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SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白?廣微測(cè)是最權(quán)威的檢測(cè)中心嗎??健明迪

SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白

Secretory Protein是指在細(xì)胞內(nèi)分解后,分泌到細(xì)胞外起作用的蛋白質(zhì)。分泌蛋白的N 端有普通由15~30 個(gè)氨基酸組成的信號(hào)肽。信號(hào)肽是引導(dǎo)新分解的蛋白質(zhì)向分泌通路轉(zhuǎn)移的短(長(zhǎng)度5-30個(gè)氨基酸)肽鏈。常指新分解多肽鏈中用于指點(diǎn)蛋白質(zhì)的跨膜轉(zhuǎn)移(定位)的N-末端的氨基酸序列(有時(shí)不一定在N端)。運(yùn)用SignalP 注釋蛋白序列能否含有信號(hào)肽結(jié)構(gòu),運(yùn)用TMHMM注釋蛋白序列能否含有跨膜結(jié)構(gòu),*終挑選出含有信號(hào)肽結(jié)構(gòu)并且不含跨膜結(jié)構(gòu)的蛋白為分泌蛋白。

軟件Software

  • SignalP V6.0
  • SignalP 6.0 預(yù)測(cè)來自古細(xì)菌、革蘭氏陽性細(xì)菌、革蘭氏陰性細(xì)菌和真核生物的蛋白質(zhì)中存在的信號(hào)肽predicts signal peptides and the location of their cleavage sites in proteins from Archaea, Gram-positive Bacteria,及其切割位點(diǎn)的位置。Gram-negative Bacteria and Eukarya.在細(xì)菌和古細(xì)菌中,SignalP 6.0 可以區(qū)分五種類型的信號(hào)肽:In Bacteria and Archaea, SignalP 6.0 can discriminate between five types of signal peptides:
    • Sec/SPI:由 Sec 轉(zhuǎn)座轉(zhuǎn)運(yùn),并由信號(hào)肽酶 I (Lep) 切割的“規(guī)范”分泌信號(hào)肽;"Standard" secretory signal peptides transported by Sec translocon and cleaved by Signal Peptidase I (Lep).
    • Sec/SPII:由 Sec 轉(zhuǎn)座子運(yùn)輸,并由信號(hào)肽酶 II (Lsp) 切割的脂蛋白信號(hào)肽;lipoprotein signal peptides transported by the Sec translocon and cleaved by Signal Peptidase II (Lsp).
    • Tat/SPI:由 Tat 轉(zhuǎn)座子轉(zhuǎn)運(yùn),并由信號(hào)肽酶 I (Lep) 切割的 Tat 信號(hào)肽;Tat signal peptides transported by the Tat translocon and cleaved by Signal Peptidase I (Lep).
    • Tat/SPII:由 Tat 轉(zhuǎn)位子轉(zhuǎn)運(yùn),并由信號(hào)肽酶 II (Lsp) 切割的 Tat 脂蛋白信號(hào)肽;Tat lipoprotein signal peptides transported by Tat translocon & cleaved by Signal Peptidase II (Lsp).
    • Sec/SPIII:由 Sec 轉(zhuǎn)位子運(yùn)輸,并由信號(hào)肽酶 III (PilD/PibD) 切割的菌毛蛋白和菌毛蛋白樣信號(hào)肽。Pilin & pilin-like signal peptides transported by Sec translocon & cleaved by Signal Peptidase III (PilD/PibD).
    • 此外,SignalP 6.0 預(yù)測(cè)信號(hào)肽的區(qū)域。Additionally, SignalP 6.0 predicts the regions of signal peptides.依據(jù)類型,預(yù)測(cè) n、h 和 c 區(qū)域以及其他顯著特征的位置。Depending on the type, the positions of n-, h- and c-regions as well as of other distinctive features are predicted.

