12 results on '"Yin-Cheng Hsieh"'
Search Results
2. FeoC from Klebsiella pneumoniae Contains a [4Fe-4S] Cluster
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Tai Huang Huang, Kuo Wei Hung, Liang Kun Yu, Yung Han Chen, Shyue chu Ke, Chun-Jung Chen, Ya Hsin Cheng, Yin Cheng Hsieh, and Kuang Lung Hsueh
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Iron-Sulfur Proteins ,Magnetic Resonance Spectroscopy ,Extended X-ray absorption fine structure ,Permease ,Stereochemistry ,Protein domain ,chemistry.chemical_element ,Articles ,Gene Expression Regulation, Bacterial ,Nuclear magnetic resonance spectroscopy ,Biology ,Microbiology ,Oxygen ,Ferrous ,law.invention ,Klebsiella pneumoniae ,Absorptiometry, Photon ,Bacterial Proteins ,chemistry ,Membrane protein ,Biochemistry ,law ,Electron paramagnetic resonance ,Oxidation-Reduction ,Molecular Biology - Abstract
Iron is essential for pathogen survival, virulence, and colonization. Feo is suggested to function as the ferrous iron (Fe 2+ ) transporter. The enterobacterial Feo system is composed of 3 proteins: FeoB is the indispensable component and is a large membrane protein likely to function as a permease; FeoA is a small Src homology 3 (SH3) domain protein that interacts with FeoB; FeoC is a winged-helix protein containing 4 conserved Cys residues in a sequence suitable for harboring a putative iron-sulfur (Fe-S) cluster. The presence of an iron-sulfur cluster on FeoC has never been shown experimentally. We report that under anaerobic conditions, the recombinant Klebsiella pneumoniae FeoC ( Kp FeoC) exhibited hyperfine-shifted nuclear magnetic resonance (NMR) and a UV-visible (UV-Vis) absorbance spectrum characteristic of a paramagnetic center. The electron paramagnetic resonance (EPR) and extended X-ray absorption fine structure (EXAFS) results were consistent only with the [4Fe-4S] clusters. Substituting the cysteinyl sulfur with oxygen resulted in significantly reduced cluster stability, establishing the roles of these cysteines as the ligands for the Fe-S cluster. When exposed to oxygen, the [4Fe-4S] cluster degraded to [3Fe-4S] and eventually disappeared. We propose that Kp FeoC may regulate the function of the Feo transporter through the oxygen- or iron-sensitive coordination of the Fe-S cluster.
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- 2013
3. Crystal Structure and Mutational Analysis of Aminoacylhistidine Dipeptidase from Vibrio alginolyticus Reveal a New Architecture of M20 Metallopeptidases
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Ting-Yi Wang, Yu Kuo Wang, Cheng-Hsiang Chang, Yi Ju Chen, Yin Cheng Hsieh, Chun-Jung Chen, Tung-Kung Wu, Yi Chin Chen, Chin-Yuan Chang, and Ting Wei Chiang
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Dipeptidase ,Dipeptidases ,Metallopeptidase ,Protein Conformation ,Stereochemistry ,DNA Mutational Analysis ,Molecular Conformation ,Crystallography, X-Ray ,Biochemistry ,Gene Expression Regulation, Enzymologic ,Substrate Specificity ,Protein structure ,Catalytic Domain ,Hydrolase ,Amino Acids ,Molecular Biology ,Vibrio alginolyticus ,biology ,PEPD ,Active site ,Hydrogen Bonding ,Gene Expression Regulation, Bacterial ,Cell Biology ,Enzyme structure ,Protein Structure, Tertiary ,Kinetics ,Protein Structure and Folding ,Mutagenesis, Site-Directed ,biology.protein - Abstract
Aminoacylhistidine dipeptidases (PepD, EC 3.4.13.3) belong to the family of M20 metallopeptidases from the metallopeptidase H clan that catalyze a broad range of dipeptide and tripeptide substrates, including L-carnosine and L-homocarnosine. Homocarnosine has been suggested as a precursor for the neurotransmitter γ-aminobutyric acid (GABA) and may mediate the antiseizure effects of GABAergic therapies. Here, we report the crystal structure of PepD from Vibrio alginolyticus and the results of mutational analysis of substrate-binding residues in the C-terminal as well as substrate specificity of the PepD catalytic domain-alone truncated protein PepD(CAT). The structure of PepD was found to exist as a homodimer, in which each monomer comprises a catalytic domain containing two zinc ions at the active site center for its hydrolytic function and a lid domain utilizing hydrogen bonds between helices to form the dimer interface. Although the PepD is structurally similar to PepV, which exists as a monomer, putative substrate-binding residues reside in different topological regions of the polypeptide chain. In addition, the lid domain of the PepD contains an "extra" domain not observed in related M20 family metallopeptidases with a dimeric structure. Mutational assays confirmed both the putative di-zinc allocations and the architecture of substrate recognition. In addition, the catalytic domain-alone truncated PepD(CAT) exhibited substrate specificity to l-homocarnosine compared with that of the wild-type PepD, indicating a potential value in applications of PepD(CAT) for GABAergic therapies or neuroprotection.
