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5o1n
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human aminoadipate semialdehyde synthase, saccharopine dehydrogenase domain with N-[(2S)-2-Pyrrolidinylmethyl]-trifluoromethanesulfonamide bound== | |
| - | + | <StructureSection load='5o1n' size='340' side='right' caption='[[5o1n]], [[Resolution|resolution]] 2.28Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[5o1n]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5O1N OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5O1N FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=9H8:1,1,1-tris(fluoranyl)-~{N}-[[(2~{S})-pyrrolidin-2-yl]methyl]methanesulfonamide'>9H8</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene></td></tr> | |
| - | [[ | + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">AASS ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> |
| - | [[ | + | <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=5o1n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5o1n OCA], [http://pdbe.org/5o1n PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5o1n RCSB], [http://www.ebi.ac.uk/pdbsum/5o1n PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5o1n ProSAT]</span></td></tr> |
| - | [[ | + | </table> |
| - | [[ | + | == Disease == |
| - | [[ | + | [[http://www.uniprot.org/uniprot/AASS_HUMAN AASS_HUMAN]] Hyperlysinemia;Saccharopinuria. The disease is caused by mutations affecting the gene represented in this entry. The protein represented in this entry is involved in disease pathogenesis. A selective decrease in mitochondrial NADP(H) levels due to NADK2 mutations causes a deficiency of NADPH-dependent mitochondrial enzymes, such as DECR1 and AASS.<ref>PMID:24847004</ref> |
| - | [[ | + | == Function == |
| - | [[ | + | [[http://www.uniprot.org/uniprot/AASS_HUMAN AASS_HUMAN]] Bifunctional enzyme that catalyzes the first two steps in lysine degradation. The N-terminal and the C-terminal contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively. |
| - | [[ | + | == References == |
| - | [[Category: | + | <references/> |
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Human]] | ||
[[Category: Arrowsmith, C]] | [[Category: Arrowsmith, C]] | ||
| - | [[Category: Talon, R]] | ||
[[Category: Arruda, P]] | [[Category: Arruda, P]] | ||
| - | [[Category: | + | [[Category: Bountra, C]] |
| + | [[Category: Brennan, P]] | ||
| + | [[Category: Burgess-Brown, N]] | ||
| + | [[Category: Collins, P]] | ||
| + | [[Category: Delft, F von]] | ||
[[Category: Edwards, A]] | [[Category: Edwards, A]] | ||
| - | [[Category: | + | [[Category: Goubin, S]] |
| + | [[Category: Kopec, J]] | ||
[[Category: Krojer, T]] | [[Category: Krojer, T]] | ||
| - | [[Category: | + | [[Category: McLaughlin, M]] |
| + | [[Category: Pena, I A]] | ||
[[Category: Rembeza, E]] | [[Category: Rembeza, E]] | ||
[[Category: Sethi, R]] | [[Category: Sethi, R]] | ||
| - | [[Category: | + | [[Category: Strain-Damerell, C]] |
| + | [[Category: Talon, R]] | ||
| + | [[Category: Velupillai, S]] | ||
| + | [[Category: Yue, W W]] | ||
| + | [[Category: Human aminoadipate semialdehyde synthase]] | ||
| + | [[Category: Oxidoreductase]] | ||
Revision as of 11:47, 16 November 2017
Crystal structure of human aminoadipate semialdehyde synthase, saccharopine dehydrogenase domain with N-[(2S)-2-Pyrrolidinylmethyl]-trifluoromethanesulfonamide bound
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Categories: Human | Arrowsmith, C | Arruda, P | Bountra, C | Brennan, P | Burgess-Brown, N | Collins, P | Delft, F von | Edwards, A | Goubin, S | Kopec, J | Krojer, T | McLaughlin, M | Pena, I A | Rembeza, E | Sethi, R | Strain-Damerell, C | Talon, R | Velupillai, S | Yue, W W | Human aminoadipate semialdehyde synthase | Oxidoreductase
