Author results

1IS7
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CRYSTAL STRUCTURE OF RAT GTPCHI/GFRP STIMULATORY COMPLEX
Descriptor:GTP Cyclohydrolase I, GTP Cyclohydrolase I Feedback Regulatory Protein, POTASSIUM ION, ...
Authors:Maita, N., Okada, K., Hatakeyama, K., Hakoshima, T.
Deposit date:2001-11-18
Release date:2002-02-20
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Crystal structure of the stimulatory complex of GTP cyclohydrolase I and its feedback regulatory protein GFRP.
Proc.Natl.Acad.Sci.USA, 99, 2002
1IS8
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CRYSTAL STRUCTURE OF RAT GTPCHI/GFRP STIMULATORY COMPLEX PLUS ZN
Descriptor:GTP Cyclohydrolase I, GTP Cyclohydrolase I Feedback Regulatory Protein, ZINC ION, ...
Authors:Maita, N., Okada, K., Hatakeyama, K., Hakoshima, T.
Deposit date:2001-11-18
Release date:2002-02-20
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Crystal structure of the stimulatory complex of GTP cyclohydrolase I and its feedback regulatory protein GFRP.
Proc.Natl.Acad.Sci.USA, 99, 2002
1UEX
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CRYSTAL STRUCTURE OF VON WILLEBRAND FACTOR A1 DOMAIN COMPLEXED WITH SNAKE VENOM BITISCETIN
Descriptor:bitiscetin alpha chain, bitiscetin beta chain, von Willebrand Factor
Authors:Maita, N., Nishio, K., Nishimoto, E., Matsui, T., Shikamoto, Y., Morita, T., Sadler, J.E., Mizuno, H.
Deposit date:2003-05-22
Release date:2003-09-30
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.85 Å)
Cite:Crystal structure of von Willebrand factor A1 domain complexed with snake venom, bitiscetin. Insight into glycoprotein Ibalpha binding mechanism induced by snake venom proteins.
J.Biol.Chem., 278, 2003
1WDU
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ENDONUCLEASE DOMAIN OF TRAS1, A TELOMERE-SPECIFIC NON-LTR RETROTRANSPOSON
Descriptor:TRAS1 ORF2p, PHOSPHATE ION, CHLORIDE ION
Authors:Maita, N., Anzai, T., Aoyagi, H., Mizuno, H., Fujiwara, H.
Deposit date:2004-05-17
Release date:2004-08-10
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Crystal structure of the endonuclease domain encoded by the telomere-specific long interspersed nuclear element, TRAS1
J.Biol.Chem., 279, 2004
1WPL
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CRYSTAL STRUCTURE OF THE INHIBITORY FORM OF RAT GTP CYCLOHYDROLASE I/GFRP COMPLEX
Descriptor:GTP cyclohydrolase I, GTP cyclohydrolase I feedback regulatory protein, ZINC ION, ...
Authors:Maita, N., Hatakeyama, K., Okada, K., Hakoshima, T.
Deposit date:2004-09-08
Release date:2004-09-28
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Structural basis of biopterin-induced inhibition of GTP cyclohydrolase I by GFRP, its feedback regulatory protein
J.Biol.Chem., 279, 2004
2EI9
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CRYSTAL STRUCTURE OF R1BM ENDONUCLEASE DOMAIN
Descriptor:Non-LTR retrotransposon R1Bmks ORF2 protein, ACETIC ACID
Authors:Maita, N., Aoyagi, H., Osanai, M., Shirakawa, M., Fujiwara, H.
Deposit date:2007-03-12
Release date:2007-07-17
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2 Å)
Cite:Characterization of the sequence specificity of the R1Bm endonuclease domain by structural and biochemical studies.
Nucleic Acids Res., 35, 2007
3AAG
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CRYSTAL STRUCTURE OF C. JEJUNI PGLB C-TERMINAL DOMAIN
Descriptor:General glycosylation pathway protein, CALCIUM ION
Authors:Maita, N., Kohda, D.
Deposit date:2009-11-16
Release date:2009-12-08
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.8 Å)
Cite:Comparative structural biology of Eubacterial and Archaeal oligosaccharyltransferases.
J.Biol.Chem., 285, 2010
3W81
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HUMAN ALPHA-L-IDURONIDASE
Descriptor:Alpha-L-iduronidase, N-ACETYL-D-GLUCOSAMINE, BETA-D-MANNOSE, ...
Authors:Maita, N., Tsukimura, T., Taniguchi, T., Saito, S., Ohno, K., Taniguchi, H., Sakuraba, H.
Deposit date:2013-03-11
Release date:2013-08-21
Last modified:2013-10-16
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Human alpha-L-iduronidase uses its own N-glycan as a substrate-binding and catalytic module
Proc.Natl.Acad.Sci.USA, 110, 2013
3W82
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HUMAN ALPHA-L-IDURONIDASE IN COMPLEX WITH IDURONIC ACID
Descriptor:Alpha-L-iduronidase, N-ACETYL-D-GLUCOSAMINE, BETA-D-MANNOSE, ...
