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1.
J Biol Inorg Chem ; 27(6): 541-551, 2022 09.
Article in English | MEDLINE | ID: mdl-35513576

ABSTRACT

Pseudomonas aeruginosa is an increasingly antibiotic-resistant pathogen that causes severe lung infections, burn wound infections, and diabetic foot infections. P. aeruginosa produces the siderophore pyochelin through the use of a non-ribosomal peptide synthetase (NRPS) biosynthetic pathway. Targeting members of siderophore NRPS proteins is one avenue currently under investigation for the development of new antibiotics against antibiotic-resistant organisms. Here, the crystal structure of the pyochelin adenylation domain PchD is reported. The structure was solved to 2.11 Å when co-crystallized with the adenylation inhibitor 5'-O-(N-salicylsulfamoyl)adenosine (salicyl-AMS) and to 1.69 Å with a modified version of salicyl-AMS designed to target an active site cysteine (4-cyano-salicyl-AMS). In the structures, PchD adopts the adenylation conformation, similar to that reported for AB3403 from Acinetobacter baumannii.


Subject(s)
Pseudomonas aeruginosa , Siderophores , Anti-Bacterial Agents/metabolism , Anti-Bacterial Agents/pharmacology , Phenols , Pseudomonas aeruginosa/metabolism , Salicylates/metabolism , Siderophores/chemistry , Thiazoles
2.
Biochemistry ; 59(21): 2022-2031, 2020 06 02.
Article in English | MEDLINE | ID: mdl-32368901

ABSTRACT

Cysteine dioxygenase (CDO) structurally resembles cupin enzymes that use a 3-His/1-Glu coordination scheme. However, the glutamate ligand is substituted with a cysteine (Cys93) residue, which forms a thioether bond with tyrosine (Tyr157) under physiological conditions. The reversion variant, C93E CDO, was generated in order to reestablish the more common 3-His/1-Glu metal ligands of the cupin superfamily. This variant provides a framework for testing the structural and functional significance of Cys93 and the cross-link in CDO. Although dioxygen consumption was observed with C93E CDO, it was not coupled with l-cysteine oxidation. Substrate analogues (d-cysteine, cysteamine, and 3-mercaptopropionate) were not viable substrates for the C93E CDO variant, although they showed variable coordinations to the iron center. The structures of C93E and cross-linked and non-cross-linked wild-type CDO were solved by X-ray crystallography to 1.91, 2.49, and 2.30 Å, respectively. The C93E CDO variant had similar overall structural properties compared to cross-linked CDO; however, the iron was coordinated by a 3-His/1-Glu geometry, leaving only two coordination sites available for dioxygen and bidentate l-cysteine binding. The hydroxyl group of Tyr157 shifted in both non-cross-linked and C93E CDO, and this displacement prevented the residue from participating in substrate stabilization. Based on these results, the divergence of the metal center of cysteine dioxygenase from the 3-His/1-Glu geometry seen with many cupin enzymes was essential for effective substrate binding. The substitution of Glu with Cys in CDO allows for a third coordination site on the iron for bidentate cysteine and monodentate oxygen binding.


Subject(s)
Cysteine Dioxygenase/metabolism , Cysteine/metabolism , Ferric Compounds/metabolism , Histidine/metabolism , Oxygen/metabolism , Crystallography, X-Ray , Cysteine/chemistry , Cysteine Dioxygenase/chemistry , Ferric Compounds/chemistry , Histidine/chemistry , Models, Molecular , Molecular Conformation , Oxidation-Reduction , Oxygen/chemistry
3.
Educ Prim Care ; 31(4): 210-217, 2020 07.
Article in English | MEDLINE | ID: mdl-32151231

