The Vps4 C-terminal helix is a critical determinant for assembly and ATPase activity and has elements conserved in other members of the meiotic clade of AAA ATPases

FEBS Journal

Volumn 275, Issue 7, 2008, Pages 1427-1449

  Vajjhala, Parimala R ^a   Nguyen, Chau H ^a   Landsberg, Michael J ^a   Kistler, Carol ^a   Gan, Ai Lin ^a   King, Glenn F ^a   Hankamer, Ben ^a   Munn, Alan L ^a,b  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b GRIFFITH UNIVERSITY   (Australia)

Author keywords

Endocytosis; Lysosome; Macromolecular complex; Membrane traffic; Vacuole

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; MEMBRANE PROTEIN; OLIGOMER; PROTEIN VPS4; PROTEIN VTA1; UNCLASSIFIED DRUG;

ALPHA HELIX; AMINO TERMINAL SEQUENCE; ANTIGEN PRESENTATION; ARTICLE; CARBOXY TERMINAL SEQUENCE; CLADISTICS; COMPLEX FORMATION; ENDOSOME; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME MECHANISM; ENZYME STRUCTURE; HYDROLYSIS; IN VITRO STUDY; IN VIVO STUDY; MEIOSIS; MEMBRANE VESICLE; MICROTUBULE; NONHUMAN; OLIGOMERIZATION; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DOMAIN; PROTEIN TARGETING; PROTEIN TRANSPORT; RECEPTOR DOWN REGULATION; VIROGENESIS; VIRUS ENVELOPE;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; CATALYSIS; CONSERVED SEQUENCE; ENDOSOMES; HUMANS; MEIOSIS; MOLECULAR SEQUENCE DATA; PROTEIN STRUCTURE, SECONDARY; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 40749161604     PISSN: 1742464X     EISSN: 17424658     Source Type: Journal    
DOI: 10.1111/j.1742-4658.2008.06300.x     Document Type: Article

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