6ee4: Difference between revisions

New page: '''Unreleased structure''' The entry 6ee4 is ON HOLD Authors: Drinkwater, N., McGowan, S. Description: X-ray crystal structure of Pf-M1 in complex with inhibitor (6m) and catalytic zin...
 
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'''Unreleased structure'''


The entry 6ee4 is ON HOLD
==X-ray crystal structure of Pf-M1 in complex with inhibitor (6m) and catalytic zinc ion==
<StructureSection load='6ee4' size='340' side='right'caption='[[6ee4]], [[Resolution|resolution]] 1.58&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6ee4]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Plasmodium_falciparum_FcB1/Columbia Plasmodium falciparum FcB1/Columbia]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6EE4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6EE4 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.58&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=J4S:(2R)-2-[(cyclopropylacetyl)amino]-N-hydroxy-2-(3,4,5-trifluoro[1,1-biphenyl]-4-yl)acetamide'>J4S</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></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=6ee4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ee4 OCA], [https://pdbe.org/6ee4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6ee4 RCSB], [https://www.ebi.ac.uk/pdbsum/6ee4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6ee4 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/AMP1_PLAFQ AMP1_PLAFQ] Displays aminopeptidase activity with a broad substrate specificity. Preferentially hydrolyzes L-Lys-AMC but also shows strong activity against L-Ala-AMC, L-Arg-AMC and L-Leu-AMC.<ref>PMID:12166515</ref> <ref>PMID:19196988</ref>


Authors: Drinkwater, N., McGowan, S.
==See Also==
 
*[[Aminopeptidase 3D structures|Aminopeptidase 3D structures]]
Description: X-ray crystal structure of Pf-M1 in complex with inhibitor (6m) and catalytic zinc ion
== References ==
[[Category: Unreleased Structures]]
<references/>
[[Category: Drinkwater, N]]
__TOC__
[[Category: Mcgowan, S]]
</StructureSection>
[[Category: Large Structures]]
[[Category: Plasmodium falciparum FcB1/Columbia]]
[[Category: Drinkwater N]]
[[Category: McGowan S]]

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