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ID   AF063097   standard; DNA; PHG; 33593 BP.
XX
AC   AF063097; J02474; L29304; M12772; M13202; M27131; M27836; M34756; M58023;
AC   M59752; M64677; U02597; X02300; X02301; X05655; X61229; X87173; X99627;
AC   X99628; Z11483;
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SV   AF063097.1
XX
DT   21-MAY-1998 (Rel. 55, Created)
DT   07-JAN-1999 (Rel. 58, Last updated, Version 2)
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DE   Bacteriophage P2, complete genome.
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KW   .
XX
OS   Enterobacteria phage P2
OC   Viruses; dsDNA viruses, no RNA stage; Caudovirales; Myoviridae;
OC   P2-like Viruses.
XX
RN   [1]
RP   1-9, 33582-33593
RX   MEDLINE; 73220701.
RA   Murray K., Murray N.E.;
RT   "Terminal nucleotide sequences of DNA from temperate coliphages";
RL   Nature New Biol. 243(126):134-139(1973).
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RN   [2]
RP   1-26, 33568-33593
RX   MEDLINE; 77209985.
RA   Murray K., Isaksson-Forsen A.G., Challberg M., Englund P.T.;
RT   "Symmetrical nucleotide sequences in the recognition sites for the ter
RT   function of bacteriophages P2, 299 and 186";
RL   J. Mol. Biol. 112(3):471-489(1977).
XX
RN   [3]
RP   1-26, 33568-33593
RX   MEDLINE; 82051282.
RA   Lindqvist B.H.;
RT   "Recombination between satellite phage P4 and its helper P2. I. In vivo and
RT   in vitro construction of P4: :P2 hybrid satellite phage";
RL   Gene 14(4):231-241(1981).
XX
RN   [4]
RP   2929-3589
RX   MEDLINE; 83268689.
RA   Christie G.E., Calendar R.;
RT   "Bacteriophage P2 late promoters. Transcription initiation sites for two
RT   late mRNAs";
RL   J. Mol. Biol. 167(4):773-790(1983).
XX
RN   [5]
RP   25456-25995
RX   MEDLINE; 84248044.
RA   Ljungquist E., Kockum K., Bertani E.L.;
RT   "DNA sequence of the repressor gene and operator region of bacteriophage
RT   P2";
RL   Proc. Natl. Acad. Sci. U.S.A. 81:3988-3992(1984).
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RN   [6]
RP   10188-10518, 17510-17996
RX   MEDLINE; 85160858.
RA   Christie G.E., Calender R.;
RT   "Bacteriophage P2 late promoters - comparison of the four late promoter
RT   sequences";
RL   J. Mol. Biol. 181:373-382(1985).
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RN   [7]
RP   23909-24339
RX   MEDLINE; 86281704.
RA   Birkeland N.K., Lindquist B.H.;
RT   "Coliphage P2 late control gene ogr. DNA sequence and product
RT   identification";
RL   J. Mol. Biol. 188(3):487-490(1986).
XX
RN   [8]
RP   23889-24333
RX   MEDLINE; 86205872.
RA   Christie G.E., Haggard-Ljungquist E., Feiwell R., Calendar R.;
RT   "Regulation of bacteriophage P2 late-gene expression: the ogr gene";
RL   Proc. Natl. Acad. Sci. U.S.A. 83(10):3238-3242(1986).
XX
RN   [9]
RP   25849-27048
RX   MEDLINE; 87286423.
RA   Haggard-Ljungquist E., Kockum K., Bertani L.E.;
RT   "DNA sequences of bacteriophage P2 early genes cox and B and their
RT   regulatory sites";
RL   Mol. Gen. Genet. 208(1-2):52-56(1987).
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RN   [10]
RP   25849-27048
RX   MEDLINE; 88082694.
RA   Saha S., Haggard-Ljungquist E., Nordstrom K.;
RT   "The cox protein of bacteriophage P2 inhibits the formation of the
RT   repressor protein and autoregulates the early operon";
RL   EMBO J. 6(10):3191-3199(1987).
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RN   [11]
RP   24252-25595
RX   MEDLINE; 90006769.
RA   Yu A., Bertani L.E., Haggard-Ljungquist E.;
RT   "Control of prophage integration and excision in bacteriophage P2:
RT   nucleotide sequences of the int gene and att sites";
RL   Gene 80(1):1-11(1989).
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RN   [12]
RP   31590-33593
RX   MEDLINE; 90152373.
RA   Haggard-Ljungquist E., Barreiro V., Calendar R., Kurnit D.M., Cheng H.;
RT   "The P2 phage old gene: sequence, transcription and translational control";
RL   Gene 85(1):25-33(1989).
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RN   [13]
RP   1-266, 33200-33593
RX   MEDLINE; 91092507.
RA   Ziermann R., Calendar R.;
RT   "Characterization of the cos sites of bacteriophages P2 and P4";
RL   Gene 96(1):9-15(1990).
XX
RN   [14]
RP   17627-19373
RX   MEDLINE; 91135001.
RA   Temple L.M., Forsburg S.L., Calendar R., Christie G.E.;
RT   "Nucleotide sequence of the genes encoding the major tail sheath and tail
RT   tube proteins of bacteriophage P2";
RL   Virology 181(1):353-358(1991).
XX
RN   [15]
RP   4050-5178
RX   MEDLINE; 91220668.
RA   Six E.W., Sunshine M.G., Williams J., Haggard-Ljungquist E.,
RA   Lindqvist B.H.;
RT   "Morphopoietic switch mutations of bacteriophage P2";
RL   Virology 182(1):34-46(1991).
XX
RN   [16]
RP   1-6551
RX   MEDLINE; 92115571.
RA   Linderoth N.A., Ziermann R., Haggard-Ljungquist E., Christie G.E.,
RA   Calendar R.;
RT   "Nucleotide sequence of the DNA packaging and capsid synthesis genes of
RT   bacteriophage P2";
RL   Nucleic Acids Res. 19(25):7207-7214(1991).
XX
RN   [17]
RP   12173-15684
RX   MEDLINE; 92165720.
RA   Haggard-Ljungquist E., Halling C., Calendar R.;
RT   "DNA sequence of two tail genes of bacteriophage P2: Further evidence for
RT   horizontal transfer of tail fiber genes among unrelated bacteriophages";
RL   J. Bacteriol. 174:1462-1477(1992).
