2A63

Solution structure of a stably monomeric mutant of lambda Cro produced by substitutions in the ball-and-socket interface

Summary for 2A63

• Entry DOI: 10.2210/pdb2a63/pdb
• NMR Information: BMRB: 6771
• Descriptor: Regulatory protein cro (1 entity in total)
• Functional Keywords: helix-turn-helix, monomer, ball-and-socket, viral protein
• Biological source: Enterobacteria phage lambda
• Total number of polymer chains: 1
• Total formula weight: 7423.48

Authors

Newlove, T.,Atkinson, K.R.,Van Dorn, L.O.,Cordes, M.H. (deposition date: 2005-07-01, release date: 2006-06-06, Last modification date: 2024-05-22)

Primary citation

Newlove, T.,Atkinson, K.R.,Van Dorn, L.O.,Cordes, M.H.
A Trade between Similar but Nonequivalent Intrasubunit and Intersubunit Contacts in Cro Dimer Evolution.
Biochemistry, 45:6379-6391, 2006

PubMed Abstract: The homodimeric lambda Cro protein has a "ball-and-socket" interface that includes insertion of an aromatic side chain, Phe 58, from each subunit into a cavity in the hydrophobic core of the other subunit. This overlap between the subunit core and dimer interface hypothetically explains the strong dimerization and weak monomer stability of lambda Cro in comparison to homologues. According to a model developed here and in a previous study [LeFevre, K. R., and Cordes, M. H. (2003) Proc. Natl. Acad. Sci. U.S.A. 100, 2345-2350], the socket cavity evolved in part by replacement of a buried tryptophan in an ancestral stable monomer with a smaller side chain (Ala 33 in lambda Cro). The resulting core defect was in effect repaired by insertion of a different side chain (Phe 58) from a second subunit, generating the ball and socket. Consistent with such an evolutionary trade between intrasubunit and intersubunit interactions, we showed in the previous study that restoration of the ancestral Trp 33 in lambda Cro stabilized the monomer and reduced the extent of dimerization. Here, we report the solution structure of a stable lambda Cro monomer containing the Ala33Trp mutation, which confirms that the restored tryptophan fulfills its ancestral role as a core side chain, filling part of the socket cavity occupied by Phe 58 in the wild-type dimer. The structure also reveals, however, that the cavity is not completely filled by Trp 33, suggesting that its formation could have involved multiple mutations that reduced side chain volume. We offer suggestive evidence of a role of mutations at a second position.

PubMed: 16700549
DOI: 10.1021/bi052541c

Experimental method

SOLUTION NMR