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6p2v
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 6p2v is ON HOLD Authors: Andorfer, M.C., Sukumar, N., Lewis, J.C. Description: RebH Variant 10S, Tryptamine 5-halogenase [[Category: Unreleased Str...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==RebH Variant 10S, Tryptamine 5-halogenase== | |
| - | + | <StructureSection load='6p2v' size='340' side='right'caption='[[6p2v]], [[Resolution|resolution]] 2.55Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6p2v]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Lentzea_aerocolonigenes Lentzea aerocolonigenes]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6P2V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6P2V 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]] 2.553Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene></td></tr> |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6p2v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6p2v OCA], [https://pdbe.org/6p2v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6p2v RCSB], [https://www.ebi.ac.uk/pdbsum/6p2v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6p2v ProSAT]</span></td></tr> |
| - | [[Category: Lewis | + | </table> |
| - | [[Category: | + | == Function == |
| + | [https://www.uniprot.org/uniprot/REBH_LENAE REBH_LENAE] Involved in the biosynthesis of the indolocarbazole antitumor agent rebeccamycin. Catalyzes the chlorination of tryptophan (Trp) at C7 position to yield 7-chlorotryptophan. The reaction between FADH2, Cl-, and O2 generates the powerful oxidant HOCl, which is presumed to carry out the chlorination reaction. The reaction of HOCl with the active site Lys-79 generates a lysine chloramine, which plays a key role in directing regiospecific chlorination of substrate in this important class of biosynthetic enzymes. It is also able to use bromide ions to generate monobrominated Trp.<ref>PMID:11983340</ref> <ref>PMID:15743914</ref> <ref>PMID:17260957</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Lentzea aerocolonigenes]] | ||
| + | [[Category: Andorfer MC]] | ||
| + | [[Category: Lewis JC]] | ||
| + | [[Category: Sukumar N]] | ||
Current revision
RebH Variant 10S, Tryptamine 5-halogenase
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