Basic Vector Information
- Vector Name:
- pNTT104
- Antibiotic Resistance:
- Ampicillin
- Length:
- 3297 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Nomura N, Nagase T.
pNTT104 vector Map
pNTT104 vector Sequence
LOCUS 40924_33617 3297 bp DNA circular SYN 18-DEC-2018 DEFINITION Cloning vector pNTT104 DNA, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 3297) AUTHORS Nomura N, Nagase T. TITLE The nucleotide sequence of the pNTT104 vector JOURNAL Published Only in Database (1999) REFERENCE 2 (bases 1 to 3297) AUTHORS Nomura N, Nagase T. TITLE Direct Submission JOURNAL Submitted (31-AUG-1999) Nobuo Nomura, Kazusa DNA Research Institute, Laboratory of Gene Structure 1; 1532-3 Yana, Kisarazu, Chiba 292-0812, Japan (E-mail:nomura@kazusa.or.jp, URL:http://www.kazusa.or.jp, Tel:81-438-52-3932, Fax:81-438-52-3931) REFERENCE 3 (bases 1 to 3297) TITLE Direct Submission REFERENCE 4 (bases 1 to 3297) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Published Only in Database (1999)" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted (31-AUG-1999) Nobuo Nomura, Kazusa DNA Research Institute, Laboratory of Gene Structure 1"; volume: " 1532-3 Yana, Kisarazu, Chiba 292-0812, Japan (E-mail:nomura@kazusa.or.jp, URL:http://www.kazusa.or.jp, Tel:81-438-52-3932, Fax"; pages: "81-438-52-3931" COMMENT SGRef: number: 3; type: "Journal Article" COMMENT pNTT104 This sequence is derived from the pUC118 sequence mainly compiled by changing the polylinker sequence (sequence at the position between 231 and 291 of the pUC118) to the 194-bp sequence (sequence at the position between 231 and 426 of the pNTT104) containing multiple restriction enzyme recognition sites. In addition to that, both the ScaI and NarI sites of the pUC118 were eliminated by nucleotide exchanges at the positions 586 (C to T) and 1802 (G to A) of the pNTT104 sequence, respectively. FEATURES Location/Qualifiers source 1..3297 /mol_type="other DNA" /organism="synthetic DNA construct" protein_bind 107..128 /label=CAP binding site /note="CAP binding activates transcription in the presence of cAMP." promoter 143..173 /label=lac promoter /note="promoter for the E. coli lac operon" protein_bind 181..197 /label=lac operator /note="The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-beta-D-thiogalactopyranoside (IPTG)." primer_bind 205..221 /label=M13 rev /note="common sequencing primer, one of multiple similar variants" primer_bind complement(426..442) /label=M13 fwd /note="common sequencing primer, one of multiple similar variants" rep_origin 655..1110 /label=f1 ori /note="f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis" promoter 1392..1496 /label=AmpR promoter CDS 1497..2354 /codon_start=1 /label=AmpR /note="beta-lactamase" /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS LIKHW" rep_origin 2528..3116 /direction=RIGHT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication"
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