Basic Vector Information
- Vector Name:
- pSKPDR5-PPUS
- Antibiotic Resistance:
- Ampicillin
- Length:
- 5654 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Host:
- Yeast
- Source/Author:
- Nakamura K, Niimi M, Niimi K, Holmes AR, Yates JE, Decottignies A, Monk BC, Goffeau A, Cannon RD.
- Promoter:
- URA3
pSKPDR5-PPUS vector Map
pSKPDR5-PPUS vector Sequence
LOCUS 40924_40597 5654 bp DNA circular SYN 18-DEC-2018 DEFINITION Cloning vector pSKPDR5-PPUS, complete sequence. ACCESSION . VERSION . KEYWORDS . SOURCE synthetic DNA construct ORGANISM synthetic DNA construct REFERENCE 1 (bases 1 to 5654) AUTHORS Nakamura K, Niimi M, Niimi K, Holmes AR, Yates JE, Decottignies A, Monk BC, Goffeau A, Cannon RD. TITLE Functional expression of Candida albicans drug efflux pump Cdr1p in a Saccharomyces cerevisiae strain deficient in membrane transporters JOURNAL Antimicrob. Agents Chemother. 45 (12), 3366-3374 (2001) PUBMED 11709310 REFERENCE 2 (bases 1 to 5654) AUTHORS Lamping E, Niimi M, Cannon RD. TITLE Small, synthetic, GC-rich mRNA stem-loop modules 5' proximal to the AUG start-codon predictably tune gene expression in yeast JOURNAL Microb. Cell Fact. 12 (1), 74 (2013) PUBMED 23895661 REFERENCE 3 (bases 1 to 5654) AUTHORS Lamping E, Niimi M, Cannon RD. TITLE Direct Submission JOURNAL Submitted (15-AUG-2011) Sir John Walsh Research Institute, University of Otago, 310 Great King Street, Dunedin, Otago 9054, New Zealand REFERENCE 4 (bases 1 to 5654) TITLE Direct Submission REFERENCE 5 (bases 1 to 5654) AUTHORS . TITLE Direct Submission COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Antimicrob. Agents Chemother."; date: "2001"; volume: "45"; issue: "12"; pages: "3366-3374" COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Microb. Cell Fact."; date: "2013"; volume: "12"; issue: "1"; pages: "74" COMMENT SGRef: number: 3; type: "Journal Article"; journalName: "Submitted (15-AUG-2011) Sir John Walsh Research Institute, University of Otago, 310 Great King Street, Dunedin, Otago 9054, New Zealand" COMMENT SGRef: number: 4; type: "Journal Article" FEATURES Location/Qualifiers source 1..5654 /mol_type="other DNA" /organism="synthetic DNA construct" rep_origin complement(3..458) /direction=LEFT /label=f1 ori /note="f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis" primer_bind 600..616 /label=M13 fwd /note="common sequencing primer, one of multiple similar variants" promoter 623..641 /label=T7 promoter /note="promoter for bacteriophage T7 RNA polymerase" primer_bind 667..683 /label=KS primer /note="common sequencing primer, one of multiple similar variants" misc_feature 1823..1864 /label=multiple cloning site /note="multiple cloning site" regulatory 1870..2069 /label=3' end of Saccharomyces cerevisiae PDR5 ORF /note="3' end of Saccharomyces cerevisiae PDR5 ORF" /regulatory_class="terminator" promoter 2106..2321 /label=URA3 promoter CDS 2322..3122 /label=URA3 /note="orotidine-5'-phosphate decarboxylase, required for uracil biosynthesis" misc_feature 3146..3423 /label=3' end of Saccharomyces cerevisiae PDR5 ORF /note="3' end of Saccharomyces cerevisiae PDR5 ORF" promoter complement(3466..3484) /label=T3 promoter /note="promoter for bacteriophage T3 RNA polymerase" primer_bind complement(3505..3521) /label=M13 rev /note="common sequencing primer, one of multiple similar variants" protein_bind complement(3529..3545) /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)." promoter complement(3553..3583) /label=lac promoter /note="promoter for the E. coli lac operon" protein_bind complement(3598..3619) /label=CAP binding site /note="CAP binding activates transcription in the presence of cAMP." rep_origin complement(3907..4495) /direction=LEFT /label=ori /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of replication" CDS complement(4669..5526) /label=AmpR /note="beta-lactamase" promoter complement(5527..5631) /label=AmpR promoter
This page is informational only.