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RN   [18]
RP   26923-30721
RX   MEDLINE; 93287108.
RA   Liu Y., Saha S., Haggard-Ljungquist E.;
RT   "Studies of bacteriophage P2 DNA replication. The DNA sequence of the
RT   cis-acting gene A and ori region and construction of a P2 mini-chromosome";
RL   J. Mol. Biol. 231(2):361-374(1993).
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RN   [19]
RP   6288-8381
RX   MEDLINE; 94327465.
RA   Ziermann R., Bartlett B., Calendar R., Christie G.E.;
RT   "Functions involved in bacteriophage P2-induced host cell lysis and
RT   identification of a new tail gene";
RL   J. Bacteriol. 176:4974-4984(1994).
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RN   [20]
RP   8376-10381
RX   MEDLINE; 94233699.
RA   Linderoth N.A., Julien B., Flick K.E., Calendar R., Christie G.E.;
RT   "Molecular cloning and characterization of bacteriophage P2 genes R and S
RT   involved in tail completion";
RL   Virology 200:347-359(1994).
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RN   [21]
RP   10276-12739
RX   MEDLINE; 96036485.
RA   Haggard-Liungquist E., Jacobsen E., Rishovd S., Six W.S., Nilssen O.,
RA   Sunshine M.G., Lindqvist B.H., Kim K.J., Barreiro V., Koonin E.V.,
RA   Calendar R.;
RT   "Bacteriophage P2: genes involved in baseplate assembly";
RL   Virology 213(1):109-121(1995).
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RN   [22]
RP   15627-17626, 30643-31622
RA   Calendar R., Yu S., Myung H., Barreiro V., Odegrip R., Bertani L.E.,
RA   Carlson K., Davenport L., Mosig G., Christie G.E., Haggard-Ljungquist E.;
RT   "The lysogenic conversion genes of coliphage P2 have unusually high AT
RT   content";
RL   (in) Syvanen M., Kado C. (eds.);
RL   HORIZONTAL GENE TRANSFER:1-1;
RL   Chapman and Hall, London (1998)
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RN   [23]
RP   19374-23954
RA   Christie G.E., Temple L.M., Bartlett B.A., Goodwin T.S.;
RT   "Bacteriophage P2 tail assembly genes: Gene organization and a programmed
RT   translational frameshift parallel those of bacteriophage lambda";
RL   Unpublished.
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RN   [24]
RP   1-33593
RA   Christie G.E., Haggard-Ljungquist E., Calendar R.;
RT   "The complete genome of bacteriophage P2";
RL   Unpublished.
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RN   [25]
RP   24351-25595
RA   Haggard-Ljungquist E.;
RT   ;
RL   Submitted (15-SEP-1989) to the EMBL/GenBank/DDBJ databases.
RL   Department of Microbial Genetics, Karolinska Institutet, Stockholm, Sweden
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RN   [26]
RP   1-6551
RA   Linderoth N.A.;
RT   ;
RL   Submitted (13-AUG-1991) to the EMBL/GenBank/DDBJ databases.
RL   Dept of Mol and Cell Biology, Div of Biochemistry and Molecular Biology,
RL   University of California, 401 Barker Hall, Berkeley, CA 94720, USA
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RN   [27]
RP   26923-30721
RA   Haggard-Ljungquist E.;
RT   ;
RL   Submitted (12-NOV-1991) to the EMBL/GenBank/DDBJ databases.
RL   Department of Microbial Genetics, Karolinska Institutet, S-10401,
RL   Stockholm, Sweden
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RN   [28]
RP   8376-10381
RA   Linderoth N.A.;
RT   ;
RL   Submitted (18-OCT-1993) to the EMBL/GenBank/DDBJ databases.
RL   Nora A. Linderoth, Laboratory of Genetics, The Rockefeller University, 1230
RL   York Avenue, New York, NY 10021, USA
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RN   [29]
RP   10276-12739
RA   Haggard E.B.;
RT   ;
RL   Submitted (12-MAY-1995) to the EMBL/GenBank/DDBJ databases.
RL   Department of Genetics, Stockholm University, S-10691, Stockholm, Sweden
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RN   [30]
RP   15627-17626, 30643-31622
RA   Haggard-Ljungquist E.;
RT   ;
RL   Submitted (30-JUL-1996) to the EMBL/GenBank/DDBJ databases.
RL   Department of Genetics, Stockholm University, S-106 91, Stockholm, Sweden
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RN   [31]
RP   17510-23954
RA   Christie G.E.;
RT   ;
RL   Submitted (21-NOV-1996) to the EMBL/GenBank/DDBJ databases.
RL   Department of Microbiology and Immunology, Virginia Commonwealth
RL   University, Box 980678, Richmond, VA 23298-0678, USA
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RN   [32]
RP   1-33593
RA   Christie G.E.;
RT   ;
RL   Submitted (05-MAY-1998) to the EMBL/GenBank/DDBJ databases.
RL   Department of Microbiology and Immunology, Virginia Commonwealth
RL   University, Richmond, VA 23298-0678, USA
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DR   SPTREMBL; O64312; O64312.
DR   SPTREMBL; O64313; O64313.
DR   SPTREMBL; O64314; O64314.
DR   SPTREMBL; O64315; O64315.
DR   SPTREMBL; P79669; P79669.
DR   SPTREMBL; P79670; P79670.
DR   SPTREMBL; Q38498; Q38498.
DR   SWISS-PROT; P04132; RPC_BPP2.
DR   SWISS-PROT; P07695; VCOX_BPP2.
DR   SWISS-PROT; P07696; VPB_BPP2.
DR   SWISS-PROT; P08762; VOGR_BPP2.
DR   SWISS-PROT; P10312; VPD_BPP2.
DR   SWISS-PROT; P13520; VOLD_BPP2.
DR   SWISS-PROT; P22501; VPF1_BPP2.
DR   SWISS-PROT; P22502; VPF2_BPP2.
DR   SWISS-PROT; P25475; VPL_BPP2.
DR   SWISS-PROT; P25476; VPM_BPP2.
DR   SWISS-PROT; P25477; VPN_BPP2.
DR   SWISS-PROT; P25478; VPO_BPP2.
DR   SWISS-PROT; P25479; VPP_BPP2.
DR   SWISS-PROT; P25480; VPQ_BPP2.
