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7F27
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BU of 7f27 by Molmil
Crystal structure of polyketide ketosynthase
分子名称: 3-oxoacyl-(Acyl-carrier-protein) synthase
著者Kim, Y, Lee, W.C.
登録日2021-06-10
公開日2022-06-15
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.806 Å)
主引用文献Structural basis of the complementary activity of two ketosynthases in aryl polyene biosynthesis.
Sci Rep, 11, 2021
7F28
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BU of 7f28 by Molmil
Crystal structure of a bacterial ketosynthase
分子名称: Ketoacyl_synth_N domain-containing protein, Putative 3-oxoacyl-[ACP] synthase FabV
著者Lee, W.C, Kim, Y.
登録日2021-06-10
公開日2022-06-15
最終更新日2023-11-29
実験手法X-RAY DIFFRACTION (1.877 Å)
主引用文献Structural basis of the complementary activity of two ketosynthases in aryl polyene biosynthesis.
Sci Rep, 11, 2021
2G1N
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BU of 2g1n by Molmil
Ketopiperazine-based renin inhibitors: Optimization of the "C" ring
分子名称: 2-acetamido-2-deoxy-beta-D-glucopyranose, N-{2-[6-(2,4-DIAMINO-6-ETHYLPYRIMIDIN-5-YL)-2,2-DIMETHYL-3-OXO-2,3-DIHYDRO-4H-1,4-BENZOTHIAZIN-4-YL]ETHYL}ACETAMIDE, Renin
著者Holsworth, D.D.
登録日2006-02-14
公開日2006-06-13
最終更新日2020-07-29
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Ketopiperazine-based renin inhibitors: Optimization of the "C" ring
BIOORG.MED.CHEM.LETT., 16, 2006
5GTI
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BU of 5gti by Molmil
Native XFEL structure of photosystem II (two flash dataset)
分子名称: 1,2-DI-O-ACYL-3-O-[6-DEOXY-6-SULFO-ALPHA-D-GLUCOPYRANOSYL]-SN-GLYCEROL, 1,2-DIPALMITOYL-PHOSPHATIDYL-GLYCEROLE, 1,2-DISTEAROYL-MONOGALACTOSYL-DIGLYCERIDE, ...
著者Suga, M, Shen, J.R.
登録日2016-08-20
公開日2017-03-15
最終更新日2020-07-29
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Light-induced structural changes and the site of O=O bond formation in PSII caught by XFEL.
Nature, 543, 2017
5GTH
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BU of 5gth by Molmil
Native XFEL structure of photosystem II (dark dataset)
分子名称: 1,2-DI-O-ACYL-3-O-[6-DEOXY-6-SULFO-ALPHA-D-GLUCOPYRANOSYL]-SN-GLYCEROL, 1,2-DIPALMITOYL-PHOSPHATIDYL-GLYCEROLE, 1,2-DISTEAROYL-MONOGALACTOSYL-DIGLYCERIDE, ...
著者Suga, M, Shen, J.R.
登録日2016-08-20
公開日2017-03-15
最終更新日2023-11-08
実験手法X-RAY DIFFRACTION (2.5 Å)
主引用文献Light-induced structural changes and the site of O=O bond formation in PSII caught by XFEL.
Nature, 543, 2017
3DM7
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BU of 3dm7 by Molmil
Crystal Structure of the Vps75 Histone Chaperone
分子名称: Vacuolar protein sorting-associated protein 75
著者Tang, Y, Marmorstein, R.
登録日2008-06-30
公開日2008-09-09
最終更新日2021-10-20
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Structure of Vps75 and implications for histone chaperone function.
Proc.Natl.Acad.Sci.Usa, 105, 2008
4DGV
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BU of 4dgv by Molmil
Structure of the Hepatitis C virus envelope glycoprotein E2 antigenic region 412-423 bound to the broadly neutralizing antibody HCV1, P2(1) form
分子名称: E2 peptide, HCV1 Heavy Chain, HCV1 Light Chain, ...
著者Kong, L, Wilson, I.A, Law, M.
登録日2012-01-26
公開日2012-05-23
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (1.805 Å)
主引用文献Structural basis of hepatitis C virus neutralization by broadly neutralizing antibody HCV1.
Proc.Natl.Acad.Sci.USA, 109, 2012
3S88
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BU of 3s88 by Molmil
Crystal structure of Sudan Ebolavirus Glycoprotein (strain Gulu) bound to 16F6
分子名称: 16F6 - Heavy chain, 16F6 - Light chain, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ...
著者Saphire, E.O, Dias, J.M, Bale, S.
登録日2011-05-27
公開日2011-12-07
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (3.351 Å)
主引用文献A shared structural solution for neutralizing ebolaviruses.
