Self-assembly of MinE on the membrane underlies formation of the MinE ring to sustain function of the Escherichia coli Min system

Journal of Biological Chemistry

Volumn 289, Issue 31, 2014, Pages 21252-21266

  Zheng, Min ^a   Chiang, Ya Ling ^b   Lee, Hsiao Lin ^a   Kong, Lih Ren ^a   Hsu, Shang Te Danny ^a,c   Hwang, Ing Shouh ^b,d   Rothfield, Lawrence I ^e   Shih, Yu Ling ^a,c  

^a INSTITUTE OF BIOLOGICAL CHEMISTRY   (Taiwan)

^b NATIONAL TSING HUA UNIVERSITY   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^d INSTITUTE OF PHYSICS   (Taiwan)

^e UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ESCHERICHIA COLI; LIPID BILAYERS; POLES; PROTEINS;

FIBRILLAR STRUCTURES; FOLDING PROPENSITIES; OSCILLATION CYCLES; POLE-TO-POLE OSCILLATIONS; POSSIBLE MECHANISMS; RING-LIKE STRUCTURES; SUBCELLULAR LOCALIZATIONS; SUPPORTED LIPID BILAYERS;

SELF ASSEMBLY;

BACTERIAL PROTEIN; MIND PROTEIN; PROTEIN MINE; UNCLASSIFIED DRUG; CELL CYCLE PROTEIN; ESCHERICHIA COLI PROTEIN; LIPID BILAYER; MINE PROTEIN, E COLI;

AMINO TERMINAL SEQUENCE; ARTICLE; ATOMIC FORCE MICROSCOPY; BACTERIAL SECRETION SYSTEM; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; DIMERIZATION; ESCHERICHIA COLI; LIPID BILAYER; MOLECULAR CLONING; MOLECULAR DYNAMICS; MORPHOLOGY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN ASSEMBLY; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; TRANSMISSION ELECTRON MICROSCOPY; ULTRACENTRIFUGATION; AMINO ACID SEQUENCE; CELL MEMBRANE; CHEMISTRY; CIRCULAR DICHROISM; MASS SPECTROMETRY; METABOLISM; MOLECULAR GENETICS; PHYSIOLOGY;

AMINO ACID SEQUENCE; CELL CYCLE PROTEINS; CELL MEMBRANE; CIRCULAR DICHROISM; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; LIPID BILAYERS; MOLECULAR SEQUENCE DATA; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; ULTRACENTRIFUGATION;

EID: 84905384791     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.571976     Document Type: Article

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