18 results on '"Shirouzu, Mikako"'
Search Results
2. Structural and Mutational Studies of the Amino Acid-Editing Domain from Archaeal/Eukaryal Phenylalanyl-tRNA Synthetase
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Sasaki, Hiroshi M., Sekine, Shun-ichi, Sengoku, Toru, Fukunaga, Ryuya, Hattori, Motoyuki, Utsunomiya, Yukiko, Kuroishi, Chizu, Kuramitsu, Seiki, Shirouzu, Mikako, and Yokoyama, Shigeyuki
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- 2006
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3. Crystal Structure of an Archaeal Tyrosyl-tRNA Synthetase Bound to Photocaged L-Tyrosine and Its Potential Application to Time-Resolved X-ray Crystallography.
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Hosaka, Toshiaki, Katsura, Kazushige, Ishizuka-Katsura, Yoshiko, Hanada, Kazuharu, Ito, Kaori, Tomabechi, Yuri, Inoue, Mio, Akasaka, Ryogo, Takemoto, Chie, and Shirouzu, Mikako
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X-ray crystallography ,CRYSTAL structure ,CYTOSKELETAL proteins ,AMINO acids ,PROTEIN synthesis - Abstract
Genetically encoded caged amino acids can be used to control the dynamics of protein activities and cellular localization in response to external cues. In the present study, we revealed the structural basis for the recognition of O-(2-nitrobenzyl)-L-tyrosine (oNBTyr) by its specific variant of Methanocaldococcus jannaschii tyrosyl-tRNA synthetase (oNBTyrRS), and then demonstrated its potential availability for time-resolved X-ray crystallography. The substrate-bound crystal structure of oNBTyrRS at a 2.79 Å resolution indicated that the replacement of tyrosine and leucine at positions 32 and 65 by glycine (Tyr32Gly and Leu65Gly, respectively) and Asp158Ser created sufficient space for entry of the bulky substitute into the amino acid binding pocket, while Glu in place of Leu162 formed a hydrogen bond with the nitro moiety of oNBTyr. We also produced an oNBTyr-containing lysozyme through a cell-free protein synthesis system derived from the Escherichia coli B95. ΔA strain with the UAG codon reassigned to the nonnatural amino acid. Another crystallographic study of the caged protein showed that the site-specifically incorporated oNBTyr was degraded to tyrosine by light irradiation of the crystals. Thus, cell-free protein synthesis of caged proteins with oNBTyr could facilitate time-resolved structural analysis of proteins, including medically important membrane proteins. [ABSTRACT FROM AUTHOR]
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- 2022
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4. Structural basis of CoA recognition by the Pyrococcus single-domain CoA-binding proteins
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Hiyama, Takuya B., Zhao, Min, Kitago, Yu, Yao, Min, Sekine, Shun-ichi, Terada, Takaho, Kuroishi, Chizu, Liu, Zhi-Jie, Rose, John P., Kuramitsu, Seiki, Shirouzu, Mikako, Watanabe, Nobuhisa, Yokoyama, Shigeyuki, Tanaka, Isao, and Wang, Bi-Cheng
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- 2006
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5. Cell-free synthesis of functional antibody fragments to provide a structural basis for antibody–antigen interaction.
