This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


5d3a

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
m (Protected "5d3a" [edit=sysop:move=sysop])
Current revision (11:46, 9 May 2024) (edit) (undo)
 
(5 intermediate revisions not shown.)
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 5d3a is ON HOLD until Aug 06 2017
+
==KIF21A regulatory coiled coil==
 +
<StructureSection load='5d3a' size='340' side='right'caption='[[5d3a]], [[Resolution|resolution]] 2.50&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[5d3a]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5D3A OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5D3A FirstGlance]. <br>
 +
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.495&#8491;</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
 +
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5d3a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5d3a OCA], [https://pdbe.org/5d3a PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5d3a RCSB], [https://www.ebi.ac.uk/pdbsum/5d3a PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5d3a ProSAT]</span></td></tr>
 +
</table>
 +
== Disease ==
 +
[https://www.uniprot.org/uniprot/KI21A_HUMAN KI21A_HUMAN] Congenital fibrosis of extraocular muscles. The disease is caused by mutations affecting the gene represented in this entry.
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/KI21A_HUMAN KI21A_HUMAN] Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity).
-
Authors: Bianchi, S., Kraatz, S., Steinmetz, M.O., Kammerer, A.R.
+
==See Also==
-
 
+
*[[Kinesin 3D Structures|Kinesin 3D Structures]]
-
Description:
+
__TOC__
-
[[Category: Unreleased Structures]]
+
</StructureSection>
-
[[Category: Kammerer, A.R]]
+
[[Category: Homo sapiens]]
-
[[Category: Steinmetz, M.O]]
+
[[Category: Large Structures]]
-
[[Category: Bianchi, S]]
+
[[Category: Bianchi S]]
-
[[Category: Kraatz, S]]
+
[[Category: Kammerer AR]]
 +
[[Category: Kraatz S]]
 +
[[Category: Steinmetz MO]]

Current revision

KIF21A regulatory coiled coil

PDB ID 5d3a

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools