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1.
J Biomol Struct Dyn ; 35(1): 26-45, 2017 Jan.
Article in English | MEDLINE | ID: mdl-26766582

ABSTRACT

Vascular endothelial growth factor (VEGF) and its co-receptor neuropilin-1 (NRP-1) are important targets of many pro-angiogenic factors. In this study, nine peptides were synthesized and evaluated for their molecular interaction with NRP-1 and compared to our previous peptide ATWLPPR. Docking study showed that the investigated peptides shared the same binding region as shown by tuftsin known to bind selectively to NRP-1. Four pentapeptides (DKPPR, DKPRR, TKPPR and TKPRR) and a hexapeptide CDKPRR demonstrated good inhibitory activity against NRP-1. In contrast, peptides having arginine residue at sites other than the C-terminus exhibited low activity towards NRP-1 and this is confirmed by their inability to displace the VEGF165 binding to NRP-1. Docking study also revealed that replacement of carboxyl to amide group at the C-terminal arginine of the peptide did not affect significantly the binding interaction to NRP-1. However, the molecular affinity study showed that these peptides have marked reduction in the activity against NRP-1. Pentapeptides having C-terminal arginine showed strong interaction and good inhibitory activity with NRP thus may be a good template for anti-angiogenic targeting agent.


Subject(s)
Angiogenesis Inhibitors/chemistry , Antineoplastic Agents/chemistry , Drug Design , Models, Molecular , Neuropilin-1/chemistry , Peptides/chemistry , Amino Acid Sequence , Angiogenesis Inhibitors/pharmacology , Antineoplastic Agents/pharmacology , Binding Sites , Humans , Ligands , Molecular Conformation , Molecular Docking Simulation , Molecular Dynamics Simulation , Neuropilin-1/antagonists & inhibitors , Peptides/pharmacology , Protein Binding , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Vascular Endothelial Growth Factor A/chemistry
2.
J Biol Chem ; 287(37): 31095-103, 2012 Sep 07.
Article in English | MEDLINE | ID: mdl-22782904

ABSTRACT

Structural dynamics associated with cofactor binding have been shown to play key roles in the catalytic mechanism of hydrolytic NAD(P)-dependent aldehyde dehydrogenases (ALDH). By contrast, no information is available for their CoA-dependent counterparts. We present here the first crystal structure of a CoA-dependent ALDH. The structure of the methylmalonate semialdehyde dehydrogenase (MSDH) from Bacillus subtilis in binary complex with NAD(+) shows that, in contrast to what is observed for hydrolytic ALDHs, the nicotinamide ring is well defined in the electron density due to direct and H(2)O-mediated hydrogen bonds with the carboxamide. The structure also reveals that a conformational isomerization of the NMNH is possible in MSDH, as shown for hydrolytic ALDHs. Finally, the adenine ring is substantially more solvent-exposed, a result that could be explained by the presence of a Val residue at position 229 in helix α(F) that reduces the depth of the binding pocket and the absence of Gly-225 at the N-terminal end of helix α(F). Substitution of glycine for Val-229 and/or insertion of a glycine residue at position 225 resulted in a significant decrease of the rate constant associated with the dissociation of NADH from the NADH/thioacylenzyme complex, thus demonstrating that the weaker stabilization of the adenine ring is a key factor in triggering the early NADH release in the MSDH-catalyzed reaction. This study provides for the first time structural insights into the mechanism whereby the cofactor binding mode is responsible at least in part for the different kinetic behaviors of the hydrolytic and CoA-dependent ALDHs.