DR   SWISS-PROT; P26699; TFA_BPP2.
DR   SWISS-PROT; P26700; VPH_BPP2.
DR   SWISS-PROT; P26701; VPI_BPP2.
DR   SWISS-PROT; P31340; VPV_BPP2.
DR   SWISS-PROT; P36932; VINT_BPP2.
DR   SWISS-PROT; P36933; VPR_BPP2.
DR   SWISS-PROT; P36934; VPS_BPP2.
DR   SWISS-PROT; P36935; YSV_BPP2.
DR   SWISS-PROT; P51767; VPJ_BPP2.
DR   SWISS-PROT; P51768; VPW_BPP2.
DR   SWISS-PROT; P51769; LYSA_BPP2.
DR   SWISS-PROT; P51770; LYSB_BPP2.
DR   SWISS-PROT; P51771; LYCV_BPP2.
DR   SWISS-PROT; P51772; VPX_BPP2.
DR   SWISS-PROT; P51773; HOLI_BPP2.
DR   SWISS-PROT; Q06419; VPA_BPP2.
DR   SWISS-PROT; Q06422; YO80_BPP2.
DR   SWISS-PROT; Q06423; YO81_BPP2.
DR   SWISS-PROT; Q06424; YO82_BPP2.
DR   SWISS-PROT; Q06425; YO83_BPP2.
DR   SWISS-PROT; Q06426; YO91_BPP2.
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CC   On May 20, 1998 this sequence version replaced gi:506838 gi:15821
CC   gi:1806573 gi:215666 gi:506836 gi:508561 gi:1061043 gi:215669
CC   gi:1769975 gi:494974 gi:215664 gi:15620 gi:393451 gi:1769977
CC   gi:215681 gi:215675 gi:215676 gi:15141 gi:414530.
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FH   Key             Location/Qualifiers
FH
FT   source          1..33593
FT                   /db_xref="taxon:10679"
FT                   /organism="Enterobacteria phage P2"
FT                   /lab_host="Escherichia coli"
FT   misc_feature    1..19
FT                   /note="cosL; left cohesive end"
FT   terminator      complement(160..181)
FT                   /note="tQ; putative rho-independent terminator for P
FT                   operon"
FT   CDS             complement(187..1221)
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25480"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="Q"
FT                   /function="presumed portal protein"
FT                   /product="gpQ"
FT                   /protein_id="AAD03268.1"
FT                   /translation="MSKKKGKTPQPAAKTMTASGPKMEAFTFGEPVPVLDRRDILDYVE
FT                   CISNGRWYEPPVSFTGLAKSLRAAVHHSSPIYVKRNILASTFIPHPWLSQQDFSRFVLD
FT                   FLVFGNAFLEKRYSTTGKVIRLETSPAKYTRRGVEEDVYWWVPSFNEPTAFAPGSVFHL
FT                   LEPDINQELYGLPEYLSALNSAWLNESATLFRRKYYENGAHAGYIMYVTDAVQDRNDIE
FT                   MLRENMVKSKGRNNFKNLFLYAPQGKADGIKIIPLSEVATKDDFFNIKKASAADLLDAH
FT                   RIPFQLMGGKPENVGSLGDIEKVAKVFVRNELIPLQDRIREINGWLGQEVIRFKNYSLD
FT                   TDND"
FT   variation       complement(653)
FT                   /note="Qam34 mutation"
FT                   /replace="t"
FT                   /gene="Q"
FT   CDS             complement(1221..2993)
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25479"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="P"
FT                   /function="terminase; DNA-dependent ATPase"
FT                   /product="gpP"
FT                   /protein_id="AAD03269.1"
FT                   /translation="MTITTDTTLLHDPRRQAALLYWQGFSVPQIAAMLQMKRPTVQSWK
FT                   QRDGWDSVAPISRVEMSLEARLTQLIIKPQKTGGDFKEIDLLGRQIERLARVNRYSQTG
FT                   NEADLNPNVANRNKGGRRKPKKNFFSDEAIEKLEQIFFEQSFDYQLHWYRAGLEHRIRD
FT                   ILKSRQIGATFYFSREALLRALKTGHNQIFLSASKTQAYVFREYIIAFARLVDVDLTGD
FT                   PIVLGNNGAKLIFLGTNSNTAQSHNGDLYVDEIFWIPNFQVLRKVASGMASQSHLRSTY
FT                   FSTPSTLAHDAYPFWSGELFNRGRASAAERVEIDVSHNALAGGLLCADGQWRQIVTIED
FT                   ALKGGCTLFDIEQLKRENSADDFKNLFMCEFVDDKASVFPFEELQRCMVDTLEEWEDYA
FT                   PFAANPFGSRPVWIGYDPSHRGDSAGCVVLAPPVVAGGKFRILERHQWKGMDFATQAES
FT                   IRKLTEKYNVEYIGIDATGLGVGVFQLVRSFYPAARDIRYTPEMKTAMVLKAKDVIRRG
FT                   CLEYDVSATDITSSFMAIRKTMTSSGRSATYEASRSEEASHADLAWATMHALLNEPLTA
FT                   GISTPLTSTILEFY"
FT   variation       complement(2210)
FT                   /note="Pam24 and Pam137 mutations"
FT                   /replace="a"
FT                   /gene="P"
FT   variation       complement(2948)
FT                   /note="Pam253 mutation"
FT                   /replace="a"
FT                   /gene="P"
FT   misc_feature    complement(3016)
FT                   /note="transcription start site for P operon; encodes P,Q"
FT                   /gene="P"
FT   misc_feature    3057..3087
FT                   /evidence=EXPERIMENTAL
FT                   /note="activator binding site; pO, pP promoters"
FT   misc_feature    3127
FT                   /evidence=EXPERIMENTAL
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FT                   /note="transcription start site for O operon; encodes O,
FT                   N, M, L, X, Y, K, lysA, lysB, R, S"
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FT   CDS             3167..4021
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25478"
FT                   /transl_table=11
FT                   /gene="O"
FT                   /function="presumed capsid scaffolding protein"
FT                   /product="gpO"
FT                   /protein_id="AAD03270.1"
FT                   /translation="MAKKVSKFFRIGVEGDTCDGRVISAQDIQEMAETFDPRVYGCRIN
FT                   LEHLRGILPDGIFKRYGDVAELKAEKIDDDSALKGKWALFAKITPTDDLIAMNKAAQKV
FT                   YTSMEIQPNFANTGKCYLVGLAVTDDPASLGTEYLEFCRTAKHNPLNRFKLSPENLISV
FT                   ATPVELEFEDLPETVFTALTEKVKSIFGRKQASDDARLNDVHEAVTAVAEHVQEKLSAT
FT                   EQRLAEMETAFSALKQEVTDRADETSQAFTRLKNSLDHTESLTQQRRSKATGGGGDALM
FT                   TNC"
FT   variation       3206
FT                   /note="Oam71 mutation"
FT                   /replace="t"
FT                   /gene="O"
FT   variation       3411
FT                   /note="Oam7 mutation"