Authors:Maita, N., Tsukimura, T., Taniguchi, T., Saito, S., Ohno, K., Taniguchi, H., Sakuraba, H.
Deposit date:2013-03-11
Release date:2013-08-21
Last modified:2013-10-16
Method:X-RAY DIFFRACTION (2.76 Å)
Cite:Human alpha-L-iduronidase uses its own N-glycan as a substrate-binding and catalytic module
Proc.Natl.Acad.Sci.USA, 110, 2013
6A42
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R1EN(5-223)-UBIQUITIN FUSION
Descriptor:RNA-directed DNA polymerase homolog (R1),Polyubiquitin-C, ACETIC ACID
Authors:Maita, N.
Deposit date:2018-06-19
Release date:2018-10-24
Last modified:2018-11-07
Method:X-RAY DIFFRACTION (1.7 Å)
Cite:Crystal Structure Determination of Ubiquitin by Fusion to a Protein That Forms a Highly Porous Crystal Lattice
J. Am. Chem. Soc., 140, 2018
6A43
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R1EN(5-225)-UBIQUITIN FUSION
Descriptor:RNA-directed DNA polymerase homolog (R1),Polyubiquitin-C, ACETIC ACID
Authors:Maita, N.
Deposit date:2018-06-19
Release date:2018-10-24
Last modified:2018-11-07
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Crystal Structure Determination of Ubiquitin by Fusion to a Protein That Forms a Highly Porous Crystal Lattice
J. Am. Chem. Soc., 140, 2018
6A44
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R1EN(5-227)-UBIQUITIN FUSION
Descriptor:RNA-directed DNA polymerase homolog (R1),Polyubiquitin-C, ACETIC ACID
Authors:Maita, N.
Deposit date:2018-06-19
Release date:2018-10-24
Last modified:2018-11-07
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Crystal Structure Determination of Ubiquitin by Fusion to a Protein That Forms a Highly Porous Crystal Lattice
J. Am. Chem. Soc., 140, 2018
2ZAG
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CRYSTAL STRUCTURE OF THE SEMET-SUBSTITUTED SOLUBLE DOMAIN OF STT3 FROM P. FURIOSUS
Descriptor:Oligosaccharyl transferase stt3 subunit related protein, CALCIUM ION, CHLORIDE ION
Authors:Maita, N.
Deposit date:2007-10-05
Release date:2007-12-11
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (3 Å)
Cite:Structure-guided identification of a new catalytic motif of oligosaccharyltransferase
Embo J., 27, 2008
2ZAI
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CRYSTAL STRUCTURE OF THE SOLUBLE DOMAIN OF STT3 FROM P. FURIOSUS
Descriptor:Oligosaccharyl transferase stt3 subunit related protein, CALCIUM ION, CHLORIDE ION
Authors:Maita, N.
Deposit date:2007-10-05
Release date:2007-12-11
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Structure-guided identification of a new catalytic motif of oligosaccharyltransferase
Embo J., 27, 2008
4Z2G
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 26
Descriptor:Chitinase B, (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-3-ethyl-2,10-dihydroxy-2,6,8,10,12,15,15,17-octamethyl-5-oxo-9-(prop-2-yn-1-yloxy)-4,14,16-trioxabicyclo[11.3.1]heptadec-7-yl {4-[N'-(methylcarbamoyl)carbamimidamido]butyl}carbamate
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
4Z2H
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 29
Descriptor:Chitinase B, (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-3-ethyl-2,10-dihydroxy-2,6,8,10,12,15,15,17-octamethyl-5-oxo-9-(prop-2-yn-1-yloxy)-4,14,16-trioxabicyclo[11.3.1]heptadec-7-yl {2-[N'-(methylcarbamoyl)carbamimidamido]ethyl}carbamate, GLYCEROL, ...
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2.35 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
4Z2I
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 30
Descriptor:Chitinase B, (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-3-ethyl-2,10-dihydroxy-2,6,8,10,12,15,15,17-octamethyl-5-oxo-9-(prop-2-yn-1-yloxy)-4,14,16-trioxabicyclo[11.3.1]heptadec-7-yl {3-[N'-(methylcarbamoyl)carbamimidamido]propyl}carbamate, SODIUM ION, ...
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
4Z2J
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 31
Descriptor:Chitinase B, (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-3-ethyl-2,10-dihydroxy-2,6,8,10,12,15,15,17-octamethyl-5-oxo-9-(prop-2-yn-1-yloxy)-4,14,16-trioxabicyclo[11.3.1]heptadec-7-yl {5-[N'-(methylcarbamoyl)carbamimidamido]pentyl}carbamate, GLYCEROL, ...