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Matsuda, Takayoshi, Ito, Takuhiro, Takemoto, Chie, Katsura, Kazushige, Ikeda, Mariko, Wakiyama, Motoaki, Kukimoto-Niino, Mutsuko, Yokoyama, Shigeyuki, Kurosawa, Yoshikazu, and Shirouzu, Mikako
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ANTIGEN-antibody reactions ,PROTEIN structure ,HEMODIALYSIS ,EPIDERMAL growth factor receptors ,TARGETED drug delivery - Abstract
Growing numbers of therapeutic antibodies offer excellent treatment strategies for many diseases. Elucidation of the interaction between a potential therapeutic antibody and its target protein by structural analysis reveals the mechanism of action and offers useful information for developing rational antibody designs for improved affinity. Here, we developed a rapid, high-yield cell-free system using dialysis mode to synthesize antibody fragments for the structural analysis of antibody–antigen complexes. Optimal synthesis conditions of fragments (Fv and Fab) of the anti-EGFR antibody 059–152 were rapidly determined in a day by using a 30-μl-scale unit. The concentration of supplemented disulfide isomerase, DsbC, was critical to obtaining soluble antibody fragments. The optimal conditions were directly applicable to a 9-ml-scale reaction, with linear scalable yields of more than 1 mg/ml. Analyses of purified 059-152-Fv and Fab showed that the cell-free synthesized antibody fragments were disulfide-bridged, with antigen binding activity comparable to that of clinical antibodies. Examination of the crystal structure of cell-free synthesized 059-152-Fv in complex with the extracellular domain of human EGFR revealed that the epitope of 059-152-Fv broadly covers the EGF binding surface on domain III, including residues that formed critical hydrogen bonds with EGF (Asp355
EGFR , Gln384EGFR , H409EGFR , and Lys465EGFR ), so that the antibody inhibited EGFR activation. We further demonstrated the application of the cell-free system to site-specific integration of non-natural amino acids for antibody engineering, which would expand the availability of therapeutic antibodies based on structural information and rational design. This cell-free system could be an ideal antibody-fragment production platform for functional and structural analysis of potential therapeutic antibodies and for engineered antibody development. [ABSTRACT FROM AUTHOR]- Published
- 2018
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6. Crystal structural characterization reveals novel oligomeric interactions of human voltage-dependent anion channel 1.
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Hosaka, Toshiaki, Okazaki, Masateru, Kimura‐Someya, Tomomi, Ishizuka‐Katsura, Yoshiko, Ito, Kaori, Yokoyama, Shigeyuki, Dodo, Kosuke, Sodeoka, Mikiko, and Shirouzu, Mikako
- Abstract
Voltage-dependent anion channel 1 (VDAC1), which is located in the outer mitochondrial membrane, plays important roles in various cellular processes. For example, oligomerization of VDAC1 is involved in the release of cytochrome c to the cytoplasm, leading to apoptosis. However, it is unknown how VDAC1 oligomerization occurs in the membrane. In the present study, we determined high-resolution crystal structures of oligomeric human VDAC1 (hVDAC1) prepared by using an Escherichia coli cell-free protein synthesis system, which avoided the need for denaturation and refolding of the protein. Broad-range screening using a bicelle crystallization method produced crystals in space groups C222 and P22
1 21 , which diffracted to a resolution of 3.10 and 3.15 Å , respectively. Each crystal contained two hVDAC1 protomers in the asymmetric unit. Dimer within the asymmetrical unit of the crystal in space group C222 were oriented parallel, whereas those of the crystal in space group P221 21 were oriented anti-parallel. From a model of the crystal in space group C222, which we constructed by using crystal symmetry operators, a heptameric structure with eight patterns of interaction between protomers, including hydrophobic interactions with β-strands, hydrophilic interactions with loop regions, and protein–lipid interactions, was observed. It is possible that by having multiple patterns of interaction, VDAC1 can form homo- or heterooligomers not only with other VDAC1 protomers but also with other proteins such as VDAC2, VDAC3 and apoptosis-regulating proteins in the Bcl-2 family. [ABSTRACT FROM AUTHOR]- Published
- 2017
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7. Mapping of the basic amino-acid residues responsible for tubulation and cellular protrusion by the EFC/F-BAR domain of pacsin2/Syndapin II