FT                   /replace="a"
FT                   /gene="O"
FT   variation       3878
FT                   /note="Oam279 mutation"
FT                   /replace="t"
FT                   /gene="O"
FT   CDS             4080..5153
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25477"
FT                   /transl_table=11
FT                   /gene="N"
FT                   /function="major capsid precursor"
FT                   /product="gpN"
FT                   /protein_id="AAD03271.1"
FT                   /translation="MRQETRFKFNAYLSRVAELNGIDAGDVSKKFTVEPSVTQTLMNTM
FT                   QESSDFLTRINIVPVSEMKGEKIGIGVTGSIASTTDTAGGTERQPKDFSKLASNKYECD
FT                   QINFDFYIRYKTLDLWARYQDFQLRIRNAIIKRQSLDFIMAGFNGVKRAETSDRSSNPM
FT                   LQDVAVGWLQKYRNEAPARVMSKVTDEEGRTTSEVIRVGKGGDYASLDALVMDATNNLI
FT                   EPWYQEDPDLVVIVGRQLLADKYFPIVNKEQDNSEMLAADVIISQKRIGNLPAVRVPYF
FT                   PADAMLITKLENLSIYYMDDSHRRVIEENPKLDRVENYESMNIDYVVEDYAAGCLVEKI
FT                   KVGDFSTPAKATAEPGA"
FT   variation       4349..4350
FT                   /note="Nam209 mutation"
FT                   /replace="at"
FT                   /gene="N"
FT   variation       4630
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FT                   /note="sir3 mutation; defective for choice of small
FT                   capsids by satellite phage P4"
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FT                   /replace="c"
FT                   /gene="N"
FT   variation       4695
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FT                   /note="sir5 mutation; defective for choice of small
FT                   capsids by satellite phage P4"
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FT                   /replace="t"
FT                   /gene="N"
FT   variation       4695..4697
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FT                   /note="sir9 mutation; defective for choice of small
FT                   capsids by satellite phage P4"
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FT                   /replace=""
FT                   /gene="N"
FT   variation       4699
FT                   /note="sir2, sir6 and sir8 mutations; defective for choice
FT                   of small capsids by satellite phage P4"
FT                   /replace="t"
FT                   /gene="N"
FT   variation       4740
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FT                   /note="sir1 mutation; defective for choice of small
FT                   capsids by satellite phage P4"
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FT                   /replace="g"
FT                   /gene="N"
FT   variation       4741
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FT                   /note="sir4 mutation; defective for choice of small
FT                   capsids by satellite phage P4"
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FT                   /replace="a"
FT                   /gene="N"
FT   CDS             5157..5900
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25476"
FT                   /transl_table=11
FT                   /gene="M"
FT                   /function="terminase"
FT                   /product="gpM"
FT                   /protein_id="AAD03272.1"
FT                   /translation="MTSPAQRHMMRVSAAMTAQREAAPLRHATVYEQMLVKLAADQRTL
FT                   KAIYSKELKAAKKRELLPFWLPWVNGVLELGKGAQDDILMTVMLWRLDTGDIAGALEIA
FT                   RYALKYGLTMPGKHRRTPPYMFTEEVALAAMRAHAAGESVDTRLLTETLELTATADMPD
FT                   EVRAKLHKITGLFLRDGGDAAGALAHLQRATQLDCQAGVKKEIERLERELKPKPEPQPK
FT                   AATRAPRKTRSVTPAKRGRPKKKAS"
FT   variation       5361
FT                   /note="Mts52 mutation"
FT                   /replace="a"
FT                   /gene="M"
FT   variation       5751
FT                   /note="Mam32 mutation"
FT                   /replace="t"
FT                   /gene="M"
FT   CDS             6000..6509
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P25475"
FT                   /transl_table=11
FT                   /gene="L"
FT                   /function="capsid completion protein"
FT                   /product="gpL"
FT                   /protein_id="AAD03273.1"
FT                   /translation="MMTLIIPRKEAPVSGEGTVVIPQPAGDEPVIKNTFFFPDIDPKRV
FT                   RERMRLEQTVAPARLREAIKSGMAETNAELYEYREQKIAAGFTRLADVPADDIDGESIK
FT                   VFYYERAVCAMATASLYERYRGVDASAKGDKKADSIDSTIDELWRDMRWAVARIQGKPR
FT                   CIVSQI"
FT   variation       6024
FT                   /note="Lam79 mutation"
FT                   /replace="t"
FT                   /gene="L"
FT   variation       6240
FT                   /note="Lam9 mutation"
FT                   /replace="t"
FT                   /gene="L"
FT   CDS             6509..6712
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51772"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="X"
FT                   /function="essential tail gene"
FT                   /product="gpX"
FT                   /protein_id="AAD03274.1"
FT                   /translation="MKTFALQGDTLDAICVRYYGRTEGVVETVLAANPGLAELGAVLPH
FT                   GTAVELPDVQTAPVAETVNLWE"
FT   variation       6562
FT                   /note="Xam95 mutation"
FT                   /replace="g"
FT                   /gene="X"
FT   CDS             6716..6997
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51773"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="Y"
FT                   /function="holin; essential for host cell cell lysis"
