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6de3

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'''Unreleased structure'''
 
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The entry 6de3 is ON HOLD until Paper Publication
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==Crystal structure of the double mutant (R39Q/D52N) of the full-length NT5C2 in the active state==
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<StructureSection load='6de3' size='340' side='right' caption='[[6de3]], [[Resolution|resolution]] 3.06&Aring;' scene=''>
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Authors: Forouhar, F., Dieck, C.L., Tzoneva, G., Carpenter, Z., Ambesi-Impiombato, A., Sanchez-Martin, M., Kirschner-Schwabe, R., Lew, S., Seetharaman, J., Ferrando, A.A., Tong, L.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6de3]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DE3 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6DE3 FirstGlance]. <br>
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Description: Crystal structure of the double mutant (R39Q/D52N) of the full-length NT5C2 in the active state
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ATP:ADENOSINE-5-TRIPHOSPHATE'>ATP</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/5'-nucleotidase 5'-nucleotidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.3.5 3.1.3.5] </span></td></tr>
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<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=6de3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6de3 OCA], [http://pdbe.org/6de3 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6de3 RCSB], [http://www.ebi.ac.uk/pdbsum/6de3 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6de3 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/5NTC_HUMAN 5NTC_HUMAN]] Autosomal recessive spastic paraplegia type 45. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:24482476</ref>
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== Function ==
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[[http://www.uniprot.org/uniprot/5NTC_HUMAN 5NTC_HUMAN]] May have a critical role in the maintenance of a constant composition of intracellular purine/pyrimidine nucleotides in cooperation with other nucleotidases. Preferentially hydrolyzes inosine 5'-monophosphate (IMP) and other purine nucleotides.
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: 5'-nucleotidase]]
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[[Category: Ambesi-Impiombato, A]]
[[Category: Carpenter, Z]]
[[Category: Carpenter, Z]]
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[[Category: Dieck, C L]]
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[[Category: Ferrando, A A]]
[[Category: Forouhar, F]]
[[Category: Forouhar, F]]
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[[Category: Kirschner-Schwabe, R]]
[[Category: Lew, S]]
[[Category: Lew, S]]
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[[Category: Sanchez-Martin, M]]
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[[Category: Seetharaman, J]]
[[Category: Tong, L]]
[[Category: Tong, L]]
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[[Category: Kirschner-Schwabe, R]]
 
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[[Category: Ferrando, A.A]]
 
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[[Category: Sanchez-Martin, M]]
 
[[Category: Tzoneva, G]]
[[Category: Tzoneva, G]]
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[[Category: Dieck, C.L]]
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[[Category: Hydrolase]]
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[[Category: Ambesi-Impiombato, A]]
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[[Category: Seetharaman, J]]
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Revision as of 07:16, 4 July 2018

Crystal structure of the double mutant (R39Q/D52N) of the full-length NT5C2 in the active state

6de3, resolution 3.06Å

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