8SOT
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5GPH
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5EZ1
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6BHF
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8HM4
| Crystal structure of PPIase | 分子名称: | Peptidylprolyl isomerase | 著者 | Xu, J.H, Chen, Z, Gao, X. | 登録日 | 2022-12-02 | 公開日 | 2023-11-29 | 最終更新日 | 2024-01-24 | 実験手法 | X-RAY DIFFRACTION (3.79 Å) | 主引用文献 | Bacteroides fragilis ubiquitin homologue drives intraspecies bacterial competition in the gut microbiome. Nat Microbiol, 9, 2024
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6DUN
| Crystal Structure Analysis of PIN1 | 分子名称: | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1, TRIHYDROXYARSENITE(III) | 著者 | Seo, H.-S, Dhe-Paganon, S. | 登録日 | 2018-06-21 | 公開日 | 2019-03-06 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.59 Å) | 主引用文献 | Arsenic targets Pin1 and cooperates with retinoic acid to inhibit cancer-driving pathways and tumor-initiating cells. Nat Commun, 9, 2018
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1J6Y
| Solution structure of Pin1At from Arabidopsis thaliana | 分子名称: | peptidyl-prolyl cis-trans isomerase | 著者 | Landrieu, I, Wieruszeski, J.M, Wintjens, R, Inze, D, Lippens, G. | 登録日 | 2001-05-15 | 公開日 | 2002-08-07 | 最終更新日 | 2022-02-23 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution Structure of the
Single-domain Prolyl Cis/Trans
Isomerase PIN1At from Arabidopsis thaliana J.Mol.Biol., 320, 2002
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5TVL
| Crystal structure of foldase protein PrsA from Streptococcus pneumoniae str. Canada MDR_19A | 分子名称: | CHLORIDE ION, Foldase protein PrsA, GLYCEROL, ... | 著者 | Borek, D, Yim, V, Kudritska, M, Wawrzak, Z, Stogios, P.J, Otwinowski, Z, Savchenko, A, Anderson, W, Center for Structural Genomics of Infectious Diseases (CSGID) | 登録日 | 2016-11-09 | 公開日 | 2016-11-23 | 最終更新日 | 2024-03-06 | 実験手法 | X-RAY DIFFRACTION (2.55 Å) | 主引用文献 | Crystal structure of foldase protein PrsA from Streptococcus pneumoniae str. Canada MDR_19A To Be Published
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6VJ4
| 1.70 Angstrom Resolution Crystal Structure of Peptidylprolyl Isomerase (PrsA) from Bacillus anthracis | 分子名称: | Peptidylprolyl isomerase PrsA | 著者 | Minasov, G, Shuvalova, L, Kiryukhina, O, Wiersum, G, Endres, M, Satchell, K.J.F, Center for Structural Genomics of Infectious Diseases (CSGID) | 登録日 | 2020-01-14 | 公開日 | 2020-02-05 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | 1.70 Angstrom Resolution Crystal Structure of Peptidylprolyl Isomerase (PrsA) from Bacillus anthracis To Be Published
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6GMP
| CRYSTAL STRUCTURE OF THE PPIASE DOMAIN OF TBPAR42 | 分子名称: | PARVULIN 42 | 著者 | Hoenig, D, Rute, A, Hofmann, E, Bayer, P, Gasper, R. | 登録日 | 2018-05-28 | 公開日 | 2019-03-20 | 最終更新日 | 2019-07-17 | 実験手法 | X-RAY DIFFRACTION (1.35 Å) | 主引用文献 | Structural Analysis of the 42 kDa Parvulin ofTrypanosoma brucei. Biomolecules, 9, 2019
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1NMW
| Solution structure of the PPIase domain of human Pin1 | 分子名称: | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1, SULFATE ION | 著者 | Bayer, E, Goettsch, S, Mueller, J.W, Griewel, B, Guiberman, E, Mayr, L, Bayer, P. | 登録日 | 2003-01-12 | 公開日 | 2003-07-15 | 最終更新日 | 2011-07-13 | 実験手法 | SOLUTION NMR | 主引用文献 | Structural Analysis of the Mitotic Regulator hPin1 in Solution: INSIGHTS INTO DOMAIN ARCHITECTURE AND SUBSTRATE BINDING. J.Biol.Chem., 278, 2003
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2JZV
| Solution structure of S. aureus PrsA-PPIase | 分子名称: | Foldase protein prsA | 著者 | Seppala, R, Tossavainen, H, Heikkinen, S, Koskela, H, Kontinen, V, Permi, P. | 登録日 | 2008-01-21 | 公開日 | 2009-01-20 | 最終更新日 | 2022-03-16 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structure of the parvulin-type PPIase domain of Staphylococcus aureus PrsA - Implications for the catalytic mechanism of parvulins. Bmc Struct.Biol., 9, 2009
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2LJ4
| Solution structure of the TbPIN1 | 分子名称: | Peptidyl-prolyl cis-trans isomerase/rotamase, putative | 著者 | Sun, L, Lin, D, Zhao, Y. | 登録日 | 2011-09-06 | 公開日 | 2012-08-22 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | Solution structural analysis of the single-domain parvulin TbPin1. Plos One, 7, 2012
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4TNS
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4TYO
| PPIase in complex with a non-phosphate small molecule inhibitor. | 分子名称: | 3-(6-fluoro-1H-benzimidazol-2-yl)-N-(naphthalen-2-ylcarbonyl)-D-alanine, GLYCEROL, Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | 著者 | Greasley, S.E, Ferre, R.A. | 登録日 | 2014-07-08 | 公開日 | 2014-08-20 | 最終更新日 | 2023-12-27 | 実験手法 | X-RAY DIFFRACTION (1.75 Å) | 主引用文献 | Structure-based design of novel human Pin1 inhibitors (III): Optimizing affinity beyond the phosphate recognition pocket. Bioorg.Med.Chem.Lett., 24, 2014
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2N87
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2PV2
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2PV1
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2RUC
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2RUQ
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2RUD
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2RUR
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3GPK
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3I6C
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3IKD
| Structure-Based Design of Novel PIN1 Inhibitors (I) | 分子名称: | (2R)-2-[(1-benzothiophen-2-ylcarbonyl)amino]-3-phenylpropyl phosphate, Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | 著者 | Matthews, D, Greasley, S, Ferre, R, Parge, H. | 登録日 | 2009-08-05 | 公開日 | 2009-09-22 | 最終更新日 | 2024-02-21 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structure-based design of novel human Pin1 inhibitors (I). Bioorg.Med.Chem.Lett., 19, 2009
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