Subject(s)
Adenine/chemistry , Bacillus subtilis/enzymology , Bacterial Proteins/chemistry , Methylmalonate-Semialdehyde Dehydrogenase (Acylating)/chemistry , NADP/chemistry , Adenine/metabolism , Bacterial Proteins/metabolism , Crystallography, X-Ray , Hydrolysis , Kinetics , Methylmalonate-Semialdehyde Dehydrogenase (Acylating)/metabolism , NADP/metabolism , Protein Structure, Secondary , Structure-Activity Relationship
3.
J Mol Biol ; 377(1): 268-80, 2008 Mar 14.
Article in English | MEDLINE | ID: mdl-18255097

ABSTRACT

The methionine sulfoxide reductases (Msrs) are thioredoxin-dependent oxidoreductases that catalyse the reduction of the sulfoxide function of the oxidized methionine residues. These enzymes have been shown to regulate the life span of a wide range of microbial and animal species and to play the role of physiological virulence determinant of some bacterial pathogens. Two structurally unrelated classes of Msrs exist, MsrA and MsrB, with opposite stereoselectivity towards the R and S isomers of the sulfoxide function, respectively. Both Msrs share a similar three-step chemical mechanism including (1) the formation of a sulfenic acid intermediate on the catalytic Cys with the concomitant release of the product-methionine, (2) the formation of an intramonomeric disulfide bridge between the catalytic and the regenerating Cys and (3) the reduction of the disulfide bridge by thioredoxin or its homologues. In this study, four structures of the MsrA domain of the PilB protein from Neisseria meningitidis, representative of four catalytic intermediates of the MsrA catalytic cycle, were determined by X-ray crystallography: the free reduced form, the Michaelis-like complex, the sulfenic acid intermediate and the disulfide oxidized forms. They reveal a conserved overall structure up to the formation of the sulfenic acid intermediate, while a large conformational switch is observed in the oxidized form. The results are discussed in relation to those proposed from enzymatic, NMR and theoretical chemistry studies. In particular, the substrate specificity and binding, the catalytic scenario of the reductase step and the relevance and role of the large conformational change observed in the oxidized form are discussed.


Subject(s)
Neisseria meningitidis/enzymology , Oxidoreductases/chemistry , Oxidoreductases/metabolism , Amino Acid Sequence , Binding Sites , Catalysis , Cysteine , Methionine Sulfoxide Reductases , Models, Molecular , Molecular Sequence Data , Oxidation-Reduction , Protein Structure, Secondary , Protein Structure, Tertiary , Sequence Alignment , Solutions , Substrate Specificity
4.
J Mol Biol ; 370(3): 512-29, 2007 Jul 13.
Article in English | MEDLINE | ID: mdl-17531267

ABSTRACT

Glutathione peroxidases (GPXs) are a group of enzymes that regulate the levels of reactive oxygen species in cells and tissues, and protect them against oxidative damage. Contrary to most of their counterparts in animal cells, the higher plant GPX homologues identified so far possess cysteine instead of selenocysteine in their active site. Interestingly, the plant GPXs are not dependent on glutathione but rather on thioredoxin as their in vitro electron donor. We have determined the crystal structures of the reduced and oxidized form of Populus trichocarpaxdeltoides GPX5 (PtGPX5), using a selenomethionine derivative. PtGPX5 exhibits an overall structure similar to that of the known animal GPXs. PtGPX5 crystallized in the assumed physiological dimeric form, displaying a pseudo ten-stranded beta sheet core. Comparison of both redox structures indicates that a drastic conformational change is necessary to bring the two distant cysteine residues together to form an intramolecular disulfide bond. In addition, a computer model of a complex of PtGPX5 and its in vitro recycling partner thioredoxin h1 is proposed on the basis of the crystal packing of the oxidized form enzyme. A possible role of PtGPX5 as a heavy-metal sink is also discussed.