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Shimada, Atsushi, Takano, Kazunori, Shirouzu, Mikako, Hanawa-Suetsugu, Kyoko, Terada, Takaho, Toyooka, Kiminori, Umehara, Takashi, Yamamoto, Masaki, Yokoyama, Shigeyuki, and Suetsugu, Shiro
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GENE mapping ,AMINO acids ,CELL membranes ,X-ray crystallography ,GENE expression ,HYDROPHOBIC surfaces - Abstract
Abstract: The extended Fes-CIP4 homology (EFC)/FCH-BAR (F-BAR) domain tubulates membranes. Overexpression of the pacsin2 EFC/F-BAR domain resulted in tubular localization inside cells and deformed liposomes into tubules in vitro. We found that overexpression of the pacsin2 EFC/F-BAR domain induced cellular microspikes, with the pacsin2 EFC/F-BAR domain concentrated at the neck. The hydrophobic loops and the basic amino-acid residues on the concave surface of the pacsin2 EFC/F-BAR domain are essential for both the microspike formation and tubulation. Since the curvature of the neck of the microspike and that of the tubulation share similar geometry, the pacsin2 EFC/F-BAR domain is considered to facilitate both microspike formation and tubulation. Structured summary: MINT-7710892: EFCS pacsin2 (uniprotkb:Q9UNF0) and EFCS pacsin2 (uniprotkb:Q9UNF0) bind (MI:0407) by X-ray crystallography (MI:0114) [Copyright &y& Elsevier]
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- 2010
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8. Crystal structure of the human receptor activity-modifying protein 1 extracellular domain.
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Kusano, Seisuke, Kukimoto-Niino, Mutsuko, Akasaka, Ryogo, Toyama, Mitsutoshi, Terada, Takaho, Shirouzu, Mikako, Shindo, Takayuki, and Yokoyama, Shigeyuki
- Abstract
Receptor activity-modifying protein (RAMP) 1 forms a heterodimer with calcitonin receptor-like receptor (CRLR) and regulates its transport to the cell surface. The CRLR·RAMP1 heterodimer functions as a specific receptor for calcitonin gene-related peptide (CGRP). Here, we report the crystal structure of the human RAMP1 extracellular domain. The RAMP1 structure is a three-helix bundle that is stabilized by three disulfide bonds. The RAMP1 residues important for cell-surface expression of the CRLR·RAMP1 heterodimer are clustered to form a hydrophobic patch on the molecular surface. The hydrophobic patch is located near the tryptophan residue essential for binding of the CGRP antagonist, BIBN4096BS. These results suggest that the hydrophobic patch participates in the interaction with CRLR and the formation of the ligand-binding pocket when it forms the CRLR·RAMP1 heterodimer. [ABSTRACT FROM AUTHOR]
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- 2008
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9. Ion binding and selectivity of the rotor ring of the Na+-transporting V-ATPase.
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Murata, Takeshi, Yamato, Ichiro, Kakinuma, Yoshimi, Shirouzu, Mikako, Walker, John E., Yokoyama, Shigeyuki, and Iwata, So
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LITHIUM ions ,MEMBRANE proteins ,X-ray crystallography ,ADENOSINE triphosphate ,ION bombardment ,RADIOISOTOPES ,DISSOCIATION (Chemistry) - Abstract
The vacuole-type ATPases (V-ATPases) are proton pumps in various intracellular compartments of eukaryotic cells. Prokaryotic V-ATPase of Enterococcus hirae, closely related to the eukaryotic enzymes, provides a unique opportunity to study ion translocation by V-ATPases because it transports Na
+ ions, which are easier to detect by x-ray crystallography and radioisotope experiments. The purified rotor ring (K-ring) of the E. hirae V-ATPase binds one Na+ ion per K-monomer with high affinity, which is competitively inhibited by Li+ or H+ , suggesting that the K-ring can also bind these ions. This finding is also supported by the K-ring structure at 2.8 Å in the presence of Li+ . Association and dissociation rates of the Na+ to and from the purified K-ring were extremely slow compared with the Na+ translocation rate estimated from the enzymatic activity, strongly suggesting that interaction with the stator subunit (I-subunit) is essential for Na+ binding to /release from the K-ring. [ABSTRACT FROM AUTHOR]- Published
- 2008
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10. Crystallization and Preliminary X-Ray Analysis of a DNA Primase from Hyperthermophilic Archaeon Pyrococcus horikoshii1.
