4h1s: Difference between revisions

<table><tr><td colspan='2'>[[4h1s]] is a 2 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=4H1S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4H1S FirstGlance]. <br>

</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=4h1s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4h1s OCA], [https://pdbe.org/4h1s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4h1s RCSB], [https://www.ebi.ac.uk/pdbsum/4h1s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4h1s ProSAT]</span></td></tr>

[https://www.uniprot.org/uniprot/5NTD_HUMAN 5NTD_HUMAN] Hereditary arterial and articular multiple calcification syndrome. The disease is caused by mutations affecting the gene represented in this entry.

[https://www.uniprot.org/uniprot/5NTD_HUMAN 5NTD_HUMAN] Hydrolyzes extracellular nucleotides into membrane permeable nucleosides. Exhibits AMP-, NAD-, and NMN-nucleosidase activities.<ref>PMID:21933152</ref>  

[[Category: Heuts DP]]

[[Category: Levy CW]]

[[Category: Olkhov RV]]

[[Category: Scrutton NS]]

[[Category: Shaw AM]]

[[Category: Weissenborn MJ]]