Toolyard

SpeI Recognition Site


SpeI at a glance

5' A|CTAGT 3'
3' TGATC|A 5'
Recognition site5'-ACTAGT-3'
CutA^CTAGT
Endsa 4-base 5' overhang (CTAG)
Expected frequencyabout once every 4,096 bp in random DNA
Compatible endsAvrII, NheI, XbaI

How to find SpeI sites in a sequence

  1. Paste a DNA sequence or FASTA record into the box above. SpeI is already entered under Only these enzymes.
  2. Tick Circular DNA for a plasmid, so a site that spans the end and the start is found.
  3. The map marks each SpeI cut with its position. Copy or download the output below it.

Frequently asked questions

What sequence does SpeI cut?

SpeI recognizes ACTAGT (written 5' to 3') and cuts the top strand at A^CTAGT.

Does SpeI leave sticky or blunt ends?

Sticky ends: a 4-base 5' overhang (CTAG).

Which enzymes leave ends compatible with SpeI?

AvrII, NheI and XbaI. Their overhangs are the same, so the ends can be ligated to each other.

How often does SpeI cut?

A site like ACTAGT turns up about once every 4,096 bp in random DNA. Real sequences vary, so check yours above.

Restriction enzymes

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