1MQB
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![BU of 1mqb by Molmil](/molmil-images/mine/1mqb) | Crystal Structure of Ephrin A2 (ephA2) Receptor Protein Kinase | 分子名称: | Ephrin type-A receptor 2, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER | 著者 | Nowakowski, J, Cronin, C.N, McRee, D.E, Knuth, M.W, Nelson, C, Pavletich, N, Rogers, J, Sang, B.C, Scheibe, D.N, Swanson, R.V, Thompson, D.A. | 登録日 | 2002-09-16 | 公開日 | 2003-09-16 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Structures of the Cancer Related Aurora-A, FAK and EphA2 Protein Kinases from Nanovolume Crystallography Structure, 10, 2003
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1MK1
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![BU of 1mk1 by Molmil](/molmil-images/mine/1mk1) | Structure of the MT-ADPRase in complex with ADPR, a Nudix enzyme | 分子名称: | ADENOSINE-5-DIPHOSPHORIBOSE, ADPR pyrophosphatase | 著者 | Kang, L.-W, Gabelli, S.B, Bianchet, M.A, Cunningham, J.E, O'Handley, S.F, Amzel, L.M. | 登録日 | 2002-08-28 | 公開日 | 2003-08-05 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Structure and mechanism of MT-ADPRase, a Nudix hydrolase from Mycobacterium tuberculosis Structure, 11, 2003
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7QPM
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![BU of 7qpm by Molmil](/molmil-images/mine/7qpm) | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate | 分子名称: | 5,7-dimethyl-2-[(1-methyl-4-phenyl-imidazol-2-yl)sulfanylmethyl]imidazo[1,2-a]pyrimidine, MAGNESIUM ION, ZINC ION, ... | 著者 | Leonard, P.M, Langgard, M. | 登録日 | 2022-01-05 | 公開日 | 2023-04-19 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.4 Å) | 主引用文献 | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate To Be Published
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1MIO
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![BU of 1mio by Molmil](/molmil-images/mine/1mio) | X-RAY CRYSTAL STRUCTURE OF THE NITROGENASE MOLYBDENUM-IRON PROTEIN FROM CLOSTRIDIUM PASTEURIANUM AT 3.0 ANGSTROMS RESOLUTION | 分子名称: | 3-HYDROXY-3-CARBOXY-ADIPIC ACID, CALCIUM ION, FE-MO-S CLUSTER, ... | 著者 | Kim, J, Woo, D, Rees, D.C. | 登録日 | 1993-03-24 | 公開日 | 1993-10-31 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (3 Å) | 主引用文献 | X-ray crystal structure of the nitrogenase molybdenum-iron protein from Clostridium pasteurianum at 3.0-A resolution. Biochemistry, 32, 1993
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5CWG
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7QOL
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![BU of 7qol by Molmil](/molmil-images/mine/7qol) | Tail assembly of the phicrAss001 virion with C6 symmetry imposed | 分子名称: | Cargo protein 1 gp45, MAGNESIUM ION, Muzzle bound helix, ... | 著者 | Bayfield, O.W, Shkoporov, A.N, Yutin, N, Khokhlova, E.V, Smith, J.L.R, Hawkins, D.E.D.P, Koonin, E.V, Hill, C, Antson, A.A. | 登録日 | 2021-12-24 | 公開日 | 2023-03-29 | 最終更新日 | 2023-05-24 | 実験手法 | ELECTRON MICROSCOPY (3.33 Å) | 主引用文献 | Structural atlas of a human gut crassvirus. Nature, 617, 2023
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5VFU
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![BU of 5vfu by Molmil](/molmil-images/mine/5vfu) | Nucleotide-driven Triple-state Remodeling of the AAA-ATPase Channel in the Activated Human 26S Proteasome | 分子名称: | 26S protease regulatory subunit 10B, 26S protease regulatory subunit 4, 26S protease regulatory subunit 6A, ... | 著者 | Zhu, Y, Wang, W.L, Yu, D, Ouyang, Q, Lu, Y, Mao, Y. | 登録日 | 2017-04-09 | 公開日 | 2018-07-18 | 最終更新日 | 2021-03-24 | 実験手法 | ELECTRON MICROSCOPY (5.8 Å) | 主引用文献 | Structural mechanism for nucleotide-driven remodeling of the AAA-ATPase unfoldase in the activated human 26S proteasome. Nat Commun, 9, 2018
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7QPV
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![BU of 7qpv by Molmil](/molmil-images/mine/7qpv) | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate | 分子名称: | 8-methyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyridine, MAGNESIUM ION, ZINC ION, ... | 著者 | Leonard, P.M, Langgard, M. | 登録日 | 2022-01-05 | 公開日 | 2023-04-19 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.3 Å) | 主引用文献 | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate To Be Published
