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PDB: 42681 results

3NJK
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D116A mutant of SO1698 protein, an aspartic peptidase from Shewanella oneidensis, at pH5.5
Descriptor: GLYCEROL, Peptidase
Authors:Osipiuk, J, Mulligan, R, Bargassa, M, Collart, F, Joachimiak, A, Midwest Center for Structural Genomics (MCSG)
Deposit date:2010-06-17
Release date:2010-07-21
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Characterization of member of DUF1888 protein family, self-cleaving and self-assembling endopeptidase.
J.Biol.Chem., 287, 2012
3NRO
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Crystal Structure of putative transcriptional factor Lmo1026 from Listeria monocytogenes (FRAGMENT 52-321), Northeast Structural Genomics Consortium Target LmR194
Descriptor: Lmo1026 protein
Authors:Kuzin, A, Su, M, Seetharaman, J, Mao, M, Xiao, R, Ciccosanti, C, Lee, D, Everett, J.K, Nair, R, Acton, T.B, Rost, B, Montelione, G.T, Hunt, J.F, Tong, L, Northeast Structural Genomics Consortium (NESG)
Deposit date:2010-06-30
Release date:2010-08-04
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.9 Å)
Cite:Northeast Structural Genomics Consortium Target LmR194
To be Published
3NTB
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Structure of 6-methylthio naproxen analog bound to mCOX-2.
Descriptor: (2S)-2-[6-(methylsulfanyl)naphthalen-2-yl]propanoic acid, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ...
Authors:Duggan, K.C, Musee, J, Walters, M.J, Harp, J.M, Kiefer, J.R, Oates, J.A, Marnett, L.J.
Deposit date:2010-07-03
Release date:2010-09-01
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.27 Å)
Cite:Molecular basis for cyclooxygenase inhibition by the non-steroidal anti-inflammatory drug naproxen.
J.Biol.Chem., 285, 2010
3NT1
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High resolution structure of naproxen:COX-2 complex.
Descriptor: (2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ...
Authors:Duggan, K.C, Musee, J, Walters, M.J, Harp, J.M, Kiefer, J.R, Oates, J.A, Marnett, L.J.
Deposit date:2010-07-02
Release date:2010-09-01
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (1.73 Å)
Cite:Molecular basis for cyclooxygenase inhibition by the non-steroidal anti-inflammatory drug naproxen.
J.Biol.Chem., 285, 2010
3NXJ
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Crystal Structure of Ketosteroid Isomerase D99N from Pseudomonas Testosteroni (tKSI)
Descriptor: SULFATE ION, Steroid Delta-isomerase
Authors:Gonzalez, A, Tsai, Y, Schwans, J, Sunden, F, Herschlag, D.
Deposit date:2010-07-13
Release date:2011-08-03
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.966 Å)
Cite:Crystal Structure of Ketosteroid Isomerase D99N from Pseudomonas Testosteroni (tKSI)
To be Published
3NZT
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BU of 3nzt by Molmil
2.0 Angstrom Crystal structure of Glutamate--Cysteine Ligase (gshA) ftom Francisella tularensis in Complex with AMP
Descriptor: ADENOSINE MONOPHOSPHATE, Glutamate--cysteine ligase, SULFATE ION
Authors:Minasov, G, Halavaty, A, Shuvalova, L, Dubrovska, I, Winsor, J, Papazisi, L, Anderson, W.F, Center for Structural Genomics of Infectious Diseases (CSGID)
Deposit date:2010-07-16
Release date:2010-07-28
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (2 Å)
Cite:2.0 Angstrom Crystal structure of Glutamate--Cysteine Ligase (gshA) ftom Francisella tularensis in Complex with AMP.
