6NL3
 
 | | Solution structure of human Coa6 | | 分子名称: | Cytochrome c oxidase assembly factor 6 homolog | | 著者 | Naik, M.T, Soma, S, Gohil, V. | | 登録日 | 2019-01-07 | | 公開日 | 2019-11-20 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | COA6 Is Structurally Tuned to Function as a Thiol-Disulfide Oxidoreductase in Copper Delivery to Mitochondrial Cytochrome c Oxidase.
Cell Rep, 29, 2019
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6NM2
 | | NMR Structure of WW291 | | 分子名称: | WW291 peptide | | 著者 | Wang, G, Zarena, D. | | 登録日 | 2019-01-10 | | 公開日 | 2020-07-15 | | 最終更新日 | 2020-09-09 | | 実験手法 | SOLUTION NMR | | 主引用文献 | The pi Configuration of the WWW Motif of a Short Trp-Rich Peptide Is Critical for Targeting Bacterial Membranes, Disrupting Preformed Biofilms, and Killing Methicillin-Resistant Staphylococcus aureus.
Biochemistry, 56, 2017
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6NM3
 | | NMR structure of WW295 | | 分子名称: | WW295 peptide | | 著者 | Wang, G, Zarena, D. | | 登録日 | 2019-01-10 | | 公開日 | 2020-07-15 | | 最終更新日 | 2020-09-09 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Two distinct amphipathic peptide antibiotics with systemic efficacy.
Proc.Natl.Acad.Sci.USA, 117, 2020
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6NNB
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6NOA
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6NOM
 | | NMR solution structure of Pisum sativum defensin 2 (Psd2) provides evidence for the presence of hydrophobic surface clusters | | 分子名称: | Defensin-2 | | 著者 | Pinheiro-Aguiar, R, Amaral, V.S.G, Bastos, I, Kurtenbach, E, Almeida, F.C.L. | | 登録日 | 2019-01-16 | | 公開日 | 2019-08-21 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Nuclear magnetic resonance solution structure of Pisum sativum defensin 2 provides evidence for the presence of hydrophobic surface-clusters.
Proteins, 88, 2020
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6NOX
 | | Solution structure of SFTI-KLK5 inhibitor | | 分子名称: | SFTI-KLK5 Peptide | | 著者 | White, A.M. | | 登録日 | 2019-01-16 | | 公開日 | 2019-04-03 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Amino Acid Scanning at P5' within the Bowman-Birk Inhibitory Loop Reveals Specificity Trends for Diverse Serine Proteases.
J. Med. Chem., 62, 2019
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6NS8
 | | RDC-refined SOLUTION NMR STRUCTURE OF PROTEIN PF2048.1 | | 分子名称: | Uncharacterized protein | | 著者 | Daigham, N.S, Liu, G, Swapna, G.V.T, Cole, C, Valafar, H, Montelione, G.T. | | 登録日 | 2019-01-24 | | 公開日 | 2020-01-29 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | REDCRAFT: A Computational Platform Using Residual Dipolar Coupling NMR Data for Determining Structures of Perdeuterated Proteins Without NOEs
To Be Published
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6NU0
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6NU4
 | | Solution structure of the Arabidopsis thaliana RALF8 peptide | | 分子名称: | Protein RALF-like 8 | | 著者 | Lee, W, Markley, J.L, Frederick, R.O, Miyoshi, H, Tonelli, M, Cornilescu, G, Cornilescu, C, Sussman, M.R. | | 登録日 | 2019-01-30 | | 公開日 | 2019-05-08 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Function and solution structure of the Arabidopsis thaliana RALF8 peptide.
Protein Sci., 28, 2019
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6NUG
 | | hGRNA4-28_3s | | 分子名称: | Granulin-4 | | 著者 | Dastpeyman, M, Bansal, P, Wilson, D, Loukas, A, Smout, M, Daly, N. | | 登録日 | 2019-02-01 | | 公開日 | 2020-02-05 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | hGRN4-28_3s
to be published
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6NUI
 | | Human Guanylate Kinase | | 分子名称: | Guanylate kinase | | 著者 | Sabo, T.M, Khan, N, Ban, D, Trigo-Mourino, P, Carneiro, M.G, Trent, J.O, Konrad, M, Lee, D. | | 登録日 | 2019-02-01 | | 公開日 | 2019-06-26 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Solution structure and functional investigation of human guanylate kinase reveals allosteric networking and a crucial role for the enzyme in cancer.
