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F100A mutant structure of MIF2 (D-DT)
分子名称:	D-dopachrome decarboxylase, SULFATE ION
著者	Murphy, E.L, Manjula, R, Murphy, J.W, Lolis, E.
登録日	2021-05-09
公開日	2021-08-18
最終更新日	2023-10-18
実験手法	X-RAY DIFFRACTION (1.57 Å)
主引用文献	A structurally preserved allosteric site in the MIF superfamily affects enzymatic activity and CD74 activation in D-dopachrome tautomerase. J.Biol.Chem., 297, 2021

5JPE

Yeast-specific serine/threonine protein phosphatase (PPZ1) of Candida albicans
分子名称:	CITRATE ANION, GLYCEROL, Serine/threonine-protein phosphatase
著者	Choy, M.S, Chen, E.H, Peti, W, Page, R.
登録日	2016-05-03
公開日	2016-08-31
最終更新日	2023-09-27
実験手法	X-RAY DIFFRACTION (2.611 Å)
主引用文献	Molecular Insights into the Fungus-Specific Serine/Threonine Protein Phosphatase Z1 in Candida albicans. Mbio, 7, 2016

5JPF

Serine/Threonine phosphatase Z1 (Candida albicans) binds to inhibitor microcystin-LR
分子名称:	MALONATE ION, MANGANESE (II) ION, Microcystin-LR, ...
著者	Choy, M.S, Chen, E.H, Peti, W, Page, R.
登録日	2016-05-03
公開日	2016-08-31
最終更新日	2023-11-15
実験手法	X-RAY DIFFRACTION (2.39929724 Å)
主引用文献	Molecular Insights into the Fungus-Specific Serine/Threonine Protein Phosphatase Z1 in Candida albicans. Mbio, 7, 2016

4K2U

Crystal structure of PfEBA-175 F1 in complex with R218 antibody Fab fragment
分子名称:	Antibody Heavy Chain, Antibody Light Chain, Erythrocyte binding antigen 175, ...
著者	Tolia, N.H.
登録日	2013-04-09
公開日	2013-06-12
最終更新日	2017-11-15
実験手法	X-RAY DIFFRACTION (2.45 Å)
主引用文献	Structural and Functional Basis for Inhibition of Erythrocyte Invasion by Antibodies that Target Plasmodium falciparum EBA-175. Plos Pathog., 9, 2013

8WZX

Cryo-EM structure of the hamster prion 23-144 fibril at pH 3.7
分子名称:	Major prion protein
著者	Lee, C.-H, Saw, J.-E, Chen, E, Wang, C.-H, Chen, R.
登録日	2023-11-02
公開日	2024-05-01
最終更新日	2024-05-08
実験手法	ELECTRON MICROSCOPY (2.88 Å)
主引用文献	The Positively Charged Cluster in the N-terminal Disordered Region may Affect Prion Protein Misfolding: Cryo-EM Structure of Hamster PrP(23-144) Fibrils. J.Mol.Biol., 436, 2024

8EKD

Cryo-EM map of SARS-CoV-2 Omicron BA.2 spike in complex with 2130-1-0114-112
分子名称:	2-acetamido-2-deoxy-beta-D-glucopyranose, Fab LLNL-199 HC, Fab LLNL-199 LC, ...
著者	Binshtein, E, Crowe, J.E.
登録日	2022-09-20
公開日	2024-02-21
最終更新日	2024-06-19
実験手法	ELECTRON MICROSCOPY (3.6 Å)
主引用文献	Computationally restoring the potency of a clinical antibody against Omicron. Nature, 629, 2024

1HSI

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES
分子名称:	HIV-2 PROTEASE
著者	Chen, Z.
登録日	1995-03-31
公開日	1996-04-03
最終更新日	2024-02-07
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	Crystal structure at 1.9-A resolution of human immunodeficiency virus (HIV) II protease complexed with L-735,524, an orally bioavailable inhibitor of the HIV proteases. J.Biol.Chem., 269, 1994

1HSG

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES
分子名称:	HIV-1 PROTEASE, N-[2(R)-HYDROXY-1(S)-INDANYL]-5-[(2(S)-TERTIARY BUTYLAMINOCARBONYL)-4(3-PYRIDYLMETHYL)PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYLPENTANAMIDE
著者	Chen, Z.
登録日	1995-03-31
公開日	1996-04-03
最終更新日	2024-02-07
実験手法	X-RAY DIFFRACTION (2 Å)
主引用文献	Crystal structure at 1.9-A resolution of human immunodeficiency virus (HIV) II protease complexed with L-735,524, an orally bioavailable inhibitor of the HIV proteases. J.Biol.Chem., 269, 1994

