6y0o
From Proteopedia
(Difference between revisions)
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==isopenicillin N synthase in complex with ACV and Fe under anaerobic environment using FT-SSX methods== | ==isopenicillin N synthase in complex with ACV and Fe under anaerobic environment using FT-SSX methods== | ||
- | <StructureSection load='6y0o' size='340' side='right'caption='[[6y0o]]' scene=''> | + | <StructureSection load='6y0o' size='340' side='right'caption='[[6y0o]], [[Resolution|resolution]] 2.20Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Y0O OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6Y0O FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6y0o]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Aspergillus_nidulans Aspergillus nidulans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6Y0O OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6Y0O FirstGlance]. <br> |
- | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6y0o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6y0o OCA], [http://pdbe.org/6y0o PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6y0o RCSB], [http://www.ebi.ac.uk/pdbsum/6y0o PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6y0o ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACV:L-D-(A-AMINOADIPOYL)-L-CYSTEINYL-D-VALINE'>ACV</scene>, <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> |
+ | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1bk0|1bk0]], [[1blz|1blz]]</td></tr> | ||
+ | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">ipnA (ips) ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=227321 Aspergillus nidulans])</td></tr> | ||
+ | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Isopenicillin-N_synthase Isopenicillin-N synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.21.3.1 1.21.3.1] </span></td></tr> | ||
+ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6y0o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6y0o OCA], [http://pdbe.org/6y0o PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6y0o RCSB], [http://www.ebi.ac.uk/pdbsum/6y0o PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6y0o ProSAT]</span></td></tr> | ||
</table> | </table> | ||
+ | == Function == | ||
+ | [[http://www.uniprot.org/uniprot/IPNS_EMENI IPNS_EMENI]] Removes, in the presence of oxygen, 4 hydrogen atoms from delta-L-(alpha-aminoadipyl)-L-cysteinyl-D-valine (ACV) to form the azetidinone and thiazolidine rings of isopenicillin. | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | Cryogenic X-ray diffraction is a powerful tool for crystallographic studies on enzymes including oxygenases and oxidases. Amongst the benefits that cryo-conditions (usually employing a nitro-gen cryo-stream at 100 K) enable, is data collection of di-oxy-gen-sensitive samples. Although not strictly anaerobic, at low temperatures the vitreous ice conditions severely restrict O2 diffusion into and/or through the protein crystal. Cryo-conditions limit chemical reactivity, including reactions that require significant conformational changes. By contrast, data collection at room temperature imposes fewer restrictions on diffusion and reactivity; room-temperature serial methods are thus becoming common at synchrotrons and XFELs. However, maintaining an anaerobic environment for di-oxy-gen-dependent enzymes has not been explored for serial room-temperature data collection at synchrotron light sources. This work describes a methodology that employs an adaptation of the 'sheet-on-sheet' sample mount, which is suitable for the low-dose room-temperature data collection of anaerobic samples at synchrotron light sources. The method is characterized by easy sample preparation in an anaerobic glovebox, gentle handling of crystals, low sample consumption and preservation of a localized anaerobic environment over the timescale of the experiment (<5 min). The utility of the method is highlighted by studies with three X-ray-radiation-sensitive Fe(II)-containing model enzymes: the 2-oxoglutarate-dependent l-arginine hy-droxy-lase VioC and the DNA repair enzyme AlkB, as well as the oxidase isopenicillin N synthase (IPNS), which is involved in the biosynthesis of all penicillin and cephalosporin antibiotics. | ||
+ | |||
+ | Anaerobic fixed-target serial crystallography.,Rabe P, Beale JH, Butryn A, Aller P, Dirr A, Lang PA, Axford DN, Carr SB, Leissing TM, McDonough MA, Davy B, Ebrahim A, Orlans J, Storm SLS, Orville AM, Schofield CJ, Owen RL IUCrJ. 2020 Aug 21;7(Pt 5):901-912. doi: 10.1107/S2052252520010374. eCollection, 2020 Sep 1. PMID:32939282<ref>PMID:32939282</ref> | ||
+ | |||
+ | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
+ | </div> | ||
+ | <div class="pdbe-citations 6y0o" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
+ | [[Category: Aspergillus nidulans]] | ||
+ | [[Category: Isopenicillin-N synthase]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Aller P]] | + | [[Category: Aller, P]] |
- | [[Category: Axford D]] | + | [[Category: Axford, D]] |
- | [[Category: Beale | + | [[Category: Beale, J H]] |
- | [[Category: Butryn A]] | + | [[Category: Butryn, A]] |
- | [[Category: Dirr | + | [[Category: Dirr, A S]] |
- | [[Category: Kamps | + | [[Category: Kamps, J J.A G]] |
- | [[Category: Lang | + | [[Category: Lang, P A]] |
- | [[Category: Leissing | + | [[Category: Leissing, T M]] |
- | [[Category: McDonough | + | [[Category: McDonough, M A]] |
- | [[Category: Orville | + | [[Category: Orville, A M]] |
- | [[Category: Owen R]] | + | [[Category: Owen, R]] |
- | [[Category: Rabe P]] | + | [[Category: Rabe, P]] |
- | [[Category: Schofield | + | [[Category: Schofield, C J]] |
+ | [[Category: Iron dependent oxygenase]] | ||
+ | [[Category: Isopenicillin n]] | ||
+ | [[Category: Oxidoreductase]] | ||
+ | [[Category: Penicillin biosynthesis]] |
Revision as of 07:46, 30 September 2020
isopenicillin N synthase in complex with ACV and Fe under anaerobic environment using FT-SSX methods
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Categories: Aspergillus nidulans | Isopenicillin-N synthase | Large Structures | Aller, P | Axford, D | Beale, J H | Butryn, A | Dirr, A S | Kamps, J J.A G | Lang, P A | Leissing, T M | McDonough, M A | Orville, A M | Owen, R | Rabe, P | Schofield, C J | Iron dependent oxygenase | Isopenicillin n | Oxidoreductase | Penicillin biosynthesis