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- 2010
4. Crystal Structures of Bacillus cereus NCTU2 Chitinase Complexes with Chitooligomers Reveal Novel Substrate Binding for Catalysis
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Keshab Lal Shrestha, Yin-Cheng Hsieh, Chueh-Yuan Kuo, Yue-Jin Wu, Yaw-Kuen Li, Chun-Jung Chen, Yen-Chieh Huang, Phimonphan Chuankhayan, Wen-guey Wu, Cheng-Fu Chao, and Tzu-Ying Chiang
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biology ,urogenital system ,Chemistry ,Stereochemistry ,Active site ,Cell Biology ,urologic and male genital diseases ,Biochemistry ,chemistry.chemical_compound ,Crystallography ,Chitin ,Chitin binding ,Hydrolase ,Chitinase ,biology.protein ,Glycoside hydrolase ,Binding site ,Molecular Biology ,Glycoside hydrolase family 18 - Abstract
Chitinases hydrolyze chitin, an insoluble linear polymer of N-acetyl-d-glucosamine (NAG)n, into nutrient sources. Bacillus cereus NCTU2 chitinase (ChiNCTU2) predominantly produces chitobioses and belongs to glycoside hydrolase family 18. The crystal structure of wild-type ChiNCTU2 comprises only a catalytic domain, unlike other chitinases that are equipped with additional chitin binding and insertion domains to bind substrates into the active site. Lacking chitin binding and chitin insertion domains, ChiNCTU2 utilizes two dynamic loops (Gly-67—Thr-69 and Ile-106–Val-112) to interact with (NAG)n, generating novel substrate binding and distortion for catalysis. Gln-109 is crucial for direct binding with substrates, leading to conformational changes of two loops with a maximum shift of ∼4.6 Å along the binding cleft. The structures of E145Q, E145Q/Y227F, and E145G/Y227F mutants complexed with (NAG)n reveal (NAG)2, (NAG)2, and (NAG)4 in the active site, respectively, implying various stages of reaction: before hydrolysis, E145G/Y227F with (NAG)4; in an intermediate state, E145Q/Y227F with a boat-form NAG at the −1 subsite, −1-(NAG); after hydrolysis, E145Q with a chair form −1-(NAG). Several residues were confirmed to play catalytic roles: Glu-145 in cleavage of the glycosidic bond between −1-(NAG) and +1-(NAG); Tyr-227 in the conformational change of −1-(NAG); Asp-143 and Gln-225 in stabilizing the conformation of −1-(NAG). Additionally, Glu-190 acts in the process of product release, and Tyr-193 coordinates with water for catalysis. Residues Asp-143, E145Q, Glu-190, and Tyr-193 exhibit multiple conformations for functions. The inhibitors zinc ions and cyclo-(l-His-l-Pro) are located at various positions and confirm the catalytic-site topology. Together with kinetics analyses of related mutants, the structures of ChiNCTU2 and its mutant complexes with (NAG)n provide new insights into its substrate binding and the mechanistic action.