FT                   /product="gpY"
FT                   /protein_id="AAD03275.1"
FT                   /translation="MTAEEKSVLSLFMIGVLIVVGKVLAGGEPITPRLFIGRMLLGGFV
FT                   SMVAGVVLVQFPDLSLPAVCGIGSMLGIAGYQVIEIAIQRRFKGRGKQ"
FT   variation       6852
FT                   /note="Yam94 mutation"
FT                   /replace="a"
FT                   /gene="Y"
FT   CDS             6997..7494
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51771"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="K"
FT                   /function="endolysin; essential for host cell lysis"
FT                   /product="gpK"
FT                   /protein_id="AAD03276.1"
FT                   /translation="MPVINTHQNIAAFLDMLAVSEGTANHPLTKNRGYDVIVTGLDGKP
FT                   EIFTDYSDHPFAHGRPAKVFNRRGEKSTASGRYQQLYLFWPHYRKQLALPDFSPLSQDR
FT                   LAIQLIRERGALDDIRAGRIERAISRCRNIWASLPGAGYGQREHSLEKLVTVWRTAGGV
FT                   PA"
FT   variation       7114
FT                   /note="Kts60 mutation"
FT                   /replace="a"
FT                   /gene="K"
FT   variation       7126
FT                   /note="Kam218 mutation"
FT                   /replace="t"
FT                   /gene="K"
FT   variation       7318
FT                   /note="Kam12 mutation"
FT                   /replace="t"
FT                   /gene="K"
FT   variation       7322
FT                   /note="Kam76 mutation"
FT                   /replace="a"
FT                   /gene="K"
FT   CDS             7509..7934
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51769"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="lysA"
FT                   /function="nonessential; affects timing of lysis"
FT                   /product="LysA"
FT                   /protein_id="AAD03277.1"
FT                   /translation="MKKLSLSLMLNVSLALMLALSLIYPQSVAVNFVAAWAILATVICV
FT                   VAGGVGVYATEYVLERYGRELPPESLAVKIVTSLFLQPVPWRRRAAALVVVVATFISLV
FT                   AAGWIFTALIYLVVSLFFRLIRKACRQRLEGREPCQG"
FT   variation       7694
FT                   /note="lysAam96 mutation"
FT                   /replace="g"
FT                   /gene="lysA"
FT   CDS             7922..8347
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51770"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="lysB"
FT                   /function="nonessential; affects timing of lysis"
FT                   /product="LysB"
FT                   /protein_id="AAD03278.1"
FT                   /translation="MSRLMIVLVVLLSLAVAGLFLVKHKNASLRASLDRANNVASGQQT
FT                   TITMLKNQLHVALTRADKNELAQVALRQELENAAKREAQREKTITRLLNENEDFRRWYG
FT                   ADLPDAVRRLHQRPACTDASDCPQRMPESEPLPDAGQ"
FT   variation       8099..8100
FT                   /note="lysBam97 mutation"
FT                   /replace="ta"
FT                   /gene="lysB"
FT   attenuator      8399..8417
FT                   /note="putative transcription attenuator; O operon"
FT   CDS             8455..8922
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P36933"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="R"
FT                   /function="essential tail gene; tail completion"
FT                   /product="gpR"
FT                   /protein_id="AAD03279.1"
FT                   /translation="MLKPDSLRRALTDAVTVLKTNPDMLRIFVDNGSIASTLAASLSFE
FT                   KRYTLNVIVTDFTGDFDLLIVPVLAWLRENQPDIMTTDEGQKKGFTFYADINNDSSFDI
FT                   SISLMLTERTLVSEVDGALHVKNISEPPPPEPVTRPMELYINGELVSKWDE"
FT   variation       8680
FT                   /note="Ram3 mutation"
FT                   /replace="t"
FT                   /gene="R"
FT   variation       8710
FT                   /note="Ram42 mutation"
FT                   /replace="t"
FT                   /gene="R"
FT   variation       8857
FT                   /note="Ram23 mutation"
FT                   /replace="t"
FT                   /gene="R"
FT   CDS             8915..9367
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P36934"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="S"
FT                   /function="essential tail gene; tail completion"
FT                   /product="gpS"
FT                   /protein_id="AAD03280.1"
FT                   /translation="MNEFKRFEDRLTGLIESLSPSGRRRLSAELAKRLRQSQQRRVMAQ
FT                   KAPDGTPYAPRQQQSVRKKTGRVKRKMFAKLITSRFLHIRASPEQASMEFYGGKSPKIA
FT                   SVHQFGLSEENRKDGKKIDYPARPLLGFTGEDVQMIEEIILAHLER"
FT   variation       9209
FT                   /note="Sam75 mutation"
FT                   /replace="t"
FT                   /gene="S"
FT   variation       9213
FT                   /note="Sam89 mutation"
FT                   /replace="a"
FT                   /gene="S"
FT   terminator      9397..9433
FT                   /note="putative rho-independent terminator for O operon"
FT   CDS             complement(9439..10224)
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P36935"
FT                   /transl_table=11
FT                   /gene="orf30"
FT                   /function="nonessential"
FT                   /product="Orf30"
FT                   /protein_id="AAD03281.1"
FT                   /translation="MVSYNVTNVWGLIVFFLCSFAVLAFFSFGKSNLMRLIAHYFNFGY
FT                   SDKKLKRLDREWRDIQLFKIINGINVSGIENVRMIQQGLIDGKLKTSYFFLTRIWGDIT
FT                   KPPHIIKTIIVILASIFYILLACYIHNEQSVIVRDATGIPYKNMMYYVYSDKVLLSFKN
FT                   KAVEFNKTYSLADCKRLQNVFIKDTLPEIACNKLLQLNEEDSEWLSQEIKDNNSHKKAL
FT                   LILSLVYFTSGLVIFLSYTKFFYANKKVLEYKASNKNHS"
FT   misc_feature    10239..10266
FT                   /evidence=EXPERIMENTAL
