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PMID: 3011407 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The integrase family of site-specific recombinases: regional similarities and global diversity.

The EMBO journal ·Vol. 5 ·No. 2 ·1986-02-00 ·Pages 433-40

Argos P, Landy A, Abremski K, Egan JB, Haggard-Ljungquist E, Hoess RH, Kahn ML, Kalionis B, Narayana SV, Pierson LS

Abstract

A combination of two methods for detecting distant relationships in protein primary sequences was used to compare the site-specific recombination proteins encoded by bacteriophage lambda, phi 80, P22, P2, 186, P4 and P1. This group of proteins exhibits an unexpectedly large diversity of sequences. Despite this diversity, all of the recombinases can be aligned in their C-terminal halves. A 40-residue region near the C terminus is particularly well conserved in all the proteins and is homologous to a region near the C terminus of the yeast 2 mu plasmid Flp protein. This family of recombinases does not appear to be related to any other site-specific recombinases. Three positions are perfectly conserved within this family: histidine, arginine and tyrosine are found at respective alignment positions 396, 399 and 433 within the well-conserved C-terminal region. We speculate that these residues contribute to the active site of this family of recombinases, and suggest that tyrosine-433 forms a transient covalent linkage to DNA during strand cleavage and rejoining.

MeSH Terms
Amino Acid Sequence Bacteriophage lambda/enzymology Coliphages/enzymology DNA Helicases/genetics DNA Nucleotidyltransferases/genetics Integrases Protein Conformation Species Specificity
Chemicals
DNA Nucleotidyltransferases Integrases DNA Helicases
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Argos P
Landy A
Abremski K
Egan J B
Haggard-Ljungquist E
Hoess R H
Kahn M L
Kalionis B
Narayana S V
Pierson L S
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Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Published
1986-02-00
Pages
433-40
Language
English
Region
England
NLM ID
8208664
PMCID
PMC1166749
Subset
IM
Grants
NIAID NIH HHS · AI 13544 · United States
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