To be Published
3O2R
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Structural flexibility in region involved in dimer formation of nuclease domain of Ribonuclase III (rnc) from Campylobacter jejuni
Descriptor: CHLORIDE ION, Ribonuclease III
Authors:Minasov, G, Halavaty, A, Shuvalova, L, Dubrovska, I, Winsor, J, Papazisi, L, Anderson, W.F, Center for Structural Genomics of Infectious Diseases (CSGID)
Deposit date:2010-07-22
Release date:2010-08-04
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.251 Å)
Cite:Structural Flexibility in Region Involved in Dimer Formation of Nuclease Domain of Ribonuclase III (rnc) from Campylobacter jejuni.
TO BE PUBLISHED
6O94
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Structure of the IRAK4 kinase domain with compound 17
Descriptor: CALCIUM ION, Interleukin-1 receptor-associated kinase 4, N-{5-[4-(hydroxymethyl)piperidin-1-yl]-1-methyl-2-(morpholin-4-yl)-1H-benzimidazol-6-yl}pyrazolo[1,5-a]pyrimidine-3-carboxamide
Authors:Yu, C, Drobnick, J, Bryan, M.C, Kiefer, J, Lupardus, P.J.
Deposit date:2019-03-13
Release date:2019-05-22
Last modified:2024-04-03
Method:X-RAY DIFFRACTION (1.98 Å)
Cite:Development of Potent and Selective Pyrazolopyrimidine IRAK4 Inhibitors.
J.Med.Chem., 62, 2019
3O6D
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Pyridoxal phosphate biosynthetic protein PdxJ from Campylobacter jejuni in complex with pyridoxine-5'-phosphate
Descriptor: PHOSPHATE ION, PYRIDOXINE-5'-PHOSPHATE, Pyridoxine 5'-phosphate synthase
Authors:Osipiuk, J, Zhou, M, Kwon, K, Anderson, W.F, Joachimiak, A, Center for Structural Genomics of Infectious Diseases (CSGID)
Deposit date:2010-07-28
Release date:2010-08-11
Last modified:2017-11-08
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:X-ray crystal structure of pyridoxal phosphate biosynthetic protein PdxJ from Campylobacter jejuni.
To be Published
3O6K
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BU of 3o6k by Molmil
Crystal structure of anti-Tat HIV Fab'11H6H1
Descriptor: 11H6H1 Fab' heavy chain, 11H6H1 Fab' light chain
Authors:Serriere, J, Gouet, P, Guillon, C.
Deposit date:2010-07-29
Release date:2010-11-10
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (2 Å)
Cite:Fab'-induced folding of antigenic N-terminal peptides from intrinsically disordered HIV-1 Tat revealed by X-ray crystallography.
J.Mol.Biol., 405, 2011
3O4R
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Crystal Structure of Human Dehydrogenase/Reductase (SDR family) member 4 (DHRS4)
Descriptor: 1,2-ETHANEDIOL, 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, Dehydrogenase/reductase SDR family member 4, ...
Authors:Ugochukwu, E, Bhatia, C, Krojer, T, Vollmar, M, Yue, W.W, Bountra, C, Arrowsmith, C.H, Weigelt, J, Edwards, A, von Delft, F, Oppermann, U, Structural Genomics Consortium (SGC)
Deposit date:2010-07-27
Release date:2010-08-04
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.7 Å)
Cite:Crystal Structure of Human Dehydrogenase/Reductase (SDR family) member 4 (DHRS4)
To be Published
3O6V
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BU of 3o6v by Molmil
Crystal structure of Uridine Phosphorylase from Vibrio cholerae O1 biovar El Tor
Descriptor: FORMIC ACID, GLYCEROL, Uridine phosphorylase
Authors:Maltseva, N, Kim, Y, Hasseman, J, Anderson, W.F, Joachimiak, A, Center for Structural Genomics of Infectious Diseases (CSGID)
Deposit date:2010-07-29
Release date:2010-10-13
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (1.695 Å)
Cite:Crystal structure of Uridine Phosphorylase from Vibrio cholerae O1 biovar El Tor
To be Published
3O7P
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BU of 3o7p by Molmil
Crystal structure of the E.coli Fucose:proton symporter, FucP (N162A)
Descriptor: L-fucose-proton symporter, nonyl beta-D-glucopyranoside
Authors:Dang, S.Y, Sun, L.F, Wang, J, Yan, N.