FT                   /note="activator binding site; activation of pV promoter"
FT   CDS             10308..10943
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P31340"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="V"
FT                   /function="baseplate assembly protein"
FT                   /product="gpV"
FT                   /protein_id="AAD03282.1"
FT                   /translation="MNTLANIQELARALRNMIRTGIIVETDLNAGRCRVQTGGMCTDWL
FT                   QWLTHRAGRSRTWWAPSVGEQVLILAVGGELDTAFVLPGIYSGDNPSPSVSADALHIRF
FT                   PDGAVIEYEPETSALTVSGIKTASVTASGSVTATVPVVMVKASTRVTLDTPEVVCTNRL
FT                   ITGTLEVQKGGTMRGNIEHTGGELSSNGKVLHTHKHPGDSGGTTGSPL"
FT   misc_feature    10308
FT                   /evidence=EXPERIMENTAL
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FT                   /note="transcription start site for V operon; encodes V,
FT                   W, J, I, H, G"
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FT                   /gene="V"
FT   variation       10329
FT                   /note="Vam42, Vam203 and Vam205 mutations"
FT                   /replace="t"
FT                   /gene="V"
FT   variation       10498
FT                   /note="Vts199 mutation"
FT                   /replace="a"
FT                   /gene="V"
FT   CDS             10940..11287
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51768"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="W"
FT                   /function="baseplate assembly protein"
FT                   /product="gpW"
FT                   /protein_id="AAD03283.1"
FT                   /translation="MTARYLGMNRSDGLTVTDLEHISQSIGDILRTPVGSRVMRRDYGS
FT                   LLASMIDQPQTPALELQIKVACYMAVLKWEPRVTLSSVTTARSFDGRMTVTLTGQHNDT
FT                   GQPLSLTIPVS"
FT   variation       11237
FT                   /note="Wam50 mutation"
FT                   /replace="t"
FT                   /gene="W"
FT   CDS             11292..12200
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P51767"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="J"
FT                   /function="baseplate assembly protein"
FT                   /product="gpJ"
FT                   /protein_id="AAD03284.1"
FT                   /translation="MPIIDLNQLPAPDVVEELDFESILAERKATLISLYPEDQQEAVAR
FT                   TLTLESEPLVKLLEENAYRELIWRQRVNEAARAVMLACAAGNDLDVIGANYNTTRLTIT
FT                   PADDSTIPPTPAVMESDTDYRLRIQQAFEGLSVAGSVGAYQYHGRSADGRVADISVTSP
FT                   SPACVTISVLSRENNGVASEDLLAVVRNALNGEDVRPVADRVTVQSAAIVEYQINATLY
FT                   LYPGPESEPIRAAAVKKLEAYITAQHRLGRDIRLSAIYAALHVEGVQRVELAAPLADIV
FT                   LNSTQASFCTEYRVVTGGSDE"
FT   variation       11937
FT                   /note="Jam31 mutation"
FT                   /replace="t"
FT                   /gene="J"
FT   CDS             12193..12723
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P26701"
FT                   /evidence=EXPERIMENTAL
FT                   /transl_table=11
FT                   /gene="I"
FT                   /function="baseplate assembly protein"
FT                   /product="gpI"
FT                   /protein_id="AAD03285.1"
FT                   /translation="MSDSRLLPTGSSPLEVAAAKACAEIEKTPVSIRELWNPDTCPANL
FT                   LPWLAWAFSVDRWDEKWPEATKRAVIRDAYFIHCHKGTIGAIRRVVEPLGYLINVTEWW
FT                   ENSDPPGTFRLDIGVLESGITEAMYQEMERLIADAKPASRHLIGLNITRDIPGYLFAGG
FT                   VAYDGDVITVYPG"
FT   variation       12235
FT                   /note="Iam78 mutation"
FT                   /replace="t"
FT                   /gene="I"
FT   CDS             12734..14743
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P26700"
FT                   /transl_table=11
FT                   /gene="H"
FT                   /function="probable tail fiber protein"
FT                   /product="gpH"
FT                   /protein_id="AAD03286.1"
FT                   /translation="MSIKFRTVITTAGAAKLAAATAPGRRKVGITTMAVGDGGGKLPVP
FT                   DAGQTGLIHEVWRHALNKISQDKRNSNYIIAELVIPPEVGGFWMRELGLYDDAGTLIAV
FT                   ANMAESYKPALAEGSGRWQTCRMVIIVSSVASVELTIDTTTVMATQDYVDDKIAEHEQS
FT                   RRHPDASLTAKGFTQLSSATNSTSETLAATPKAVKAAYDLANGKYTAQDATTARKGLVQ
FT                   LSSATNSTSETLAATPKAVKTVMDETNKKAPLNSPALTGTPTTPTARQGTNNTQIANTA
FT                   FVMAAIAALVDSSPDALNTLNELAAALGNDPNFATTMTNALAGKQPKDATLTALAGLAT
FT                   AADRFPYFTGNDVASLATLTKVGRDILAKSTVAAVIEYLGLQETVNRAGNAVQKNGDTL
FT                   SGGLTFENDSILAWIRNTDWAKIGFKNDADGDTDSYMWFETGDNGNEYFKWRSRQSTTT
FT                   KDLMTLKWDALNILVNAVINGCFGVGTTNALGGSSIVLGDNDTGFKQNGDGILDVYANS
FT                   QRVFRFQNGVAIAFKNIQAGDSKKFSLSSSNTSTKNITFNLWGASTRPVVAELGDEAGW
FT                   HFYSQRNTDNSVIFAVNGQMQPSNWGNFDSRYVKDVRLGTRVVQLMARGGRYEKAGHTI
FT                   TGLRIIGEVDGDDEAIFRPIQKYINGTWYNVAQV"
FT   variation       13994
FT                   /note="Ham72 mutation"
FT                   /replace="t"
FT                   /gene="H"
FT   variation       14336
FT                   /note="Ham59 mutation"
FT                   /replace="t"
FT                   /gene="H"
FT   CDS             14747..15274
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P26699"
FT                   /transl_table=11
FT                   /gene="G"
FT                   /function="probable tail fiber assembly protein"
FT                   /product="gpG"
FT                   /protein_id="AAD03287.1"
FT                   /translation="MQHLKNIKSGNPKTKEQYQLTKNFDVIWLWSEDGKNWYEEVKNFQ
