The role of the hypervariable C-terminal domain in Rab GTPases membrane targeting

Proceedings of the National Academy of Sciences of the United States of America

Volumn 111, Issue 7, 2014, Pages 2572-2577

  Li, Fu ^a,b   Yi, Long ^a   Zhao, Lei ^a,b   Itzen, Aymelt ^a,c   Goody, Roger S ^a   Wu, Yao Wen ^a,b  

^a MAX PLANCK INSTITUTE OF MOLECULAR PHYSIOLOGY   (Germany)

^b CHEMICAL GENOMICS CENTRE OF THE MAX PLANCK SOCIETY   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Chemical protein modification; RILP; Synthetic protein probe

Indexed keywords

ISOPRENE; LIPID; MACROGOL; OXIME; RAB PROTEIN; RAB1 PROTEIN; RAB35 PROTEIN; RAB5 PROTEIN; RAB7 PROTEIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; ENDOSOME; ENZYME LOCALIZATION; HUMAN; HUMAN CELL; INTRACELLULAR MEMBRANE; LYSOSOME; MEMBRANE TRANSPORT; NONHUMAN; PRENYLATION; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FAMILY; PROTEIN LIPID INTERACTION;

CHEMICAL PROTEIN MODIFICATION; RILP; SYNTHETIC PROTEIN PROBE;

ANIMALS; CELL MEMBRANE; DOGS; GENETIC VARIATION; HELA CELLS; HUMANS; MADIN DARBY CANINE KIDNEY CELLS; MODELS, BIOLOGICAL; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; RAB GTP-BINDING PROTEINS;

EID: 84894332323     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1313655111     Document Type: Article

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