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8KF5
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The cryo-EM structure of type1 amyloid beta 42 fibril in AD3.
分子名称: Amyloid-beta precursor protein
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-15
公開日2024-08-21
実験手法ELECTRON MICROSCOPY (3.4 Å)
主引用文献The cryo-EM structure of type1 amyloid beta 42 fibril in AD3.
To Be Published
8KF4
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The cryo-EM structure of type1 amyloid beta 42 fibril in AD2 patient.
分子名称: Amyloid-beta precursor protein
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-15
公開日2024-08-21
実験手法ELECTRON MICROSCOPY (3 Å)
主引用文献The cryo-EM structure of type1 amyloid beta 42 fibril in AD2 patient.
To Be Published
8KF3
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BU of 8kf3 by Molmil
The cryo-EM structure of type3 amyloid beta 42 fibril.
分子名称: Amyloid-beta precursor protein
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-15
公開日2024-08-21
実験手法ELECTRON MICROSCOPY (3.5 Å)
主引用文献The cryo-EM structure of type1 amyloid beta 42 fibril.
To Be Published
8KF6
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BU of 8kf6 by Molmil
The cryo-EM structure of AV-45 bound type3 amyloid beta 42 fibril.
分子名称: P3(40)
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-15
公開日2024-08-21
実験手法ELECTRON MICROSCOPY (3.7 Å)
主引用文献The cryo-EM structure of type1 amyloid beta 42 fibril.
To Be Published
8KEW
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BU of 8kew by Molmil
The cryo-EM structure of type1 amyloid beta 42 fibril.
分子名称: P3(40)
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-13
公開日2024-08-14
実験手法ELECTRON MICROSCOPY (3.3 Å)
主引用文献The cryo-EM structure of type1 amyloid beta 42 fibril.
To Be Published
8KF1
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BU of 8kf1 by Molmil
The cryo-EM structure of AV-45 bound type1 amyloid beta 42 fibril.
分子名称: 4-[2-[6-[2-[2-(2-fluoranylethoxy)ethoxy]ethoxy]pyridin-3-yl]ethyl]-~{N}-methyl-aniline, P3(40)
著者Zhao, Q.Y, Tao, Y.Q, Liu, C, Li, D.
登録日2023-08-15
公開日2024-08-21
実験手法ELECTRON MICROSCOPY (3.3 Å)
主引用文献The cryo-EM structure of AV-45 bound type1 amyloid beta 42 fibril.
To Be Published
8P5F
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BU of 8p5f by Molmil
Human wild-type GAPDH,orthorhombic form
分子名称: ACETATE ION, Glyceraldehyde-3-phosphate dehydrogenase, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ...
著者Samygina, V.R, Muronetz, V.I, Schmalhausen, E.V.
登録日2023-05-24
公開日2023-07-05
最終更新日2023-07-12
実験手法X-RAY DIFFRACTION (1.82 Å)
主引用文献S-nitrosylation and S-glutathionylation of GAPDH: Similarities, differences, and relationships.
Biochim Biophys Acta Gen Subj, 1867, 2023
1L4D
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BU of 1l4d by Molmil
CRYSTAL STRUCTURE OF MICROPLASMINOGEN-STREPTOKINASE ALPHA DOMAIN COMPLEX
分子名称: PLASMINOGEN, STREPTOKINASE, SULFATE ION
著者Wakeham, N, Terzyan, S, Zhai, P, Loy, J.A, Tang, J, Zhang, X.C.
登録日2002-03-04
公開日2002-12-11
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Effects of deletion of streptokinase residues 48-59 on plasminogen activation
PROTEIN ENG., 15, 2002
8P4K
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BU of 8p4k by Molmil
Vaccinia Virus palisade layer A10 trimer
分子名称: Core protein OPG136
著者Datler, J, Hansen, J.M, Thader, A, Schloegl, A, Hodirnau, V.V, Schur, F.K.M.
登録日2023-05-22
公開日2024-01-17
最終更新日2024-07-31
実験手法ELECTRON MICROSCOPY (3.8 Å)
主引用文献Multi-modal cryo-EM reveals trimers of protein A10 to form the palisade layer in poxvirus cores.
Nat.Struct.Mol.Biol., 31, 2024
8OVB
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BU of 8ovb by Molmil
Human Complement C3b in complex with Trypanosoma brucei ISG65.
分子名称: Complement C3, Complement C3f fragment, ISG65 G
著者Cook, A.D, Higgins, M.K.