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7QPF
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![BU of 7qpf by Molmil](/molmil-images/mine/7qpf) | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate | 分子名称: | 2-(1~{H}-benzimidazol-2-ylsulfanylmethyl)-3-bromanyl-5,7-dimethyl-imidazo[1,2-a]pyrimidine, MAGNESIUM ION, ZINC ION, ... | 著者 | Leonard, P.M, Langgard, M. | 登録日 | 2022-01-04 | 公開日 | 2023-04-19 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (1.7 Å) | 主引用文献 | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate To Be Published
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1MPB
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7QPQ
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![BU of 7qpq by Molmil](/molmil-images/mine/7qpq) | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate | 分子名称: | 2-[(1-methyl-4-phenyl-imidazol-2-yl)methylsulfanyl]-[1,2,4]triazolo[1,5-a]pyridine, MAGNESIUM ION, ZINC ION, ... | 著者 | Leonard, P.M, Langgard, M. | 登録日 | 2022-01-05 | 公開日 | 2023-04-19 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.2 Å) | 主引用文献 | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate To Be Published
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7QQ4
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![BU of 7qq4 by Molmil](/molmil-images/mine/7qq4) | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate | 分子名称: | 5,8-dimethyl-2-[2-(1-methyl-4-phenyl-imidazol-2-yl)ethyl]-[1,2,4]triazolo[1,5-a]pyrazine, MAGNESIUM ION, ZINC ION, ... | 著者 | Leonard, P.M, Langgard, M. | 登録日 | 2022-01-06 | 公開日 | 2023-04-19 | 最終更新日 | 2024-02-07 | 実験手法 | X-RAY DIFFRACTION (2.45 Å) | 主引用文献 | Discovery of Lu AF11167, a Phosphodiesterase 10A inhibitor clinical candidate To Be Published
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1MPY
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![BU of 1mpy by Molmil](/molmil-images/mine/1mpy) | STRUCTURE OF CATECHOL 2,3-DIOXYGENASE (METAPYROCATECHASE) FROM PSEUDOMONAS PUTIDA MT-2 | 分子名称: | ACETONE, CATECHOL 2,3-DIOXYGENASE, FE (II) ION | 著者 | Kita, A, Kita, S, Fujisawa, I, Inaka, K, Ishida, T, Horiike, K, Nozaki, M, Miki, K. | 登録日 | 1998-10-20 | 公開日 | 1999-05-18 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | An archetypical extradiol-cleaving catecholic dioxygenase: the crystal structure of catechol 2,3-dioxygenase (metapyrocatechase) from Ppseudomonas putida mt-2. Structure Fold.Des., 7, 1999
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5VPJ
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![BU of 5vpj by Molmil](/molmil-images/mine/5vpj) | The crystal structure of a thioesteras from Actinomadura verrucosospora. | 分子名称: | CHLORIDE ION, TETRAETHYLENE GLYCOL, Thioesterase | 著者 | Tan, K, Joachimiak, G, Endres, M, Phillips Jr, G.N, Joachmiak, A, Midwest Center for Structural Genomics (MCSG), Enzyme Discovery for Natural Product Biosynthesis (NatPro) | 登録日 | 2017-05-05 | 公開日 | 2017-07-19 | 最終更新日 | 2019-12-04 | 実験手法 | X-RAY DIFFRACTION (2.35 Å) | 主引用文献 | The crystal structure of a thioesteras from Actinomadura verrucosospora. To Be Published
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1M9S
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![BU of 1m9s by Molmil](/molmil-images/mine/1m9s) | Crystal structure of Internalin B (InlB), a Listeria monocytogenes virulence protein containing SH3-like domains. | 分子名称: | Internalin B, SULFATE ION, TERBIUM(III) ION | 著者 | Marino, M, Banerjee, M, Jonquieres, R, Cossart, P, Ghosh, P. | 登録日 | 2002-07-29 | 公開日 | 2002-11-06 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (2.65 Å) | 主引用文献 | GW domains of the Listeria monocytogenes invasion protein InlB are SH3-like and mediate binding to host ligands Embo J., 21, 2002
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1MA2
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7QD7
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![BU of 7qd7 by Molmil](/molmil-images/mine/7qd7) | TarM(Se)_G117R | 分子名称: | CHLORIDE ION, GLYCEROL, PENTAETHYLENE GLYCOL, ... | 著者 | Guo, Y, Stehle, T. | 登録日 | 2021-11-26 | 公開日 | 2023-05-10 | 最終更新日 | 2023-12-06 | 実験手法 | X-RAY DIFFRACTION (2.06 Å) | 主引用文献 | Invasive Staphylococcus epidermidis uses a unique processive wall teichoic acid glycosyltransferase to evade immune recognition. Sci Adv, 9, 2023