FT                   PDTIKIVYDENNIIVAITRDASTLNPEGFSVVEVPDITSNRRADDSGKWMFKDGAVVKR
FT                   IYTADEQQQQAESQKAALLSEAENVIQPLERAVRLNMATDEERARLESWERYSVLVSRV
FT                   DPANPEWPEMPQ"
FT   variation       14879
FT                   /note="Gam1 mutation"
FT                   /replace="t"
FT                   /gene="G"
FT   variation       15294..17233
FT                   /note="del2 deletion"
FT                   /replace=""
FT   terminator      15639..15666
FT                   /note="putative rho-independent terminator for V operon"
FT   CDS             complement(15675..17261)
FT                   /codon_start=1
FT                   /db_xref="SPTREMBL:P79669"
FT                   /note="cloned gene blocks growth of T5"
FT                   /transl_table=11
FT                   /gene="fun(Z)"
FT                   /function="nonessential; lysogenic conversion; confers
FT                   sensitivity to FUdR"
FT                   /product="Fun(Z)"
FT                   /protein_id="AAD03288.1"
FT                   /translation="MIPIKDLTLGYADAENYKRRENKELLNKVFIRDNHLSRLCEPNIS
FT                   FLVGEKGTGKTAYSIYLSNNNINNTLATTKYIRETEYQKFITLKSEKHLNLSDFSGIWK
FT                   VILYLLISKQVLDKEGKISKLLNYSKFSSLNDAIDEYYLKAFSPEIIQALSFVQESKVA
FT                   AELLHKHATLKGEERESLSFSESRFQINLFYIQKKFEEAFSQIRLSQNHILFIDGIDIR
FT                   PSSIPYDDYLECIKGLAHAVWEINNDFFPSIKGGKGRMKAVLLIRPDIFESIGLQNQNA
FT                   KIRDNSVFLDWRTEYVNHRSSQLFEVLDHLLRTQQDMALKKGQAWDHYFPWDSPNVHDN
FT                   YNHPTSFINFLRWSYYRPRDILRMLEIIKSHASGDDGKNQFSLDDFESPSMQRDYSNYL
FT                   LGEIKDHLSFYYGSEHYEIFLKFFEFLSGKDTFDYAEYLLAYKQLETHISSISTTKPKF
FT                   MTTANDFLQFLFGLNVICYIETTEDNNRFIRWCFRERSYANISPKIKTGMKYQIFYGLA
FT                   KSLNVGKALKK"
FT   variation       complement(15784)
FT                   /note="Z81su3 mutation"
FT                   /replace="a"
FT                   /gene="fun(Z)"
FT   variation       complement(15872)
FT                   /note="Z20 mutation"
FT                   /replace="t"
FT                   /gene="fun(Z)"
FT   variation       complement(15944)
FT                   /note="Z81 mutation"
FT                   /replace="t"
FT                   /gene="fun(Z)"
FT   variation       complement(15946)
FT                   /note="fun1 mutation"
FT                   /replace="t"
FT                   /gene="fun(Z)"
FT   variation       complement(16079)
FT                   /note="csZ150 mutation"
FT                   /replace="t"
FT                   /gene="fun(Z)"
FT   variation       complement(16266)
FT                   /note="fun99 mutation"
FT                   /replace="t"
FT                   /gene="fun(Z)"
FT   variation       16267..17299
FT                   /note="del5 deletion"
FT                   /replace=""
FT   variation       complement(16638)
FT                   /note="csZ150 mutation"
FT                   /replace="a"
FT                   /gene="fun(Z)"
FT   misc_feature    17555..17583
FT                   /evidence=EXPERIMENTAL
FT                   /note="activator binding site; activation of pF promoter"
FT   misc_feature    17626..17628
FT                   /evidence=EXPERIMENTAL
FT                   /note="transcription start site for F operon; encodes FI,
FT                   FII, E, E', T, U, D"
FT   CDS             17652..18842
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P22501"
FT                   /transl_table=11
FT                   /gene="FI"
FT                   /function="essential tail protein; tail sheath"
FT                   /product="gpFI"
FT                   /protein_id="AAD03289.1"
FT                   /translation="MSDYHHGVQVLEINEGTRVISTVSTAIVGMVCTASDADAETFPLN
FT                   KPVLITNVQSAISKAGKKGTLAASLQAIADQSKPVTVVMRVEDGTGDDEETKLAQTVSN
FT                   IIGTTDENGQYTGLKAMLAAESVTGVKPRILGVPGLDTKEVAVALASVCQKLRAFGYIS
FT                   AWGCKTISEVKAYRQNFSQRELMVIWPDFLAWDTVTSTTATAYATARALGLRAKIDQEQ
FT                   GWHKTLSNVGVNGVTGISASVFWDLQESGTDADLLNESGVTTLIRRDGFRFWGNRTCSD
FT                   DPLFLFENYTRTAQVVADTMAEAHMWAVDKPITATLIRDIVDGINAKFRELKTNGYIVD
FT                   ATCWFSEESNDAETLKAGKLYIDYDYTPVPPLENLTLRQRITDKYLANLVTSVNSN"
FT   variation       18183
FT                   /note="Fam4 mutation"
FT                   /replace="t"
FT                   /gene="FI"
FT   CDS             18855..19373
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P22502"
FT                   /transl_table=11
FT                   /gene="FII"
FT                   /function="essential tail protein; tail tube"
FT                   /product="gpFII"
FT                   /protein_id="AAD03290.1"
FT                   /translation="MAMPRKLKLMNVFLNGYSYQGVAKSVTLPKLTRKLENYRGAGMNG
FT                   SAPVDLGLDDDALSMEWSLGGFPDSVIWELYAATGVDAVPIRFAGSYQRDDTGETVAVE
FT                   VVMRGRQKEIDTGEGKQGEDTESKISVVCTYFRLTMDGKELVEIDTINMIEKVNGVDRL
FT                   EQHRRNIGL"
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FT   CDS             19430..19705
FT                   /codon_start=1
FT                   /db_xref="SPTREMBL:O64313"
FT                   /transl_table=11
FT                   /gene="E"
FT                   /function="essential tail protein"
FT                   /product="gpE"
FT                   /protein_id="AAD03291.1"
FT                   /translation="MNKENVITLDNPVKRGEQVIEQVTLMKPSAGTLRGVSLAAVANSE
FT                   VDALIKVLPRMTAPMLTEQEVAALELPDLVALAGKVVGFLSPNSVQ"
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FT   CDS             join(19430..19684,19684..19857)