登録日2023-04-25
公開日2024-02-14
最終更新日2024-05-15
実験手法ELECTRON MICROSCOPY (3.4 Å)
主引用文献Molecular mechanism of complement inhibition by the trypanosome receptor ISG65.
Elife, 12, 2024
8OTF
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Ab typeII filament from Guam ALS/PDC
分子名称: Amyloid-beta precursor protein
著者Qi, C, Yang, S, Scheres, S.H.W, Goedert, M.
登録日2023-04-20
公開日2024-03-27
実験手法ELECTRON MICROSCOPY (3.3 Å)
主引用文献Tau filaments from amyotrophic lateral sclerosis/parkinsonism-dementia complex adopt the CTE fold.
Proc.Natl.Acad.Sci.USA, 120, 2023
8PE9
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BU of 8pe9 by Molmil
Complex between DDR1 DS-like domain and PRTH-101 Fab
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ...
著者Liu, J, Chiang, H, Xiong, W, Laurent, V, Griffiths, S.C, Duelfer, J, Deng, H, Sun, X, Yin, Y.W, Li, W, Audoly, L.P, An, Z, Schuerpf, T, Li, R, Zhang, N.
登録日2023-06-13
公開日2023-06-28
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.152 Å)
主引用文献A highly selective humanized DDR1 mAb reverses immune exclusion by disrupting collagen fiber alignment in breast cancer.
J Immunother Cancer, 11, 2023
1AO5
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BU of 1ao5 by Molmil
MOUSE GLANDULAR KALLIKREIN-13 (PRORENIN CONVERTING ENZYME)
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, GLANDULAR KALLIKREIN-13
著者Timm, D.E.
登録日1997-07-16
公開日1997-10-15
最終更新日2023-08-02
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献The crystal structure of the mouse glandular kallikrein-13 (prorenin converting enzyme)
Protein Sci., 6, 1997
2J15
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BU of 2j15 by Molmil
Cyclic MrIA: An exceptionally stable and potent cyclic conotoxin with a novel topological fold that targets the norepinephrine transporter.
分子名称: MAI126P
著者Lovelace, E.S, Armishaw, C.J, Colgrave, M.L, Walstrom, M.E, Alewood, P.F, Daly, N.L, Craik, D.J.
登録日2006-08-09
公開日2006-11-01
最終更新日2018-05-09
実験手法SOLUTION NMR
主引用文献Cyclic MrIA: a stable and potent cyclic conotoxin with a novel topological fold that targets the norepinephrine transporter.
J. Med. Chem., 49, 2006
1EB1
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BU of 1eb1 by Molmil
Complex structure of human thrombin with N-methyl-arginine inhibitor
分子名称: 3-CYCLOHEXYL-D-ALANYL-L-PROLYL-N~2~-METHYL-L-ARGININE, PEPTIDE INHIBITOR, THROMBIN HEAVY CHAIN, ...
著者Friedrich, R, Steinmetzer, T, Bode, W.
登録日2001-07-18
公開日2002-01-28
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献The Methyl Group of N(Alpha)(Me)Arg-Containing Peptides Disturbs the Active-Site Geometry of Thrombin, Impairing Efficient Cleavage
J.Mol.Biol., 316, 2002
5E7F
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BU of 5e7f by Molmil
Complex between lactococcal phage Tuc2009 RBP head domain and a nanobody (L06)
分子名称: Major structural protein 1, nanobody L06
著者Legrand, P, Collins, B, Blangy, S, Murphy, J, Spinelli, S, Gutierrez, C, Richet, N, Kellenberger, C, Desmyter, A, Mahony, J, van Sinderen, D, Cambillau, C.
登録日2015-10-12
公開日2015-12-30
最終更新日2024-01-10
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献The Atomic Structure of the Phage Tuc2009 Baseplate Tripod Suggests that Host Recognition Involves Two Different Carbohydrate Binding Modules.
Mbio, 7, 2016
3MG7
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BU of 3mg7 by Molmil
Structure of yeast 20S open-gate proteasome with Compound 8
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, 4-(benzyloxy)-N-[(1S,2R)-2-hydroxy-1-({(1S)-1-[(2-methylbenzyl)carbamoyl]-3-phenylpropyl}carbamoyl)propyl]benzamide, MAGNESIUM ION, ...
著者Sintchak, M.D.
登録日2010-04-05
公開日2011-05-18
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.78 Å)
主引用文献Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit.
