📄 iep.txt
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iep Function Calculates the isoelectric point of a proteinDescription This calculates the isoelectric point of a protein from its amino acid composition assuming that no electrostatic interactions change the propensity for ionization. Adjusting the pH of an aqueous protein solution to the point where the numbers of positive and negative charges on the protein are equal brings the protein to its isoelectric point. This is often the point of lowest solubility, presumably because it is the point at which there are fewest intermolecular repulsions, so that the molecules tend to form aggregates. The application can make a plot of the ionization curve with respect to pH and can write an output file of the data.Usage Here is a sample session with iep% iep tsw:laci_ecoli Calculates the isoelectric point of a proteinOutput file [laci_ecoli.iep]: Go to the input files for this example Go to the output files for this example Example 2% iep tsw:ifna2_human -disulphide 2 -lysinemodified 2 Calculates the isoelectric point of a proteinOutput file [ifna2_human.iep]: Go to the input files for this example Go to the output files for this exampleCommand line arguments Standard (Mandatory) qualifiers (* if not always prompted): [-sequence] seqall Protein sequence(s) filename and optional format, or reference (input USA)* -graph xygraph [$EMBOSS_GRAPHICS value, or x11] Graph type (ps, hpgl, hp7470, hp7580, meta, cps, x11, tekt, tek, none, data, xterm, png)* -outfile outfile [*.iep] Output file name Additional (Optional) qualifiers: -amino integer [1] Number of N-termini (Integer 0 or more) -[no]termini boolean [Y] Include charge at N and C terminus -lysinemodified integer [0] Number of modified lysines (Integer 0 or more) -disulphides integer [0] Number of disulphide bridges (Integer 0 or more) Advanced (Unprompted) qualifiers: -step float [.5] Step value for pH (Number from 0.010 to 1.000) -plot toggle [N] Plot charge vs pH -[no]report toggle [Y] Write results to a file Associated qualifiers: "-sequence" associated qualifiers -sbegin1 integer Start of each sequence to be used -send1 integer End of each sequence to be used -sreverse1 boolean Reverse (if DNA) -sask1 boolean Ask for begin/end/reverse -snucleotide1 boolean Sequence is nucleotide -sprotein1 boolean Sequence is protein -slower1 boolean Make lower case -supper1 boolean Make upper case -sformat1 string Input sequence format -sdbname1 string Database name -sid1 string Entryname -ufo1 string UFO features -fformat1 string Features format -fopenfile1 string Features file name "-graph" associated qualifiers -gprompt boolean Graph prompting -gdesc string Graph description -gtitle string Graph title -gsubtitle string Graph subtitle -gxtitle string Graph x axis title -gytitle string Graph y axis title -goutfile string Output file for non interactive displays -gdirectory string Output directory "-outfile" associated qualifiers -odirectory string Output directory General qualifiers: -auto boolean Turn off prompts -stdout boolean Write standard output -filter boolean Read standard input, write standard output -options boolean Prompt for standard and additional values -debug boolean Write debug output to program.dbg -verbose boolean Report some/full command line options -help boolean Report command line options. More information on associated and general qualifiers can be found with -help -verbose -warning boolean Report warnings -error boolean Report errors -fatal boolean Report fatal errors -die boolean Report dying program messagesInput file format iep reads in any protein sequence USA. Input files for usage example 'tsw:laci_ecoli' is a sequence entry in the example protein database 'tsw' Database entry: tsw:laci_ecoliID LACI_ECOLI STANDARD; PRT; 360 AA.AC P03023; P71309; Q47338; O09196;DT 21-JUL-1986 (Rel. 01, Created)DT 01-NOV-1997 (Rel. 35, Last sequence update)DT 15-DEC-1998 (Rel. 37, Last annotation update)DE LACTOSE OPERON REPRESSOR.GN LACI.OS Escherichia coli.OC Bacteria; Proteobacteria; gamma subdivision; Enterobacteriaceae;OC Escherichia.RN [1]RP SEQUENCE FROM N.A.RX MEDLINE; 78246991.RA FARABAUGH P.J.;RT "Sequence of the lacI gene.";RL