Nat.Struct.Mol.Biol., 18, 2011
2KSE
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BU of 2kse by Molmil
Backbone structure of the membrane domain of E. coli histidine kinase receptor QseC, Center for Structures of Membrane Proteins (CSMP) target 4311C
分子名称: Sensor protein qseC
著者Maslennikov, I, Klammt, C, Kefala, G, Esquivies, L, Kwiatkowski, W, Choe, S, Center for Structures of Membrane Proteins (CSMP)
登録日2010-01-02
公開日2010-03-02
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Membrane domain structures of three classes of histidine kinase receptors by cell-free expression and rapid NMR analysis.
Proc.Natl.Acad.Sci.USA, 107, 2010
2MJ6
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BU of 2mj6 by Molmil
Solution structure of the extracellular sensor domain of DraK histidine kinase
分子名称: Putative two-component system histidine kinase
著者Yeo, K, Cheong, H.
登録日2013-12-25
公開日2014-09-24
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Mechanism of the pH-Induced Conformational Change in the Sensor Domain of the DraK Histidine Kinase via the E83, E105, and E107 Residues
Plos One, 9, 2014
3UK8
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BU of 3uk8 by Molmil
The crystal structure of the cd-bound domain 3 of the cadmium carbonic anhydrase from marine diatom Thalassiosira weissflogii
分子名称: ACETATE ION, CADMIUM ION, Cadmium-specific carbonic anhydrase
著者Alterio, V, De Simone, G.
登録日2011-11-09
公開日2012-07-11
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogii.
Biochimie, 94, 2012
2M36
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BU of 2m36 by Molmil
Solution structure of the insecticidal spider-venom peptide Aps III
分子名称: U2-cyrtautoxin-As1a
著者King, G.F, Bende, N.S, Mobli, M.
登録日2013-01-10
公開日2013-03-27
最終更新日2023-06-14
実験手法SOLUTION NMR
主引用文献The insecticidal neurotoxin Aps III is an atypical knottin peptide that potently blocks insect voltage-gated sodium channels.
Biochem Pharmacol, 85, 2013
2XXN
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BU of 2xxn by Molmil
Structure of the vIRF4-HAUSP TRAF domain complex
分子名称: K10, UBIQUITIN CARBOXYL-TERMINAL HYDROLASE 7
著者Choi, W.C, Hwang, J, Kim, M.H.
登録日2010-11-11
公開日2011-11-09
最終更新日2023-12-20
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Bilateral Inhibition of Hausp Deubiquitinase by a Viral Interferon Regulatory Factor Protein
Nat.Struct.Mol.Biol., 18, 2011
2V6I
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BU of 2v6i by Molmil
Kokobera Virus Helicase
分子名称: PYROPHOSPHATE 2-, RNA HELICASE
著者Speroni, S, De Colibus, L, Coutard, B, Canard, B, Mattevi, A.
登録日2007-07-18
公開日2008-03-25
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Structure and Biochemical Analysis of Kokobera Virus Helicase
Proteins: Struct., Funct., Bioinf., 70, 2008
4PX6
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BU of 4px6 by Molmil
SYK catalytic domain in complex with a potent pyridopyrimidinone inhibitor
分子名称: 7-{[(1R,2S)-2-aminocyclohexyl]amino}-5-(1H-indol-7-ylamino)pyrido[4,3-d]pyrimidin-4(3H)-one, Tyrosine-protein kinase SYK
著者Lee, C.C.
登録日2014-03-21
公開日2014-04-23
最終更新日2023-09-20
実験手法X-RAY DIFFRACTION (1.6 Å)
主引用文献Syk inhibitors with high potency in presence of blood.
Bioorg.Med.Chem.Lett., 24, 2014
2V37
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BU of 2v37 by Molmil
Solution structure of the N-terminal extracellular domain of human T- cadherin
分子名称: CADHERIN-13
著者Dames, S.A, Bang, E.J, Ahrens, T, Haeussinger, D, Grzesiek, S.
登録日2007-06-13
公開日2008-06-10
最終更新日2024-05-15
実験手法SOLUTION NMR
主引用文献Insights into the low adhesive capacity of human T-cadherin from the NMR structure of Its N-terminal extracellular domain.
J. Biol. Chem., 283, 2008
2V6J
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BU of 2v6j by Molmil
Kokobera Virus Helicase: Mutant Met47Thr
分子名称: RNA HELICASE
著者Speroni, S, De Colibus, L, Coutard, B, Canard, B, Mattevi, A.
登録日2007-07-18
公開日2008-03-25
最終更新日2023-12-13
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structure and Biochemical Analysis of Kokobera Virus Helicase
Proteins: Struct., Funct., Bioinf., 70, 2008
2HLS
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BU of 2hls by Molmil
The crystal structure of a protein disulfide oxidoreductase from Aeropyrum pernix k1
分子名称: CHLORIDE ION, protein disulfide oxidoreductase
著者D'Ambrosio, K, De Simone, G.
