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
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