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。
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)。
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。
Segmentation fault (core dumped)
錯(cuò)誤,暫時(shí)無解。各位可以運(yùn)用其在線版。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. txt
produces 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.
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
*代表輸入文件的名字。
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。
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)
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 (
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
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!
原文鏈接:SignalP+TMHMM預(yù)測(cè)微生物分泌蛋白 | liaochenlanruo
轉(zhuǎn)載請(qǐng)注明出處!
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
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。
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)Copyright ? 2023.廣州市健明迪檢測(cè)有限公司 .粵ICP備2022046874號(hào)技術(shù)文章 檢測(cè)服務(wù) 相關(guān)資訊