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5t3d

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m (Protected "5t3d" [edit=sysop:move=sysop])
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'''Unreleased structure'''
 
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The entry 5t3d is ON HOLD
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==Crystal structure of holo-EntF a nonribosomal peptide synthetase in the thioester-forming conformation==
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<StructureSection load='5t3d' size='340' side='right' caption='[[5t3d]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
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Authors: Miller, B.R., Drake, E.J., Sundlov, J.A., Gulick, A.M.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5t3d]] is a 1 chain structure. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=4zxj 4zxj]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5T3D OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5T3D FirstGlance]. <br>
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Description: Crystal structure of holo-EntF a nonribosomal peptide synthetase in the thioester-forming conformation
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=75C:5-({[(2R,3S)-3-AMINO-4-HYDROXY-2-{[2-({N-[(2R)-2-HYDROXY-3,3-DIMETHYL-4-(PHOSPHONOOXY)BUTANOYL]-BETA-ALANYL}AMINO)ETHYL]SULFANYL}BUTYL]SULFONYL}AMINO)-5-DEOXYADENOSINE'>75C</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5t3d FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5t3d OCA], [http://pdbe.org/5t3d PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5t3d RCSB], [http://www.ebi.ac.uk/pdbsum/5t3d PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5t3d ProSAT]</span></td></tr>
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[[Category: Drake, E.J]]
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</table>
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[[Category: Sundlov, J.A]]
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== Function ==
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[[Category: Gulick, A.M]]
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[[http://www.uniprot.org/uniprot/ENTF_ECOLI ENTF_ECOLI]] Activates the carboxylate group of L-serine via ATP-dependent PPi exchange reactions to the aminoacyladenylate, preparing that molecule for the final stages of enterobactin synthesis. Holo-EntF acts as the catalyst for the formation of the three amide and three ester bonds present in the cyclic (2,3-dihydroxybenzoyl)serine trimer enterobactin, using seryladenylate and acyl-holo-EntB (acylated with 2,3-dihydroxybenzoate by EntE).
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[[Category: Miller, B.R]]
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__TOC__
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</StructureSection>
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[[Category: Drake, E J]]
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[[Category: Gulick, A M]]
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[[Category: Miller, B R]]
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[[Category: Sundlov, J A]]
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[[Category: Adenylation]]
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[[Category: Biosynthetic protein]]
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[[Category: Condensation]]
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[[Category: Nonribosomal peptide synthetase]]
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[[Category: Nrp]]
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[[Category: Pcp]]
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[[Category: Phosphopantetheine]]
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[[Category: Thioesterase]]

Revision as of 13:32, 21 September 2016

Crystal structure of holo-EntF a nonribosomal peptide synthetase in the thioester-forming conformation

5t3d, resolution 2.80Å

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