c端和n端幾乎沒有同源性。 mwyb蛋白的c一端還含有一個富含脯氨酸區，這樣的結構基序可能具有激活轉錄的功能。 -
It contained 187 amino acids deduced from the nucleotide sequence, and showed 65 % amino acid sequence identity with human aoeb166. the analysis of n - and c - terminal domains revealed amino acid sequences characteristic of features of mitochondrial and peroxisomal targetin
原位雜交分析表明從受精卵到神經胚， aophihmgb基因廣泛表達，但隨著發育的進行，中胚層、內胚層和神經管的表達減弱，到1天幼蟲期，僅在表皮可檢測到表達。 -
In this paper, we mainly optimize the flight profile of the aircraft, simulate the 4d - flight of them and research the application of sequence in arrival aircraft scheduling in terminal area. firstly, we create the mathematics models for simulating 4d - flight
本文主要對按給定航線飛行的航班的飛行剖面進行優化設計，模擬航班的四維飛行，同時對到達航班隊列排序優化演算法進行設計、研究和實現。 -
It is shown that the obtained proteins ( hq - 5 & tsk - 2 ) can be identified as novel components of anti - coagulation enzyme family in the venom of agkistrodon acutus by the analysis of the n - terminal sequence of tsk - 2
其一級序列為rtefqrymeivv 。與從蘄蛇蛇毒中分離出的其它組分相比， hq - 5及其降解產生的組分（ tsk - 2 ）為新的抗凝血組分。 -
Unified power flow controller ( upfc ) is one of the most powerful and most promising controllers of facts. if we use upfc to control the transmission parameters, terminal voltage, line impedance and phase angle in normal situation and use it to compensate zero sequence and negative sequence currents when one of transmission lines is cut off, we can implement two phases operating in high voltage transmission lines, which can improve stability and reliability for the transmission system
統一潮流控制器（ upfc ）是功能最強、最具發展潛力的靈活交流輸電系統（ facts ）控制器之一，如果在常規條件下，用upfc實現輸電線路的電壓調節、移相、潮流控制、阻尼振蕩等功能，在發生單相永久性接地或單相斷路故障時，由傳統的三相跳閘改為單相跳閘，用upfc的並補來濾除兩端系統的零序和負序電流，用upfc的串補來提高輸電線的傳輸功率，以實現兩相長期運行，那麼輸電系統的穩定性、可靠性將大大提高。 -
The decoder is compiled and simulated in ep1c12q240c by quartusii - 5. 0. the different error style is added to the sequence received in emulated channel. correspondingly, the correct decoding results are attained at the output terminal
在quartusii - 5 . 0模擬環境下以cyclone系列的ep1c12q240c為目標晶元對譯碼器進行了編譯和模擬，在接收序列中加入不同的錯誤類型，相應的在譯碼器輸出端得出了譯碼后的正確譯碼結果，驗證了設計方案的正確性。 -
Tams, terminal - age main sequence
終齡主序 -
The sequence encodes an open reading frame of 518 amino acids. there is a transit peptide of 74 amino acids in the n terminal of the putative amino acids sequence coded by the cdna
該序列長為1758hp ，起始密碼子位於84 86hp ，終止密碼子為1658 166fop ，開放閱讀框長為1557hp ，編碼58個氨基酸序列，其中n末端含有74個氨基酸的轉運肽。 -
A pair of primers were designed according to the published sequence of gnrh2 ' s gene mrna and transporter gene with oligo version 4. 1 softwarre, they were annealed by their 3 ' terminal brief complementary base sequence to form small segment double chain, therery, they serve mutually as template and primer, and their extension were carried out to synthesize 90 bp " gnrh / trs
本研究根據genbank中已發表的人gnrh2基因mrna序列以及轉運肽（ transporter ， trs ）基因核苷酸序列，藉助oligo4 . 1設計了一對寡核苷酸引物，以引物3末端的短互補序列退火形成小段雙鏈，從而互為模板和引物，通過引導合成長達90bp的gnrh trs序列gnrh trs 。 -