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
4Z2K
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 32
Descriptor:Chitinase B, (1R,2R,3R,6R,7S,8S,9R,10R,12R,13S,17S)-3-ethyl-2,10-dihydroxy-2,6,8,10,12,15,15,17-octamethyl-5-oxo-9-(prop-2-yn-1-yloxy)-4,14,16-trioxabicyclo[11.3.1]heptadec-7-yl {7-[N'-(methylcarbamoyl)carbamimidamido]heptyl}carbamate, GLYCEROL
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
4Z2L
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SERRATIA MARCESCENS CHITINASE B COMPLEXED WITH MACROLIDE INHIBITOR 33
Descriptor:Chitinase B, (3R,4S,5S,6R,7R,9R,10S,11S,12R,13S,14R)-14-ethyl-7,10,12,13-tetrahydroxy-3,5,7,9,11,13-hexamethyl-2-oxo-6-(prop-2-yn-1-yloxy)oxacyclotetradecan-4-yl {3-[N'-(methylcarbamoyl)carbamimidamido]propyl}carbamate, GLYCEROL, ...
Authors:Maita, N., Sugawara, A., Sunazuka, T.
Deposit date:2015-03-30
Release date:2015-07-01
Last modified:2015-07-08
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase
J.Med.Chem., 58, 2015
1WLF
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STRUCTURE OF THE N-TERMINAL DOMAIN OF PEX1 AAA-ATPASE: CHARACTERIZATION OF A PUTATIVE ADAPTOR-BINDING DOMAIN
Descriptor:Peroxisome biogenesis factor 1, SULFATE ION
Authors:Shiozawa, K., Maita, N., Tomii, K., Seto, A., Goda, N., Tochio, H., Akiyama, Y., Shimizu, T., Shirakawa, M., Hiroaki, H.
Deposit date:2004-06-25
Release date:2004-09-07
Last modified:2017-10-11
Method:X-RAY DIFFRACTION (2.05 Å)
Cite:Structure of the N-terminal Domain of PEX1 AAA-ATPase: CHARACTERIZATION OF A PUTATIVE ADAPTOR-BINDING DOMAIN
J.Biol.Chem., 279, 2004
5ZJ9
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HUMAN D-AMINO ACID OXIDASE COMPLEXED WITH 5-CHLOROTHIOPHENE-3-CARBOXYLIC ACID
Descriptor:D-amino-acid oxidase, FLAVIN-ADENINE DINUCLEOTIDE, 5-chloro thiophene-3-carboxylic acid
Authors:Kato, Y., Hin, N., Maita, N., Thomas, A.G., Kurosawa, S., Rojas, C., Yorita, K., Slusher, B.S., Fukui, K., Tsukamoto, T.
Deposit date:2018-03-19
Release date:2018-10-10
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Structural basis for potent inhibition of d-amino acid oxidase by thiophene carboxylic acids
Eur J Med Chem, 159, 2018
5ZJA
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HUMAN D-AMINO ACID OXIDASE COMPLEXED WITH 5-CHLOROTHIOPHENE-2-CARBOXYLIC ACID
Descriptor:D-amino-acid oxidase, FLAVIN-ADENINE DINUCLEOTIDE, 5-chloro thiophene-2-carboxylic acid
Authors:Kato, Y., Hin, N., Maita, N., Thomas, A.G., Kurosawa, S., Rojas, C., Yorita, K., Slusher, B.S., Fukui, K., Tsukamoto, T.
Deposit date:2018-03-19
Release date:2018-10-10
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Structural basis for potent inhibition of d-amino acid oxidase by thiophene carboxylic acids
Eur J Med Chem, 159, 2018
1ISN
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CRYSTAL STRUCTURE OF MERLIN FERM DOMAIN
Descriptor:merlin
Authors:Shimizu, T., Seto, A., Maita, N., Hamada, K., Tsukita, S., Tsukita, S., Hakoshima, T.
Deposit date:2001-12-13
Release date:2002-04-03
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.9 Å)
Cite:Structural basis for neurofibromatosis type 2. Crystal structure of the merlin FERM domain.
J.Biol.Chem., 277, 2002
1WYW
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CRYSTAL STRUCTURE OF SUMO1-CONJUGATED THYMINE DNA GLYCOSYLASE
Descriptor:G/T mismatch-specific thymine DNA glycosylase, Ubiquitin-like protein SMT3C, CHLORIDE ION, ...
Authors:Baba, D., Maita, N., Jee, J.G., Uchimura, Y., Saitoh, H., Sugasawa, K., Hanaoka, F., Tochio, H., Hiroaki, H., Shirakawa, M.
Deposit date:2005-02-17
Release date:2005-06-21
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Crystal structure of thymine DNA glycosylase conjugated to SUMO-1.
Nature, 435, 2005
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