8xv5
From Proteopedia
(Difference between revisions)
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8xv5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xv5 OCA], [https://pdbe.org/8xv5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xv5 RCSB], [https://www.ebi.ac.uk/pdbsum/8xv5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xv5 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=8xv5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xv5 OCA], [https://pdbe.org/8xv5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xv5 RCSB], [https://www.ebi.ac.uk/pdbsum/8xv5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xv5 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| - | == Disease == | ||
| - | [https://www.uniprot.org/uniprot/S19A3_HUMAN S19A3_HUMAN] Thiamine-responsive encephalopathy;Infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome;Biotin-thiamine-responsive basal ganglia disease. The disease is caused by variants affecting the gene represented in this entry. | ||
| - | == Function == | ||
| - | [https://www.uniprot.org/uniprot/S19A3_HUMAN S19A3_HUMAN] Mediates high affinity thiamine uptake, probably via a proton anti-port mechanism (PubMed:11731220, PubMed:33008889, PubMed:35512554, PubMed:35724964). Has no folate transport activity (PubMed:11731220). Mediates H(+)-dependent pyridoxine transport (PubMed:33008889, PubMed:35512554, PubMed:35724964, PubMed:36456177).<ref>PMID:11731220</ref> <ref>PMID:33008889</ref> <ref>PMID:35512554</ref> <ref>PMID:35724964</ref> <ref>PMID:36456177</ref> [https://www.uniprot.org/uniprot/C562_ECOLX C562_ECOLX] Electron-transport protein of unknown function. | ||
| - | == References == | ||
| - | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
Current revision
Pyridoxamine-bound human SLC19A3
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