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Ito, Nobutoshi, Nureki, Osamu, Shirouzu, Mikako, Yokoyama, Shigeyuki, and Hanaoka, Fumio
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DNA primase ,DNA replication ,PYROCOCCUS horikoshii ,CRYSTALLIZATION ,ESCHERICHIA coli ,CRYSTALS - Abstract
At the initiation of chromosomal DNA replication, DNA primases synthesize short RNA primers, which are subsequently elongated by DNA polymerases. To understand the structural basis for the primer synthesis by archaeal/eukaryotic-type primases, the gene of the DNA primase from hyperthermophilic archaeon Pyrococcus horikoshii was cloned and overexpressed in Escherichia coli as a fusion protein with a hexa-histidine tag at its amino terminus. The recombinant DNA primase was purified and crystallized by the hanging-drop vapor diffusion method at 293K, with polyethylene glycol 8000 as the precipitant. The crystals belong to the PS2l space group with unit-cell parameters a = b = 77.8, c = 129.6 A, and α = β = 90°, y = 120°. Crystals of the selenomethionine derivative were obtained by means of a cross-seeding method using native crystals. The data for the native and selenomethionine-substituted crystals were collected to 1.8 and 2.2 A resolution, respectively, with synchrotron radiation at SPring-8 under flash-frozen conditions at 100K. The four wavelength MAD data provided a phase to determine the structure of the primase at 2.2 A resolution [ABSTRACT FROM AUTHOR]
- Published
- 2001
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11. Structural genomics projects in Japan.
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Yokoyama, Shigeyuki, Hirota, Hiroshi, Kigawa, Takanori, Yabuki, Takashi, Shirouzu, Mikako, Terada, Takaho, Ito, Yutaka, Matsuo, Yo, Kuroda, Yutaka, Nishimura, Yoshifumi, Kyogoku, Yoshimasa, Miki, Kunio, Masui, Ryoji, and Kuramitsu, Seiki
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GENOMES ,X-ray crystallography ,NUCLEAR magnetic resonance spectroscopy - Abstract
Two major structural genomics projects exist in Japan. The oldest, the RIKEN Structural Genomics Initiative, has two major goals: to determine bacterial, mammalian, and plant protein structures by X-ray crystallography and NMR spectroscopy and to perform functional analyses with the target proteins. The newest, the structural genomics project at the Biological Information Research Center, focuses on human membrane proteins. [ABSTRACT FROM AUTHOR]
- Published
- 2000
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12. Protein stabilization utilizing a redefined codon.
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Ohtake, Kazumasa, Yamaguchi, Atsushi, Mukai, Takahito, Kashimura, Hiroki, Hirano, Nobutaka, Haruki, Mitsuru, Kohashi, Sosuke, Yamagishi, Kenji, Murayama, Kazutaka, Tomabechi, Yuri, Itagaki, Takashi, Akasaka, Ryogo, Kawazoe, Masahito, Takemoto, Chie, Shirouzu, Mikako, Yokoyama, Shigeyuki, and Sakamoto, Kensaku
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AMINO acids ,GENETIC code ,GLUTATHIONE transferase ,TYROSINE ,X-ray crystallography ,HALOGENS - Abstract
Recent advances have fundamentally changed the ways in which synthetic amino acids are incorporated into proteins, enabling their efficient and multiple-site incorporation, in addition to the 20 canonical amino acids. This development provides opportunities for fresh approaches toward addressing fundamental problems in bioengineering. In the present study, we showed that the structural stability of proteins can be enhanced by integrating bulky halogenated amino acids at multiple selected sites. Glutathione S-transferase was thus stabilized significantly (by 5.2 and 5.6 kcal/mol) with 3-chloro- and 3-bromo-l-tyrosines, respectively, incorporated at seven selected sites. X-ray crystallographic analyses revealed that the bulky halogen moieties filled internal spaces within the molecules, and formed non-canonical stabilizing interactions with the neighboring residues. This new mechanism for protein stabilization is quite simple and applicable to a wide range of proteins, as demonstrated by the rapid stabilization of the industrially relevant azoreductase. [ABSTRACT FROM AUTHOR]
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- 2015
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13. Structure-based development of novel substrate-type G9a inhibitors as epigenetic modulators for sickle cell disease treatment.