  • TMHMM V2.0c
    • 用于預(yù)測(cè)蛋白質(zhì)中的跨膜螺旋。

  • Python

SignalP和TMHMM關(guān)于學(xué)術(shù)用戶收費(fèi),但是需求填寫相關(guān)信息和郵箱,以接納下載鏈接(4h有效時(shí)間)。

軟件裝置Installation of Softwares

裝置SignalP 6.0

  • 下載 訪問SignalP V6.0網(wǎng)站,找到“Download”,填寫相關(guān)信息,獲取下載鏈接,下載失掉“signalp-6.0.fast.tar.gz”。有兩個(gè)形式可以選擇——“slow_sequential”和“fast"。前者runs the full model sequentially, taking the same amount of RAM as fast but being 6 times slower;后者uses a smaller model that approximates the performance of the full model, requiring a fraction of the resources and being significantly faste。本教程下載的是fast形式。
  • 裝置Installation
    • 裝置依賴Dependencies
      • Python
      • matplotlib>3.3.2
      • numpy>1.19.2
      • torch>1.7.0 pip install torch
      • tqdm>4.46.1

    • 裝置SignalP 6.0 # 解緊縮裝置文件 tar zxvf signalp-6.0.fast.tar.gz # 進(jìn)入解壓后的軟件目錄,在終端運(yùn)轉(zhuǎn) python setup.py install # 測(cè)試裝置 signalp6 --help

裝置TMHMM V2.0c

  • 下載 訪問TMHMM V2.0c網(wǎng)站,找到“Download”,填寫相關(guān)信息,獲取下載鏈接,下載失掉“tmhmm-2.0c.Linux.tar.gz”。
  • 裝置 # 解緊縮 tar zxvf tmhmm-2.0c.Linux.tar.gz # 進(jìn)入解壓后的目錄 cd tmhmm-2.0c # 獲取以后途徑,我的是“/home/liu/tools/tmhmm-2.0c/bin” pwd # 將該途徑參與到系統(tǒng)的環(huán)境變量中,參考我之前的文章來(編輯~/.bashrc)liaochenlanruo.github.io # 修正bin目錄下的tmhmm和tmhmmformat.pl的首行為“#!/usr/bin/perl”
  • 運(yùn)轉(zhuǎn)錯(cuò)誤 運(yùn)轉(zhuǎn)軟件時(shí)總報(bào)Segmentation fault (core dumped)錯(cuò)誤,暫時(shí)無解。各位可以運(yùn)用其在線版。

軟件用法Usage

SignalP 6.0

預(yù)測(cè)Prediction

A command takes the following form

signalp6 --fastafile /path/to/input.fasta --organism other --output_dir path/to/be/saved --format txt --mode fast

  • fastafile 輸入文件為FASTA格式的蛋白序列文件Specifies the fasta file with the sequences to be predicted.。
  • organism is either other or Eukarya. Specifying Eukarya triggers post-processing of the SP predictions to prevent spurious results (only predicts type Sec/SPI).
  • format can take the values txt, png, eps, all. It defines what output files are created for individual sequences. txtproduces a tabular .gff file with the per-position predictions for each sequence. png, eps, all additionally produce probability plots in the requested format. For larger prediction jobs, plotting will slow down the processing speed significantly.
  • mode is either fast, slow or slow-sequential. Default is fast, which uses a smaller model that approximates the performance of the full model, requiring a fraction of the resources and being significantly faster. slow runs the full model in parallel, which requires more than 14GB of RAM to be available. slow-sequential runs the full model sequentially, taking the same amount of RAM as fast but being 6 times slower. If the specified model is not installed, SignalP will abort with an error.

輸入Outputs

  • output_dir/output.gff3:僅包括含有信號(hào)肽的序列信息;

  • output_dir/prediction_results.txt:包括了輸入文件中的一切序列(不重要);
  • output_dir/region_output.gff3:包括一切的信號(hào)肽區(qū)域信息。
    • n-region: The n-terminal region of the signal peptide. Reported for Sec/SPI, Sec/SPII, Tat/SPI and Tat/SPII. Labeled as N
    • h-region: The center hydrophobic region of the signal peptide. Reported for Sec/SPI, Sec/SPII, Tat/SPI and Tat/SPII. Labeled as H
    • c-region: The c-terminal region of the signal peptide, reported for Sec/SPI and Tat/SPI.
    • Cysteine: The conserved cysteine in +1 of the cleavage site of Lipoproteins that is used for Lipidation. Labeled as c.
    • Twin-arginine motif: The twin-arginine motif at the end of the n-region that is characteristic for Tat signal peptides. Labeled as R.
    • Sec/SPIII: These signal peptides have no known region structure.

