نتایج جستجو برای: cargo terminal

تعداد نتایج: 159678  

Journal: :The Journal of Cell Biology 2005
Kevin C. Slep Stephen L. Rogers Sarah L. Elliott Hiroyuki Ohkura Peter A. Kolodziej Ronald D. Vale

EB1 is a member of a conserved protein family that localizes to growing microtubule plus ends. EB1 proteins also recruit cell polarity and signaling molecules to microtubule tips. However, the mechanism by which EB1 recognizes cargo is unknown. Here, we have defined a repeat sequence in adenomatous polyposis coli (APC) that binds to EB1's COOH-terminal domain and identified a similar sequence i...

2015
Andreea Popa Wei Zhang Megan S. Harrison Kylia Goodner Teymur Kazakov Edward C. Goodwin Alex Lipovsky Christopher G. Burd Daniel DiMaio

Trafficking of human papillomaviruses to the Golgi apparatus during virus entry requires retromer, an endosomal coat protein complex that mediates the vesicular transport of cellular transmembrane proteins from the endosome to the Golgi apparatus or the plasma membrane. Here we show that the HPV16 L2 minor capsid protein is a retromer cargo, even though L2 is not a transmembrane protein. We sho...

2010
Kaitlyn M. Dykstra Jacqueline E. Pokusa Joseph Suhan Tina H. Lee

The structure of the endoplasmic reticulum (ER) undergoes highly regulated changes in specialized cell types. One frequently observed type of change is its reorganization into stacked and concentrically whorled membranes, but the underlying mechanisms and functional relevance for cargo export are unknown. Here, we identify Yip1A, a conserved membrane protein that cycles between the ER and early...

Journal: :The Journal of biological chemistry 2004
João Costa-Rodrigues Andreia F Carvalho Alexandra M Gouveia Marc Fransen Clara Sá-Miranda Jorge E Azevedo

Most newly synthesized peroxisomal matrix proteins are transported to the organelle by Pex5p, a remarkable multidomain protein involved in an intricate network of transient protein-protein interactions. Presently, our knowledge regarding the structure/function of amino acid residues 118 to the very last residue of mammalian Pex5p is quite vast. Indeed, the cargo-protein receptor domain as well ...

Journal: :The Journal of Cell Biology 2007
Hwajin Kim Shuo-Chien Ling Gregory C. Rogers Comert Kural Paul R. Selvin Stephen L. Rogers Vladimir I. Gelfand

Dynactin links cytoplasmic dynein and other motors to cargo and is involved in organizing radial microtubule arrays. The largest subunit of dynactin, p150(glued), binds the dynein intermediate chain and has an N-terminal microtubule-binding domain. To examine the role of microtubule binding by p150(glued), we replaced the wild-type p150(glued) in Drosophila melanogaster S2 cells with mutant Del...

ژورنال: :journal of biotechnology and health sciences 0
masoud rahmati department of physical education and sport sciences, faculty of literature and humanities, lorestan university, khorramabad, ir iran; department of physical education and sport sciences, faculty of literature and humanities, lorestan university, khorramabad, ir iran. tel: +98-9124525538, fax: +98-4215393

conclusions in summary, the current review article demonstrated that some proteins such as adaptors, scaffolds, chaperons and microtubule associated proteins and some metabolites, hormones, protein kinases and exercise training can regulate kinesin-1 traffic control in neuronal highway. these findings open exciting new areas of kinesin-1 research. context the current study aimed to review resea...

2017
Yuqing Hou George B. Witman

Cilia are assembled via intraflagellar transport (IFT). The IFT machinery is composed of motors and multisubunit particles, termed IFT-A and IFT-B, that carry cargo into the cilium. Knowledge of how the IFT subunits interact with their cargo is of critical importance for understanding how the unique ciliary domain is established. We previously reported a Chlamydomonas mutant, ift46-1, that fail...

Journal: :The Journal of biological chemistry 2004
Hsiangling Teo Dmitry B Veprintsev Roger L Williams

The endosomal sorting complex required for transport (ESCRT-I) is a 350-kDa complex of three proteins, Vps23, Vps28, and Vps37. The N-terminal ubiquitin-conjugating enzyme E2 variant (UEV) domain of Vps23 is required for sorting ubiquitinated proteins into the internal vesicles of multivesicular bodies. UEVs are homologous to E2 ubiquitin ligases but lack the conserved cysteine residue required...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Johann Urschitz Miyuri Kawasumi Jesse Owens Kazuto Morozumi Hideaki Yamashiro Ilko Stoytchev Joel Marh James A Dee Kris Kawamoto Craig J Coates Joseph M Kaminski Pawel Pelczar Ryuzo Yanagimachi Stefan Moisyadi

Efficient integration of functional genes is an essential prerequisite for successful gene delivery such as cell transfection, animal transgenesis, and gene therapy. Gene delivery strategies based on viral vectors are currently the most efficient. However, limited cargo capacity, host immune response, and the risk of insertional mutagenesis are limiting factors and of concern. Recently, several...

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