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Nishigaya, Yosuke, Takase, Shohei, Sumiya, Tatsunobu, Sato, Tomohiro, Niwa, Hideaki, Sato, Shin, Nakata, Akiko, Matsuoka, Seiji, Maemoto, Yuki, Hashimoto, Noriaki, Namie, Ryosuke, Honma, Teruki, Umehara, Takashi, Shirouzu, Mikako, Koyama, Hiroo, Yoshida, Minoru, Ito, Akihiro, and Shirai, Fumiyuki
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SICKLE cell anemia , *SURFACE plasmon resonance , *THERAPEUTICS , *X-ray crystallography , *PROTEIN-ligand interactions , *GLOBIN genes - Abstract
[Display omitted] The discovery and development of structurally distinct lysine methyltransferase G9a inhibitors have been the subject of intense research in epigenetics. Structure-based optimization was conducted, starting with the previously reported seed compound 7a and lead to the identification of a highly potent G9a inhibitor, compound 7i (IC 50 = 0.024 μM). X-ray crystallography for the ligand–protein interaction and kinetics study, along with surface plasmon resonance (SPR) analysis, revealed that compound 7i interacts with G9a in a unique binding mode. In addition, compound 7i caused attenuation of cellular H3K9me2 levels and induction of γ-globin mRNA expression in HUDEP-2 cells in a dose-dependent manner. [ABSTRACT FROM AUTHOR]
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- 2024
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14. Phosphorylated and non-phosphorylated HCK kinase domains produced by cell-free protein expression.
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Katsura, Kazushige, Tomabechi, Yuri, Matsuda, Takayoshi, Yonemochi, Mayumi, Mikuni, Junko, Ohsawa, Noboru, Terada, Takaho, Yokoyama, Shigeyuki, Kukimoto-Niino, Mutsuko, Takemoto, Chie, and Shirouzu, Mikako
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HEMATOPOIETIC stem cells , *KINASES , *PHOSPHORYLATION , *PROTEIN expression , *DRUG development , *PHYSIOLOGY - Abstract
Since phosphorylation is involved in various physiological events, kinases and interacting factors can be potential targets for drug discovery. For the development and improvement of inhibitors from the point of view of mechanistic enzymology, a cell-free protein synthesis system would be advantageous, since it could prepare mutant proteins easily. However, especially in the case of protein kinase, product solubility remains one of the major challenges. To overcome this problem, we prepared a chaperone-supplemented extract from Escherichia coli BL21 cells harboring a plasmid encoding a set of chaperone genes, dnaK , dnaJ , and grpE . We explored cell-disruption procedures and constructed an efficient protein synthesis system. Employing this system, we produced the kinase domain of human hematopoietic cell kinase (HCK) to obtain further structural information about its molecular interaction with one of its inhibitors, previously developed by our group (RK-20449). Lower reaction temperature improved the solubility, and addition of a protein phosphatase (YpoH) facilitated the homogeneous production of the non-phosphorylated kinase domain. Crystals of the purified product were obtained and the kinase-inhibitor complex structure was solved at 1.7 Å resolution. In addition, results of kinase activity measurement, using a synthetic substrate, showed that the kinase activity was facilitated by autophosphorylation at Tyr416, as confirmed by the peptide mass mapping. [ABSTRACT FROM AUTHOR]
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- 2018
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15. Cryo-EM structure of a monomeric RC-LH1-PufX supercomplex with high-carotenoid content from Rhodobacter capsulatus.