Subject(s)
Glutathione Peroxidase/chemistry , Peroxidases/chemistry , Plant Proteins/chemistry , Populus/enzymology , Protein Structure, Tertiary , Amino Acid Sequence , Animals , Binding Sites , Cadmium/metabolism , Crystallography, X-Ray , Cysteine/metabolism , Glutathione Peroxidase/metabolism , Humans , Models, Molecular , Molecular Sequence Data , Oxidation-Reduction , Peroxidases/genetics , Peroxidases/metabolism , Peroxiredoxins , Plant Proteins/genetics , Plant Proteins/metabolism , Protein Folding , Protein Structure, Quaternary , Protein Structure, Secondary , Protein Subunits/chemistry , Protein Subunits/genetics , Protein Subunits/metabolism , Sequence Alignment
5.
Chem Commun (Camb) ; (39): 4069-71, 2006 Oct 21.
Article in English | MEDLINE | ID: mdl-17024251

ABSTRACT

Enantiopure dipeptide-derived 1,3,5-triazepan-2,6-diones and form H-bonded 3(1) helical molecular tapes with P chirality in the solid state; in the case of , these columnar tapes self-assemble through aromatic-aromatic interactions to give hollow tubular structures.


Subject(s)
Azepines , Dipeptides/chemistry , Azepines/chemical synthesis , Azepines/chemistry , Crystallography, X-Ray , Hydrogen Bonding , Microscopy, Electron, Transmission , Models, Molecular , Molecular Structure , Porosity , Solvents/chemistry , Stereoisomerism
6.
Chemistry ; 12(33): 8498-512, 2006 Nov 15.
Article in English | MEDLINE | ID: mdl-16927352

ABSTRACT

The development of the 1,3,5-triazepane-2,6-dione system as a novel, conformationally restricted, and readily accessible class of dipeptidomimetics is reported. The synthesis of the densely functionalized 1,3,5-triazepane-2,6-dione skeleton was achieved in only four steps from a variety of simple linear dipeptide precursors. To extend the practical value of 1,3,5-triazepane-2,6-diones, a general polymer-assisted solution-phase synthesis approach amenable to library production in a multiparallel format was developed. The conformational preferences of the 1,3,5-triazepane-2,6-dione skeleton were investigated in detail by NMR spectroscopy and X-ray diffraction. The ring exhibits a characteristic folded conformation which was compared to that of related dipeptide-derived scaffolds including the more planar 2,5-diketopiperazine (DKP). Molecular and structural diversity was increased further through post-cyclization appending operations at urea nitrogens. Preliminary biological screens of a small collection of 1,3,5-triazepane-2,6-diones revealed inhibitors of the underexplored malaria liver stage and suggest strong potential for this dipeptide-derived scaffold to interfere with and to modulate biological pathways.


Subject(s)
Combinatorial Chemistry Techniques/methods , Dipeptides/chemistry , Heterocyclic Compounds/chemical synthesis , Molecular Mimicry , Peptide Library , Enzyme Inhibitors/analysis , Liver/parasitology , Liver/pathology , Magnetic Resonance Spectroscopy , Malaria/pathology , Molecular Conformation , Pilot Projects , X-Ray Diffraction
7.
J Mol Biol ; 358(2): 443-54, 2006 Apr 28.
Article in English | MEDLINE | ID: mdl-16530221

ABSTRACT

The secreted form of the PilB protein was recently shown to be bound to the outer membrane of Neisseria gonorrhoeae and proposed to be involved in survival of the pathogen to the host's oxidative burst. PilB is composed of three domains. The central and the C-terminal domains display methionine sulfoxide reductase (Msr) A and B activities respectively, i.e. the ability to reduce specifically the S and the R enantiomers of the sulfoxide function of the methionine sulfoxides, which are easily formed upon oxidation of methionine residues. The N-terminal domain of PilB (Dom1(PILB)) of N.meningitidis, which possesses a CXXC motif, was recently shown to recycle the oxidized forms of the PilB Msr domains in vitro, as the Escherichia coli thioredoxin (Trx) 1 does. The X-ray structure of Dom1(PILB) of N.meningitidis determined here shows a Trx-fold, in agreement with the biochemical properties of Dom1(PILB). However, substantial structural differences with E.coli Trx1 exist. Dom1(PILB) displays more structural homologies with the periplasmic disulfide oxidoreductases involved in cytochrome maturation pathways in bacteria. The active site of the reduced form of Dom1(PILB) reveals a high level of stabilization of the N-terminal catalytic cysteine residue and a hydrophobic environment of the C-terminal recycling cysteine in the CXXC motif, consistent with the pK(app) values measured for Cys67 (<6) and Cys70 (9.3), respectively. Compared to cytochrome maturation disulfide oxidoreductases and to Trx1, one edge of the active site is covered by four additional residues (99)FLHE(102). The putative role of the resulting protuberance is discussed in relation to the disulfide reductase properties of Dom1(PILB).