FT                   /codon_start=1
FT                   /db_xref="SPTREMBL:O64312"
FT                   /note="shares amino terminus with gpE; -1 frameshift"
FT                   /transl_table=11
FT                   /gene="E+E'"
FT                   /function="essential tail protein"
FT                   /product="gpE+E'"
FT                   /protein_id="AAD03292.1"
FT                   /translation="MNKENVITLDNPVKRGEQVIEQVTLMKPSAGTLRGVSLAAVANSE
FT                   VDALIKVLPRMTAPMLTEQEVAALELPDLVALAGKVVGFLVAELGAVTFPKNLSVDDLM
FT                   ADVAVIFHWPPSELYPMSLTELITWREKALRRSGNTNE"
FT   variation       19473
FT                   /note="Ets55 mutation"
FT                   /replace="a"
FT                   /gene="E"
FT   variation       19619
FT                   /note="Eam30 mutation"
FT                   /replace="t"
FT                   /gene="E"
FT   misc_feature    19685
FT                   /evidence=EXPERIMENTAL
FT                   /note="site of -1 translational frameshift"
FT                   /gene="E+E'"
FT   CDS             19850..22297
FT                   /codon_start=1
FT                   /db_xref="SPTREMBL:O64314"
FT                   /transl_table=11
FT                   /gene="T"
FT                   /function="essential tail protein; putative tail length
FT                   determinator"
FT                   /product="gpT"
FT                   /protein_id="AAD03293.1"
FT                   /translation="MSNNVKLQVLLRAVDQASRPFKSIRTASKSLSGDIRETQKSLREL
FT                   NGHASRIEGFRKTSAQLAVTGHALEKARQEAEALATQFKNTERPTRAQAKVLESAKRAA
FT                   EDLQAKYNRLTDSVKRQQRELAAVGINTRNLAHDEQGLKNRISETTAQLNRQRDALVRV
FT                   SAQQAKLNAVKQRYQAGKELAGNMASVGAAGVGIAAAGTMAGVKLLMPGYEFAQKNSEL
FT                   QAVIGVAKDSAEMAALRKQARQLGDNTAASADDAAGAQIIIAKAGGDVDAIQAATPVTL
FT                   NMALANRRTMEENAALLMGMKSAFQLSNDKVAHIGDVLSMTMNKTAADFDGMSDALTYA
FT                   APVAKNAGVSIEETAAMVGALHDAKITGSMAGTGSRAVLSRLQAPTGKAWDALKELGVK
FT                   TSDSKGNTRPIFTILKEMQASFEKNRLGTAQQAEYMKTIFGEEASSAAAVLMTAASTGK
FT                   LDKLTAAFKASDGKTAELVNIMQDNLGGDFKAFQSAYEAVGTDLFDQQEGALRKLTQTA
FT                   TKYVLKLDGWIQKNKSLASTIGIIAGGALALTGIIGAIGLVAWPVITGINAIIAAAGAM
FT                   GAVFTTVGSAVMTAIGAISWPVVAVVAAIVAGALLIRKYWEPVSAFFGGVVEGLKAAFA
FT                   PVGELFTPLKPVFDWLGEKLQAAWQWFKNLIAPVKATQDTLNRCRDTGVMFGQALADAL
FT                   MLPLNAFNKLRSGIDWVLEKLGVINKESDTLDQTAARTHTATYGTGDYIPATSSYAGYQ
FT                   AYQPVTAPAGRSYVDQSKNEYHISLTGGTAPGTQLDRQLQDALEKYERDKRARARASMM
FT                   HDG"
FT   variation       20669
FT                   /note="Tam215 mutation"
FT                   /replace="t"
FT                   /gene="T"
FT   variation       21101
FT                   /note="Tam5 mutation"
FT                   /replace="t"
FT                   /gene="T"
FT   variation       21528
FT                   /note="Tam64 mutation"
FT                   /replace="a"
FT                   /gene="T"
FT   CDS             22312..22791
FT                   /codon_start=1
FT                   /db_xref="SPTREMBL:O64315"
FT                   /transl_table=11
FT                   /gene="U"
FT                   /function="essential tail protein"
FT                   /product="gpU"
FT                   /protein_id="AAD03294.1"
FT                   /translation="MMLALGMFVFMRQTLPHQTMQRESDYRWPSNSRIGKRDAFQFLGV
FT                   GEENITLAGVLYPELTGGKLTMTTLRLMAEEGRAWPLLDGTGMIYGMYVISRVSETGSI
FT                   FFADGTPRKIDFTLSLTRVDESLAALYGDIGKQAESLIGKAGSMATRFTGMTGAG"
FT   variation       22363
FT                   /note="Uam25 mutation"
FT                   /replace="t"
FT                   /gene="U"
FT   variation       22501
FT                   /note="Uam77 and Uam92 mutations"
FT                   /replace="t"
FT                   /gene="U"
FT   CDS             22791..23954
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P10312"
FT                   /transl_table=11
FT                   /gene="D"
FT                   /function="essential tail protein"
FT                   /product="gpD"
FT                   /protein_id="AAD03295.1"
FT                   /translation="MLDALTFDAGSTLTPDYMLMLDSRDITGNISDRLMSMTLTDNRGF
FT                   EADQLDIELNDADGQVGLPVRGAVLTVYIGWKGFALVCKGKFTVDEVEHRGAPDVVTIR
FT                   ARSADFRGTLNSRREGSWHDTTLGAIVKAIATRNRLEASVAPSLAGIKIPHIDQSQESD
FT                   AKFLTRLAERNGGEVSVKMGKLLFLKAGQGVTASGKKIPQVTITRSDGDRHHFAIADRG
FT                   AYTGVTAKWLHTKDPKPQKQKVKLKRKKKEKHLRALEHPKAKPVRQKKAPKVPEAREGE
FT                   YMAGEADNVFALTTVYATKAQAMRAAQAKWDKLQRGVAEFSISLATGRADIYTETPVKV
FT                   SGFKRVIDEQDWTITKVTHFLNNSGFTTSLELEVRLSDVEYETEDDE"
FT   variation       23592
FT                   /note="Dam6 mutation"
FT                   /replace="t"
FT                   /gene="D"
FT   -35_signal      23973..23975
FT   -10_signal      23996..24002
FT   prim_transcript 24008..24288
FT                   /note="putative"
FT   CDS             24036..24254
FT                   /codon_start=1
FT                   /db_xref="SWISS-PROT:P08762"
FT                   /transl_table=11
FT                   /gene="ogr"
FT                   /product="Ogr"
FT                   /protein_id="AAD03296.1"
FT                   /translation="MFHCPLCQHAAHARTSRYITDTTKERYHQCQNVNCSATFITYESV
FT                   QRYIVKPGEVHAVRPHPLPSGQQIMWM"
FT   variation       24148..25274
FT                   /note="del15 deletion"
FT                   /replace=""
FT   variation       24160
FT                   /note="ogr1 and ogr52 mutations"