Deposit date:2010-07-30
Release date:2010-09-15
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (3.196 Å)
Cite:Structure of a fucose transporter in an outward-open conformation
Nature, 467, 2010
3NR6
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BU of 3nr6 by Molmil
Crystal structure of xenotropic murine leukemia virus-related virus (XMRV) protease
Descriptor: PHOSPHATE ION, POTASSIUM ION, Protease p14
Authors:Lubkowski, J, Li, M, Gustchina, A, Zhou, D, Dauter, Z, Wlodawer, A.
Deposit date:2010-06-30
Release date:2011-02-02
Last modified:2024-04-03
Method:X-RAY DIFFRACTION (1.97 Å)
Cite:Crystal structure of XMRV protease differs from the structures of other retropepsins.
Nat.Struct.Mol.Biol., 18, 2011
3NZL
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BU of 3nzl by Molmil
Crystal Structure of the N-terminal domain of DNA-binding protein SATB1 from Homo sapiens, Northeast Structural Genomics Consortium Target HR4435B
Descriptor: DNA-binding protein SATB1
Authors:Forouhar, F, Abashidze, M, Seetharaman, J, Kuzin, A.P, Patel, P, Xiao, R, Ciccosanti, C, Shastry, R, Everett, J.K, Nair, R, Acton, T.B, Rost, B, Montelione, G.T, Hunt, J.F, Tong, L, Northeast Structural Genomics Consortium (NESG)
Deposit date:2010-07-16
Release date:2010-09-22
Last modified:2019-07-17
Method:X-RAY DIFFRACTION (1.199 Å)
Cite:Crystal Structure of the N-terminal domain of DNA-binding protein SATB1 from Homo sapiens, Northeast Structural Genomics Consortium Target HR4435B (CASP Target)
To be Published
3O4C
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BU of 3o4c by Molmil
Crystal structure of Symfoil-4V: de novo designed beta-trefoil architecture with symmetric primary structure
Descriptor: 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, CHLORIDE ION, SULFATE ION, ...
Authors:Lee, J, Blaber, M.
Deposit date:2010-07-26
Release date:2010-12-22
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (1.75 Å)
Cite:Experimental support for the evolution of symmetric protein architecture from a simple peptide motif.
Proc.Natl.Acad.Sci.USA, 108, 2011
7MSA
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BU of 7msa by Molmil
GDC-9545 in complex with estrogen receptor alpha
Descriptor: (2S)-3-(3-hydroxyphenyl)-2-(4-iodophenyl)-4-methyl-2H-1-benzopyran-6-ol, 3-[(1R,3R)-1-(2,6-difluoro-4-{[1-(3-fluoropropyl)azetidin-3-yl]amino}phenyl)-3-methyl-1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl]-2,2-difluoropropan-1-ol, Estrogen receptor
Authors:Kiefer, J.R, Vinogradova, M, Liang, J, Zbieg, J.R, Wang, X, Ortwine, D.F.
Deposit date:2021-05-10
Release date:2021-06-02
Last modified:2024-05-22
Method:X-RAY DIFFRACTION (2.24 Å)
Cite:GDC-9545 (Giredestrant): A Potent and Orally Bioavailable Selective Estrogen Receptor Antagonist and Degrader with an Exceptional Preclinical Profile for ER+ Breast Cancer.
J.Med.Chem., 64, 2021
3O5Y
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BU of 3o5y by Molmil
The Crystal Structure of the GAF domain of a two-component sensor histidine kinase from Bacillus halodurans to 2.45A
Descriptor: ACETATE ION, Sensor protein
Authors:Stein, A.J, Mack, J, Buck, K, Joachimiak, A, Midwest Center for Structural Genomics (MCSG)
Deposit date:2010-07-28
Release date:2010-08-11
Last modified:2017-11-08
Method:X-RAY DIFFRACTION (2.45 Å)
Cite:The Crystal Structure of the GAF domain of a two-component sensor histidine kinase from Bacillus halodurans to 2.45A
To be Published
3O4F
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Crystal Structure of Spermidine Synthase from E. coli
Descriptor: SULFATE ION, Spermidine synthase
Authors:Zhou, X, Tkaczuk, K.L, Chruszcz, M, Chua, T.K, Minor, W, Sivaraman, J.