ABSTRACT

BACKGROUND: Undergraduate (UG) General Practice (GP) tutors have been identified in the literature and in key UK workforce planning documents as one of the main influences on medical students' decisions about pursuing a career in GP. AIM: To explore the attitudes and educational approaches of UG GP tutors in promoting GP as a career. DESIGN AND SETTING: A pragmatic constructivist qualitative study, interviewing 8 UG GP tutors supervising undergraduate final year medical students on placement. METHOD: Interviews were transcribed, coded and grouped into themes using NVIVO11. Analysis was descriptive and interpretive using principles of thematic analysis. RESULTS: Tutors saw their role as promoting GP, supporting informed career decisions, correcting misconceptions and giving honest views. They used tutorials, critical reflection, exposure to authentic GP and role-modelling to promote GP, challenge misconceptions, and showcase managing complexities.. DISCUSSION: By guiding students to identify, discuss and reflect on their beliefs and by using clinical encounters and role modelling with further reflection, tutors enabled students to get a true picture of GP to identify if they could handle the challenges and complexities of the job. Kolb's experiential learning cycle could form a framework to guide tutors in clinical settings supporting students making informed career decisions.


Subject(s)
Career Choice , Education, Medical, Undergraduate/methods , General Practitioners/education , Students, Medical , Attitude of Health Personnel , Female , Humans , Male , Problem-Based Learning , Qualitative Research , United Kingdom
4.
Acta Crystallogr F Struct Biol Commun ; 75(Pt 6): 461-469, 2019 Jun 01.
Article in English | MEDLINE | ID: mdl-31204694

ABSTRACT

Human liver pyruvate kinase (hLPYK) converts phosphoenolpyruvate to pyruvate in the final step of glycolysis. hLPYK is allosterically activated by fructose-1,6-bisphosphate (Fru-1,6-BP). The allosteric site, as defined by previous structural studies, is located in domain C between the phosphate-binding loop (residues 444-449) and the allosteric loop (residues 527-533). In this study, the X-ray crystal structures of four hLPYK variants were solved to make structural correlations with existing functional data. The variants are D499N, W527H, Δ529/S531G (called GGG here) and S531E. The results revealed a conformational toggle between the open and closed positions of the allosteric loop. In the absence of Fru-1,6-BP the open position is stabilized, in part, by a cation-π bond between Trp527 and Arg538' (from an adjacent monomer). In the S531E variant glutamate binds in place of the 6'-phosphate of Fru-1,6-BP in the allosteric site, leading to partial allosteric activation. Finally, the structure of the D499N mutant does not provide structural evidence for the previously observed allosteric activation of the D499N variant.


Subject(s)
Cations/chemistry , Fructosediphosphates/metabolism , Liver/enzymology , Mutation , Pyruvate Kinase/chemistry , Pyruvate Kinase/metabolism , Allosteric Site , Binding Sites , Crystallography, X-Ray , Fructosediphosphates/chemistry , Humans , Models, Molecular , Protein Conformation , Protein Subunits , Pyruvate Kinase/genetics
5.
Protein Sci ; 28(1): 123-134, 2019 01.
Article in English | MEDLINE | ID: mdl-30171650

ABSTRACT

The π-helix located at the tetramer interface of two-component FMN-dependent reductases contributes to the structural divergence from canonical FMN-bound reductases within the NADPH:FMN reductase family. The π-helix in the SsuE FMN-dependent reductase of the alkanesulfonate monooxygenase system has been proposed to be generated by the insertion of a Tyr residue in the conserved α4-helix. Variants of Tyr118 were generated, and their X-ray crystal structures determined, to evaluate how these alterations affect the structural integrity of the π-helix. The structure of the Y118A SsuE π-helix was converted to an α-helix, similar to the FMN-bound members of the NADPH:FMN reductase family. Although the π-helix was altered, the FMN binding region remained unchanged. Conversely, deletion of Tyr118 disrupted the secondary structural properties of the π-helix, generating a random coil region in the middle of helix 4. Both the Y118A and Δ118 SsuE SsuE variants crystallize as a dimer. The MsuE FMN reductase involved in the desulfonation of methanesulfonates is structurally similar to SsuE, but the π-helix contains a His insertional residue. Exchanging the π-helix insertional residue of each enzyme did not result in equivalent kinetic properties. Structure-based sequence analysis further demonstrated the presence of a similar Tyr residue in an FMN-bound reductase in the NADPH:FMN reductase family that is not sufficient to generate a π-helix. Results from the structural and functional studies of the FMN-dependent reductases suggest that the insertional residue alone is not solely responsible for generating the π-helix, and additional structural adaptions occur to provide the altered gain of function.


