Sandbox 666

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spinqualitylabelsall models PDB ID 1eri Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image
1eri, resolution 2.50Å ()
Structural annotation: Resources: CATH : 1Eria00 InterPro : Ipr011335, Ipr004221, Ipr011336 Pfam : PF02963 SCOP : d1eria_ UniProt : P00642
Functional annotation: Biological process: DNA restriction-modification system Molecular function: hydrolase activity Type II site-specific deoxyribonuclease activity metal ion binding DNA binding nuclease activity endonuclease activity magnesium ion binding
Resources:	FirstGlance, OCA, PDBsum, RCSB
Coordinates:	save as pdb, mmCIF, xml

Contents 1 Presentation 2 Reaction 3 Structure 4 Application of EcoRI in molecular biology 5 Links 6 References

Presentation

EcoRI is a type II restriction endonuclease. It recognizes and cleaves DNA on a specific palindromic sequence: GAATTC. EcoRI has been extracted from strain R Escherichia coli, a common bacterium which populates the intestine of mammalians. In bacteria, restriction enzymes protect the cell by cutting foreign DNA from bacteriophages (specific bacterial viruses).

Reaction

EcoRI (E.C. 3.1.21.4) is a hydrolase and its substrate is a double-strand DNA molecule and two water molecules. For its catalytic activity, EcoRI needs a cofactor which is the divalent ion Mg²⁺. EcoRI hydrolyses the phosphodiester bond between the guanylic and adenylic residues resulting in 5’-phosphate sticky ends which are complementary.

Structure

EcoRI is a homodimer, so it has two identical subunits (Representation of one ) of 31 kDa, but it possible to have homotetramers at high concentrations. The constitutive monomers are 276 amino acids long. EcoRI and all the other restriction enzymes show a common structural core which is a α/β domain. The constitutive subunits of EcoRI are organized into a single α/β domain (five stranded sheet which is surrounded by ). Four of these five β strands are parallel whereas the fourth (β4) is in an anti-parallel orientation to the others.^[1]

The N-terminal section of each subunit forms, with a β-hairpin, an “arm” which wraps around the DNA molecule. (The arm brings the DNA molecule to the catalytic cleft.)

The specific recognition of EcoRI of the GAATTC sequence is mediated by twelve hydrogen bonds (six bonds per subunit) originating from α helical recognition modules. Three amino acids are responsible for the recognition:Arg²⁰⁰, Glu¹⁴⁴ and Arg¹⁴⁵. These aminoacids are shown in red .Each residue form two hydrogen bonds with Guanine and the adjacent Adenosine residues respectively.

The reaction is due to a catalytic sequence motif which is found in most type II restriction endonucleases: the PD…D/EXK motif. For EcoRI, this catalytic sequence is PD⁹¹ …E¹¹¹AK.. This motif is also responsible for Mg2+ binding(Asp90 and Glu111). ^[2]

Application of EcoRI in molecular biology

Type II restriction endonuclease like EcoRI are often used in molecular biology for their capacity to cut precisely DNA on specific restriction site. That makes them useful tools for gene cloning. By using two different restriction enzymes, it is possible to do directional cloning which is very important if you want to insert a gene in an expression vector.

Links

[1]

References

1. ↑ Refinement of Eco RI endonuclease crystal structure: a revised protein chain tracing. Kim YC, Grable JC, Love R, Greene PJ, Rosenberg JM.
2. ↑ Structure and function of type II restriction endonucleases Alfred Pingoud, Albert Jeltsch Nucleic Acids Res. 2001 September 15; 29(18): 3705–3727. PMCID: PMC55916