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Bracun, Laura, Yamagata, Atsushi, Christianson, Bern M., Shirouzu, Mikako, and Liu, Lu-Ning
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PHOTOSYNTHETIC bacteria , *ELECTRON transport , *BACTERIOCHLOROPHYLLS , *CAROTENOIDS , *MONOMERS , *ELECTRON microscopes , *X-ray crystallography - Abstract
In purple photosynthetic bacteria, the photochemical reaction center (RC) and light-harvesting complex 1 (LH1) assemble to form monomeric or dimeric RC-LH1 membrane complexes, essential for bacterial photosynthesis. Here, we report a 2.59-Å resolution cryoelectron microscopy (cryo-EM) structure of the RC-LH1 supercomplex from Rhodobacter capsulatus. We show that Rba. capsulatus RC-LH1 complexes are exclusively monomers in which the RC is surrounded by a 15-subunit LH1 ring. Incorporation of a transmembrane polypeptide PufX leads to a large opening within the LH1 ring. Each LH1 subunit associates two carotenoids and two bacteriochlorophylls, which is similar to Rba. sphaeroides RC-LH1 but more than one carotenoid per LH1 in Rba. veldkampii RC-LH1 monomer. Collectively, the unique Rba. capsulatus RC-LH1-PufX represents an intermediate structure between Rba. sphaeroides and Rba. veldkampii RC-LH1-PufX. Comparison of PufX from the three Rhodobacter species indicates the important residues involved in dimerization of RC-LH1. [Display omitted] • The photosynthetic RC-LH1 core complex of Rhodobacter capsulatus forms a monomer • The LH1 ring surrounding RC contains 15 LH1 subunits and PufX, mediating an opening • Each LH1 αβ subunit contains two BChls and two carotenoids • Structural flexibility of the last LH1 subunits results in varying degrees of opening Bracun et al. report the cryo-EM structure of the reaction center-light-harvesting-1-PufX supercomplex, a key photosynthetic complex in the phototropic purple bacterium R. capsulatus. The detailed structural analysis provides insights into light harvesting, electron transport, and the structural diversity of the photosynthetic core complexes from various bacterial species. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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16. Structural Basis for the Specific Recognition of the Major Antigenic Peptide from the Japanese Cedar Pollen Allergen Cry j 1 by HLA-DP5.
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Seisuke Kusano, Kukimoto-Niino, Mutsuko, Yoko Satta, Noboru Ohsawa, Uchikubo-Kamo, Tomomi, Wakiyama, Motoaki, Mariko Ikeda, Takaho Terada, Yamamoto, Ken, Nishimura, Yasuharu, Shirouzu, Mikako, Sasazuki, Takehiko, and Yokoyama, Shigeyuki
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EPITOPES , *PEPTIDES , *CRYPTOMERIA japonica , *ALLERGIC rhinitis , *IMMUNOGLOBULIN E - Abstract
The major allergen, Cry j 1, was isolated from Japanese cedar Cryptomeria japonica (Cry j) pollen and was shown to react with immunoglobulin E antibodies in the sera from pollinosis patients. We previously reported that the frequency of HLA-DP5 was significantly higher in pollinosis patients and the immunodominant peptides from Cry j 1 bound to HLA-DP5 to activate Th2 cells. In the present study, we determined the crystal structure of the HLA-DP5 heterodimer in complex with a Cry j 1-derived nine-residue peptide, at 2.4 Å resolution. The peptide-binding groove recognizes the minimal peptide with 10 hydrogen bonds, including those between the negatively charged P1 pocket and the Lys side chain at the first position in the peptide sequence. We confirmed that HLA-DP5 exhibits the same Cry j 1-binding mode in solution, through pull-down experiments using structure-based mutations of Cry j 1. We also identified the characteristic residues of HLA-DP5 that are responsible for the distinct properties of the groove, by comparing the structure of HLA-DP5 and the previously reported structures of HLA-DP2 in complexes with pDRA of the self-antigen. The comparison revealed that the HLA-DP5·pCry j 1 complex forms several hydrogen bond/salt bridge networks between the receptor and the antigen that were not observed in the HLA-DP2·pDRA complex. Evolutionary considerations have led us to conclude that HLA-DP5 and HLA-DP2 represent two major groups of the HLA-DP family, in which the properties of the P1 and P4 pockets have evolved and acquired the present ranges of epitope peptide-binding specificities. [ABSTRACT FROM AUTHOR]
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- 2014
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17. Crystal structure of the guanylate kinase domain from discs large homolog 1 (DLG1/SAP97).
