Small-angle X-ray scattering analysis reveals the ATP-bound monomeric state of the ATPase domain from the homodimeric MutL endonuclease, a GHKL phosphotransferase superfamily protein

Extremophiles

Volumn 19, Issue 3, 2015, Pages 643-656

  Iino, Hitoshi ^a   Hikima, Takaaki ^a   Nishida, Yuya ^b   Yamamoto, Masaki ^a   Kuramitsu, Seiki ^b   Fukui, Kenji ^c  

^a RIKEN SPring 8 Center   (Japan)

^b OSAKA UNIVERSITY   (Japan)

^c OSAKA MEDICAL COLLEGE   (Japan)

Author keywords

ATPase; DNA mismatch repair; Endonuclease; GHKL superfamily; Small angle X ray scattering

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; BACTERIAL PROTEIN; PROTEIN BINDING; PROTEIN SUBUNIT;

AMINO ACID SEQUENCE; BACTERIUM; BINDING SITE; CHEMISTRY; ENZYMOLOGY; METABOLISM; MOLECULAR GENETICS; PROTEIN SUBUNIT; SMALL ANGLE SCATTERING; X RAY DIFFRACTION;

ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; AMINO ACID SEQUENCE; BACTERIA; BACTERIAL PROTEINS; BINDING SITES; MOLECULAR SEQUENCE DATA; PROTEIN BINDING; PROTEIN SUBUNITS; SCATTERING, SMALL ANGLE; X-RAY DIFFRACTION;

EID: 84939977299     PISSN: 14310651     EISSN: 14334909     Source Type: Journal    
DOI: 10.1007/s00792-015-0745-2     Document Type: Article

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