Basic Vector Information
- Vector Name:
- pKW3_MB1Amp_TracrK_Spacer
- Antibiotic Resistance:
- Ampicillin
- Length:
- 3246 bp
- Type:
- Cloning vector
- Replication origin:
- ori
- Source/Author:
- Wang K, de la Torre D, Robertson WE, Chin JW.
- Promoter:
- PLtetO-1
pKW3_MB1Amp_TracrK_Spacer vector Map
pKW3_MB1Amp_TracrK_Spacer vector Sequence
LOCUS 62056_13610 3246 bp DNA circular SYN 30-AUG-2019
DEFINITION Cloning vector pKW3_MB1Amp_TracrK_Spacer, complete sequence.
ACCESSION MN226641
VERSION .
KEYWORDS .
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 3246)
AUTHORS Wang K, de la Torre D, Robertson WE, Chin JW.
TITLE Programmed chromosome fission and fusion enable precise large-scale
genome rearrangement and assembly
JOURNAL Science 365 (6456), 922-926 (2019)
REFERENCE 2 (bases 1 to 3246)
AUTHORS Wang K, de la Torre D, Robertson WE, Chin JW.
TITLE Direct Submission
JOURNAL Submitted (24-JUL-2019) Protein and Nucleic Acid Chemistry, MRC
Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge,
Cambridgeshire CB2 0QH, United Kingdom
REFERENCE 3 (bases 1 to 3246)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"; journalName: "Science";
date: "2019"; volume: "365"; issue: "6456"; pages: "922-926"
COMMENT SGRef: number: 2; type: "Journal Article"; journalName: "Submitted
(24-JUL-2019) Protein and Nucleic Acid Chemistry, MRC Laboratory of
Molecular Biology, Francis Crick Avenue, Cambridge, Cambridgeshire
CB2 0QH, United Kingdom"
COMMENT ##Assembly-Data-START##
Sequencing Technology :: Sanger dideoxy sequencing
##Assembly-Data-END##
FEATURES Location/Qualifiers
source 1..3246
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 104..208
/label=AmpR promoter
CDS 209..1066
/label=AmpR
/note="beta-lactamase"
rep_origin 1240..1828
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
terminator complement(1992..2078)
/label=rrnB T1 terminator
/note="transcription terminator T1 from the E. coli rrnB
gene"
regulatory 2234..2268
/label=Cas9 promoter predicted
/note="Cas9 promoter predicted"
/regulatory_class="promoter"
regulatory 2300..2327
/label=putative tracrRNA promoter
/note="putative tracrRNA promoter"
/regulatory_class="promoter"
misc_RNA 2381..2459
/label=tracrRNA
/note="trans-activating CRISPR RNA for the Streptococcus
pyogenes CRISPR/Cas9 system"
misc_feature 2571..2702
/label=crRNA leader
/note="crRNA leader sequence for the Streptococcus pyogenes
CRISPR/Cas system"
repeat_region 2703..2738
/label=DR
/note="direct repeat for the Streptococcus pyogenes
CRISPR/Cas system"
gap 2739..2768
/estimated_length=30
gap 2805..2834
/estimated_length=30
gap 2871..2900
/estimated_length=30
gap 2937..2966
/estimated_length=30
gap 3003..3032
/estimated_length=30
gap 3069..3098
/estimated_length=30
promoter complement(3167..3240)
/label=PLtetO-1 promoter
/note="modified phage lambda PL promoter with tet operator
sites (Lutz and Bujard, 1997)"
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