- Author
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Mori, Shinji, Tezuka, Yuta, Arakawa, Akihiko, Handa, Noriko, Shirouzu, Mikako, Akiyama, Tetsu, and Yokoyama, Shigeyuki
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CRYSTAL structure , *PROTEIN kinases , *HOMOLOGY (Biochemistry) , *BINDING sites , *PEPTIDES , *PHOSPHORYLATION - Abstract
Highlights: [•] The crystal structure of the human DLG1 GK domain was solved at 2.2Å resolution. [•] The peptide-binding site is bound to the C-terminal tail of another DLG1 molecule. [•] The main-chain direction of the tail is opposite to that of LGN bound to DLG1. [•] The side-chain interactions of DLG1 with the C-terminal tail resemble those with LGN. [ABSTRACT FROM AUTHOR]
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- 2013
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18. Structure of Selenophosphate Synthetase Essential for Selenium Incorporation into Proteins and RNAs
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Itoh, Yuzuru, Sekine, Shun-ichi, Matsumoto, Eiko, Akasaka, Ryogo, Takemoto, Chie, Shirouzu, Mikako, and Yokoyama, Shigeyuki
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LIGASES , *SELENIDES , *GENETIC mutation , *ADENOSINE triphosphate , *SELENOPROTEINS , *POLYETHYLENE glycol , *X-ray crystallography , *BINDING sites - Abstract
Abstract: Selenophosphate synthetase (SPS) catalyzes the activation of selenide with adenosine 5′-triphosphate (ATP) to generate selenophosphate, the essential reactive selenium donor for the formation of selenocysteine (Sec) and 2-selenouridine residues in proteins and RNAs, respectively. Many SPS are themselves Sec-containing proteins, in which Sec replaces Cys in the catalytically essential position (Sec/Cys). We solved the crystal structures of Aquifex aeolicus SPS and its complex with adenosine 5′-(α,β-methylene) triphosphate (AMPCPP). The ATP-binding site is formed at the subunit interface of the homodimer. Four Asp residues coordinate four metal ions to bind the phosphate groups of AMPCPP. In the free SPS structure, the two loop regions in the ATP-binding site are not ordered, and no enzyme-associated metal is observed. This suggests that ATP binding, metal binding, and the formation of their binding sites are interdependent. To identify the amino-acid residues that contribute to SPS activity, we prepared six mutants of SPS and examined their selenide-dependent ATP consumption. Mutational analyses revealed that Sec/Cys13 and Lys16 are essential. In SPS·AMPCPP, the N-terminal loop, including the two residues, assumes different conformations (“open” and “closed”) between the two subunits. The AMPCPP γ-phosphate group is solvent-accessible, suggesting that a putative nucleophile could attack the ATP γ-phosphate group to generate selenophosphate and adenosine 5′-diphosphate (ADP). Selenide attached to Sec/Cys13 as –Se–Se−/–S–Se− could serve as the nucleophile in the “closed” conformation. A water molecule, fixed close to the β-phosphate group, could function as the nucleophile in subsequent ADP hydrolysis to orthophosphate and adenosine 5′-monophosphate. [Copyright &y& Elsevier]
- Published
- 2009
- Full Text
- View/download PDF
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