7NUY
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1KGM
| SOLUTION STRUCTURE OF THE SMALL SERINE PROTEASE INHIBITOR SGCI | 分子名称: | SERINE PROTEASE INHIBITOR I | 著者 | Gaspari, Z, Patthy, A, Graf, L, Perczel, A. | 登録日 | 2001-11-28 | 公開日 | 2001-12-12 | 最終更新日 | 2022-02-23 | 実験手法 | SOLUTION NMR | 主引用文献 | Comparative structure analysis of proteinase inhibitors from the desert locust, Schistocerca gregaria. Eur.J.Biochem., 269, 2002
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3H13
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1MIQ
| Crystal structure of proplasmepsin from the human malarial pathogen Plasmodium vivax | 分子名称: | plasmepsin | 著者 | Bernstein, N.K, Cherney, M.M, Yowell, C.A, Dame, J.B, James, M.N. | 登録日 | 2002-08-23 | 公開日 | 2002-09-18 | 最終更新日 | 2018-01-31 | 実験手法 | X-RAY DIFFRACTION (2.5 Å) | 主引用文献 | Structural insights into the activation of P. vivax plasmepsin. J.Mol.Biol., 329, 2003
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1M22
| X-ray structure of native peptide amidase from Stenotrophomonas maltophilia at 1.4 A | 分子名称: | 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, peptide amidase | 著者 | Labahn, J, Neumann, S, Buldt, G, Kula, M.-R, Granzin, J. | 登録日 | 2002-06-21 | 公開日 | 2002-10-16 | 最終更新日 | 2024-03-13 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | An alternative mechanism for amidase signature enzymes J.MOL.BIOL., 322, 2002
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1WIP
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6I9A
| Porphyromonas gingivalis gingipain K (Kgp) in complex with inhibitor KYT-36 | 分子名称: | (2S,3S)-1,4-DIMERCAPTOBUTANE-2,3-DIOL, 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, CALCIUM ION, ... | 著者 | Gomis-Ruth, F.X, Guevara, T, Rofdriguez-Banqueri, A. | 登録日 | 2018-11-22 | 公開日 | 2019-03-13 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (1.2 Å) | 主引用文献 | Structural determinants of inhibition of Porphyromonas gingivalis gingipain K by KYT-36, a potent, selective, and bioavailable peptidase inhibitor. Sci Rep, 9, 2019
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1NUG
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7POO
| Crystal structure of profragilysin-3 (proBFT-3) from Bacteroides fragilis in complex with foliosidine in P212121. | 分子名称: | ACETATE ION, BFT-3, PROLINE, ... | 著者 | Eckhard, U, Guevara, T, Gomis-Ruth, F.X. | 登録日 | 2021-09-09 | 公開日 | 2022-09-14 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (2.7 Å) | 主引用文献 | Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilis. Protein Sci., 31, 2022
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7POQ
| Crystal structure of profragilysin-3 (proBFT-3) from Bacteroides fragilis in complex with foliosidine in P41212. | 分子名称: | 1,2-ETHANEDIOL, BFT-3, CHLORIDE ION, ... | 著者 | Eckhard, U, Guevara, T, Gomis-Ruth, F.X. | 登録日 | 2021-09-09 | 公開日 | 2022-09-14 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilis. Protein Sci., 31, 2022
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7PND
| Crystal structure of profragilysin-3 (proBFT-3) from Bacteroides fragilis at 1.85 A resolution. | 分子名称: | BFT-3, DIMETHYL SULFOXIDE, FORMIC ACID, ... | 著者 | Eckhard, U, Guevara, T, Gomis-Ruth, F.X. | 登録日 | 2021-09-06 | 公開日 | 2022-09-14 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.85 Å) | 主引用文献 | Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilis. Protein Sci., 31, 2022
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7POL
| Crystal structure of profragilysin-3 (proBFT-3) from Bacteroides fragilis in complex with flumequine | 分子名称: | (12~{R})-7-fluoranyl-12-methyl-4-oxidanylidene-1-azatricyclo[7.3.1.0^{5,13}]trideca-2,5(13),6,8-tetraene-3-carboxylic acid, BFT-3, CHLORIDE ION, ... | 著者 | Eckhard, U, Guevara, T, Gomis-Ruth, F.X. | 登録日 | 2021-09-09 | 公開日 | 2022-09-14 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilis. Protein Sci., 31, 2022
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7POU