Nature 274:765-769(1978).RN [2]RP SEQUENCE FROM N.A.RC STRAIN=K12 / MG1655;RX MEDLINE; 97426617.RA BLATTNER F.R., PLUNKETT G. III, BLOCH C.A., PERNA N.T., BURLAND V.,RA RILEY M., COLLADO-VIDES J., GLASNER F.D., RODE C.K., MAYHEW G.F.,RA GREGOR J., DAVIS N.W., KIRKPATRICK H.A., GOEDEN M.A., ROSE D.J.,RA MAU B., SHAO Y.;RT "The complete genome sequence of Escherichia coli K-12.";RL Science 277:1453-1474(1997).RN [3]RP SEQUENCE FROM N.A.RC STRAIN=K12 / MG1655;RA DUNCAN M., ALLEN E., ARAUJO R., APARICIO A.M., CHUNG E., DAVIS K.,RA FEDERSPIEL N., HYMAN R., KALMAN S., KOMP C., KURDI O., LEW H.,RA LIN D., NAMATH A., OEFNER P., ROBERTS D., SCHRAMM S., DAVIS R.W.;RL Submitted (NOV-1996) to the EMBL/GenBank/DDBJ databases.RN [4]RP SEQUENCE FROM N.A.RA CHEN J., MATTHEWS K.K.S.M.;RL Submitted (MAY-1991) to the EMBL/GenBank/DDBJ databases.RN [5]RP SEQUENCE FROM N.A.RA MARSH S.;RL Submitted (JAN-1997) to the EMBL/GenBank/DDBJ databases.RN [6]RP SEQUENCE OF 1-147; 159-230 AND 233-360.RX MEDLINE; 76091932.RA BEYREUTHER K., ADLER K., FANNING E., MURRAY C., KLEMM A., GEISLER N.;RT "Amino-acid sequence of lac repressor from Escherichia coli.RT Isolation, sequence analysis and sequence assembly of trypticRT peptides and cyanogen-bromide fragments.";RL Eur. J. Biochem. 59:491-509(1975).RN [7] [Part of this file has been deleted for brevity]CC between the Swiss Institute of Bioinformatics and the EMBL outstation -CC the European Bioinformatics Institute. There are no restrictions on itsCC use by non-profit institutions as long as its content is in no wayCC modified and this statement is not removed. Usage by and for commercialCC entities requires a license agreement (See http://www.isb-sib.ch/announce/CC or send an email to license@isb-sib.ch).CC --------------------------------------------------------------------------DR EMBL; V00294; CAA23569.1; -.DR EMBL; J01636; AAA24052.1; -.DR EMBL; AE000141; AAC73448.1; -.DR EMBL; U73857; AAB18069.1; ALT_INIT.DR EMBL; X58469; CAA41383.1; -.DR EMBL; U86347; AAB47270.1; ALT_INIT.DR EMBL; U72488; AAB36549.1; -.DR EMBL; U78872; AAB37348.1; -.DR EMBL; U78873; AAB37351.1; -.DR EMBL; U78874; AAB37354.1; -.DR PIR; A03558; RPECL.DR PIR; S02540; S02540.DR PDB; 1LCC; 31-JAN-94.DR PDB; 1LCD; 31-JAN-94.DR PDB; 1LTP; 31-OCT-93.DR PDB; 1TLF; 31-JUL-95.DR PDB; 1LBG; 11-JUL-96.DR PDB; 1LBH; 11-JUL-96.DR PDB; 1LBI; 11-JUL-96.DR PDB; 1LQC; 12-FEB-97.DR ECO2DBASE; H039.0; 6TH EDITION.DR ECOGENE; EG10525; LACI.DR PFAM; PF00356; lacI; 1.DR PFAM; PF00532; Peripla_BP_like; 1.DR PROSITE; PS00356; HTH_LACI_FAMILY; 1.KW Transcription regulation; DNA-binding; Repressor; 3D-structure.FT DNA_BIND 6 25 H-T-H MOTIF.FT MUTAGEN 17 17 Y->H: BROADENING OF SPECIFICITY.FT MUTAGEN 22 22 R->N: RECOGNIZE AN OPERATOR VARIANT.FT VARIANT 282 282 Y -> D (IN T41 MUTANT).FT CONFLICT 286 286 S -> L (IN AAA24052, REF. 2, 4 AND 5).FT HELIX 6 13FT TURN 14 14FT HELIX 17 24FT HELIX 32 44FT TURN 49 50SQ SEQUENCE 360 AA; 38564 MW; 4CA5A1D6 CRC32; MKPVTLYDVA EYAGVSYQTV SRVVNQASHV SAKTREKVEA AMAELNYIPN RVAQQLAGKQ SLLIGVATSS LALHAPSQIV AAIKSRADQL GASVVVSMVE RSGVEACKAA VHNLLAQRVS GLIINYPLDD QDAIAVEAAC TNVPALFLDV SDQTPINSII FSHEDGTRLG VEHLVALGHQ QIALLAGPLS SVSARLRLAG WHKYLTRNQI QPIAEREGDW SAMSGFQQTM QMLNEGIVPT AMLVANDQMA LGAMRAITES GLRVGADISV VGYDDTEDSS CYIPPSTTIK QDFRLLGQTS VDRLLQLSQG QAVKGNQLLP VSLVKRKTTL APNTQTASPR ALADSLMQLA RQVSRLESGQ// Input files for usage example 2 Database entry: tsw:ifna2_humanID IFNA2_HUMAN STANDARD; PRT; 188 AA.AC P01563; P01564; Q14606; Q96KI6;DT 21-JUL-1986, integrated into UniProtKB/Swiss-Prot.DT 21-JUL-1986, sequence version 1.DT 27-JUN-2006, entry version 72.DE Interferon alpha-2 precursor (Interferon alpha-A) (LeIF A).GN Name=IFNA2;OS Homo sapiens (Human).OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;OC Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;OC Catarrhini; Hominidae; Homo.OX NCBI_TaxID=9606;RN [1]RP NUCLEOTIDE SEQUENCE.RX MEDLINE=81052322; PubMed=6159538; DOI=10.1038/287411a0;RA Goeddel D.V., Yelverton E., Ullrich A., Heyneker H.L., Miozzari G.,RA Holmes W., Seeburg P.H., Dull T.J., May L., Stebbing N., Crea R.,RA Maeda S., McCandliss R., Sloma A., Tabor J.M., Gross M.,
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