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5CTG
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BU of 5ctg by Molmil
The 3.1 A resolution structure of a eukaryotic SWEET transporter
分子名称: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 3,6,9,12,15,18,21,24-OCTAOXAHEXACOSAN-1-OL, Bidirectional sugar transporter SWEET2b, ...
著者Tao, Y, Perry, K, Feng, L.
登録日2015-07-24
公開日2015-10-28
最終更新日2024-03-06
実験手法X-RAY DIFFRACTION (3.103 Å)
主引用文献Structure of a eukaryotic SWEET transporter in a homotrimeric complex.
Nature, 527, 2015
3ID2
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BU of 3id2 by Molmil
Crystal Structure of RseP PDZ2 domain
分子名称: IODIDE ION, Regulator of sigma E protease
著者Li, X, Wang, B, Feng, L, Wang, J, Shi, Y.
登録日2009-07-20
公開日2009-08-11
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (3.089 Å)
主引用文献Cleavage of RseA by RseP requires a carboxyl-terminal hydrophobic amino acid following DegS cleavage
Proc.Natl.Acad.Sci.USA, 106, 2009
3ID4
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BU of 3id4 by Molmil
Crystal Structure of RseP PDZ2 domain fused GKASPV peptide
分子名称: Regulator of sigma E protease
著者Li, X, Wang, B, Feng, L, Wang, J, Shi, Y.
登録日2009-07-20
公開日2009-08-11
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (1.604 Å)
主引用文献Cleavage of RseA by RseP requires a carboxyl-terminal hydrophobic amino acid following DegS cleavage
Proc.Natl.Acad.Sci.USA, 106, 2009
3ID1
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BU of 3id1 by Molmil
Crystal Structure of RseP PDZ1 domain
分子名称: Regulator of sigma E protease
著者Li, X, Wang, B, Feng, L, Wang, J, Shi, Y.
登録日2009-07-20
公開日2009-08-11
最終更新日2024-03-20
実験手法X-RAY DIFFRACTION (1.67 Å)
主引用文献Cleavage of RseA by RseP requires a carboxyl-terminal hydrophobic amino acid following DegS cleavage
Proc.Natl.Acad.Sci.USA, 106, 2009
3ID3
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BU of 3id3 by Molmil
Crystal Structure of RseP PDZ2 I304A domain
分子名称: Regulator of sigma E protease
著者Li, X, Wang, B, Feng, L, Wang, J, Shi, Y.
登録日2009-07-20
公開日2009-08-11
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (2.01 Å)
主引用文献Cleavage of RseA by RseP requires a carboxyl-terminal hydrophobic amino acid following DegS cleavage
Proc.Natl.Acad.Sci.USA, 106, 2009
6C5R
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BU of 6c5r by Molmil
Crystal structure of the soluble domain of the mitochondrial calcium uniporter
分子名称: calcium uniporter
著者Fan, C, Fan, M, Fastman, N, Zhang, J, Feng, L.
登録日2018-01-16
公開日2018-07-11
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (3.09608316 Å)
主引用文献X-ray and cryo-EM structures of the mitochondrial calcium uniporter.
Nature, 559, 2018
8JJT
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BU of 8jjt by Molmil
Structure of SenB in complex with UDP-GlcNAc at 1.88 Angstroms resolution
分子名称: TIGR04348 family glycosyltransferase, URIDINE-DIPHOSPHATE-N-ACETYLGLUCOSAMINE
著者Wei, H, Feng, L.
登録日2023-05-31
公開日2024-02-07
実験手法X-RAY DIFFRACTION (1.88 Å)
主引用文献Structure of SenB in complex with UDP-GlcNAc at 1.88 Angstroms resolution
To be published
7CIR
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BU of 7cir by Molmil
Peptide phosphorylation modification of MHC class I molecules
分子名称: ARG-ARG-PHE-SEP-ARG-SER-PRO-ILE-ARG-ARG, Beta-2-microglobulin, MHC class I antigen
著者Sun, M.W, Feng, L, Qi, J.X, Liu, W.J, Gao, G.F.
登録日2020-07-08
公開日2022-03-09
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.81 Å)
主引用文献Phosphosite-dependent presentation of dual phosphorylated peptides by MHC class I molecules.
Iscience, 25, 2022
7CIS
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BU of 7cis by Molmil
Peptide modification of MHC class I molecules
分子名称: ARG-ARG-PHE-SEP-ARG-SEP-PRO-ILE-ARG, Beta-2-microglobulin, MHC class I antigen
著者Sun, M.W, Feng, L, Qi, J.X, Liu, W.J, Gao, G.F.