| Crystal structure of profragilysin-3 (proBFT-3) from Bacteroides fragilis in complex with hesperetin. | 分子名称: | (2S)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one, BFT-3, DIMETHYL SULFOXIDE, ... | 著者 | Eckhard, U, Guevara, T, Gomis-Ruth, F.X. | 登録日 | 2021-09-09 | 公開日 | 2022-09-14 | 最終更新日 | 2024-01-31 | 実験手法 | X-RAY DIFFRACTION (2.03 Å) | 主引用文献 | Repositioning small molecule drugs as allosteric inhibitors of the BFT-3 toxin from enterotoxigenic Bacteroides fragilis. Protein Sci., 31, 2022
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1WIQ
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1NUD
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4Q7O
| The crystal structure of an immunity protein NMB0503 from Neisseria meningitidis MC58 | 分子名称: | BROMIDE ION, FORMIC ACID, Immunity protein | 著者 | Tan, K, Stols, L, Eschenfeldt, W, Babnigg, G, Low, D.A, Hayes, C.S, Goulding, C.W, Joachimiak, A, Midwest Center for Structural Genomics (MCSG), Structure-Function Analysis of Polymorphic CDI Toxin-Immunity Protein Complexes (UC4CDI) | 登録日 | 2014-04-25 | 公開日 | 2014-05-14 | 最終更新日 | 2024-02-28 | 実験手法 | X-RAY DIFFRACTION (1.45 Å) | 主引用文献 | The structure of a contact-dependent growth-inhibition (CDI) immunity protein from Neisseria meningitidis MC58. Acta Crystallogr F Struct Biol Commun, 71, 2015
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4HXD
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1NUF
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5Y9L
| Human kallikrein 7 in complex with 1,3,6-trisubstituted 1,4-diazepane-7-one | 分子名称: | 3-[2-[(3Z,6R)-6-[(5-chloranyl-2-methoxy-phenyl)methyl]-3-(dimethylhydrazinylidene)-7-oxidanylidene-1,4-diazepan-1-yl]ethanoylamino]benzoic acid, CHLORIDE ION, Kallikrein-7 | 著者 | Sugawara, H. | 登録日 | 2017-08-25 | 公開日 | 2017-11-29 | 最終更新日 | 2023-11-22 | 実験手法 | X-RAY DIFFRACTION (2.15 Å) | 主引用文献 | Discovery and structure-activity relationship study of 1,3,6-trisubstituted 1,4-diazepane-7-ones as novel human kallikrein 7 inhibitors Bioorg. Med. Chem. Lett., 27, 2017
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5YCZ
| Crystal structure of Alocasin, protease inhibitor from Giant Taro (Arum macrorrhizon) | 分子名称: | Trypsin/chymotrypsin inhibitor | 著者 | Vajravijayan, S, Pletnev, S, Nandhagopal, N, Gunasekaran, K. | 登録日 | 2017-09-08 | 公開日 | 2018-06-13 | 最終更新日 | 2018-11-28 | 実験手法 | X-RAY DIFFRACTION (2.502 Å) | 主引用文献 | Crystal structure of a novel Kunitz type inhibitor, alocasin with anti-Aedes aegypti activity targeting midgut proteases. Pest Manag. Sci., 74, 2018
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6GWV
| Molybdenum storage protein without polymolybdate clusters and ATP | 分子名称: | ADENOSINE-5'-TRIPHOSPHATE, CHLORIDE ION, Molybdenum storage protein subunit alpha, ... | 著者 | Ermler, U, Poppe, J, Bruenle, S. | 登録日 | 2018-06-26 | 公開日 | 2018-11-07 | 最終更新日 | 2024-05-15 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | The Molybdenum Storage Protein: A soluble ATP hydrolysis-dependent molybdate pump. FEBS J., 285, 2018
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5YJK
| Human kallikrein 7 in complex with 1,4-diazepane-7-one 1-acetamide derivative | 分子名称: | (R)-2-(6-(5-chloro-2-methoxybenzyl)-3-(2,2-dimethylhydrazono)-7-oxo-1,4-diazepan-1-yl)-N-(3-(methylsulfonyl)phenyl)acetamide, CHLORIDE ION, Kallikrein-7 | 著者 | Sugawara, H. | 登録日 | 2017-10-11 | 公開日 | 2017-12-06 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Discovery and structure-activity relationship study of 1,3,6-trisubstituted 1,4-diazepane-7-ones as novel human kallikrein 7 inhibitors Bioorg. Med. Chem. Lett., 27, 2017
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5YPT
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4GWN
| Crystal structure of human mature meprin beta | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... | 著者 | Arolas, J.L, Broder, C, Jefferson, T, Guevara, T, Sterchi, E.E, Bode, W, Stocker, W, Becker-Pauly, C, Gomis-Ruth, F.X. | 登録日 | 2012-09-03 | 公開日 | 2012-09-19 | 最終更新日 | 2023-11-08 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | Structural basis for the sheddase function of human meprin beta metalloproteinase at the plasma membrane Proc.Natl.Acad.Sci.USA, 109, 2012
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5WOT
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