Deposit date:2010-07-27
Release date:2010-08-18
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.9 Å)
Cite:The crystal structure of Escherichia coli spermidine synthase SpeE reveals a unique substrate-binding pocket
J.Struct.Biol., 169, 2010
3O7Q
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Crystal structure of a Major Facilitator Superfamily (MFS) transporter, FucP, in the outward conformation
Descriptor: L-fucose-proton symporter, nonyl beta-D-glucopyranoside
Authors:Sun, L.F, Dang, S.Y, Wang, J, Yan, N.
Deposit date:2010-07-30
Release date:2010-09-15
Last modified:2024-03-20
Method:X-RAY DIFFRACTION (3.143 Å)
Cite:Structure of a fucose transporter in an outward-open conformation
Nature, 467, 2010
3NQX
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Crystal structure of vibriolysin MCP-02 mature enzyme, a zinc metalloprotease from M4 family
Descriptor: CALCIUM ION, Secreted metalloprotease Mcp02, ZINC ION
Authors:Gao, X, Wang, J, Wu, J.-W, Zhang, Y.-Z.
Deposit date:2010-06-30
Release date:2010-10-06
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.7 Å)
Cite:Structural basis for the autoprocessing of zinc metalloproteases in the thermolysin family
Proc.Natl.Acad.Sci.USA, 107, 2010
3NNC
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Crystal Structure of CUGBP1 RRM1/2-RNA Complex
Descriptor: CUGBP Elav-like family member 1, RNA (5'-R(*UP*GP*UP*GP*UP*GP*UP*UP*GP*UP*GP*UP*G)-3')
Authors:Teplova, M, Song, J, Gaw, H, Teplov, A, Patel, D.J.
Deposit date:2010-06-23
Release date:2010-10-27
Last modified:2023-09-06
Method:X-RAY DIFFRACTION (2.2005 Å)
Cite:Structural Insights into RNA Recognition by the Alternate-Splicing Regulator CUG-Binding Protein 1.
Structure, 18, 2010
3NVR
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BU of 3nvr by Molmil
Modulating Heme Redox Potential Through Protein-Induced Porphyrin Distortion
Descriptor: CHLORIDE ION, Methyl-accepting chemotaxis protein, OXYGEN MOLECULE, ...
Authors:Olea Jr, C, Kuriyan, J, Marletta, M.A.
Deposit date:2010-07-08
Release date:2010-09-08
Last modified:2024-02-21
Method:X-RAY DIFFRACTION (2.148 Å)
Cite:Modulating heme redox potential through protein-induced porphyrin distortion
J.Am.Chem.Soc., 132, 2010
3NNU
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Crystal structure of P38 alpha in complex with DP1376
Descriptor: 2-{3-[(5E)-5-{[(2,3-dichlorophenyl)carbamoyl]imino}-3-thiophen-2-yl-2,5-dihydro-1H-pyrazol-1-yl]phenyl}acetamide, Mitogen-activated protein kinase 14
Authors:Abendroth, J.
Deposit date:2010-06-24
Release date:2010-09-15
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Switch control pocket inhibitors of p38-MAP kinase. Durable type II inhibitors that do not require binding into the canonical ATP hinge region
Bioorg.Med.Chem.Lett., 20, 2010
3NOF
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Mycobacterium tuberculosis thioredoxin C C40S mutant
Descriptor: THIOCYANATE ION, Thioredoxin TrxC
Authors:Hall, G, Emsley, J.
Deposit date:2010-06-25
Release date:2010-11-10
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (1.6 Å)
Cite:Structure of Mycobacterium tuberculosis thioredoxin in complex with quinol inhibitor PMX464
Protein Sci., 20, 2011

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