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Lactobacillus casei Y261M in complex with substrate, dUMP
分子名称:	2'-DEOXYURIDINE 5'-MONOPHOSPHATE, thymidylate synthase
著者	Finer-Moore, J.S, Stroud, R.M.
登録日	2006-03-02
公開日	2006-03-14
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	The role of protein dynamics in thymidylate synthase catalysis: variants of conserved 2'-deoxyuridine 5'-monophosphate (dUMP)-binding Tyr-261 Biochemistry, 45, 2006

8QRN

mt-SSU in GTPBP8 knock-out cells, state 4
分子名称:	12S mitochondrial rRNA, 28S ribosomal protein S10, mitochondrial, ...
著者	Valentin Gese, G, Cipullo, M, Rorbach, J, Hallberg, B.M.
登録日	2023-10-09
公開日	2024-06-26
最終更新日	2024-07-17
実験手法	ELECTRON MICROSCOPY (2.98 Å)
主引用文献	GTPBP8 plays a role in mitoribosome formation in human mitochondria. Nat Commun, 15, 2024

8QRK

mt-SSU assembly intermediate in GTPBP8 knock-out cells, state 1
分子名称:	12S mitochondrial rRNA, 28S ribosomal protein S10, mitochondrial, ...
著者	Valentin Gese, G, Cipullo, M, Rorbach, J, Hallberg, B.M.
登録日	2023-10-09
公開日	2024-06-26
最終更新日	2024-07-17
実験手法	ELECTRON MICROSCOPY (6.69 Å)
主引用文献	GTPBP8 plays a role in mitoribosome formation in human mitochondria. Nat Commun, 15, 2024

8QRL

mt-SSU assembly intermediate in GTPBP8 knock-out cells, state 2
分子名称:	12S mitochondrial rRNA, 12S rRNA N4-methylcytidine (m4C) methyltransferase, 28S ribosomal protein S10, ...
著者	Valentin Gese, G, Cipullo, M, Rorbach, J, Hallberg, B.M.
登録日	2023-10-09
公開日	2024-06-26
最終更新日	2024-07-17
実験手法	ELECTRON MICROSCOPY (3.34 Å)
主引用文献	GTPBP8 plays a role in mitoribosome formation in human mitochondria. Nat Commun, 15, 2024

8QU1

mt-LSU assembly intermediate in GTPBP8 knock-out cells, state 1
分子名称:	16S ribosomal RNA, 39S ribosomal protein L10, mitochondrial, ...
著者	Valentin Gese, G, Cipullo, M, Rorbach, J, Hallberg, B.M.
登録日	2023-10-13
公開日	2024-06-26
最終更新日	2024-07-17
実験手法	ELECTRON MICROSCOPY (2.74 Å)
主引用文献	GTPBP8 plays a role in mitoribosome formation in human mitochondria. Nat Commun, 15, 2024

2FS9

Human beta tryptase II with inhibitor CRA-28427
分子名称:	ETHYL {(1S)-5-AMINO-1-[(5-{4-[(2,3-DIHYDRO-1H-INDEN-2-YLAMINO)CARBONYL]BENZYL}-1,2,4-OXADIAZOL-3-YL)CARBONYL]PENTYL}CARBAMATE, Tryptase beta-2
著者	Somoza, J.R.
登録日	2006-01-21
公開日	2006-03-07
最終更新日	2017-10-18
実験手法	X-RAY DIFFRACTION (2.3 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

2FXR

human beta tryptase II complexed with activated ketone inhibitor CRA-29382
分子名称:	ALLYL {(1S)-1-[(5-{4-[(2,3-DIHYDRO-1H-INDEN-2-YLAMINO)CARBONYL]BENZYL}-1,2,4-OXADIAZOL-3-YL)CARBONYL]-3-PYRROLIDIN-3-YLPROPYL}CARBAMATE, Tryptase beta-2
著者	Katz, B.A.
登録日	2006-02-06
公開日	2006-02-09
最終更新日	2023-08-30
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

2FX6

bovine trypsin complexed with 2-aminobenzamidazole
分子名称:	2H-BENZOIMIDAZOL-2-YLAMINE, CALCIUM ION, Trypsin
著者	Katz, B.A.
登録日	2006-02-03
公開日	2006-02-14
最終更新日	2017-10-18
実験手法	X-RAY DIFFRACTION (1.57 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