Subject(s)
Bacterial Proteins/chemistry , Neisseria meningitidis/chemistry , Oxidoreductases/chemistry , Thioredoxins/chemistry , Amino Acid Sequence , Binding Sites , Crystallography, X-Ray , Cysteine/chemistry , Cysteine/metabolism , Methionine/chemistry , Molecular Sequence Data , Protein Folding , Protein Structure, Tertiary , Sequence Homology, Amino Acid
8.
Biochemistry ; 45(9): 2978-86, 2006 Mar 07.
Article in English | MEDLINE | ID: mdl-16503652

ABSTRACT

Crystal structures of several members of the nonphosphorylating CoA-independent aldehyde dehydrogenase (ALDH) family have shown that the peculiar binding mode of the cofactor to the Rossmann fold results in a conformational flexibility for the nicotinamide moiety of the cofactor. This has been hypothesized to constitute an essential feature of the catalytic mechanism because the conformation of the cofactor required for the acylation step is not appropriate for the deacylation step. In the present study, the structure of a reaction intermediate of the E268A-glyceraldehyde 3-phosphate dehydrogenase (GAPN) from Streptococcus mutans, obtained by soaking the crystals of the enzyme/NADP complex with the natural substrate, is reported. The substrate is bound covalently in the four monomers and presents the geometric characteristics expected for a thioacylenzyme intermediate. Control experiments assessed that reduction of the coenzyme has occurred within the crystal. The structure reveals that reduction of the cofactor upon acylation leads to an extensive motion of the nicotinamide moiety with a flip of the reduced pyridinium ring away from the active site without significant changes of the protein structure. This event positions the reduced nicotinamide moiety in a pocket that likely constitutes the exit door for NADPH. Arguments are provided that the structure reported here constitutes a reasonable picture of the first thioacylenzyme intermediate characterized thus far in the ALDH family and that the position of the reduced nicotinamide moiety observed in GAPN is the one suitable for the deacylation step within all of the nonphosphorylating CoA-independent ALDH family.


Subject(s)
Aldehyde Dehydrogenase/chemistry , Coenzymes/chemistry , Acylation , Aldehyde Dehydrogenase/metabolism , Binding Sites , Catalysis , Coenzymes/metabolism , Crystallography, X-Ray , Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)/chemistry , Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)/metabolism , Isomerism , Kinetics , NADP/chemistry , NADP/metabolism , Nicotinamide Mononucleotide/chemistry , Oxidation-Reduction , Protein Conformation , Streptococcus mutans/enzymology , Streptococcus mutans/metabolism
9.
Biochim Biophys Acta ; 1703(2): 249-60, 2005 Jan 17.
Article in English | MEDLINE | ID: mdl-15680233

ABSTRACT

Methionine sulfoxides are easily formed in proteins exposed to reactive oxidative species commonly present in cells. Their reduction back to methionine residues is catalyzed by peptide methionine sulfoxide reductases. Although grouped in a unique family with respect to their biological function, these enzymes are divided in two classes named MsrA and MsrB, depending on the sulfoxide enantiomer of the substrate they reduce. This specificity-based classification differentiates enzymes which display no sequence homology. Several three-dimensional structures of peptide methionine sulfoxide reductases have been determined, so that members of both classes are known to date. These crystal structures are reviewed in this paper. The folds and active sites of MsrAs and MsrBs are discussed in the light of the methionine sulfoxide reductase sequence diversity.


