📄 backtranambig.input
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<a name="input.1"></a><h3>Input files for usage example </h3>'tsw:opsd_human' is a sequence entry in the example protein database 'tsw'<p><p><h3>Database entry: tsw:opsd_human</h3><table width="90%"><tr><td bgcolor="#FFCCFF"><pre>ID OPSD_HUMAN STANDARD; PRT; 348 AA.AC P08100; Q16414;DT 01-AUG-1988 (Rel. 08, Created)DT 01-AUG-1988 (Rel. 08, Last sequence update)DT 15-JUL-1999 (Rel. 38, Last annotation update)DE RHODOPSIN.GN RHO.OS Homo sapiens (Human).OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Mammalia;OC Eutheria; Primates; Catarrhini; Hominidae; Homo.RN [1]RP SEQUENCE FROM N.A.RX MEDLINE; 84272729.RA NATHANS J., HOGNESS D.S.;RT "Isolation and nucleotide sequence of the gene encoding humanRT rhodopsin.";RL Proc. Natl. Acad. Sci. U.S.A. 81:4851-4855(1984).RN [2]RP SEQUENCE OF 1-120 FROM N.A.RA BENNETT J., BELLER B., SUN D., KARIKO K.;RL Submitted (NOV-1994) to the EMBL/GenBank/DDBJ databases.RN [3]RP REVIEW ON ADRP VARIANTS.RX MEDLINE; 94004905.RA AL-MAGHTHEH M., GREGORY C., INGLEHEARN C., HARDCASTLE A.,RA BHATTACHARYA S.;RT "Rhodopsin mutations in autosomal dominant retinitis pigmentosa.";RL Hum. Mutat. 2:249-255(1993).RN [4]RP VARIANT ADRP HIS-23.RX MEDLINE; 90136922.RA DRYJA T.P., MCGEE T.L., REICHEI E., HAHN L.B., COWLEY G.S.,RA YANDELL D.W., SANDBERG M.A., BERSON E.L.;RT "A point mutation of the rhodopsin gene in one form of retinitisRT pigmentosa.";RL Nature 343:364-366(1990).RN [5]RP VARIANTS ADRP.RX MEDLINE; 91051574.RA FARRAR G.J., KENNA P., REDMOND R., MCWILLIAM P., BRADLEY D.G.,RA HUMPHRIES M.M., SHARP E.M., INGLEHEARN C.F., BASHIR R., JAY M.,RA WATTY A., LUDWIG M., SCHINZEL A., SAMANNS C., GAL A.,RA BHATTACHARYA S.S., HUMPHRIES P.;RT "Autosomal dominant retinitis pigmentosa: absence of the rhodopsinRT proline-->histidine substitution (codon 23) in pedigrees fromRT Europe.";RL Am. J. Hum. Genet. 47:941-945(1990).RN [6]RP VARIANTS ADRP HIS-23; ARG-58; LEU-347 AND SER-347.RX MEDLINE; 91015273.<font color=red> [Part of this file has been deleted for brevity]</font>FT /FTId=VAR_004816.FT VARIANT 209 209 V -> M (EFFECT NOT KNOWN).FT /FTId=VAR_004817.FT VARIANT 211 211 H -> P (IN ADRP).FT /FTId=VAR_004818.FT VARIANT 211 211 H -> R (IN ADRP).FT /FTId=VAR_004819.FT VARIANT 216 216 M -> K (IN ADRP).FT /FTId=VAR_004820.FT VARIANT 220 220 F -> C (IN ADRP).FT /FTId=VAR_004821.FT VARIANT 222 222 C -> R (IN ADRP).FT /FTId=VAR_004822.FT VARIANT 255 255 MISSING (IN ADRP).FT /FTId=VAR_004823.FT VARIANT 264 264 MISSING (IN ADRP).FT /FTId=VAR_004824.FT VARIANT 267 267 P -> L (IN ADRP).FT /FTId=VAR_004825.FT VARIANT 267 267 P -> R (IN ADRP).FT /FTId=VAR_004826.FT VARIANT 292 292 A -> E (IN CSNB4).FT /FTId=VAR_004827.FT VARIANT 296 296 K -> E (IN ADRP).FT /FTId=VAR_004828.FT VARIANT 297 297 S -> R (IN ADRP).FT /FTId=VAR_004829.FT VARIANT 342 342 T -> M (IN ADRP).FT /FTId=VAR_004830.FT VARIANT 345 345 V -> L (IN ADRP).FT /FTId=VAR_004831.FT VARIANT 345 345 V -> M (IN ADRP).FT /FTId=VAR_004832.FT VARIANT 347 347 P -> A (IN ADRP).FT /FTId=VAR_004833.FT VARIANT 347 347 P -> L (IN ADRP; COMMON VARIANT).FT /FTId=VAR_004834.FT VARIANT 347 347 P -> Q (IN ADRP).FT /FTId=VAR_004835.FT VARIANT 347 347 P -> R (IN ADRP).FT /FTId=VAR_004836.FT VARIANT 347 347 P -> S (IN ADRP).FT /FTId=VAR_004837.SQ SEQUENCE 348 AA; 38892 MW; 07443BEA CRC32; MNGTEGPNFY VPFSNATGVV RSPFEYPQYY LAEPWQFSML AAYMFLLIVL GFPINFLTLY VTVQHKKLRT PLNYILLNLA VADLFMVLGG FTSTLYTSLH GYFVFGPTGC NLEGFFATLG GEIALWSLVV LAIERYVVVC KPMSNFRFGE NHAIMGVAFT WVMALACAAP PLAGWSRYIP EGLQCSCGID YYTLKPEVNN ESFVIYMFVV HFTIPMIIIF FCYGQLVFTV KEAAAQQQES ATTQKAEKEV TRMVIIMVIA FLICWVPYAS VAFYIFTHQG SNFGPIFMTI PAFFAKSAAI YNPVIYIMMN KQFRNCMLTT ICCGKNPLGD DEASATVSKT ETSQVAPA//</pre></td></tr></table><p>
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