1AB8

RAT TYPE II ADENYLYL CYCLASE C2 DOMAIN/FORSKOLIN COMPLEX
分子名称:	ADENYLYL CYCLASE, FORSKOLIN
著者	Zhang, G, Hurley, J.H.
登録日	1997-02-04
公開日	1997-05-15
最終更新日	2024-02-07
実験手法	X-RAY DIFFRACTION (2.2 Å)
主引用文献	Structure of the adenylyl cyclase catalytic core. Nature, 386, 1997

2FWW

human beta-tryptase II complexed with 4-piperidinebutyrate to make acylenzyme
分子名称:	4-PIPERIDINEBUTYRATE, Tryptase beta-2
著者	Katz, B.A.
登録日	2006-02-03
公開日	2006-02-14
最終更新日	2017-10-18
実験手法	X-RAY DIFFRACTION (2.25 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

2FPZ

Human tryptase with 2-amino benzimidazole
分子名称:	2H-BENZOIMIDAZOL-2-YLAMINE, Tryptase beta-2
著者	Somoza, J.R.
登録日	2006-01-17
公開日	2006-03-07
最終更新日	2011-07-13
実験手法	X-RAY DIFFRACTION (2 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

2FS8

Human beta-tryptase II with inhibitor CRA-29382
分子名称:	ALLYL {(1S)-1-[(5-{4-[(2,3-DIHYDRO-1H-INDEN-2-YLAMINO)CARBONYL]BENZYL}-1,2,4-OXADIAZOL-3-YL)CARBONYL]-3-PYRROLIDIN-3-YLPROPYL}CARBAMATE, Tryptase beta-2
著者	Somoza, J.R.
登録日	2006-01-21
公開日	2006-03-21
最終更新日	2017-10-18
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	Structure-guided design of Peptide-based tryptase inhibitors. Biochemistry, 45, 2006

2G89

L. casei thymidylate synthase Y261A in complex with substrate, dUMP
分子名称:	2'-DEOXYURIDINE 5'-MONOPHOSPHATE, thymidylate synthase
著者	Finer-Moore, J.S, Stroud, R.M.
登録日	2006-03-02
公開日	2006-03-14
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.5 Å)
主引用文献	The role of protein dynamics in thymidylate synthase catalysis: variants of conserved 2'-deoxyuridine 5'-monophosphate (dUMP)-binding Tyr-261 Biochemistry, 45, 2006

2G86

L. casei thymidylate synthase Y261F in complex with substrate, dUMP
分子名称:	2'-DEOXYURIDINE 5'-MONOPHOSPHATE, Thymidylate synthase
著者	Finer-Moore, J.S, Stroud, R.M.
登録日	2006-03-01
公開日	2006-03-14
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	The role of protein dynamics in thymidylate synthase catalysis: variants of conserved 2'-deoxyuridine 5'-monophosphate (dUMP)-binding Tyr-261 Biochemistry, 45, 2006

2G8D

Lactobacillus casei thymidylate synthase Y261W-dUMP complex
分子名称:	2'-DEOXYURIDINE 5'-MONOPHOSPHATE, thymidylate synthase
著者	Finer-Moore, J.S, Stroud, R.M.
登録日	2006-03-02
公開日	2006-03-14
最終更新日	2024-02-14
実験手法	X-RAY DIFFRACTION (2.4 Å)
主引用文献	The role of protein dynamics in thymidylate synthase catalysis: variants of conserved 2'-deoxyuridine 5'-monophosphate (dUMP)-binding Tyr-261 Biochemistry, 45, 2006

2G8X

Escherichia coli Y209W apoprotein
分子名称:	2,3-DIHYDROXY-1,4-DITHIOBUTANE, CARBONATE ION, PHOSPHATE ION, ...
著者	Lee, T.T, Finer-Moore, J.S, Stroud, R.M.
登録日	2006-03-03
公開日	2006-03-14
最終更新日	2023-08-30
実験手法	X-RAY DIFFRACTION (1.83 Å)
主引用文献	The role of protein dynamics in thymidylate synthase catalysis: Variants of conserved dUMP-binding Tyr-261 TO BE PUBLISHED

8TL7

CryoEM Structure of a Computationally Designed T3 Tetrahedral Nanocage
分子名称:	Computationally designed protein
著者	Weidle, C, Borst, A.J.
登録日	2023-07-26
公開日	2024-03-13
最終更新日	2024-04-10
実験手法	ELECTRON MICROSCOPY (4.05 Å)
主引用文献	Blueprinting extendable nanomaterials with standardized protein blocks. Nature, 627, 2024