Subject(s)
Oxidoreductases/chemistry , Amino Acid Sequence , Binding Sites , Methionine Sulfoxide Reductases , Molecular Sequence Data , Protein Conformation , Protein Folding , Sequence Homology, Amino Acid
10.
Biochemistry ; 44(6): 1755-67, 2005 Feb 15.
Article in English | MEDLINE | ID: mdl-15697201

ABSTRACT

Peroxiredoxins (Prxs) constitute a family of thiol peroxidases that reduce hydrogen peroxide, peroxinitrite, and hydroperoxides using a strictly conserved cysteine. Very abundant in all organisms, Prxs are produced as diverse isoforms characterized by different catalytic mechanisms and various thiol-containing reducing agents. The oligomeric state of Prxs and the link with their functionality is a subject of intensive research. We present here a combined X-ray and nuclear magnetic resonance (NMR) study of a plant Prx that belongs to the D-Prx (type II) subfamily. The Populus trichocarpa Prx is the first Prx shown to be regenerated in vitro by both the glutaredoxin and thioredoxin systems. The crystal structure and solution NMR provide evidence that the reduced protein is a specific noncovalent homodimer both in the crystal and in solution. The dimer interface is roughly perpendicular to the plane of the central beta sheet and differs from the interface of A- and B-Prx dimers, where proteins associate in the plane parallel to the beta sheet. The homodimer interface involves residues strongly conserved in the D (type II) Prxs, suggesting that all Prxs of this family can homodimerize. The study provides a new insight into the Prx oligomerism and the basis for protein-protein and enzyme-substrate interaction studies by NMR.


Subject(s)
Nuclear Magnetic Resonance, Biomolecular , Oxidoreductases/chemistry , Peroxidases/chemistry , Plant Proteins/chemistry , Populus/enzymology , Thermodynamics , Thioredoxins/chemistry , Amino Acid Sequence , Binding Sites , Consensus Sequence , Crystallization , Crystallography, X-Ray , Dimerization , Glutaredoxins , Molecular Sequence Data , Nuclear Magnetic Resonance, Biomolecular/methods , Oxidoreductases/metabolism , Peroxidases/metabolism , Peroxiredoxins , Plant Proteins/metabolism , Solutions , Surface Properties , Thioredoxins/metabolism
11.
Org Lett ; 6(20): 3449-52, 2004 Sep 30.
Article in English | MEDLINE | ID: mdl-15387520

ABSTRACT

[structure: see text] Bicyclic hexapeptides 1a-c were synthesized via an intramolecular ring-closing metathesis reaction on solid phase followed by an N- to C-terminal cyclization in solution. Structural elucidation showed that these compounds assumed a C2-symmetrical structure with two beta-turns. The trans-ethylene plane was found to occupy two positions in rapid interconversion. One of the bicyclic hexapeptides crystallized with five water molecules, which made an arch above the ethylene group.


Subject(s)
Peptides, Cyclic/chemical synthesis , Protein Conformation , Cyclization , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Peptides, Cyclic/chemistry , Stereoisomerism
12.
Acta Crystallogr D Biol Crystallogr ; 60(Pt 8): 1435-7, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15272169

ABSTRACT

Methylmalonate-semialdehyde dehydrogenase from Bacillus subtilis was cloned and overexpressed in Escherichia coli. Suitable crystals for X-ray diffraction experiments were obtained by the hanging-drop vapour-diffusion method using ammonium sulfate as precipitant. The crystals belong to space group P2(1)2(1)2(1), with unit-cell parameters a = 195.2, b = 192.5, c = 83.5 A, and contain one tetramer per asymmetric unit. X-ray diffraction data were collected to 2.5 A resolution using a synchrotron-radiation source. The crystal structure was solved by the molecular-replacement method.