- Published
- 2010
5. Structural insights into the enzyme catalysis from comparison of three forms of dissimilatory sulphite reductase from Desulfovibrio gigas
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En-Huang Liu, Yin-Cheng Hsieh, Sunney I. Chan, Yen-Lung Chiang, Vincent C.-C. Wang, Chun-Jung Chen, Ming-Yih Liu, and Wen-guey Wu
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Stereochemistry ,Substrate (chemistry) ,Crystal structure ,Biology ,Microbiology ,Sulfite reductase ,law.invention ,Enzyme catalysis ,chemistry.chemical_compound ,Thioether ,chemistry ,Biochemistry ,Covalent bond ,law ,Desulfovibrio gigas ,Electron paramagnetic resonance ,Molecular Biology - Abstract
The crystal structures of two active forms of dissimilatory sulphite reductase (Dsr) from Desulfovibrio gigas, Dsr-I and Dsr-II, are compared at 1.76 and 2.05 A resolution respectively. The dimeric α_2β_2γ_2 structure of Dsr-I contains eight [4Fe–4S] clusters, two saddle-shaped sirohaems and two flat sirohydrochlorins. In Dsr-II, the [4Fe–4S] cluster associated with the sirohaem in Dsr-I is replaced by a [3Fe–4S] cluster. Electron paramagnetic resonance (EPR) of the active Dsr-I and Dsr-II confirm the co-factor structures, whereas EPR of a third but inactive form, Dsr-III, suggests that the sirohaem has been demetallated in addition to its associated [4Fe–4S] cluster replaced by a [3Fe–4S] centre. In Dsr-I and Dsr-II, the sirohydrochlorin is located in a putative substrate channel connected to the sirohaem. The γ-subunit C-terminus is inserted into a positively charged channel formed between the α- and β-subunits, with its conserved terminal Cysγ104 side-chain covalently linked to the CHA atom of the sirohaem in Dsr-I. In Dsr-II, the thioether bond is broken, and the Cysγ104 side-chain moves closer to the bound sulphite at the sirohaem pocket. These different forms of Dsr offer structural insights into a mechanism of sulphite reduction that can lead to S_3O_6^(2−), S_2O_3^(2−) and S^(2−).
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- 2010
6. Crystal Structure of Adenylylsulfate Reductase from Desulfovibrio gigas Suggests a Potential Self-Regulation Mechanism Involving the C Terminus of the β-Subunit
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En-Hong Liu, Jeyaraman Jeyakanthan, Ming-Yih Liu, Chun-Jung Chen, Phimonphan Chuankhayan, Yuan-Lan Chiang, Jou-Yin Fang, Sunney I. Chan, Yen-Chieh Huang, and Yin-Cheng Hsieh
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Models, Molecular ,Stereochemistry ,Molecular Sequence Data ,Sequence alignment ,Random hexamer ,Crystallography, X-Ray ,Spectrum Analysis, Raman ,Microbiology ,chemistry.chemical_compound ,Structural Biology ,Desulfovibrio gigas ,Oxidoreductases Acting on Sulfur Group Donors ,Amino Acid Sequence ,Protein Structure, Quaternary ,Molecular Biology ,Peptide sequence ,Flavin adenine dinucleotide ,biology ,C-terminus ,Archaeoglobus fulgidus ,Active site ,Social Control, Informal ,Adenosine Monophosphate ,Protein Subunits ,chemistry ,Biochemistry ,Flavin-Adenine Dinucleotide ,biology.protein ,Sequence Alignment ,Ultracentrifugation ,Protein Binding - Abstract
Adenylylsulfate reductase (adenosine 5′-phosphosulfate [APS] reductase [APSR]) plays a key role in catalyzing APS to sulfite in dissimilatory sulfate reduction. Here, we report the crystal structure of APSR from Desulfovibrio gigas at 3.1-Å resolution. Different from the α 2 β 2 -heterotetramer of the Archaeoglobus fulgidus , the overall structure of APSR from D. gigas comprises six αβ-heterodimers that form a hexameric structure. The flavin adenine dinucleotide is noncovalently attached to the α-subunit, and two [4Fe-4S] clusters are enveloped by cluster-binding motifs. The substrate-binding channel in D. gigas is wider than that in A. fulgidus because of shifts in the loop (amino acid 326 to 332) and the α-helix (amino acid 289 to 299) in the α-subunit. The positively charged residue Arg160 in the structure of D. gigas likely replaces the role of Arg83 in that of A. fulgidus for the recognition of substrates. The C-terminal segment of the β-subunit wraps around the α-subunit to form a functional unit, with the C-terminal loop inserted into the active-site channel of the α-subunit from another αβ-heterodimer. Electrostatic interactions between the substrate-binding residue Arg282 in the α-subunit and Asp159 in the C terminus of the β-subunit affect the binding of the substrate. Alignment of APSR sequences from D. gigas and A. fulgidus shows the largest differences toward the C termini of the β-subunits, and structural comparison reveals notable differences at the C termini, activity sites, and other regions. The disulfide comprising Cys156 to Cys162 stabilizes the C-terminal loop of the β-subunit and is crucial for oligomerization. Dynamic light scattering and ultracentrifugation measurements reveal multiple forms of APSR upon the addition of AMP, indicating that AMP binding dissociates the inactive hexamer into functional dimers, presumably by switching the C terminus of the β-subunit away from the active site. The crystal structure of APSR, together with its oligomerization properties, suggests that APSR from sulfate-reducing bacteria might self-regulate its activity through the C terminus of the β-subunit.
