5fwb

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (13:29, 26 July 2023) (edit) (undo)
 
(2 intermediate revisions not shown.)
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 5fwb is ON HOLD until Paper Publication
+
==Human Spectrin SH3 domain D48G, E7F, K60F==
 +
<StructureSection load='5fwb' size='340' side='right'caption='[[5fwb]], [[Resolution|resolution]] 1.50&Aring;' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[5fwb]] is a 1 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=5FWB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5FWB 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]] 1.5&#8491;</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=5fwb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5fwb OCA], [https://pdbe.org/5fwb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5fwb RCSB], [https://www.ebi.ac.uk/pdbsum/5fwb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5fwb ProSAT]</span></td></tr>
 +
</table>
 +
== Disease ==
 +
[https://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN] West syndrome. The disease is caused by mutations affecting the gene represented in this entry.
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/SPTN1_HUMAN SPTN1_HUMAN] Fodrin, which seems to be involved in secretion, interacts with calmodulin in a calcium-dependent manner and is thus candidate for the calcium-dependent movement of the cytoskeleton at the membrane.
-
Authors: Gallego, P., Navarro, S., Ventura, S., Reverter, D.
+
==See Also==
-
 
+
*[[Spectrin 3D structures|Spectrin 3D structures]]
-
Description: Human Spectrin SH3 domain D48G, E7F, K60F
+
__TOC__
-
[[Category: Unreleased Structures]]
+
</StructureSection>
-
[[Category: Gallego, P]]
+
[[Category: Homo sapiens]]
-
[[Category: Reverter, D]]
+
[[Category: Large Structures]]
-
[[Category: Navarro, S]]
+
[[Category: Gallego P]]
-
[[Category: Ventura, S]]
+
[[Category: Navarro S]]
 +
[[Category: Reverter D]]
 +
[[Category: Ventura S]]

Current revision

Human Spectrin SH3 domain D48G, E7F, K60F

PDB ID 5fwb

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools