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PDB: 42507 件

1F4Q
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CRYSTAL STRUCTURE OF APO GRANCALCIN
分子名称: GRANCALCIN
著者Jia, J, Han, Q, Borregaard, N, Lollike, K, Cygler, M.
登録日2000-06-08
公開日2000-09-27
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 of human grancalcin, a member of the penta-EF-hand protein family.
J.Mol.Biol., 300, 2000
7SD1
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Crystal structure of SHOC2
分子名称: Leucine-rich repeat protein SHOC-2
著者Liau, N.P.D, Hymowitz, S.G, Sudhamsu, J.
登録日2021-09-29
公開日2022-04-20
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (3.19 Å)
主引用文献Structural basis for SHOC2 modulation of RAS signalling.
Nature, 609, 2022
8OZ0
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Structure of a human 48S translation initiation complex with eIF4F and eIF4A
分子名称: 18S rRNA, 40S ribosomal protein S10, 40S ribosomal protein S11, ...
著者Brito Querido, J, Sokabe, M, Diaz-Lopez, I, Gordiyenko, Y, Fraser, C.S, Ramakrishnan, V.
登録日2023-05-06
公開日2024-02-07
最終更新日2024-04-24
実験手法ELECTRON MICROSCOPY (3.5 Å)
主引用文献The structure of a human translation initiation complex reveals two independent roles for the helicase eIF4A.
Nat.Struct.Mol.Biol., 31, 2024
3N1C
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Crystal structure of the phosphofructokinase-2 from Escherichia coli in complex with fructose-6-phosphate
分子名称: 6-O-phosphono-beta-D-fructofuranose, 6-phosphofructokinase isozyme 2
著者Pereira, H.M, Cabrera, R, Caniuguir, A, Garratt, R.C, Babul, J.
登録日2010-05-15
公開日2010-12-08
最終更新日2023-09-06
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献The Crystal Complex of Phosphofructokinase-2 of Escherichia coli with Fructose-6-phosphate: KINETIC AND STRUCTURAL ANALYSIS OF THE ALLOSTERIC ATP INHIBITION.
J.Biol.Chem., 286, 2011
6TW9
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HumRadA22F in complex with CAM833
分子名称: CALCIUM ION, DNA repair and recombination protein RadA, GLYCEROL, ...
著者Fischer, G, Marsh, M.E, Scott, D.E, Coyne, A.G, Skidmore, J, Abell, C, Hyvonen, M.
登録日2020-01-12
公開日2021-01-27
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (1.52 Å)
主引用文献A small-molecule inhibitor of the BRCA2-RAD51 interaction modulates RAD51 assembly and potentiates DNA damage-induced cell death.
Cell Chem Biol, 28, 2021
7SKK
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pertussis toxin in complex with ADPR and Nicotinamide
分子名称: NICOTINAMIDE, Pertussis toxin subunit 1, SULFATE ION, ...
著者Littler, D.R, Beddoe, T, Pulliainen, A, Rossjohn, J.
登録日2021-10-21
公開日2022-04-13
最終更新日2023-10-18
実験手法X-RAY DIFFRACTION (1.65000772 Å)
主引用文献Crystal structures of pertussis toxin with NAD + and analogs provide structural insights into the mechanism of its cytosolic ADP-ribosylation activity.
J.Biol.Chem., 298, 2022
7SD0
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Cryo-EM structure of the SHOC2:PP1C:MRAS complex
分子名称: Leucine-rich repeat protein SHOC-2, MAGNESIUM ION, MANGANESE (II) ION, ...
著者Liau, N.P.D, Johnson, M.C, Hymowitz, S.G, Sudhamsu, J.
登録日2021-09-29
公開日2022-04-20
最終更新日2023-11-29
実験手法ELECTRON MICROSCOPY (2.95 Å)
主引用文献Structural basis for SHOC2 modulation of RAS signalling.
Nature, 609, 2022
6TXO
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Crystal structure of the haemagglutinin mutant (Gln226Leu, Del228) from an H10N7 seal influenza virus isolated in Germany in complex with avian receptor analogue 3'-SLN
分子名称: 1,2-ETHANEDIOL, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ...
著者Zhang, J, Xiong, X, Purkiss, A, Walker, P, Gamblin, S, Skehel, J.J.
登録日2020-01-14
公開日2020-10-21
最終更新日2024-01-24
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Hemagglutinin Traits Determine Transmission of Avian A/H10N7 Influenza Virus between Mammals.
Cell Host Microbe, 28, 2020
6U0I
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Putative Antitoxin HicB3 from Escherichia coli str. K-12 substr. DH10B
分子名称: Antitoxin HicB, CHLORIDE ION
著者Osipiuk, J, Tesar, C, Endres, M, Joachimiak, A, Center for Structural Genomics of Infectious Diseases (CSGID)
登録日2019-08-14
公開日2019-08-28
最終更新日2019-12-18
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Putative Antitoxin HicB3 from Escherichia coli str. K-12 substr. DH10B
to be published
6U0T
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Protofilament Ribbon Flagellar Proteins Rib43a-S
分子名称: GUANOSINE-5'-DIPHOSPHATE, GUANOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ...
著者Ichikawa, M, Khalifa, A.A.Z, Vargas, J, Basu, K, Bui, K.H.
登録日2019-08-14
公開日2019-09-25
最終更新日2024-03-13
実験手法ELECTRON MICROSCOPY (4.16 Å)
主引用文献Tubulin lattice in cilia is in a stressed form regulated by microtubule inner proteins.
Proc.Natl.Acad.Sci.USA, 116, 2019
6TYX
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Structure of Ku80 von Willebrand domain S229A mutant complexed with XLF Ku Binding Motif
分子名称: LYS-GLY-LEU-PHE-MET, X-ray repair cross-complementing protein 5
著者Min, J, Pedersen, L.C.
登録日2019-08-09
公開日2019-11-27
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.89944351 Å)
主引用文献Ligand binding characteristics of the Ku80 von Willebrand domain.
DNA Repair (Amst.), 85, 2019
8P61
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Crystal structure of O'nyong'nyong virus capsid protease (106-256)
分子名称: Capsid protein, GLYCEROL, SULFATE ION
著者Plewka, J, Chykunova, Y, Wilk, P, Sienczyk, M, Dubin, G, Pyrc, K.
登録日2023-05-24
公開日2024-03-06
最終更新日2024-05-15
実験手法X-RAY DIFFRACTION (1.9 Å)
主引用文献Autoinhibition of suicidal capsid protease from O'nyong'nyong virus.
Int.J.Biol.Macromol., 262, 2024
8P7L
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Cryo-EM structure of CDK7 subunit of CAK in complex with inhibitor LDC4297
分子名称: 2-[(3S)-piperidin-3-yl]oxy-8-propan-2-yl-N-[(2-pyrazol-1-ylphenyl)methyl]pyrazolo[1,5-a][1,3,5]triazin-4-amine, CDK-activating kinase assembly factor MAT1, Cyclin-dependent kinase 7
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2.1 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
1F4O
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CRYSTAL STRUCTURE OF GRANCALCIN WITH BOUND CALCIUM
分子名称: CALCIUM ION, GRANCALCIN
著者Jia, J, Han, Q, Borregaard, N, Lollike, K, Cygler, M.
登録日2000-06-08
公開日2000-09-27
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 of human grancalcin, a member of the penta-EF-hand protein family.
J.Mol.Biol., 300, 2000
7S3L
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Structure of Bacillus subtilis CcrZ (previously called YtmP)
分子名称: Aminoglycoside phosphotransferase family protein, PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
著者Nandakumar, J, Wozniak, K.J.
登録日2021-09-07
公開日2022-05-11
最終更新日2022-06-01
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Structure and kinase activity of bacterial cell cycle regulator CcrZ.
Plos Genet., 18, 2022
8P64
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Co-crystal structure of PD-L1 with low molecular weight inhibitor
分子名称: Programmed cell death 1 ligand 1, ~{N}-[[1-[(~{E})-2-(2-methyl-3-phenyl-phenyl)ethenyl]-1,2,3,4-tetrazol-5-yl]methyl]ethanamine
著者Plewka, J, Magiera-Mularz, K, van der Straat, R, Draijer, R, Surmiak, E, Butera, R, Land, L, Musielak, B, Domling, A.
登録日2023-05-25
公開日2024-03-06
最終更新日2024-05-15
実験手法X-RAY DIFFRACTION (3.312 Å)
主引用文献1,5-Disubstituted tetrazoles as PD-1/PD-L1 antagonists.