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- 2009
7. Stereoselective Esterase from Pseudomonas putida IFO12996 Reveals α/β Hydrolase Folds for <scp>d</scp> -β-Acetylthioisobutyric Acid Synthesis
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Yu Jen Chen, Shyh Yu Shaw, Fatemeh Elmi, Hsin Tai Lee, Jen Yeng Huang, Chun-Jung Chen, Yu Ling Wang, and Yin Cheng Hsieh
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DNA, Bacterial ,Models, Molecular ,Protein Folding ,Protein Conformation ,Stereochemistry ,Molecular Sequence Data ,Crystallography, X-Ray ,Microbiology ,Esterase ,Substrate Specificity ,Bacterial Proteins ,Structural Biology ,Enzyme Stability ,Catalytic triad ,Hydrolase ,Escherichia coli ,Moiety ,Cloning, Molecular ,Enantiomeric excess ,Molecular Biology ,chemistry.chemical_classification ,Binding Sites ,biology ,Pseudomonas putida ,Esterases ,Temperature ,food and beverages ,Active site ,Stereoisomerism ,Sequence Analysis, DNA ,Hydrogen-Ion Concentration ,biology.organism_classification ,Protein Structure, Tertiary ,Molecular Weight ,Butyrates ,Protein Subunits ,Enzyme ,Biochemistry ,chemistry ,biology.protein - Abstract
Esterase (EST) from Pseudomonas putida IFO12996 catalyzes the stereoselective hydrolysis of methyl dl -β-acetylthioisobutyrate ( dl -MATI) to produce d -β-acetylthioisobutyric acid (DAT), serving as a key intermediate for the synthesis of angiotensin-converting enzyme inhibitors. The EST gene was cloned and expressed in Escherichia coli ; the recombinant protein is a non-disulfide-linked homotrimer with a monomer molecular weight of 33,000 in both solution and crystalline states, indicating that these ESTs function as trimers. EST hydrolyzed dl -MATI to produce DAT with a degree of conversion of 49.5% and an enantiomeric excess value of 97.2% at an optimum pH of about 8 to 10 and an optimum temperature of about 57 to 67°C. The crystal structure of EST has been determined by X-ray diffraction to a resolution of 1.6 Å, confirming that EST is a member of the α/β hydrolase fold superfamily of enzymes and includes a catalytic triad of Ser97, Asp227, and His256. The active site is located approximately in the middle of the molecule at the end of a pocket ∼12 Å deep. EST can hydrolyze the methyl ester group without affecting the acetylthiol ester moiety in dl -MATI. The examination of substrate specificity of EST toward other linear esters revealed that the enzyme showed specific activity toward methyl esters and that it recognized the configuration at C-2.
