Addgene mCherry-Rab9a Sequencing Result - Sequence Analyzer Skip to main content
Addgene

Sequence Analyzer: mCherry-Rab9a Sequencing Result


Map View

600 400 200 End (780) SacI (766) Eco53kI (764) SmlI - XhoI - PaeR7I (759) BglII (755) BspEI (746) TatI - BsrGI (738) NmeAIII (726) XcmI (724) SgrAI (719) HincII (637) AccI (636) SalI (635) BsgI (632) PvuII - MspA1I (616) DrdI (578) BbvCI - Bpu10I (576) AlwNI (544) BsrBI (496) PspFI (481) PflMI - BseYI (477) BtsI - BtsαI (467) PstI - SbfI (393) SfcI (389) MfeI (325) BsaAI (268) AhdI (232) mCherry-R (183 .. 201) BssSI - BssSαI (125) ApaLI (98) MscI (68) BsiEI (30) AgeI (25) AfeI (21) BmtI (20) NheI (16) Start (0) mCherry2 Kozak sequence mCherry-Rab9a 780 bp

Sequence View

BsiEIAgeINheIBmtIAfeIStart (0) 60 1 5 MVSKGEED mCherry2 Kozak sequence EPSDPLALPVATMVSKGEED *RDGGHHALALLI t g a a c c g t c a g a t c c g c t a g c g c t a c c g g t c g c c a c c a t g g t g a g c a a g g g c g a g g a g g a a c t t g g c a g t c t a g g c g a t c g c g a t g g c c a g c g g t g g t a c c a c t c g t t c c c g c t c c t c c t

ApaLIMscI 120 10 15 20 25 NMAIIKEFMRFKVHMEGSVN mCherry2 NMAIIKEFMRFKVHMEGSVN VHGDDLLEHAELHVHLAGHV t a a c a t g g c c a t c a t c a a g g a g t t c a t g c g c t t c a a g g t g c a c a t g g a g g g c t c c g t g a a a t t g t a c c g g t a g t a g t t c c t c a a g t a c g c g a a g t t c c a c g t g t a c c t c c c g a g g c a c t t

BssSαIBssSI 180 30 35 40 45 GHEFEIEGEGEGRPYEGTQT mCherry2 GHEFEIEGEGEGRPYEGTQT AVLELDLALALAAGVLAGLG c g g c c a c g a g t t c g a g a t c g a g g g c g a g g g c g a g g g c c g c c c c t a c g a g g g c a c c c a g a c g c c g g t g c t c a a g c t c t a g c t c c c g c t c c c g c t c c c g g c g g g g a t g c t c c c g t g g g t c t g

AhdI 240 50 55 60 65 AKLKVTKGGPLPFAWDILSP mCherry2 G G T T C G A C T T C C A C T G G T T mCherry-R AKLKVTKGGPLPFAWDILSP GLQLHGLTAGQGEGPVDQGR c g c c a a g c t g a a g g t g a c c a a g g g t g g c c c c c t g c c c t t c g c c t g g g a c a t c c t g t c c c c g c g g t t c g a c t t c c a c t g g t t c c c a c c g g g g g a c g g g a a g c g g a c c c t g t a g g a c a g g g g

BsaAI 300 70 75 80 85 QFMYGSKAYVKHPADIPDYL mCherry2 QFMYGSKAYVKHPADIPDYL LEHVAGLGVHLVGGVDGVVQ t c a g t t c a t g t a c g g c t c c a a g g c c t a c g t g a a g c a c c c c g c c g a c a t c c c c g a c t a c t t a g t c a a g t a c a t g c c g a g g t t c c g g a t g c a c t t c g t g g g g c g g c t g t a g g g g c t g a t g a a

MfeI 360 90 95 100 105 KLSFPEGFNWERVMNFEDGG mCherry2 KLSFPEGFNWERVMNFEDGG LQGEGLAEIPLAHHVELVAA g a a g c t g t c c t t c c c c g a g g g c t t c a a t t g g g a g c g c g t g a t g a a c t t c g a g g a c g g c g g c t t c g a c a g g a a g g g g c t c c c g a a g t t a a c c c t c g c g c a c t a c t t g a a g c t c c t g c c g c c

SbfIPstISfcI 420 110 115 120 125 VVTVTQDSSLQDGEFIYKVK mCherry2 VVTVTQDSSLQDGEFIYKVK HHGHGLVGGQLVALEDVLHL c g t g g t g a c c g t g a c c c a g g a c t c c t c c c t g c a g g a c g g c g a g t t c a t c t a c a a g g t g a a g c a c c a c t g g c a c t g g g t c c t g a g g a g g g a c g t c c t g c c g c t c a a g t a g a t g t t c c a c t t

BseYIPflMIBtsαIBtsI 480 130 135 140 145 LRGTNFPSDGPVMQCRTMGW mCherry2 LRGTNFPSDGPVMQCRTMGW QAAGVEGGVAGYHLTTGHAP g c t g c g c g g c a c c a a c t t c c c c t c c g a c g g c c c c g t a a t g c a g t g t c g t a c c a t g g g c t g c g a c g c g c c g t g g t t g a a g g g g a g g c t g c c g g g g c a t t a c g t c a c a g c a t g g t a c c c g a c

