6dd3: Difference between revisions

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'''Unreleased structure'''


The entry 6dd3 is ON HOLD  until Paper Publication
==Crystal structure of the double mutant (D52N/D407A) of NT5C2-537X in the active state==
 
<StructureSection load='6dd3' size='340' side='right'caption='[[6dd3]], [[Resolution|resolution]] 1.98&Aring;' scene=''>
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.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6dd3]] is a 1 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=6DD3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DD3 FirstGlance]. <br>
Description: Crystal structure of the double mutant (D52N/D407A) of NT5C2-537X in the active state
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.98&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
[[Category: Carpenter, Z]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6dd3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dd3 OCA], [https://pdbe.org/6dd3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6dd3 RCSB], [https://www.ebi.ac.uk/pdbsum/6dd3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6dd3 ProSAT]</span></td></tr>
[[Category: Forouhar, F]]
</table>
[[Category: Lew, S]]
== Disease ==
[[Category: Tong, L]]
[https://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>
[[Category: Kirschner-Schwabe, R]]
== Function ==
[[Category: Ferrando, A.A]]
[https://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.
[[Category: Sanchez-Martin, M]]
== References ==
[[Category: Tzoneva, G]]
<references/>
[[Category: Dieck, C.L]]
__TOC__
[[Category: Ambesi-Impiombato, A]]
</StructureSection>
[[Category: Seetharaman, J]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Ambesi-Impiombato A]]
[[Category: Carpenter Z]]
[[Category: Dieck CL]]
[[Category: Ferrando AA]]
[[Category: Forouhar F]]
[[Category: Kirschner-Schwabe R]]
[[Category: Lew S]]
[[Category: Sanchez-Martin M]]
[[Category: Seetharaman J]]
[[Category: Tong L]]
[[Category: Tzoneva G]]

Latest revision as of 14:33, 13 March 2024

Crystal structure of the double mutant (D52N/D407A) of NT5C2-537X in the active state

6dd3, resolution 1.98Å

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