The complete human znf325 cdna sequence is 2697bp and contains a 1389 - bp open reading frame ( orf ) that encodes a 462 amino acid protein with 15 zinc finger c2h2 motifs. the complete human znf359 cdna sequence is 3270bp and contains a 1932 - bp open read ing frame ( orf ) that encodes a 643 amino acid protein with an n - terminal krab domain and 16 c - terminus zinc finger c2h2 motifs. the zfp28 cdna sequence is 4104bp and contains a 2076 - bp open reading frame ( orf ) that encodes an 868 amino acid protein with an n - terminal signal peptide, two krab domains and 14 c - terminal c2h2 zinc finger motifs
Znf325長2697個堿基，含有一個長為1389個堿基的開放閱讀框，編碼一個長為462個氨基酸的蛋白質，它包含15個c2h2型鋅指結構； znf359長3270個堿基，含有一個長為1932個堿基的開放閱讀框，編碼一個長為643個氨基酸的蛋白質，它包含一個n -端krab結構域和16個c -端c2h2型鋅指結構； zfp28長4104個堿基，含有一個長為2076個堿基的開放閱讀框，編碼一個長為868個氨基酸的蛋白質，它包含一個n -端信號肽，兩個krab結構域和14個c -端c2h2型鋅指結構。 -
Mass spectrometry technique will play more and more role in the field of sequence analysis. standard amino acid thiohydantoins are required as reference standard for development of c - terminal protein sequencing based on the thiohydantoin procedure
在蛋白質c端（異）硫氰酸法順序測定技術中，標準氨基酸乙內酰硫脲（ th - aa ）的制備是必須首先要解決的問題。 -
Not only sequence information from the c - terminus of proteins and peptides is of especial interest in the investigation of n - terminally blocked proteins and peptides, but also c - terminal sequence analysis can facilitate the production of more specific probes for gene cloning
C端與n端一樣，在蛋白質分子結構分析中具有重要的地位，對其順序測定具有重要的意義，不僅可以對n端封閉的蛋白質進行序列測定，而且對基因克隆有指導意義。 -
Sequence analysis showed highly similarity to other plants such as narcissus pseudonarcissus., and they all possess a short highly conserved n - terminal sequence encoding a dinucleotide cofactor binding site. thus it is a new member of phytoene desaturase gene family
由此可認為該番紅花八氫番茄紅素脫氫酶基因在結構上與其它植物八氫番茄紅素脫氫酶基因是同源的，是八氫番茄紅素脫氫酶基因家族中的一個新成員。 -
Its molecular weight was determined to be 26. 8kda by sds - page and the same under reduced conditions. its anti - coagulation activity was characterized. the n - terminal sequence of tsk - 2 is rtefqrymeiw
該組分為單鏈蛋白質，分子量為26 . 8kda ，具有抗凝血活性，是嗜硫色譜洗脫峰降解后新產生的蛋白組分。 -
The first 24 amino acid residues of the n - terminal sequence of ba - dfe were aqsvpygvsqikapalhsqgftgs, which is different from those fibrinolytic enzymes, such as nk ( nattokinase ), ck ( a fibrinolytic enzyme from chungkook - jang ) and kk ( katsuwokinase )
Ba - dfe能直接降解纖維蛋白，不能激活纖溶酶原形成纖溶酶。蛋白質測序結果顯示，該酶n -端24個氨基酸序列為aqsvpygvsqikapalhsqgftgs 。 -
The homologous analysis showed that the n - terminal sequence of dhap is identical to that of serine protease from another b. pumilus strain tyo - 67 and has high homology with those from other bacillus species. based on the homologous analysis, three pairs of primers were designed and synthesized
該序列與來自其它芽抱桿菌屬菌株的絲氨酸蛋白酶的n一末端氨基酸序列有較高的同源性，並和另一株短小芽抱桿菌的絲氨酸蛋白酶n一末端氨基酸序列完全一致。 -
But in recent developments, especially in derivatizing reagents, have demonstrated that this method appears very promising in the field of protein c - terminal sequence analysis in future. furthermore, with the significant improvements of mass spectrometry technologies, which facilitate analysis of large biological molecules
同時近十年來隨著質譜技術的發展，使得質譜在分析大分子化學物質成為可能后，在蛋白質順序分析領域里取得了很多重要進展。
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