Subject(s)
Aldehyde Oxidoreductases/chemistry , Aldehyde Oxidoreductases/isolation & purification , Bacillus subtilis/enzymology , Aldehyde Oxidoreductases/biosynthesis , Aldehyde Oxidoreductases/genetics , Bacillus subtilis/genetics , Crystallization , Crystallography, X-Ray , Gene Expression , Methylmalonate-Semialdehyde Dehydrogenase (Acylating)
13.
Acta Crystallogr C ; 60(Pt 3): o200-3, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15004383

ABSTRACT

X-ray studies reveal that tert-butyl (6S)-6-isobutyl-2,4-dioxopiperidine-1-carboxylate occurs in the 4-enol form, viz. tert-butyl (6S)-4-hydroxy-6-isobutyl-2-oxo-1,2,5,6-tetrahydropyridine-1-carboxylate, C14H23NO4, when crystals are grown from a mixture of dichloromethane and pentane, and has an axial orientation of the isobutyl side chain at the 6-position of the piperidine ring. Reduction of the keto functionality leads predominantly to the corresponding beta-hydroxylated delta-lactam, tert-butyl (4R,6S)-4-hydroxy-6-isobutyl-2-oxopiperidine-1-carboxylate, C14H25NO4, with a cis configuration of the 4-hydroxy and 6-isobutyl groups. The two compounds show similar molecular packing driven by strong O-H...O=C hydrogen bonds, leading to infinite chains in the crystal structure.

14.
Acta Crystallogr C ; 60(Pt 3): o204-7, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15004384

ABSTRACT

The crystal structure of (6S)-6-isobutylpiperidine-2,4-dione, C9H15NO2, shows that the keto tautomer is favoured in the solid state. The reduction of the keto functionality leads to the corresponding 4-hydroxy-6-isobutylpiperidin-2-one, C9H17NO2, with an 84:16 cis/trans ratio, containing the 4R,6S and 4S,6S isomers; the ratio of the two isomers was determined by NMR analysis of the reaction mixture. Crystals obtained from the mixture of both isomers have been studied and shown to contain the isomers in a 86:14 ratio. Hence, both X-ray and NMR analyses show that crystallization does not select the major diastereomer formed by the reduction. In both crystal structures, the two independent molecules dimerize through an R2(2)(8) hydrogen-bond motif between adjacent amide groups.

15.
Acta Crystallogr D Biol Crystallogr ; 60(Pt 1): 122-4, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14684904

ABSTRACT

The L7Ae sRNP core protein from Pyrococcus abyssii was crystallized using the sitting-drop vapour-diffusion method. Crystals were obtained in the presence of MgCl(2), PEG 2000 MME and acetate buffer at pH 4.0. A native data set has been collected at 2.9 A resolution using a rotating-anode generator at room temperature. Crystals belong to the orthorhombic space group P2(1)2(1)2, with unit-cell parameters a = 70.7, b = 112.9, c = 34.8 A. There are two monomers of MW 14 200 Da per asymmetric unit and the packing density V(M) is 2.45 A(3) Da(-1). A molecular-replacement analysis gave solutions for the rotation and translation functions.


Subject(s)
Archaeal Proteins/chemistry , Pyrococcus/chemistry , Ribonucleoproteins/chemistry , Archaeal Proteins/genetics , Archaeal Proteins/isolation & purification , Crystallization , Crystallography, X-Ray , DNA, Archaeal/chemistry , DNA, Archaeal/genetics , Escherichia coli/genetics , Polymerase Chain Reaction , Pyrococcus/genetics , Pyrococcus/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Ribonucleoproteins/genetics , Ribonucleoproteins/isolation & purification
16.
Acta Crystallogr D Biol Crystallogr ; 59(Pt 6): 1043-5, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12777768

ABSTRACT

A monocysteinic mutant of poplar glutaredoxin (C30S) has been overproduced and purified. The protein has been crystallized in complex with glutathione using the hanging-drop vapour-diffusion technique in the presence of PEG 4000 as a precipitating agent. A native data set was collected at 1.55 A resolution. The crystals belong to space group P2(1)2(1)2(1), with unit-cell parameters a = 45.7, b = 49.1, c = 104.8 A. Isomorphous crystals of a selenomethionine derivative were grown under the same conditions. Three data sets were collected at 1.73 A using the FIP synchrotron beamline at the ESRF. The positions of the Se atoms were determined and model rebuilding and refinement are in progress.


