5nb1: Difference between revisions

Line 1:

~~'''Unreleased structure'''~~

~~The entry~~ 5nb1 is ~~ON HOLD until Paper Publication~~

==Crystal structures of homooligomers of collagen type IV. alpha4NC1==

~~Authors~~: ~~Casino~~, P., ~~Marina~~, A.

== Structural highlights ==

<table><tr><td colspan='2'>[[5nb1]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5NB1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5NB1 FirstGlance]. <br>

~~Description~~: ~~Crystal structures of homooligomers of collagen type IV~~. ~~alpha4NC1~~

</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5nb1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5nb1 OCA], [http://pdbe.org/5nb1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5nb1 RCSB], [http://www.ebi.ac.uk/pdbsum/5nb1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5nb1 ProSAT]</span></td></tr>

[[~~Category~~: ~~Unreleased Structures~~]]

</table>

== Disease ==

[[http://www.uniprot.org/uniprot/CO4A4_HUMAN CO4A4_HUMAN]] Benign familial hematuria;Autosomal dominant Alport syndrome;Autosomal recessive Alport syndrome. 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.

== Function ==

[[http://www.uniprot.org/uniprot/CO4A4_HUMAN CO4A4_HUMAN]] Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen.

__TOC__

</StructureSection>

[[Category: Casino, P]]

[[Category: Marina, A]]

[[Category: Non-collagenous domain of collagen type iv. a principal structural component of basement membrane]]

[[Category: Structural protein]]

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@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
-The entry 5nb1 is ON HOLD  until Paper Publication
+==Crystal structures of homooligomers of collagen type IV. alpha4NC1==
+<StructureSection load='5nb1' size='340' side='right' caption='[[5nb1]], [[Resolution|resolution]] 2.82&Aring;' scene=''>
-Authors: Casino, P., Marina, A.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[5nb1]] is a 6 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5NB1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5NB1 FirstGlance]. <br>
-Description: Crystal structures of homooligomers of collagen type IV. alpha4NC1
+</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5nb1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5nb1 OCA], [http://pdbe.org/5nb1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5nb1 RCSB], [http://www.ebi.ac.uk/pdbsum/5nb1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5nb1 ProSAT]</span></td></tr>
-[[Category: Unreleased Structures]]
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/CO4A4_HUMAN CO4A4_HUMAN]] Benign familial hematuria;Autosomal dominant Alport syndrome;Autosomal recessive Alport syndrome. 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.
+== Function ==
+[[http://www.uniprot.org/uniprot/CO4A4_HUMAN CO4A4_HUMAN]] Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen.
+__TOC__
+</StructureSection>
 [[Category: Casino, P]]
 [[Category: Marina, A]]
+[[Category: Non-collagenous domain of collagen type iv. a principal structural component of basement membrane]]
+[[Category: Structural protein]]