J.Biol.Chem., 294, 2019
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6NVZ
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6NW8
 | | SOLUTION STRUCTURE OF CN29, A TOXIN FROM CENTRUROIDES NOXIUS SCORPION VENOM | | 分子名称: | Cn29 | | 著者 | Delepierre, M, Gurrola, G.B, Possani, L.D, Guijarro, J.I. | | 登録日 | 2019-02-06 | | 公開日 | 2019-07-03 | | 最終更新日 | 2023-06-14 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Cn29, a novel orphan peptide found in the venom of the scorpion Centruroides noxius: Structure and function.
Toxicon, 167, 2019
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6NX4
 | | Structure of the C-terminal Helical Repeat Domain of Eukaryotic Elongation Factor 2 Kinase (eEF-2K) | | 分子名称: | Eukaryotic elongation factor 2 kinase | | 著者 | Piserchio, A, Will, N, Giles, D.H, Hajredini, F, Dalby, K.N, Ghose, R. | | 登録日 | 2019-02-08 | | 公開日 | 2019-05-29 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Solution Structure of the Carboxy-Terminal Tandem Repeat Domain of Eukaryotic Elongation Factor 2 Kinase and Its Role in Substrate Recognition.
J.Mol.Biol., 431, 2019
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6NZ2
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6NZL
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6NZN
 | | Dimer-of-dimer amyloid fibril structure of glucagon | | 分子名称: | Glucagon | | 著者 | Gelenter, M.D, Smith, K.J, Liao, S.Y, Mandala, V.S, Dregni, A.J, Lamm, M.S, Tian, Y, Wei, X, Pochan, D.J, Tucker, T.J, Su, Y, Hong, M. | | 登録日 | 2019-02-14 | | 公開日 | 2019-06-05 | | 最終更新日 | 2024-05-15 | | 実験手法 | SOLID-STATE NMR | | 主引用文献 | The peptide hormone glucagon forms amyloid fibrils with two coexisting beta-strand conformations.
Nat.Struct.Mol.Biol., 26, 2019
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6O0C
 | | NMR ensemble of computationally designed protein XAA_GVDQ mutant M4L | | 分子名称: | Design construct XAA_GVDQ mutant M4L | | 著者 | Wei, K.Y, Moschidi, D, Nerli, S, Sgourakis, N, Baker, D. | | 登録日 | 2019-02-15 | | 公開日 | 2020-04-22 | | 最終更新日 | 2024-05-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Computational design of closely related proteins that adopt two well-defined but structurally divergent folds.
Proc.Natl.Acad.Sci.USA, 117, 2020
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6O0I
 | | NMR ensemble of computationally designed protein XAA | | 分子名称: | Design construct XAA | | 著者 | Wei, K.Y, Moschidi, D, Nerli, S, Sgourakis, N, Baker, D. | | 登録日 | 2019-02-16 | | 公開日 | 2020-04-22 | | 最終更新日 | 2024-05-15 | | 実験手法 | SOLUTION NMR | | 主引用文献 | Computational design of closely related proteins that adopt two well-defined but structurally divergent folds.
Proc.Natl.Acad.Sci.USA, 117, 2020
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6O1Q
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6O22
 | | Structure of Asf1-H3:H4-Rtt109-Vps75 histone chaperone-lysine acetyltransferase complex with the histone substrate. | | 分子名称: | Histone H3.2, Histone H4, Histone acetyltransferase RTT109, ... | | 著者 | Danilenko, N, Carlomagno, T, Kirkpatrick, J.P. | | 登録日 | 2019-02-22 | | 公開日 | 2019-07-31 | | 最終更新日 | 2024-05-01 | | 実験手法 | SOLUTION NMR, SOLUTION SCATTERING | | 主引用文献 | Histone chaperone exploits intrinsic disorder to switch acetylation specificity.
Nat Commun, 10, 2019
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6O2L
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6O3Q
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6O3S
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