Subject(s)
Glutathione/chemistry , Oxidoreductases , Proteins/chemistry , Cloning, Molecular , Crystallization , Crystallography, X-Ray , Electrophoresis, Polyacrylamide Gel , Glutaredoxins , Mutagenesis, Site-Directed , Selenomethionine/chemistry , Trees
17.
J Biol Chem ; 278(34): 32219-26, 2003 Aug 22.
Article in English | MEDLINE | ID: mdl-12794088

ABSTRACT

The human beta 1,3-glucuronosyltransferase I (GlcAT-I) is the key enzyme responsible for the completion of glycosaminoglycan-protein linkage tetrasaccharide of proteoglycans (GlcA beta 1,3Gal beta 1,3Gal beta 1,4Xyl beta 1-O-serine). We have investigated the role of aspartate residues Asp194-Asp195-Asp196 corresponding to the glycosyltransferase DXD signature motif, in GlcAT-I function by UDP binding experiments, kinetic analyses, and site-directed mutagenesis. We presented the first evidence that Mn2+ is not only essential for GlcAT-I activity but is also required for cosubstrate binding. In agreement, kinetic studies were consistent with a metal-activated enzyme model whereby activation probably occurs via binding of a Mn2+.UDP-GlcA complex to the enzyme. Mutational analysis showed that the Asp194-Asp195-Asp196 motif is a major element of the UDP/Mn2+ binding site. Furthermore, determination of the individual role of each aspartate showed that substitution of Asp195 as well as Asp196 to alanine strongly impaired GlcAT-I activity, whereas Asp194 replacement produced only a moderate alteration of the enzyme activity. These findings along with molecular modeling and three-dimensional structure comparison of the GlcAT-I catalytic center with that of the Bacillus subtilis glycosyltransferase SpsA provided evidence that the interactions of Asp195 with the ribose moiety of UDP and of Asp196 with the metal cation Mn2+ were crucial for GlcAT-I function. Altogether, these results indicated that, similarly to the SpsA enzyme, the nucleotide binding site of GlcAT-I contains a XDD motif rather than a DXD motif.


Subject(s)
Amino Acid Motifs , Glucuronosyltransferase/metabolism , Base Sequence , DNA Primers , Enzyme Activation , Glucuronosyltransferase/chemistry , Glucuronosyltransferase/genetics , Humans , Kinetics , Manganese/metabolism , Models, Molecular , Mutagenesis, Site-Directed , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Substrate Specificity
18.
J Biol Chem ; 278(15): 12968-76, 2003 Apr 11.
Article in English | MEDLINE | ID: mdl-12569100

ABSTRACT

The crystal structure of the phosphorylating glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from Bacillus stearothermophilus was solved in complex with its cofactor, NAD, and its physiological substrate, D-glyceraldehyde 3-phosphate (D-G3P). To isolate a stable ternary complex, the nucleophilic residue of the active site, Cys(149), was substituted with alanine or serine. The C149A and C149S GAPDH ternary complexes were obtained by soaking the crystals of the corresponding binary complexes (enzyme.NAD) in a solution containing G3P. The structures of the two binary and the two ternary complexes are presented. The D-G3P adopts the same conformation in the two ternary complexes. It is bound in a non-covalent way, in the free aldehyde form, its C-3 phosphate group being positioned in the P(s) site and not in the P(i) site. Its C-1 carbonyl oxygen points toward the essential His(176), which supports the role proposed for this residue along the two steps of the catalytic pathway. Arguments are provided that the structures reported here are representative of a productive enzyme.NAD.D-G3P complex in the ground state (Michaelis complex).