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- 2005
8. Crystal Structures of Vertebrate Dihydropyrimidinase and Complexes from Tetraodon nigroviridis with Lysine Carbamylation
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Chun-Jung Chen, Yuh-Shyong Yang, Yin Cheng Hsieh, Sunney I. Chan, Mei Chun Chen, and Ching Chen Hsu
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chemistry.chemical_classification ,Imino acid ,biology ,Stereochemistry ,Lysine ,Substrate (chemistry) ,Hydantoin ,Cell Biology ,Tetraodon nigroviridis ,biology.organism_classification ,Biochemistry ,Metal ,chemistry.chemical_compound ,Crystallography ,chemistry ,visual_art ,Dihydropyrimidinase ,visual_art.visual_art_medium ,Protein carboxylation ,Molecular Biology - Abstract
Lysine carbamylation, a post-translational modification, facilitates metal coordination for specific enzymatic activities. We have determined structures of the vertebrate dihydropyrimidinase from Tetraodon nigroviridis (TnDhp) in various states: the apoenzyme as well as two forms of the holoenzyme with one and two metals at the catalytic site. The essential active-site structural requirements have been identified for the possible existence of four metal-mediated stages of lysine carbamylation. Only one metal is sufficient for stabilizing lysine carbamylation; however, the post-translational lysine carbamylation facilitates additional metal coordination for the regulation of specific enzymatic activities through controlling the conformations of two dynamic loops, Ala^(69)–Arg^(74) and Met^(158)–Met^(165), located in the tunnel for the substrate entrance. The substrate/product tunnel is in the “open form” in the apo-TnDhp, in the “intermediate state” in the monometal TnDhp, and in the “closed form” in the dimetal TnDhp structure, respectively. Structural comparison also suggests that the C-terminal tail plays a role in the enzymatic function through interactions with the Ala^(69)–Arg^(74) dynamic loop. In addition, the structures of the dimetal TnDhp in complexes with hydantoin, N-carbamyl-β-alanine, and N-carbamyl-β-amino isobutyrate as well as apo-TnDhp in complex with a product analog, N-(2-acetamido)-iminodiacetic acid, have been determined. These structural results illustrate how a protein exploits unique lysines and the metal distribution to accomplish lysine carbamylation as well as subsequent enzymatic functions.
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- 2013
9. Crystal structure of dimeric flavodoxin from Desulfovibrio gigas suggests a potential binding region for the electron-transferring partner
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Hoong-Kun Fun, Yin-Cheng Hsieh, Tze Shyang Chia, and Chun-Jung Chen
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Models, Molecular ,crystal structure ,Semiquinone ,Flavodoxin ,Stereochemistry ,Flavin Mononucleotide ,Dimer ,Molecular Sequence Data ,flavodoxin (Fld) ,flavin mononucleotide (FMN) ,dimer ,binding region ,Flavin mononucleotide ,Crystallography, X-Ray ,Catalysis ,Article ,Inorganic Chemistry ,lcsh:Chemistry ,Electron Transport ,chemistry.chemical_compound ,Protein structure ,Desulfovibrio gigas ,Amino Acid Sequence ,Physical and Theoretical Chemistry ,Binding site ,Protein Structure, Quaternary ,Molecular Biology ,lcsh:QH301-705.5 ,Spectroscopy ,Binding Sites ,biology ,Sequence Homology, Amino Acid ,Chemistry ,Organic Chemistry ,fungi ,Active site ,General Medicine ,Computer Science Applications ,Protein Structure, Tertiary ,Crystallography ,lcsh:Biology (General) ,lcsh:QD1-999 ,Mutation ,biology.protein ,Protein Multimerization ,Protein Binding - Abstract
Flavodoxins, which exist widely in microorganisms, have been found in various pathways with multiple physiological functions. The flavodoxin (Fld) containing the cofactor flavin mononucleotide (FMN) from sulfur-reducing bacteria Desulfovibrio gigas (D. gigas) is a short-chain enzyme that comprises 146 residues with a molecular mass of 15 kDa and plays important roles in the electron-transfer chain. To investigate its structure, we purified this Fld directly from anaerobically grown D. gigas cells. The crystal structure of Fld, determined at resolution 1.3 Å, is a dimer with two FMN packing in an orientation head to head at a distance of 17 Å, which generates a long and connected negatively charged region. Two loops, Thr59–Asp63 and Asp95–Tyr100, are located in the negatively charged region and between two FMN, and are structurally dynamic. An analysis of each monomer shows that the structure of Fld is in a semiquinone state; the positions of FMN and the surrounding residues in the active site deviate. The crystal structure of Fld from D. gigas agrees with a dimeric form in the solution state. The dimerization area, dynamic characteristics and structure variations between monomers enable us to identify a possible binding area for its functional partners.