登録日2020-07-08
公開日2022-03-09
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Phosphosite-dependent presentation of dual phosphorylated peptides by MHC class I molecules.
Iscience, 25, 2022
7CIQ
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BU of 7ciq by Molmil
Phosphorylation modification of MHC I polypeptide
分子名称: ARG-ARG-PHE-SER-ARG-SER-PRO-ILE-ARG-ARG, Beta-2-microglobulin, MHC class I antigen
著者Sun, M.W, Feng, L, Qi, J.X, Liu, W.J, Gao, G.F.
登録日2020-07-08
公開日2022-03-09
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.59 Å)
主引用文献Phosphosite-dependent presentation of dual phosphorylated peptides by MHC class I molecules.
Iscience, 25, 2022
7DYN
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BU of 7dyn by Molmil
Phosphorylation of MHC I peptide
分子名称: ARG-ARG-PHE-SEP-ARG-SEP-PRO-ILE-ARG-ARG, Beta-2-microglobulin, MHC class I antigen
著者Sun, M.W, Feng, L, Qi, J.X, Liu, W.J.
登録日2021-01-22
公開日2022-03-09
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Phosphosite-dependent presentation of dual phosphorylated peptides by MHC class I molecules.
Iscience, 25, 2022
7YLQ
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BU of 7ylq by Molmil
Crystal structure of Microcystinase C from Sphingomonas sp. ACM-3962 at 2.6 A resolution
分子名称: CALCIUM ION, Microcystinase C, ZINC ION
著者Guo, X, Li, Z, Ding, W, Yin, P, Feng, L.
登録日2022-07-26
公開日2023-08-09
実験手法X-RAY DIFFRACTION (2.68 Å)
主引用文献Crystal structure of Microcystin C from Sphingomonas sp. ACM-3962 at 2.6 A resolution
To Be Published
3PUP
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BU of 3pup by Molmil
Structure of Glycogen Synthase Kinase 3 beta (GSK3B) in complex with a ruthenium octasporine ligand (OS1)
分子名称: Glycogen synthase kinase-3 beta, Ruthenium octasporine
著者Filippakopoulos, P, Kraling, K, Essen, L.O, Meggers, E, Knapp, S.
登録日2010-12-06
公開日2010-12-22
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.99 Å)
主引用文献Structurally sophisticated octahedral metal complexes as highly selective protein kinase inhibitors.
J.Am.Chem.Soc., 133, 2011
5JL4
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BU of 5jl4 by Molmil
Inhibitor resistant mutant catalytic core domain of HIV-1 Integrase
分子名称: Integrase, SULFATE ION
著者Feng, L, Kobe, M, Kvaratskhelia, M.
登録日2016-04-26
公開日2017-10-04
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (1.758 Å)
主引用文献Resistance to pyridine-based inhibitor KF116 reveals an unexpected role of integrase in HIV-1 Gag-Pol polyprotein proteolytic processing.
J. Biol. Chem., 292, 2017
8IN7
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BU of 8in7 by Molmil
Crystal structure of UGT74AN3-UDP
分子名称: Glycosyltransferase, URIDINE-5'-DIPHOSPHATE-GLUCOSE
著者Feng, L, Wei, H.
登録日2023-03-08
公開日2024-03-13
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Crystal structure of UGT74AN3-UDP
To Be Published
7QK4
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BU of 7qk4 by Molmil
EED in complex with PRC2 allosteric inhibitor compound 22 (MAK683)
分子名称: CHLORIDE ION, Histone-lysine N-methyltransferase EZH2, N-[(5-fluoranyl-2,3-dihydro-1-benzofuran-4-yl)methyl]-8-(2-methylpyridin-3-yl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, ...
著者Zhao, K, Zhao, M, Luo, X, Zhang, H, Scheufler, C.
登録日2021-12-17
公開日2022-04-13
最終更新日2024-01-31
実験手法X-RAY DIFFRACTION (1.602 Å)
主引用文献Discovery of the Clinical Candidate MAK683: An EED-Directed, Allosteric, and Selective PRC2 Inhibitor for the Treatment of Advanced Malignancies.
J.Med.Chem., 65, 2022
7QJG
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BU of 7qjg by Molmil
EED in complex with PRC2 allosteric inhibitor compound 6
分子名称: CHLORIDE ION, Histone-lysine N-methyltransferase EZH2, N-(2,3-dihydro-1-benzofuran-7-ylmethyl)-8-[4-[(dimethylamino)methyl]phenyl]-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, ...
著者Zhao, K, Zhao, M, Luo, X, Zhang, H, Scheufler, C.
登録日2021-12-16
公開日2022-04-13
最終更新日2024-01-31
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Discovery of the Clinical Candidate MAK683: An EED-Directed, Allosteric, and Selective PRC2 Inhibitor for the Treatment of Advanced Malignancies.