登録日2006-07-10
公開日2006-10-03
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (1.93 Å)
主引用文献A Novel Member of the Protein Disulfide Oxidoreductase Family from Aeropyrum pernix K1: Structure, Function and Electrostatics.
J.Mol.Biol., 362, 2006
3UGC
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BU of 3ugc by Molmil
Structural basis of Jak2 inhibition by the type II inhibtor NVP-BBT594
分子名称: 5-{[6-(acetylamino)pyrimidin-4-yl]oxy}-N-{4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl}-2,3-dihydro-1H-indole-1-carboxamide, MALONATE ION, Tyrosine-protein kinase JAK2
著者Scheufler, C, Tavares, G.A, Manley, P.W, Pissot-Soldermann, C, Kroemer, M.
登録日2011-11-02
公開日2012-05-16
最終更新日2023-09-13
実験手法X-RAY DIFFRACTION (1.34 Å)
主引用文献Modulation of activation-loop phosphorylation by JAK inhibitors is binding mode dependent.
Cancer Discov, 2, 2012
7F8K
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BU of 7f8k by Molmil
Room temperature structure of bacterial copper amine oxidase determined by serial femtosecond crystallography
分子名称: COPPER (II) ION, Phenylethylamine oxidase
著者Murakawa, T, Okajima, T.
登録日2021-07-02
公開日2021-09-08
最終更新日2021-10-13
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Microcrystal preparation for serial femtosecond X-ray crystallography of bacterial copper amine oxidase
Acta Crystallogr.,Sect.F, 77, 2021
3U6B
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BU of 3u6b by Molmil
Ef-tu (escherichia coli) in complex with nvp-ldi028
分子名称: Elongation factor Tu 1, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ...
著者Palestrant, D.J.
登録日2011-10-12
公開日2012-02-08
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.12 Å)
主引用文献Antibacterial optimization of 4-aminothiazolyl analogues of the natural product GE2270 A: identification of the cycloalkylcarboxylic acids.
J.Med.Chem., 54, 2011
3U6K
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Ef-tu (escherichia coli) in complex with nvp-ldk733
分子名称: Elongation factor Tu 1, GUANOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ...
著者Palestrant, D.J.
登録日2011-10-12
公開日2012-02-08
最終更新日2023-11-15
実験手法X-RAY DIFFRACTION (2.45 Å)
主引用文献Antibacterial optimization of 4-aminothiazolyl analogues of the natural product GE2270 A: identification of the cycloalkylcarboxylic acids.
J.Med.Chem., 54, 2011
1A5G
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BU of 1a5g by Molmil
HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN
分子名称: (1S,7S)-7-amino-7-benzyl-N-[(1S)-4-carbamimidamido-1-{(1S)-1-hydroxy-2-oxo-2-[(2-phenylethyl)amino]ethyl}butyl]-8-oxohexahydro-1H-pyrazolo[1,2-a]pyridazine-1-carboxamide, ALPHA-THROMBIN (LARGE SUBUNIT), ALPHA-THROMBIN (SMALL SUBUNIT), ...
著者St Charles, R, Tulinsky, A, Kahn, M.
登録日1998-02-16
公開日1998-05-27
最終更新日2024-06-05
実験手法X-RAY DIFFRACTION (2.06 Å)
主引用文献Bound structures of novel P3-P1' beta-strand mimetic inhibitors of thrombin.
J.Med.Chem., 42, 1999
1B5G
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BU of 1b5g by Molmil
HUMAN THROMBIN COMPLEXED WITH NOVEL SYNTHETIC PEPTIDE MIMETIC INHIBITOR AND HIRUGEN
分子名称: ALPHA-THROMBIN, HIRUGEN, SODIUM ION, ...
著者St Charles, R, Tulinsky, A, Kahn, M.
登録日1998-03-05
公開日1998-05-27
最終更新日2024-06-05
実験手法X-RAY DIFFRACTION (2.07 Å)
主引用文献Bound structures of novel P3-P1' beta-strand mimetic inhibitors of thrombin.
J.Med.Chem., 42, 1999
3TXO
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PKC eta kinase in complex with a naphthyridine
分子名称: 2-methyl-N~1~-[3-(pyridin-4-yl)-2,6-naphthyridin-1-yl]propane-1,2-diamine, Protein kinase C eta type
著者Stark, W, Rummel, G, Cowan-Jacob, S.W.
登録日2011-09-23
公開日2011-11-30
最終更新日2011-12-07
実験手法X-RAY DIFFRACTION (2.05 Å)
主引用文献2,6-Naphthyridines as potent and selective inhibitors of the novel protein kinase C isozymes.
Bioorg.Med.Chem.Lett., 21, 2011

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