6c3t: Difference between revisions
From Proteopedia
Jump to navigationJump to search
m Protected "6c3t" [edit=sysop:move=sysop] |
No edit summary |
||
| (3 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
==AMYLOID FORMING PEPTIDE AADTWE FROM TRANSTHYRETIN WITH ATTR-D38A MUTATION ASSOCIATED WITH A FAMILIAL FORM OF TRANSTHYRETIN AMYLOIDOSIS== | |||
<StructureSection load='6c3t' size='340' side='right'caption='[[6c3t]], [[Resolution|resolution]] 1.00Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6c3t]] 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=6C3T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6C3T 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]] 1Å</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=6c3t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6c3t OCA], [https://pdbe.org/6c3t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6c3t RCSB], [https://www.ebi.ac.uk/pdbsum/6c3t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6c3t ProSAT]</span></td></tr> | |||
</table> | |||
==See Also== | |||
*[[Transthyretin 3D structures|Transthyretin 3D structures]] | |||
__TOC__ | |||
[[Category: | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: | [[Category: Large Structures]] | ||
[[Category: | [[Category: Eisenberg DS]] | ||
[[Category: | [[Category: Saelices L]] | ||
[[Category: Sawaya MR]] | |||
[[Category: Sievers SA]] | |||
Latest revision as of 14:26, 13 March 2024
AMYLOID FORMING PEPTIDE AADTWE FROM TRANSTHYRETIN WITH ATTR-D38A MUTATION ASSOCIATED WITH A FAMILIAL FORM OF TRANSTHYRETIN AMYLOIDOSIS
| ||||||||||||
