2f5i: Difference between revisions
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<StructureSection load='2f5i' size='340' side='right'caption='[[2f5i]], [[Resolution|resolution]] 2.30Å' scene=''> | <StructureSection load='2f5i' size='340' side='right'caption='[[2f5i]], [[Resolution|resolution]] 2.30Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2f5i]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2f5i]] 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=2F5I OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2F5I FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.3Å</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=2f5i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2f5i OCA], [https://pdbe.org/2f5i PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2f5i RCSB], [https://www.ebi.ac.uk/pdbsum/2f5i PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2f5i ProSAT]</span></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=2f5i FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2f5i OCA], [https://pdbe.org/2f5i PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2f5i RCSB], [https://www.ebi.ac.uk/pdbsum/2f5i PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2f5i ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/SAT1_HUMAN SAT1_HUMAN] Defects in SAT1 may be a cause of keratosis follicularis spinulosa decalvans X-linked (KFSDX) [MIM:[https://omim.org/entry/308800 308800]. A rare disorder affecting the skin and the eye. Affected men show thickening of the skin of the neck, ears, and extremities, especially the palms and soles, loss of eyebrows, eyelashes and beard, thickening of the eyelids with blepharitis and ectropion, and corneal degeneration.<ref>PMID:9341865</ref> <ref>PMID:12215835</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/SAT1_HUMAN SAT1_HUMAN] Enzyme which catalyzes the acetylation of polyamines. Substrate specificity: norspermidine = spermidine >> spermine > N(1)-acetylspermine > putrescine. This highly regulated enzyme allows a fine attenuation of the intracellular concentration of polyamines. Also involved in the regulation of polyamine transport out of cells. Acts on 1,3-diaminopropane, 1,5-diaminopentane, putrescine, spermidine (forming N(1)- and N(8)-acetylspermidine), spermine, N(1)-acetylspermidine and N(8)-acetylspermidine. | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Vonrhein | [[Category: Vonrhein C]] | ||
[[Category: Wang | [[Category: Wang DC]] | ||
[[Category: Zhu | [[Category: Zhu DY]] | ||
[[Category: Zhu | [[Category: Zhu YQ]] | ||