- Published
- 2012
10. Crystal structures of complexes of the branched-chain aminotransferase from Deinococcus radiodurans with α-ketoisocaproate and L-glutamate suggest the radiation resistance of this enzyme for catalysis
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Yen-Chieh Huang, Tien-Feng Huang, Chung-De Chen, Hong-Hsiang Guan, Chih Hao Lin, Wen Chang Chang, Chun-Jung Chen, Phimonphan Chuankhayan, Yin-Cheng Hsieh, and Ming-Yih Liu
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Models, Molecular ,Stereochemistry ,Protein Conformation ,Branched chain aminotransferase ,Molecular Sequence Data ,Glutamic Acid ,Crystallography, X-Ray ,Microbiology ,Catalysis ,Gene Expression Regulation, Enzymologic ,Substrate Specificity ,Catalytic Domain ,Enzyme Stability ,Amino Acid Sequence ,Molecular Biology ,Transaminases ,chemistry.chemical_classification ,biology ,Active site ,Deinococcus radiodurans ,Gene Expression Regulation, Bacterial ,Articles ,Thermus thermophilus ,biology.organism_classification ,Keto Acids ,Amino acid ,Biochemistry ,chemistry ,Spectrophotometry ,biology.protein ,Salt bridge ,Deinococcus ,Leucine ,Isoleucine ,Crystallization - Abstract
Branched-chain aminotransferases (BCAT), which utilize pyridoxal 5′-phosphate (PLP) as a cofactor, reversibly catalyze the transfer of the α-amino groups of three of the most hydrophobic branched-chain amino acids (BCAA), leucine, isoleucine, and valine, to α-ketoglutarate to form the respective branched-chain α-keto acids and glutamate. The BCAT from Deinococcus radiodurans ( Dr BCAT), an extremophile, was cloned and expressed in Escherichia coli for structure and functional studies. The crystal structures of the native Dr BCAT with PLP and its complexes with l -glutamate and α-ketoisocaproate (KIC), respectively, have been determined. The Dr BCAT monomer, comprising 358 amino acids, contains large and small domains connected with an interdomain loop. The cofactor PLP is located at the bottom of the active site pocket between two domains and near the dimer interface. The substrate ( l -glutamate or KIC) is bound with key residues through interactions of the hydrogen bond and the salt bridge near PLP inside the active site pocket. Mutations of some interaction residues, such as Tyr71, Arg145, and Lys202, result in loss of the specific activity of the enzymes. In the interdomain loop, a dynamic loop (Gly173 to Gly179) clearly exhibits open and close conformations in structures of Dr BCAT without and with substrates, respectively. Dr BCAT shows the highest specific activity both in nature and under ionizing radiation, but with lower thermal stability above 60°C, than either BCAT from Escherichia coli ( e BCAT) or from Thermus thermophilus (HB8BCAT). The dimeric molecular packing and the distribution of cysteine residues at the active site and the molecular surface might explain the resistance to radiation but small thermal stability of Dr BCAT.
- Published
- 2012
11. Cobra CRISP Functions as an Inflammatory Modulator via a Novel Zn2+- and Heparan Sulfate-dependent Transcriptional Regulation of Endothelial Cell Adhesion Molecules*
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Je Hung Kuo, Chun-Jung Chen, Jai Shin Liu, Yin Cheng Hsieh, Jeng Jiann Chiu, Wen-guey Wu, Shao Chen Lee, Yu Ling Wang, and Yu Tsung Shih
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Transcription, Genetic ,Molecular Conformation ,Glycobiology and Extracellular Matrices ,Gene Expression ,Plasma protein binding ,Biology ,Biochemistry ,Cell Line ,chemistry.chemical_compound ,Protein structure ,X-Ray Diffraction ,Cell Adhesion ,Animals ,Humans ,Elapidae ,Binding site ,Cell adhesion ,Molecular Biology ,Cells, Cultured ,Elapid Venoms ,Binding Sites ,Kinase ,Cell adhesion molecule ,Endothelial Cells ,NF-κB ,Cell Biology ,Heparan sulfate ,Cell biology ,Protein Structure, Tertiary ,Zinc ,chemistry ,Heparitin Sulfate ,Inflammation Mediators ,Cell Adhesion Molecules ,Protein Binding - Abstract
Cysteine-rich secretory proteins (CRISPs) have been identified as a toxin family in most animal venoms with biological functions mainly associated with the ion channel activity of cysteine-rich domain (CRD). CRISPs also bind to Zn(2+) at their N-terminal pathogenesis-related (PR-1) domain, but their function remains unknown. Interestingly, similar the Zn(2+)-binding site exists in all CRISP family, including those identified in a wide range of organisms. Here, we report that the CRISP from Naja atra (natrin) could induce expression of vascular endothelial cell adhesion molecules, i.e. intercellular adhesion molecule-1, vascular adhesion molecule-1, and E-selectin, to promote monocytic cell adhesion in a heparan sulfate (HS)- and Zn(2+)-dependent manner. Using specific inhibitors and small interfering RNAs, the activation mechanisms are shown to involve both mitogen-activated protein kinases and nuclear factor-κB. Biophysical characterization of natrin by using fluorescence, circular dichroism, and x-ray crystallographic methods further reveals the presence of two Zn(2+)-binding sites for natrin. The strong binding site is located near the putative Ser-His-Glu catalytic triad of the N-terminal domain. The weak binding site remains to be characterized, but it may modulate HS binding by enhancing its interaction with long chain HS. Our results strongly suggest that natrin may serve as an inflammatory modulator that could perturb the wound-healing process of the bitten victim by regulating adhesion molecule expression in endothelial cells. Our finding uncovers a new aspect of the biological role of CRISP family in immune response and is expected to facilitate future development of new therapeutic strategy for the envenomed victims.