Subject(s)
Geobacillus stearothermophilus/enzymology , Glyceraldehyde 3-Phosphate/chemistry , Glyceraldehyde-3-Phosphate Dehydrogenases/chemistry , Amino Acid Substitution , Binding Sites , Crystallography, X-Ray , Glyceraldehyde 3-Phosphate/metabolism , Glyceraldehyde-3-Phosphate Dehydrogenases/metabolism , Models, Molecular , Mutagenesis, Site-Directed , Phosphorylation , Protein Conformation , Recombinant Proteins/chemistry
19.
Biopolymers ; 65(4): 263-73, 2002 Nov 15.
Article in English | MEDLINE | ID: mdl-12382287

ABSTRACT

To gain insight into the molecular determinants of thermoadaptation within the family of archaeal glyceraldehyde-3-phosphate dehydrogenases (GAPDH), a homology-based 3-D model of the mesophilic GAPDH from Methanobacterium bryantii was built and compared with the crystal structure of the thermophilic GAPDH from Methanothermus fervidus. The homotetrameric model of the holoenzyme was initially assembled from identical subunits completed with NADP molecules. The structure was then refined by energy minimization and simulated-annealing procedures. PROCHECK and the 3-D profile method were used to appraise the model reliability. Striking molecular features underlying the difference in stability between the enzymes were deduced from their structural comparison. First, both the increase in hydrophobic contacts and the decrease in accessibility to the protein core were shown to discriminate in favor of the thermophilic enzyme. Besides, but to a lesser degree, the number of ion pairs involved in cooperative clusters appeared to correlate with thermostability. Finally, the decreased stability of the mesophilic enzyme was also predicted to proceed from both the lack of charge-dipole interactions within alpha-helices and the enhanced entropy of unfolding due to an increase in chain flexibility. Thus, archaeal GAPDHs appear to be governed by thermoadaptation rules that differ in some aspects from those previously observed within their eubacterial counterparts.


Subject(s)
Glyceraldehyde-3-Phosphate Dehydrogenases/chemistry , Methanobacteriales/enzymology , Methanobacterium/enzymology , Adaptation, Physiological , Amino Acid Sequence , Enzyme Stability , Glyceraldehyde-3-Phosphate Dehydrogenases/genetics , Methanobacteriales/genetics , Methanobacterium/genetics , Models, Molecular , Molecular Sequence Data , Protein Structure, Quaternary , Sequence Homology, Amino Acid , Thermodynamics
20.
Biochem Pharmacol ; 64(5-6): 1065-9, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12213606

ABSTRACT

Thioredoxins are small molecular weight disulfide oxidoreductases specialized in the reduction of disulfide bonds on other proteins. Generally, the enzymes which are selectively and reversibly reduced by these proteins oscillate between an oxidized and inactive conformation and a reduced and active conformation. Thioredoxin constitutes the archetype of a family of protein disulfide oxidoreductases which comprises glutaredoxin and protein disulfide isomerase. Thioredoxin and glutaredoxin serve many roles in the cell, including the redox regulation of target enzymes and transcription factors. They can also serve as hydrogen donors to peroxiredoxins, recently discovered heme free peroxidases, the function of which is to get rid of hydroperoxides in the cell. This review describes the molecular basis for the functioning and interaction between these enzymes in photosynthetic organisms.


Subject(s)
Oxidoreductases , Photosynthesis/physiology , Sulfhydryl Compounds/metabolism , Thioredoxins/metabolism , Animals , Catalysis , Forecasting , Glutaredoxins , Humans , Models, Molecular , Oxidation-Reduction , Peroxidases/metabolism , Peroxiredoxins , Plants , Protein Disulfide Reductase (Glutathione)/metabolism , Protein Disulfide-Isomerases/metabolism , Proteins/metabolism
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