Subject(s)
Bacterial Proteins/chemistry , FMN Reductase/chemistry , Flavin Mononucleotide/chemistry , Mutation, Missense , NADP/chemistry , Protein Multimerization , Pseudomonas aeruginosa/enzymology , Amino Acid Substitution , Bacterial Proteins/genetics , Crystallography, X-Ray , FMN Reductase/genetics , Protein Structure, Secondary , Pseudomonas aeruginosa/genetics
6.
Acta Crystallogr F Struct Biol Commun ; 70(Pt 10): 1328-32, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25286934

ABSTRACT

The Aspergillus fumigatus old yellow enzyme (OYE) EasA reduces chanoclavine-I aldehyde to dihydrochanoclavine aldehyde and works in conjunction with festuclavine synthase at the branchpoint for ergot alkaloid pathways. The crystal structure of the FMN-loaded EasA was determined to 1.8 Šresolution. The active-site amino acids of OYE are conserved, supporting a similar mechanism for reduction of the α/ß-unsaturated aldehyde. The C-terminal tail of one monomer packs into the active site of a monomer in the next asymmetric unit, which is most likely to be a crystallization artifact and not a mechanism of self-regulation.


Subject(s)
Aspergillus fumigatus/enzymology , Ergot Alkaloids/biosynthesis , Fungal Proteins/chemistry , NADPH Dehydrogenase/chemistry , Catalytic Domain , Crystallography, X-Ray , Flavin Mononucleotide/chemistry , Models, Molecular , Protein Structure, Secondary
7.
J Biol Chem ; 286(36): 31789-98, 2011 Sep 09.
Article in English | MEDLINE | ID: mdl-21757711

ABSTRACT

The ornithine hydroxylase from Pseudomonas aeruginosa (PvdA) catalyzes the FAD-dependent hydroxylation of the side chain amine of ornithine, which is subsequently formylated to generate the iron-chelating hydroxamates of the siderophore pyoverdin. PvdA belongs to the class B flavoprotein monooxygenases, which catalyze the oxidation of substrates using NADPH as the electron donor and molecular oxygen. Class B enzymes include the well studied flavin-containing monooxygenases and Baeyer-Villiger monooxygenases. The first two structures of a class B N-hydroxylating monooxygenase were determined with FAD in oxidized (1.9 Å resolution) and reduced (3.03 Å resolution) states. PvdA has the two expected Rossmann-like dinucleotide-binding domains for FAD and NADPH and also a substrate-binding domain, with the active site at the interface between the three domains. The structures have NADP(H) and (hydroxy)ornithine bound in a solvent-exposed active site, providing structural evidence for substrate and co-substrate specificity and the inability of PvdA to bind FAD tightly. Structural and biochemical evidence indicates that NADP(+) remains bound throughout the oxidative half-reaction, which is proposed to shelter the flavin intermediates from solvent and thereby prevent uncoupling of NADPH oxidation from hydroxylated product formation.


Subject(s)
Mixed Function Oxygenases/chemistry , Oxygenases/chemistry , Pseudomonas aeruginosa/enzymology , Catalysis , Catalytic Domain , Crystallography, X-Ray , Flavin-Adenine Dinucleotide , NADP , Ornithine , Oxidation-Reduction , Protein Conformation , Substrate Specificity
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