批處置與結(jié)果優(yōu)化

腳本名:run_SignalP.pl

#!/usr/bin/perl

use strict;

use warnings;

# Author: Liu Hualin

# Date: Oct 14, 2021

open IDNOSEQ, ">IDNOSEQ.txt" || die;

my @faa = glob("*.faa");

foreach (@faa) {

$_ =~ /(.+).faa/;

my $str = $1;

my $out = $1 . ".nodesc";

my $sigseq = $1 . ".sigseq";

my $outdir = $1 . "_signalp";

open IN, $_ || die;

open OUT, ">$out" || die;

while () {

chomp;

if (/^(>\S+)/) {

print OUT $1 . "\n";

}else {

print OUT $_ . "\n";

}

}

close IN;

close OUT;

my %hash = idseq($out);

system("signalp6 --fastafile $out --organism other --output_dir $outdir --format txt --mode fast");

my $gff = $outdir . "/output.gff3";

if (! -z $gff) {

open IN, "$gff" || die;

;

open OUT, ">$sigseq" || die;

while () {

chomp;

my @lines = split /\t/;

if (exists $hash{$lines[0]}) {

print OUT ">$lines[0]\n$hash{$lines[0]}\n";

}else {

print IDNOSEQ $str . "\t" . "$lines[0]\n";

}

}

close IN;

close OUT;

}

system("rm $out");

system("mv $sigseq $outdir");

}

close IDNOSEQ;

sub idseq {

my ($fasta) = @_;

my %hash;

local $/ = ">";

open IN, $fasta || die;

;

while () {

chomp;

my ($header, $seq) = split (/\n/, $_, 2);

$header =~ /(\S+)/;

my $id = $1;

$hash{$id} = $seq;

}

close IN;

return (%hash);

}

將run_SignalP.pl與后綴名為“.faa”的FASTA格式文件放在同一目錄下,在終端中運(yùn)轉(zhuǎn)如下代碼:

perl run_SignalP.pl

結(jié)果解讀Output interpretation

*代表輸入文件的名字。

  • *_signalp/output.gff3:僅包括含有信號(hào)肽的序列信息;
  • *_signalp/prediction_results.txt:包括了輸入文件中的一切序列(不重要);
  • *_signalp/region_output.gff3:包括一切的信號(hào)肽區(qū)域信息;
  • *_signalp/*.sigseq:存儲(chǔ)一切信號(hào)肽的氨基酸序列文件,可用作TMHMM的輸入文件。

TMHMM

預(yù)測(cè)

離線版總是報(bào)錯(cuò),找不出緣由,因此運(yùn)用網(wǎng)頁效勞器停止,輸入文件為上述生成的“*_signalp/*.sigseq”,將其上傳至網(wǎng)頁版TMHMM,提交義務(wù),等候結(jié)果即可。

結(jié)果展現(xiàn)

TMHMM可以輸入多種格式的結(jié)果文件,詳細(xì)請(qǐng)參考其官方說明。

在TMHMM網(wǎng)站提交義務(wù)

  • Long output format
    • Length: 蛋白序列的長(zhǎng)度。The length of the protein sequence.
    • Number of predicted TMHs:預(yù)測(cè)到的跨膜螺旋的數(shù)量。The number of predicted transmembrane helices.
    • Exp number of AAs in TMHs:跨膜螺旋中氨基酸的預(yù)期數(shù)量。The expected number of amino acids intransmembrane helices. 假設(shè)此數(shù)字大于 18,則很能夠是跨膜蛋白(或具有信號(hào)肽)。If this number is larger than 18 it is very likely to be a transmembrane protein (OR have a signal peptide).
    • Exp number, first 60 AAs:在蛋白的前60個(gè)氨基酸中跨膜螺旋中氨基酸的預(yù)期數(shù)量。The expected number of amino acids in transmembrane helices in the first 60 amino acids of the protein.假設(shè)該數(shù)字超越幾個(gè),你應(yīng)該被正告在 N 端預(yù)測(cè)的跨膜螺旋能夠是一個(gè)信號(hào)肽。If it more than a few, you are warned that a predicted transmembrane helix in the N-term could be a signal peptide.
    • Total prob of N-in:N端在膜的細(xì)胞質(zhì)一側(cè)的總概率。The total probability that the N-term is on the cytoplasmic side of the membrane.
    • POSSIBLE N-term signal sequence:當(dāng)“Exp number, first 60 AAs”大于 10 時(shí)發(fā)生的正告。A warning that is produced when "Exp number, first 60 AAs" is larger than 10.