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5CZL
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![BU of 5czl by Molmil](/molmil-images/mine/5czl) | Crystal structure of a novel GH8 endo-beta-1,4-glucanase from an Achatina fulica gut metagenomic library | 分子名称: | Glucanase, PHOSPHATE ION | 著者 | Scapin, S.M.N, Souza, F.H.M, Zanphorlin, L.M, Almeida, T.S, Sade, Y.B, Cardoso, A.M, Pinheiro, G.L, Murakami, M.T. | 登録日 | 2015-07-31 | 公開日 | 2016-08-03 | 最終更新日 | 2024-03-06 | 実験手法 | X-RAY DIFFRACTION (2.391 Å) | 主引用文献 | Crystal structure of a novel GH8 endo-beta-1,4-glucanase from an Achatina fulica gut metagenomic library To Be Published
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1MB0
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![BU of 1mb0 by Molmil](/molmil-images/mine/1mb0) | CRYSTAL STRUCTURE OF THE RESPONSE REGULATOR DIVK AT PH 8.0 IN COMPLEX WITH MN2+ | 分子名称: | MANGANESE (II) ION, cell division response regulator DivK | 著者 | Guillet, V, Ohta, N, Cabantous, S, Newton, A, Samama, J.-P, Structural Proteomics in Europe (SPINE) | 登録日 | 2002-08-02 | 公開日 | 2002-12-04 | 最終更新日 | 2024-04-03 | 実験手法 | X-RAY DIFFRACTION (2 Å) | 主引用文献 | Crystallographic and Biochemical Studies of DivK Reveal Novel Features of
an Essential Response Regulator in Caulobacter crescentus. J.Biol.Chem., 277, 2002
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1MBL
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7QH9
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![BU of 7qh9 by Molmil](/molmil-images/mine/7qh9) | TarM(Se)_G117R-4RboP | 分子名称: | 1,2-ETHANEDIOL, CHLORIDE ION, TarM(Se)_G117R-4RboP, ... | 著者 | Guo, Y, Stehle, T. | 登録日 | 2021-12-10 | 公開日 | 2023-05-10 | 最終更新日 | 2023-12-06 | 実験手法 | X-RAY DIFFRACTION (2.689 Å) | 主引用文献 | Invasive Staphylococcus epidermidis uses a unique processive wall teichoic acid glycosyltransferase to evade immune recognition. Sci Adv, 9, 2023
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7QNT
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![BU of 7qnt by Molmil](/molmil-images/mine/7qnt) | TarM(Se) native | 分子名称: | 1,2-ETHANEDIOL, BETA-MERCAPTOETHANOL, CHLORIDE ION, ... | 著者 | Guo, Y, Stehle, T. | 登録日 | 2021-12-22 | 公開日 | 2023-05-10 | 最終更新日 | 2023-12-06 | 実験手法 | X-RAY DIFFRACTION (3.21 Å) | 主引用文献 | Invasive Staphylococcus epidermidis uses a unique processive wall teichoic acid glycosyltransferase to evade immune recognition. Sci Adv, 9, 2023
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1MDW
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![BU of 1mdw by Molmil](/molmil-images/mine/1mdw) | Crystal Structure of Calcium-Bound Protease Core of Calpain II Reveals the Basis for Intrinsic Inactivation | 分子名称: | CALCIUM ION, Calpain II, catalytic subunit | 著者 | Moldoveanu, T, Hosfield, C.M, Lim, D, Jia, Z, Davies, P.L. | 登録日 | 2002-08-07 | 公開日 | 2003-04-29 | 最終更新日 | 2024-02-14 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Calpain silencing by a reversible intrinsic mechanism. Nat.Struct.Biol., 10, 2003
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7QTT
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1MF4
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![BU of 1mf4 by Molmil](/molmil-images/mine/1mf4) | Structure-based design of potent and selective inhibitors of phospholipase A2: Crystal structure of the complex formed between phosholipase A2 from Naja Naja sagittifera and a designed peptide inhibitor at 1.9 A resolution | 分子名称: | CALCIUM ION, Phospholipase A2, VAL-ALA-PHE-ARG-SER | 著者 | Singh, R.K, Vikram, P, Paramsivam, M, Jabeen, T, Sharma, S, Makker, J, Dey, S, Kaur, P, Srinivasan, A, Singh, T.P. | 登録日 | 2002-08-09 | 公開日 | 2003-09-30 | 最終更新日 | 2011-07-13 | 実験手法 | X-RAY DIFFRACTION (1.9 Å) | 主引用文献 | Design of specific peptide inhibitors for group I phospholipase A2: structure of a complex formed between phospholipase A2 from Naja naja sagittifera (group I) and a designed peptide inhibitor Val-Ala-Phe-Arg-Ser (VAFRS) at 1.9 A resolution reveals unique features Biochemistry, 42, 2003
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