J.Med.Chem., 65, 2022
7QJU
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BU of 7qju by Molmil
EED in complex with PRC2 allosteric inhibitor compound 7
分子名称: CHLORIDE ION, Histone-lysine N-methyltransferase EZH2, N-(2,3-dihydro-1-benzofuran-4-ylmethyl)-8-[4-[(dimethylamino)methyl]phenyl]-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, ...
著者Zhao, K, Zhao, M, Luo, X, Zhang, H, Scheufler, C.
登録日2021-12-17
公開日2022-04-13
最終更新日2024-01-31
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Discovery of the Clinical Candidate MAK683: An EED-Directed, Allosteric, and Selective PRC2 Inhibitor for the Treatment of Advanced Malignancies.
J.Med.Chem., 65, 2022
3A9U
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BU of 3a9u by Molmil
Crystal structures and enzymatic mechanisms of a Populus tomentosa 4-coumarate--CoA ligase
分子名称: 4-coumarate--CoA ligase
著者Hu, Y.
登録日2009-11-06
公開日2010-09-08
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Crystal structures of a Populus tomentosa 4-coumarate:CoA ligase shed light on its enzymatic mechanisms
Plant Cell, 22, 2010
3A9V
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BU of 3a9v by Molmil
Crystal structures and enzymatic mechanisms of a Populus tomentosa 4-coumarate--CoA ligase
分子名称: 4-coumarate--CoA ligase, ADENOSINE MONOPHOSPHATE
著者Hu, Y.
登録日2009-11-06
公開日2010-09-08
最終更新日2023-11-01
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Crystal structures of a Populus tomentosa 4-coumarate:CoA ligase shed light on its enzymatic mechanisms
Plant Cell, 22, 2010
4WYU
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BU of 4wyu by Molmil
Crystal Structure of Scribble PDZ34 tandem in complex with its target peptide
分子名称: IODIDE ION, Protein scribble homolog, peptide SER-TRP-PHE-GLN-THR-ASP-LEU
著者Ren, J.Q, Pei, H.H, Feng, W.
登録日2014-11-18
公開日2015-10-21
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Interdomain interface-mediated target recognition by the Scribble PDZ34 supramodule.
Biochem.J., 468, 2015
4WYT
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BU of 4wyt by Molmil
Crystal Structure of Scribble PDZ34 tandem at 2.6 Angstroms
分子名称: CHLORIDE ION, Protein scribble homolog
著者Ren, J.Q, Feng, W.
登録日2014-11-18
公開日2015-10-21
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Interdomain interface-mediated target recognition by the Scribble PDZ34 supramodule.
Biochem.J., 468, 2015
5H19
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BU of 5h19 by Molmil
EED in complex with PRC2 allosteric inhibitor EED162
分子名称: 5-(furan-2-ylmethylamino)-9-(phenylmethyl)-8,10-dihydro-7H-[1,2,4]triazolo[3,4-a][2,7]naphthyridine-6-carbonitrile, Histone-lysine N-methyltransferase EZH2, Polycomb protein EED
著者Zhao, K, Zhao, M, Luo, X, Zhang, H.
登録日2016-10-08
公開日2017-01-25
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Discovery and Molecular Basis of a Diverse Set of Polycomb Repressive Complex 2 Inhibitors Recognition by EED
PLoS ONE, 12, 2017
5GSA
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BU of 5gsa by Molmil
EED in complex with an allosteric PRC2 inhibitor
分子名称: Histone-lysine N-methyltransferase EZH2, N-(furan-2-ylmethyl)-8-(4-methylsulfonylphenyl)-[1,2,4]triazolo[4,3-c]pyrimidin-5-amine, Polycomb protein EED
著者Zhao, K, Zhao, M, Luo, X, Zhang, H.
登録日2016-08-15
公開日2017-02-01
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.49 Å)
主引用文献An allosteric PRC2 inhibitor targeting the H3K27me3 binding pocket of
Nat. Chem. Biol., 13, 2017
5H14
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EED in complex with an allosteric PRC2 inhibitor EED666
分子名称: 2-[3-(3,5-dimethylpyrazol-1-yl)-4-nitro-phenyl]-3,4-dihydro-1H-isoquinoline, GLYCEROL, Histone-lysine N-methyltransferase EZH2, ...
著者Zhao, K, Zhao, M, Luo, X, Zhang, H.
登録日2016-10-08
公開日2017-01-25
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Discovery and Molecular Basis of a Diverse Set of Polycomb Repressive Complex 2 Inhibitors Recognition by EED
PLoS ONE, 12, 2017

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