  • 蛋白F01_bin.1_00110合計(jì)436個(gè)氨基酸,有5個(gè)跨膜螺旋結(jié)構(gòu)。

  • 蛋白F01_bin.1_00142合計(jì)557個(gè)氨基酸,一切序列均在膜外,即該序列編碼的是分泌蛋白。

  • Short output format
    • "len=": 蛋白序列的長(zhǎng)度。The length of the protein sequence.
    • "ExpAA=":跨膜螺旋中氨基酸的預(yù)期數(shù)量。The expected number of amino acids intransmembrane helices.假設(shè)此數(shù)字大于 18,則很能夠是跨膜蛋白(或具有信號(hào)肽)。If this number is larger than 18 it is very likely to be a transmembrane protein (OR have a signal peptide).
    • "First60=":在蛋白的前60個(gè)氨基酸中跨膜螺旋中氨基酸的預(yù)期數(shù)量。The expected number of amino acids in transmembrane helices in the first 60 amino acids of the protein.假設(shè)該數(shù)字超越幾個(gè),你應(yīng)該被正告在 N 端預(yù)測(cè)的跨膜螺旋能夠是一個(gè)信號(hào)肽。If it more than a few, you are warned that a predicted transmembrane helix in the N-term could be a signal peptide.
    • "PredHel=":預(yù)測(cè)到的跨膜螺旋的數(shù)量。The number of predicted transmembrane helices by N-best.
    • "Topology=":N-best 預(yù)測(cè)的拓?fù)浣Y(jié)構(gòu)。The topology predicted by N-best.拓?fù)涫怯煽缒ぢ菪奈恢媒o出的,假設(shè)螺旋在外部,則由“i”分隔,假設(shè)螺旋在外部,則由“o”分隔。'i7-29o44-66i87-109o'意味著它從膜內(nèi)末尾,在位置7到29有一個(gè)預(yù)測(cè)的TMH,30-43在膜外,然后是位置44-66的TMH。

結(jié)果匯總

經(jīng)過網(wǎng)頁版預(yù)測(cè)我們僅失掉了一個(gè)列表文件(Short output format),該文件需求自己復(fù)制網(wǎng)頁內(nèi)容粘貼到新文件中,我將其命名為*_TMHMM_SHORT.txt,并將其寄存在*_signalp目錄中,該目錄是由run_SignalP.pl生成的。下面我將會(huì)統(tǒng)計(jì)各個(gè)基因組中信號(hào)肽蛋白的總數(shù)量、分泌蛋白數(shù)量和跨膜蛋白數(shù)量到文件Statistics.txt中,并區(qū)分提取每個(gè)基因組的分泌蛋白序列到*_signalp/*.secretory.faa文件中,提取跨膜蛋白序列到*_signalp/*.membrane.faa文件中。該進(jìn)程將經(jīng)過tmhmm_parser.pl完成。

#!/usr/bin/perl use strict; use warnings; # Author: Liu Hualin # Date: Oct 15, 2021 open OUT, ">Statistics.txt" || die; print OUT "Strain name\tSignal peptide numbers\tSecretory protein numbers\tMembrane protein numbers\n"; my @sig = glob("*_signalp"); foreach my $sig (@sig) { $sig=~/(.+)_signalp/; my $str = $1; my $tmhmm = $sig . "/$str" . "_TMHMM_SHORT.txt"; my $fasta = $sig . "/$str" . ".sigseq"; my $secretory = $str . ".secretory.faa"; my $membrane = $str . ".membrane.faa"; open SEC, ">$secretory" || die; open MEM, ">$membrane" || die; my $out = 0; my $on = 0; my %hash = idseq($fasta); open IN, $tmhmm || die; while () { chomp; $_=~s/[\r\n]+//g; # print $_ . "\n"; my @lines = split /\t/; if ($lines[5] eq "Topology=o") { $out++; print SEC ">$lines[0]\n$hash{$lines[0]}\n"; }else { $on++; print MEM ">$lines[0]\n$hash{$lines[0]}\n"; } } close IN; close SEC; close MEM; system("mv $secretory $membrane $sig"); my $total = $out + $on; print OUT "$str\t$total\t$out\t$on\n"; } close OUT; sub idseq { my ($fasta) = @_; my %hash; local $/ = ">"; open IN, $fasta || die; ; while () { chomp; my ($header, $seq) = split (/\n/, $_, 2); $header =~ /(\S+)/; my $id = $1; $hash{$id} = $seq; } close IN; return (%hash); }