Rsc Med Chem, 15, 2024
8P71
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Cryo-EM structure of CAK in complex with inhibitor ICEC0574
分子名称: (3R,4S)-4-[[7-[(phenylmethyl)amino]-3-propan-2-yl-pyrazolo[1,5-a]pyrimidin-5-yl]amino]pyrrolidin-3-ol, CDK-activating kinase assembly factor MAT1, Cyclin-H, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
8P79
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Cryo-EM structure of CAK with averaged inhibitor density
分子名称: CDK-activating kinase assembly factor MAT1, Cyclin-H, Cyclin-dependent kinase 7
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (1.7 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
7SGS
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Cryo-EM structure of full-length MAP7 bound to the microtubule
分子名称: Ensconsin, GUANOSINE-5'-DIPHOSPHATE, GUANOSINE-5'-TRIPHOSPHATE, ...
著者Ferro, L.S, Fang, Q, Eshun-Wilson, L, Fernandes, J, Jack, A, Farrell, D.P, Golcuk, M, Huijben, T, Costa, K, Gur, M, DiMaio, F, Nogales, E, Yildiz, A.
登録日2021-10-07
公開日2022-05-18
最終更新日2024-06-05
実験手法ELECTRON MICROSCOPY (3.3 Å)
主引用文献Structural and functional insight into regulation of kinesin-1 by microtubule-associated protein MAP7.
Science, 375, 2022
8P6Z
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Cryo-EM structure of CAK in complex with inhibitor ICEC0510-R
分子名称: CDK-activating kinase assembly factor MAT1, Cyclin-H, Cyclin-dependent kinase 7, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2.1 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
8P6W
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Cryo-EM structure of CAK in complex with inhibitor BS-181
分子名称: CDK-activating kinase assembly factor MAT1, Cyclin-H, Cyclin-dependent kinase 7, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (1.9 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
6ZUF
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Urea-based Foldamer Inhibitor chimera C2 in complex with ASF1 Histone chaperone
分子名称: C2 foldamer/peptide hybrid inhibitor of histone chaperone ASF1, GLYCEROL, Histone chaperone ASF1A, ...
著者Bakail, M, Mbianda, J, Perrin, E.M, Guerois, R, Legrand, P, Traore, S, Douat, C, Guichard, G, Ochsenbein, F.
登録日2020-07-22
公開日2021-06-09
最終更新日2024-07-10
実験手法X-RAY DIFFRACTION (1.798 Å)
主引用文献Optimal anchoring of a foldamer inhibitor of ASF1 histone chaperone through backbone plasticity.
Sci Adv, 7, 2021
8P70
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Cryo-EM structure of CAK in complex with inhibitor ICEC0510-S
分子名称: CDK-activating kinase assembly factor MAT1, Cyclin-H, Cyclin-dependent kinase 7, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
8P73
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Cryo-EM structure of CAK in complex with inhibitor ICEC0829
分子名称: (3R,4R)-4-[[[7-[(phenylmethyl)amino]-3-propan-2-yl-pyrazolo[1,5-a]pyrimidin-5-yl]amino]methyl]piperidine-3,4-diol, (3S,4S)-4-[[[7-[(phenylmethyl)amino]-3-propan-2-yl-pyrazolo[1,5-a]pyrimidin-5-yl]amino]methyl]piperidine-3,4-diol, CDK-activating kinase assembly factor MAT1, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024
8P74
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Cryo-EM structure of CAK in complex with inhibitor ICEC0880 (ring-up conformation)
分子名称: (2S,3S)-3-[[7-[(2-bromophenyl)methylamino]-3-propan-2-yl-pyrazolo[1,5-a]pyrimidin-5-yl]amino]butane-1,2,4-triol, CDK-activating kinase assembly factor MAT1, Cyclin-H, ...
著者Cushing, V.I, Koh, A.F, Feng, J, Jurgaityte, K, Bahl, A.K, Ali, S, Kotecha, A, Greber, B.J.
登録日2023-05-30
公開日2024-03-20
最終更新日2024-03-27
実験手法ELECTRON MICROSCOPY (2.2 Å)
主引用文献High-resolution cryo-EM of the human CDK-activating kinase for structure-based drug design.
Nat Commun, 15, 2024

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件を2024-08-14に公開中

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