1HSH

CRYSTAL STRUCTURE AT 1.9 ANGSTROMS RESOLUTION OF HUMAN IMMUNODEFICIENCY VIRUS (HIV) II PROTEASE COMPLEXED WITH L-735,524, AN ORALLY BIOAVAILABLE INHIBITOR OF THE HIV PROTEASES
分子名称:	HIV-II PROTEASE, N-[2(R)-HYDROXY-1(S)-INDANYL]-5-[(2(S)-TERTIARY BUTYLAMINOCARBONYL)-4(3-PYRIDYLMETHYL)PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYLPENTANAMIDE
著者	Chen, Z.
登録日	1995-03-31
公開日	1996-04-03
最終更新日	2024-02-07
実験手法	X-RAY DIFFRACTION (1.9 Å)
主引用文献	Crystal structure at 1.9-A resolution of human immunodeficiency virus (HIV) II protease complexed with L-735,524, an orally bioavailable inhibitor of the HIV proteases. J.Biol.Chem., 269, 1994

4KF8

Nup188(aa1445-1827) from Myceliophthora thermophila
分子名称:	Nup188
著者	Schwartz, T.U, Andersen, K.R.
登録日	2013-04-26
公開日	2013-06-19
最終更新日	2013-08-14
実験手法	X-RAY DIFFRACTION (3 Å)
主引用文献	Scaffold nucleoporins Nup188 and Nup192 share structural and functional properties with nuclear transport receptors. Elife, 2, 2013

4KF7

Nup188(aa1-1160) from Myceliophthora thermophila
分子名称:	Nup188
著者	Schwartz, T.U, Andersen, K.R.
登録日	2013-04-26
公開日	2013-06-19
最終更新日	2024-02-28
実験手法	X-RAY DIFFRACTION (2.65 Å)
主引用文献	Scaffold nucleoporins Nup188 and Nup192 share structural and functional properties with nuclear transport receptors. Elife, 2, 2013

2BPV

HIV-1 protease-inhibitor complex
分子名称:	1-[2-HYDROXY-4-(2-HYDROXY-5-METHYL-CYCLOPENTYLCARBAMOYL)5-PHENYL-PENTYL]-4-(3-PYRIDIN-3-YL-PROPIONYL)-PIPERAZINE-2-CARB OXYLIC ACID TERT-BUTYLAMIDE, HIV-1 PROTEASE
著者	Munshi, S, Chen, Z.
登録日	1998-01-22
公開日	1999-02-23
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (1.9 Å)
主引用文献	Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme. Acta Crystallogr.,Sect.D, 54, 1998

2BPY

HIV-1 protease-inhibitor complex
分子名称:	HIV-1 PROTEASE, N-[2(S)-CYCLOPENTYL-1(R)-HYDROXY-3(R)METHYL]-5-[(2(S)-TERTIARY-BUTYLAMINO-CARBONYL)-4-(N1-(2)-(N-METHYLPIPERAZINYL)-3-CHLORO-PYRAZINYL-5-CARBONYL)-PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYL-PENTANAMIDE
著者	Munshi, S, Chen, Z.
登録日	1998-01-22
公開日	1999-02-23
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (1.9 Å)
主引用文献	Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme. Acta Crystallogr.,Sect.D, 54, 1998

2BPX

HIV-1 protease-inhibitor complex
分子名称:	HIV-1 PROTEASE, N-[2(R)-HYDROXY-1(S)-INDANYL]-5-[(2(S)-TERTIARY BUTYLAMINOCARBONYL)-4(3-PYRIDYLMETHYL)PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYLPENTANAMIDE
著者	Munshi, S, Chen, Z.
登録日	1998-01-22
公開日	1999-02-23
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme. Acta Crystallogr.,Sect.D, 54, 1998

2BPZ

HIV-1 protease-inhibitor complex
分子名称:	HIV-1 PROTEASE, N-[2(S)-CYCLOPENTYL-1(R)-HYDROXY-3(R)METHYL]-5-[(2(S)-TERTIARY-BUTYLAMINO-CARBONYL)-4-(N1-(2)-(N-METHYLPIPERAZINYL)-3-CHLORO-PYRAZINYL-5-CARBONYL)-PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYL-PENTANAMIDE
著者	Munshi, S, Chen, Z.
登録日	1998-01-22
公開日	1999-02-23
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme. Acta Crystallogr.,Sect.D, 54, 1998

2BPW

HIV-1 protease-inhibitor complex
分子名称:	1-[2-HYDROXY-4-(2-HYDROXY-5-METHYL-CYCLOPENTYLCARBAMOYL)5-PHENYL-PENTYL]-4-(3-PYRIDIN-3-YL-PROPIONYL)-PIPERAZINE-2-CARB OXYLIC ACID TERT-BUTYLAMIDE, HIV-1 PROTEASE
著者	Munshi, S, Chen, Z.
登録日	1998-01-22
公開日	1999-02-23
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	Rapid X-ray diffraction analysis of HIV-1 protease-inhibitor complexes: inhibitor exchange in single crystals of the bound enzyme. Acta Crystallogr.,Sect.D, 54, 1998

1C6X

ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP.
分子名称:	N-[2(S)-CYCLOPENTYL-1(R)-HYDROXY-3(R)METHYL]-5-[(2(S)-TERTIARY-BUTYLAMINO-CARBONYL)-4-(N1-(2)-(N-METHYLPIPERAZINYL)-3-CHLORO-PYRAZINYL-5-CARBONYL)-PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYL-PENTANAMIDE, PROTEIN (PROTEASE)
著者	Munshi, S.
登録日	1999-12-28
公開日	2000-12-28
最終更新日	2023-12-27
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	An alternate binding site for the P1-P3 group of a class of potent HIV-1 protease inhibitors as a result of concerted structural change in the 80s loop of the protease. Acta Crystallogr.,Sect.D, 56, 2000

1C6Y

ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP.
分子名称:	N-[2(R)-HYDROXY-1(S)-INDANYL]-5-[(2(S)-TERTIARY BUTYLAMINOCARBONYL)-4(3-PYRIDYLMETHYL)PIPERAZINO]-4(S)-HYDROXY-2(R)-PHENYLMETHYLPENTANAMIDE, PROTEIN (PROTEASE)
著者	Munshi, S.
登録日	1999-12-28
公開日	2000-12-28
最終更新日	2023-12-27
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	An alternate binding site for the P1-P3 group of a class of potent HIV-1 protease inhibitors as a result of concerted structural change in the 80s loop of the protease. Acta Crystallogr.,Sect.D, 56, 2000

6QT0

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S rRNA, 5.8S rRNA, 5S rRNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-02-22
公開日	2019-06-26
最終更新日	2024-05-15
実験手法	ELECTRON MICROSCOPY (3.4 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

6RZZ

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S ribosomal RNA, 5.8S ribosomal RNA, 5S ribosomal RNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-06-13
公開日	2019-06-26
最終更新日	2024-05-22
実験手法	ELECTRON MICROSCOPY (3.2 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

6QTZ

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S rRNA, 5.8S rRNA, 5S rRNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-02-26
公開日	2019-06-26
最終更新日	2024-05-15
実験手法	ELECTRON MICROSCOPY (3.5 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

6S05

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S ribosomal RNA, 5.8S ribosomal RNA, 5S ribosomal RNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-06-13
公開日	2019-06-26
最終更新日	2024-05-22
実験手法	ELECTRON MICROSCOPY (3.9 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

6RI5

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S RNA, 5.8S rRNA, 5S rRNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-04-23
公開日	2019-06-26
最終更新日	2024-05-22
実験手法	ELECTRON MICROSCOPY (3.3 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

6OSW

An order-to-disorder structural switch activates the FoxM1 transcription factor
分子名称:	Forkhead box M1
著者	Marceau, A.H, Rubin, S.M, Nerli, S, McShane, A.C, Sgourakis, N.G.
登録日	2019-05-02
公開日	2019-05-29
最終更新日	2024-05-15
実験手法	SOLUTION NMR
主引用文献	An order-to-disorder structural switch activates the FoxM1 transcription factor. Elife, 8, 2019

6QIK

Cryo-EM structures of Lsg1-TAP pre-60S ribosomal particles
分子名称:	25S ribosomal RNA, 5.8S ribosomal RNA, 5S ribosomal RNA, ...
著者	Kargas, V, Warren, A.J.
登録日	2019-01-20
公開日	2019-06-26
最終更新日	2024-05-15
実験手法	ELECTRON MICROSCOPY (3.1 Å)
主引用文献	Mechanism of completion of peptidyltransferase centre assembly in eukaryotes. Elife, 8, 2019

<123 4 5 6 >

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