BsrBIPspFI 540 150 155 160 165 EASTERMYPEDGALKGEIKQ mCherry2 EASTERMYPEDGALKGEIKQ LGGSLPHVGLVAGQLALDLL g g a g g c c t c c a c t g a g c g g a t g t a c c c c g a g g a c g g c g c c c t g a a g g g c g a g a t c a a g c a c c t c c g g a g g t g a c t c g c c t a c a t g g g g c t c c t g c c g c g g g a c t t c c c g c t c t a g t t c g t

Bpu10IBbvCIDrdIAlwNI 600 170 175 180 185 RLKLKDGGHYDAEVKTTYKA mCherry2 RLKLKDGGHYDAEVKTTYKA PQLQLVAAVVVSLDLGGVLG g a g g c t g a a g c t g a a g g a c g g c g g c c a c t a c g a c g c t g a g g t c a a g a c c a c c t a c a a g g c c t c c g a c t t c g a c t t c c t g c c g c c g g t g a t g c t g c g a c t c c a g t t c t g g t g g a t g t t c c g

BsgISalIAccIHincIIMspA1IPvuII 660 190 195 200 205 KKPVQLPGAYNVDIKLDILS mCherry2 KKPVQLPGAYNVDIKLDILS LLGHLQGAGVVDVDLQVDKG c a a g a a g c c c g t g c a g c t g c c c g g c g c c t a c a a c g t c g a c a t c a a g t t g g a c a t c c t t t c g t t c t t c g g g c a c g t c g a c g g g c c g c g g a t g t t g c a g c t g t a g t t c a a c c t g t a g g a a a g

SgrAI 720 210 215 220 225 HNEDYTIVEQYERAEGRHST mCherry2 HNEDYTIVEQYERAEGRHST VVLVVGDHFLVFAGLAAVGG c c a c a a c g a g g a c t a c a c c a t c g t g g a a c a g t a c g a a c g c g c c g a g g g c c g c c a c t c c a c g g t g t t g c t c c t g a t g t g g t a g c a c c t t g t c a t g c t t g c g c g g c t c c c g g c g g t g a g g t g

End (780) BglIIPaeR7IXhoISmlIEco53kISacIBspEIBsrGITatIXcmINmeAIII 780 230 235 GGMDELYK (in frame with mCherry2) SGLRSRARMAG mCherry2 GGMDELYKSGLRSRARMAG AAHVLQVLGSESRSSAHCS c g g c g g c a t g g a c g a g c t g t a c a a g t c c g g a c t c a g a t c t c g a g c t c g c a t g g c a g g a a a g c c g c c g t a c c t g c t c g a c a t g t t c a g g c c t g a g t c t a g a g c t c g a g c g t a c c g t c c t t t

Restriction Enzymes

Instructions: By default, all cutters are shown. Filter on number of cut sites or search by enzyme name.

Filter

Features

Primers

BLAST

BLAST (Basic Local Alignment Search Tool) finds regions of similarity between biological sequences. Click on the buttons below to submit a BLAST search to NCBI. The results will appear in a new window. See your recent BLAST results on NCBI's website.

  • Nucleotide-Nucleotide BLAST (BLASTN)

  • Translated Nucleotide-Protein BLAST (BLASTX)

  • Sequence alignment using BLAST (BLAST2)

Sequence Analyzer Guide

Map

Displays a graphical map based on nucleotide sequence data labeled with restriction enzymes, plasmid features, ORFs (theoretical open reading frames) and primers. Hovering over data labels will display additional information (e.g. cut site)

To select a portion of sequence, click one location on the plasmid and then a second location to display the sequence between the two locations.

Sequence

Displays both strands of base paired nucleotide sequences with annotated enzymes, plasmid features, ORFs (theoretical open reading frames) and primers. Hovering over data labels will display additional information (e.g. cut site).

To select a portion of sequence, click one location on the sequence and then a second location to display the sequence between the two locations.

Enzymes

List of restriction enzymes that can cut a given nucleotide sequence. Table lists enzyme name and the sequence location of the cut.

Features

List of common features detected in a given nucleotide sequence. Table lists feature name, location, size, color used to indicate its position on the map, and direction (if relevant).

Primers

List of commonly used primers detected in a given nucleotide sequence. Table lists primer name, sequence, length, binding site location, and direction.

BLAST

Use Basic Local Alignment Search Tool (BLAST) via the NCBI website to determine similarity between a given sequence and nucleotide (BLASTN) or protein (BLASTX) sequence databases. Additionally, align a custom nucleotide sequence against a given sequence using BLAST2.

File Downloads

GenBank

File contains the nucleotide sequence and annotated features in GenBank flat file format. Open the file with a text editor or plasmid mapping software to view the sequence.

SnapGene

File contains the nucleotide sequence and enhanced annotations from SnapGene Server. Open the file with SnapGene software or the free Viewer to view the plasmid map, sequence, and perform additional sequence analysis.