5BMS

Crystal structure of P21-activated kinase 4 in complex with an inhibitor compound 29
分子名称:	N~2~-[(7-chloro-1H-benzimidazol-6-yl)methyl]-N~4~-(5-cyclopropyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamine, Serine/threonine-protein kinase PAK 4
著者	Rouge, L, Wang, W.
登録日	2015-05-22
公開日	2015-07-01
最終更新日	2015-07-15
実験手法	X-RAY DIFFRACTION (2.903 Å)
主引用文献	Structure-Guided Design of Group I Selective p21-Activated Kinase Inhibitors. J.Med.Chem., 58, 2015

8FJ5

Structure of the Haloferax volcanii archaeal type IV pilus
分子名称:	Pilin_N domain-containing protein
著者	Wang, F, Kreutzberger, M.A, Baquero, D.P, Krupovic, M, Egelman, E.H.
登録日	2022-12-19
公開日	2023-06-28
最終更新日	2024-06-19
実験手法	ELECTRON MICROSCOPY (2.9 Å)
主引用文献	The evolution of archaeal flagellar filaments. Proc.Natl.Acad.Sci.USA, 120, 2023

8FJS

Structure of the Saccharolobus solfataricus archaeal type IV pilus at 3 Angstrom resolution
分子名称:	Pilin_N domain-containing protein
著者	Kreutzberger, M.A, Wang, F, Krupovic, M, Egelman, E.H.
登録日	2022-12-20
公開日	2023-06-28
最終更新日	2024-06-19
実験手法	ELECTRON MICROSCOPY (3 Å)
主引用文献	The evolution of archaeal flagellar filaments. Proc.Natl.Acad.Sci.USA, 120, 2023

8FK0

Asymmetric cryo-EM structure of a curved Saccharolobus solfataricus type IV pilus
分子名称:	Pilin_N domain-containing protein
著者	Kreutzberger, M.A, Wang, F, Krupovic, M, Egelman, E.H.
登録日	2022-12-20
公開日	2023-06-28
最終更新日	2024-06-19
実験手法	ELECTRON MICROSCOPY (4 Å)
主引用文献	The evolution of archaeal flagellar filaments. Proc.Natl.Acad.Sci.USA, 120, 2023

8FK7

Structure of the Pyrobaculum calidifontis flagellar-like archaeal type IV pilus
分子名称:	Flagellin
著者	Wang, F, Kreutzberger, M.A, Cvirkaite-Krupovic, V, Krupovic, M, Egelman, E.H.
登録日	2022-12-20
公開日	2023-06-28
最終更新日	2023-07-19
実験手法	ELECTRON MICROSCOPY (4.3 Å)
主引用文献	The evolution of archaeal flagellar filaments. Proc.Natl.Acad.Sci.USA, 120, 2023

4ZY6

Crystal structure of P21-activated kinase 1 in complex with an inhibitor compound 29
分子名称:	N~2~-[(7-chloro-1H-benzimidazol-6-yl)methyl]-N~4~-(5-cyclopropyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamine, SULFATE ION, Serine/threonine-protein kinase PAK 1
著者	Rouge, L, Wang, W.
登録日	2015-05-21
公開日	2015-07-01
最終更新日	2015-12-16
実験手法	X-RAY DIFFRACTION (2.15 Å)
主引用文献	Structure-Guided Design of Group I Selective p21-Activated Kinase Inhibitors. J.Med.Chem., 58, 2015

4ZY5

Crystal Structure of p21-activated kinase 1 in complex with an inhibitor compound 17
分子名称:	DIMETHYL SULFOXIDE, N~2~-[(trans-4-aminocyclohexyl)methyl]-N~4~-(3-cyclopropyl-1H-pyrazol-5-yl)pyrimidine-2,4-diamine, SULFATE ION, ...
著者	Rouge, L, Wang, W.
登録日	2015-05-21
公開日	2015-07-01
最終更新日	2015-07-15
実験手法	X-RAY DIFFRACTION (2.35 Å)
主引用文献	Structure-Guided Design of Group I Selective p21-Activated Kinase Inhibitors. J.Med.Chem., 58, 2015

3R1G

Structure Basis of Allosteric Inhibition of BACE1 by an Exosite-Binding Antibody
分子名称:	Beta-secretase 1, FAB of YW412.8.31 antibody heavy chain, FAB of YW412.8.31 antibody light chain
著者	Wang, W, Rouge, L, Wu, P, Chiu, C, Chen, Y, Wu, Y, Watts, R.J.
登録日	2011-03-10
公開日	2011-06-08
最終更新日	2011-07-13
実験手法	X-RAY DIFFRACTION (2.8 Å)
主引用文献	A Therapeutic Antibody Targeting BACE1 Inhibits Amyloid-{beta} Production in Vivo. Sci Transl Med, 3, 2011

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