1nf5: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px<br /><applet load="1nf5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1nf5, resolution 2.00Å" /> '''Crystal Structure of...
 
OCA (talk | contribs)
No edit summary
 
(30 intermediate revisions by the same user not shown)
Line 1: Line 1:
[[Image:1nf5.gif|left|200px]]<br /><applet load="1nf5" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1nf5, resolution 2.00&Aring;" />
'''Crystal Structure of Lactose Synthase, Complex with Glucose'''<br />


==Overview==
==Crystal Structure of Lactose Synthase, Complex with Glucose==
The lactose synthase (LS) enzyme is a 1:1 complex of a catalytic, component, beta1,4-galactosyltransferse (beta4Gal-T1) and a regulatory, component, alpha-lactalbumin (LA), a mammary gland-specific protein. LA, promotes the binding of glucose (Glc) to beta4Gal-T1, thereby altering its, sugar acceptor specificity from N-acetylglucosamine (GlcNAc) to glucose, which enables LS to synthesize lactose, the major carbohydrate component, of milk. The crystal structures of LS bound with various substrates were, solved at 2 A resolution. These structures reveal that upon substrate, binding to beta4Gal-T1, a large conformational change occurs in the region, comprising residues 345 to 365. This repositions His347 in such a way that, it can participate in the coordination of a metal ion, and creates a sugar, and LA-binding site. At the sugar-acceptor binding site, a hydrophobic, N-acetyl group-binding pocket is found, formed by residues Arg359, Phe360, and Ile363. In the Glc-bound structure, this hydrophobic pocket is absent., For the binding of Glc to LS, a reorientation of the Arg359 side-chain, occurs, which blocks the hydrophobic pocket and maximizes the interactions, with the Glc molecule. Thus, the role of LA is to hold Glc by hydrogen, bonding with the O-1 hydroxyl group in the acceptor-binding site on, beta4Gal-T1, while the N-acetyl group-binding pocket in beta4Gal-T1, adjusts to maximize the interactions with the Glc molecule. This study, provides details of a structural basis for the partially ordered kinetic, mechanism proposed for lactose synthase.
<StructureSection load='1nf5' size='340' side='right'caption='[[1nf5]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1nf5]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=1j8w 1j8w]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NF5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1NF5 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&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BGC:BETA-D-GLUCOSE'>BGC</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=PG4:TETRAETHYLENE+GLYCOL'>PG4</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=1nf5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1nf5 OCA], [https://pdbe.org/1nf5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1nf5 RCSB], [https://www.ebi.ac.uk/pdbsum/1nf5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1nf5 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/LALBA_MOUSE LALBA_MOUSE] Regulatory subunit of lactose synthase, changes the substrate specificity of galactosyltransferase in the mammary gland making glucose a good acceptor substrate for this enzyme. This enables LS to synthesize lactose, the major carbohydrate component of milk. In other tissues, galactosyltransferase transfers galactose onto the N-acetylglucosamine of the oligosaccharide chains in glycoproteins.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/nf/1nf5_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1nf5 ConSurf].
<div style="clear:both"></div>


==About this Structure==
==See Also==
1NF5 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [http://en.wikipedia.org/wiki/Mus_musculus Mus musculus] with GLC, CA, PG4 and EDO as [http://en.wikipedia.org/wiki/ligands ligands]. This structure superseeds the now removed PDB entry 1J8W. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1NF5 OCA].
*[[Alpha-lactalbumin 3D structures|Alpha-lactalbumin 3D structures]]
 
*[[Glycosyltransferase 3D structures|Glycosyltransferase 3D structures]]
==Reference==
__TOC__
Crystal structure of lactose synthase reveals a large conformational change in its catalytic component, the beta1,4-galactosyltransferase-I., Ramakrishnan B, Qasba PK, J Mol Biol. 2001 Jun 29;310(1):205-18. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11419947 11419947]
</StructureSection>
[[Category: Bos taurus]]
[[Category: Bos taurus]]
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Protein complex]]
[[Category: Qasba PK]]
[[Category: Qasba, P.K.]]
[[Category: Ramakrishnan B]]
[[Category: Ramakrishnan, B.]]
[[Category: CA]]
[[Category: EDO]]
[[Category: GLC]]
[[Category: PG4]]
[[Category: conformational change]]
[[Category: glucose binding]]
[[Category: lactose synhtase]]
[[Category: transferase modulator]]
 
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 22:12:31 2007''

Latest revision as of 08:49, 10 April 2024

Crystal Structure of Lactose Synthase, Complex with Glucose

1nf5, resolution 2.00Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA