6fwu: Difference between revisions

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-'''Unreleased structure'''
-The entry 6fwu is ON HOLD  until Paper Publication
+==Crystal structure of human wild type beta-1,4-galactosyltransferase-1 (B4GalT1) in apo-closed dimeric form==
+<StructureSection load='6fwu' size='340' side='right' caption='[[6fwu]], [[Resolution|resolution]] 2.35&Aring;' scene=''>
-Authors: Harrus, D., Kellokumpu, S., Glumoff, T.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[6fwu]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6FWU OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6FWU FirstGlance]. <br>
-Description: Crystal structure of human wild type beta-1,4-galactosyltransferase-1 (B4GalT1) in apo-closed dimeric form
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NO3:NITRATE+ION'>NO3</scene></td></tr>
-[[Category: Unreleased Structures]]
+<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=6fwu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6fwu OCA], [http://pdbe.org/6fwu PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6fwu RCSB], [http://www.ebi.ac.uk/pdbsum/6fwu PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6fwu ProSAT]</span></td></tr>
+</table>
+== Disease ==
+[[http://www.uniprot.org/uniprot/B4GT1_HUMAN B4GT1_HUMAN]] Defects in B4GALT1 are the cause of congenital disorder of glycosylation type 2D (CDG2D) [MIM:[http://omim.org/entry/607091 607091]]. CDGs are a family of severe inherited diseases caused by a defect in protein N-glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.
+== Function ==
+[[http://www.uniprot.org/uniprot/B4GT1_HUMAN B4GT1_HUMAN]] The Golgi complex form catalyzes the production of lactose in the lactating mammary gland and could also be responsible for the synthesis of complex-type N-linked oligosaccharides in many glycoproteins as well as the carbohydrate moieties of glycolipids.  The cell surface form functions as a recognition molecule during a variety of cell to cell and cell to matrix interactions, as those occurring during development and egg fertilization, by binding to specific oligosaccharide ligands on opposing cells or in the extracellular matrix.
+__TOC__
+</StructureSection>
+[[Category: Glumoff, T]]
+[[Category: Harrus, D]]
 [[Category: Kellokumpu, S]]
-[[Category: Harrus, D]]
+[[Category: 4-galactosyltransferase i]]
-[[Category: Glumoff, T]]
+[[Category: Apo]]
+[[Category: B4galt1]]
+[[Category: Beta-1]]
+[[Category: Galactosyltransferase]]
+[[Category: Galt1]]
+[[Category: Glycosyltransferase]]
+[[Category: Monomer]]
+[[Category: Monomeric]]
+[[Category: N-linked glycosylation]]
+[[Category: Open conformation]]
+[[Category: Transferase]]