2byl: Difference between revisions

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<StructureSection load='2byl' size='340' side='right'caption='[[2byl]], [[Resolution|resolution]] 2.15&Aring;' scene=''>
<StructureSection load='2byl' size='340' side='right'caption='[[2byl]], [[Resolution|resolution]] 2.15&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2byl]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2BYL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2BYL FirstGlance]. <br>
<table><tr><td colspan='2'>[[2byl]] is a 3 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=2BYL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2BYL FirstGlance]. <br>
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PLP:PYRIDOXAL-5-PHOSPHATE'>PLP</scene></td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.15&#8491;</td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1gbn|1gbn]], [[1oat|1oat]], [[2byj|2byj]], [[2can|2can]], [[2oat|2oat]]</div></td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PLP:PYRIDOXAL-5-PHOSPHATE'>PLP</scene></td></tr>
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Ornithine_aminotransferase Ornithine aminotransferase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.6.1.13 2.6.1.13] </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=2byl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2byl OCA], [https://pdbe.org/2byl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2byl RCSB], [https://www.ebi.ac.uk/pdbsum/2byl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2byl 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=2byl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2byl OCA], [https://pdbe.org/2byl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2byl RCSB], [https://www.ebi.ac.uk/pdbsum/2byl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2byl ProSAT]</span></td></tr>
</table>
</table>
== Disease ==
== Disease ==
[[https://www.uniprot.org/uniprot/OAT_HUMAN OAT_HUMAN]] Defects in OAT are the cause of hyperornithinemia with gyrate atrophy of choroid and retina (HOGA) [MIM:[https://omim.org/entry/258870 258870]]. HOGA is a slowly progressive blinding autosomal recessive disorder.<ref>PMID:3375240</ref> <ref>PMID:2793865</ref> <ref>PMID:1612597</ref> <ref>PMID:1737786</ref> <ref>PMID:7887415</ref> <ref>PMID:7668253</ref>
[https://www.uniprot.org/uniprot/OAT_HUMAN OAT_HUMAN] Defects in OAT are the cause of hyperornithinemia with gyrate atrophy of choroid and retina (HOGA) [MIM:[https://omim.org/entry/258870 258870]. HOGA is a slowly progressive blinding autosomal recessive disorder.<ref>PMID:3375240</ref> <ref>PMID:2793865</ref> <ref>PMID:1612597</ref> <ref>PMID:1737786</ref> <ref>PMID:7887415</ref> <ref>PMID:7668253</ref>  
== Function ==
[https://www.uniprot.org/uniprot/OAT_HUMAN OAT_HUMAN]
== 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: Human]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Large Structures]]
[[Category: Ornithine aminotransferase]]
[[Category: Hewlins MJE]]
[[Category: Hewlins, M J.E]]
[[Category: John RA]]
[[Category: John, R A]]
[[Category: Markova M]]
[[Category: Markova, M]]
[[Category: Peneff C]]
[[Category: Peneff, C]]
[[Category: Schirmer T]]
[[Category: Schirmer, T]]
[[Category: Disease mutation]]
[[Category: Mitochondrion]]
[[Category: Polymorphism]]
[[Category: Pyridoxal phosphate]]
[[Category: Transferase]]
[[Category: Transit peptide plp-dependent enzyme]]

Latest revision as of 13:58, 13 December 2023

Structure of ornithine aminotransferase triple mutant Y85I Y55A G320F

2byl, resolution 2.15Å

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