4lx1: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
Line 1: Line 1:
'''Unreleased structure'''
{{STRUCTURE_4lx1|  PDB=4lx1  |  SCENE=  }}
===Crystal structure of Myo5a globular tail domain===


The entry 4lx1 is ON HOLD until Paper Publication
==Disease==
[[http://www.uniprot.org/uniprot/MYO5A_HUMAN MYO5A_HUMAN]] Griscelli disease type 3;Neuroectodermal melanolysosomal disease;Griscelli disease type 1. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry.


Authors: Pylypenko, O., Attanda, W., Coulibaly, D., Gauquelin, C., Houdusse, A.
==Function==
[[http://www.uniprot.org/uniprot/MYO5A_HUMAN MYO5A_HUMAN]] Processive actin-based motor that can move in large steps approximating the 36-nm pseudo-repeat of the actin filament. Involved in melanosome transport. Also mediates the transport of vesicles to the plasma membrane. May also be required for some polarization process involved in dendrite formation.<ref>PMID:10448864</ref> 


Description: Crystal structure of Myo5a globular tail domain
==About this Structure==
[[4lx1]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LX1 OCA].
 
==Reference==
<references group="xtra"/><references/>
[[Category: Attanda, W.]]
[[Category: Coulibaly, D.]]
[[Category: Gauquelin, C.]]
[[Category: Houdusse, A.]]
[[Category: Pylypenko, O.]]
[[Category: Dil]]
[[Category: Transport protein]]
Retrieved from "https://proteopedia.org/4lx1"