運(yùn)轉(zhuǎn)方法:將tmhmm_parser.pl放在*_signalp的上一級(jí)目錄下,*_signalp目錄中必需包括*_TMHMM_SHORT.txt文件和*.sigseq文件。在終端運(yùn)轉(zhuǎn)如下代碼:

perl tmhmm_parser.pl

腳本獲取

本文腳本見GitHub。

敬告:運(yùn)用文中腳本請(qǐng)?jiān)帽疚木W(wǎng)址,請(qǐng)尊重自己的休息效果,謝謝!Notice: When you use the scripts in this article, please cite the link of this webpage. Thank you!

參考

原文鏈接:SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白 | liaochenlanruo

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編輯于 2021-12-28 09:33
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SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白?廣微測(cè)是*威望的檢測(cè)中心嗎??健明迪

如何檢測(cè)純真水設(shè)備能否有細(xì)菌繁殖呢

保證產(chǎn)出水質(zhì)的潔凈是純真水設(shè)備消費(fèi)的關(guān)鍵,但是有時(shí)分也會(huì)出現(xiàn)純真水細(xì)菌繁殖的狀況,那么純真水設(shè)備如何檢測(cè)能否有細(xì)菌繁殖呢?罕見的有三種方法:

  一、經(jīng)典微生物培育法:微生物培育法的要素包括:培育基的類型、培育溫度和培育時(shí)間。培育方法包括:燒注皿培育法、鋪平皿法、膜過濾法。

  二、儀器法主要有:顯微鏡直接計(jì)數(shù)法、放射法、阻抗法以及多種生化方法。

1、優(yōu)點(diǎn)是精度好,準(zhǔn)確度高,可以在較短時(shí)間內(nèi)取得檢測(cè)結(jié)果, 有利于停止及時(shí)控制。

2、缺陷是需人工處置樣品,任務(wù)量大,樣品處置量小,易受儀器等其他方面的制約,并且儀器法對(duì)微生物是破壞性的,它無法對(duì)污染菌作進(jìn)一步的分別和鑒別。

  三、慣例方法:微生物的鑒別是一項(xiàng)專業(yè)性很強(qiáng)的任務(wù),需少量任務(wù)閱歷及專業(yè)知識(shí)。

  掌握純真水設(shè)備細(xì)菌檢測(cè)方法,足以可以看出各種不利于設(shè)備產(chǎn)水規(guī)范的現(xiàn)象,檢測(cè)出危機(jī)產(chǎn)水質(zhì)量的污染細(xì)菌種類,保證用戶可以及時(shí)處置效果,結(jié)合純真水設(shè)備運(yùn)轉(zhuǎn)條件保證系統(tǒng)產(chǎn)水動(dòng)搖、牢靠。

發(fā)布于 2022-11-13 15:33?IP 屬地山東
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SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白?廣微測(cè)是*威望的檢測(cè)中心嗎??健明迪

健明迪微生物:例磺胺、抗生素等對(duì)生物體外部被微生物感染的組織或病變細(xì)胞停止治療,以殺死組織內(nèi)的病原微生物或病變細(xì)胞,但對(duì)無機(jī)體無毒害作用的治療措施。 來源:健明迪轉(zhuǎn)載于食品微生物檢測(cè)群眾號(hào)
SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白?廣微測(cè)是最權(quán)威的檢測(cè)中心嗎??健明迪
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健明迪檢測(cè)提供的SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白?廣微測(cè)是最權(quán)威的檢測(cè)中心嗎??健明迪,預(yù)測(cè)微生物分泌蛋白了塵蘭若了塵蘭若了塵蘭若華中農(nóng)業(yè)大學(xué)微生物學(xué)博士華中農(nóng)業(yè)大學(xué)微生物學(xué)博士
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