Biochem.J., 430, 2010
5DVH
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BU of 5dvh by Molmil
Structure of the Kunitz-type cysteine protease inhibitor PCPI-3 from potato
分子名称: CHLORIDE ION, PCPI-3
著者Brynda, J, Mishra, M, Mares, M.
登録日2015-09-21
公開日2016-10-12
最終更新日2017-09-06
実験手法X-RAY DIFFRACTION (1.8 Å)
主引用文献Structure of the Kunitz-type cysteine protease inhibitor PCPI-3 from potato
To Be Published
3MG4
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Structure of yeast 20S proteasome with Compound 1
分子名称: (2S)-2-amino-N-[(1S)-1-({(1S)-1-[(4-methylbenzyl)carbamoyl]-3-phenylpropyl}carbamoyl)-3-phenylpropyl]-4-phenylbutanamide, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, MAGNESIUM ION, ...
著者Sintchak, M.D.
登録日2010-04-05
公開日2011-04-27
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (3.11 Å)
主引用文献Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit.
Biochem.J., 430, 2010
3MG8
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BU of 3mg8 by Molmil
Structure of yeast 20S open-gate proteasome with Compound 16
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, MAGNESIUM ION, N-(2,2-dimethylpropyl)-N~2~-[1H-indol-3-yl(oxo)acetyl]-L-asparaginyl-N-(2-methylbenzyl)-3-pyridin-4-yl-L-alaninamide, ...
著者Sintchak, M.D.
登録日2010-04-05
公開日2011-05-18
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.59 Å)
主引用文献Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit.
Biochem.J., 430, 2010
5E3H
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BU of 5e3h by Molmil
Structural Basis for RNA Recognition and Activation of RIG-I
分子名称: ADENOSINE-5'-DIPHOSPHATE, BERYLLIUM TRIFLUORIDE ION, GLYCEROL, ...
著者Jiang, F, Miller, M.T, Marcotrigiano, J.
登録日2015-10-02
公開日2015-11-18
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structural basis of RNA recognition and activation by innate immune receptor RIG-I.
Nature, 479, 2011
5DSS
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BU of 5dss by Molmil
MP-4 contributes to snake venom neutralization by Mucuna pruriens seeds through stimulation of cross-reactive antibodies
分子名称: MP-4
著者Kumar, A, Nair, D.T, Salunke, D.M.
登録日2015-09-17
公開日2016-03-30
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献MP-4 Contributes to Snake Venom Neutralization by Mucuna pruriens Seeds through an Indirect Antibody-mediated Mechanism.
J.Biol.Chem., 291, 2016
5DT7
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BU of 5dt7 by Molmil
Crystal structure of the GH1 beta-glucosidase from Exiguobacterium antarcticum B7 in space group C2221
分子名称: 3-CYCLOHEXYL-1-PROPYLSULFONIC ACID, Beta-glucosidase, GLYCEROL, ...
著者Zanphorlin, L.M, Giuseppe, P.O, Tonoli, C.C.C, Murakami, M.T.
登録日2015-09-17
公開日2016-04-13
最終更新日2023-09-27
実験手法X-RAY DIFFRACTION (2.15 Å)
主引用文献Oligomerization as a strategy for cold adaptation: Structure and dynamics of the GH1 beta-glucosidase from Exiguobacterium antarcticum B7.
Sci Rep, 6, 2016
1ELT
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BU of 1elt by Molmil
STRUCTURE OF NATIVE PANCREATIC ELASTASE FROM NORTH ATLANTIC SALMON AT 1.61 ANGSTROMS RESOLUTION
分子名称: CALCIUM ION, ELASTASE
著者Berglund, G.I, Smalaas, A.O.
登録日1995-01-02
公開日1996-01-01
最終更新日2018-04-18
実験手法X-RAY DIFFRACTION (1.61 Å)
主引用文献Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution.
Acta Crystallogr.,Sect.D, 51, 1995
3MG6
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BU of 3mg6 by Molmil
Structure of yeast 20S open-gate proteasome with Compound 6
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, MAGNESIUM ION, N~2~-{[(1S)-6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl]acetyl}-N-{(1S)-1-[(4-methylbenzyl)carbamoyl]-3-phenylpropyl}-L-threoninamide, ...
著者Sintchak, M.D.
登録日2010-04-05
公開日2011-05-18
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit.
Biochem.J., 430, 2010

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