- Published
- 2010
12. Crystal Structures of Aspergillus japonicus Fructosyltransferase Complex with Donor/Acceptor Substrates Reveal Complete Subsites in the Active Site for Catalysis*
- Author
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Chung-De Chen, Hong-Hsiang Guan, Yen-Chieh Huang, Yi-You Hsieh, Chun-Jung Chen, Chih-Yu Hsieh, Phimonphan Chuankhayan, Yueh-Chu Tien, Chien-Min Chiang, and Yin-Cheng Hsieh
- Subjects
Models, Molecular ,Glycoside Hydrolases ,Stereochemistry ,Molecular Sequence Data ,Crystallography, X-Ray ,Biochemistry ,chemistry.chemical_compound ,Structure-Activity Relationship ,Protein structure ,Fructan ,Hexosyltransferases ,Catalytic Domain ,Hydrolase ,Glycoside hydrolase ,Amino Acid Sequence ,Raffinose ,Enzyme Inhibitors ,Molecular Biology ,chemistry.chemical_classification ,biology ,Active site ,Cell Biology ,Enzyme ,Aspergillus ,Glucose ,chemistry ,Protein Structure and Folding ,biology.protein ,Biocatalysis - Abstract
Fructosyltransferases catalyze the transfer of a fructose unit from one sucrose/fructan to another and are engaged in the production of fructooligosaccharide/fructan. The enzymes belong to the glycoside hydrolase family 32 (GH32) with a retaining catalytic mechanism. Here we describe the crystal structures of recombinant fructosyltransferase (AjFT) from Aspergillus japonicus CB05 and its mutant D191A complexes with various donor/acceptor substrates, including sucrose, 1-kestose, nystose, and raffinose. This is the first structure of fructosyltransferase of the GH32 with a high transfructosylation activity. The structure of AjFT comprises two domains with an N-terminal catalytic domain containing a five-blade beta-propeller fold linked to a C-terminal beta-sandwich domain. Structures of various mutant AjFT-substrate complexes reveal complete four substrate-binding subsites (-1 to +3) in the catalytic pocket with shapes and characters distinct from those of clan GH-J enzymes. Residues Asp-60, Asp-191, and Glu-292 that are proposed for nucleophile, transition-state stabilizer, and general acid/base catalyst, respectively, govern the binding of the terminal fructose at the -1 subsite and the catalytic reaction. Mutants D60A, D191A, and E292A completely lost their activities. Residues Ile-143, Arg-190, Glu-292, Glu-318, and His-332 combine the hydrophobic Phe-118 and Tyr-369 to define the +1 subsite for its preference of fructosyl and glucosyl moieties. Ile-143 and Gln-327 define the +2 subsite for raffinose, whereas Tyr-404 and Glu-405 define the +2 and +3 subsites for inulin-type substrates with higher structural flexibilities. Structural geometries of 1-kestose, nystose and raffinose are different from previous data. All results shed light on the catalytic mechanism and substrate recognition of AjFT and other clan GH-J fructosyltransferases.
- Published
- 2010
Catalog
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