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PDB: 8 results

5F9K
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BU of 5f9k by Molmil
Dictyostelium discoideum dUTPase at 2.2 Angstrom
Descriptor: 2'-DEOXYURIDINE 5'-ALPHA,BETA-IMIDO-TRIPHOSPHATE, Deoxyuridine 5'-triphosphate nucleotidohydrolase, MAGNESIUM ION, ...
Authors:Inoguchi, N, Chia, C.P, Heck, K, Moriyama, H.
Deposit date:2015-12-09
Release date:2016-12-14
Last modified:2023-09-27
Method:X-RAY DIFFRACTION (2.179 Å)
Cite:Mitochondrial localization of Dictyostelium discoideum dUTPase mediated by its N-terminus.
Bmc Res Notes, 13, 2020
1Z8V
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The Structure of d(GGCCAATTGG) Complexed with Netropsin
Descriptor: (5'-D(*GP*GP*CP*CP*AP*AP*TP*TP*GP*G)-3'), NETROPSIN
Authors:Van Hecke, K, Nam, P.C, Nguyen, M.T, Van Meervelt, L.
Deposit date:2005-03-31
Release date:2006-03-14
Last modified:2024-04-03
Method:X-RAY DIFFRACTION (1.75 Å)
Cite:Netropsin interactions in the minor groove of d(GGCCAATTGG) studied by a combination of resolution enhancement and ab initio calculations.
Febs J., 272, 2005
3L1Q
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BU of 3l1q by Molmil
The crystal structure of the undecamer d(TGGCCTTAAGG)
Descriptor: 5'-D(*TP*GP*GP*CP*CP*TP*TP*AP*AP*GP*G)-3'
Authors:Van Hecke, K.
Deposit date:2009-12-14
Release date:2010-10-27
Last modified:2023-11-01
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Designing Triple Helical Fragments: The Crystal Structure of the Undecamer d(TGGCCTTAAGG) Mimicking T·AT Base Triplets
Cryst.Growth Des., 10, 2010
1OMK
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The Crystal Structure of d(CACG(5IU)G)
Descriptor: 5'-D(*CP*AP*CP*GP*(5IU)P*G)-3', COBALT HEXAMMINE(III)
Authors:Schuerman, G, Van Hecke, K, Van Meervelt, L.
Deposit date:2003-02-25
Release date:2003-11-04
Last modified:2024-04-03
Method:X-RAY DIFFRACTION (1.3 Å)
Cite:Exploration of the influence of 5-iodo-2'-deoxyuridine incorporation on the structure of d[CACG(IDU)G].
Acta Crystallogr.,Sect.D, 59, 2003
4EMQ
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BU of 4emq by Molmil
Crystal structure of a single mutant of Dronpa, the green-on-state PDM1-4
Descriptor: 4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID, DI(HYDROXYETHYL)ETHER, Fluorescent protein Dronpa, ...
Authors:Ngan, N.B, Van Hecke, K, Van Meervelt, L.
Deposit date:2012-04-12
Release date:2012-11-21
Last modified:2024-10-09
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Structural basis for the influence of a single mutation K145N on the oligomerization and photoswitching rate of Dronpa.
Acta Crystallogr.,Sect.D, 68, 2012
3V3D
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Crystal Structure of an eYFP single mutant
Descriptor: SULFATE ION, Yellow fluorescent protein
Authors:Ngan, N.B, Van Hecke, K, Van Meervelt, L.
Deposit date:2011-12-13
Release date:2012-12-26
Last modified:2024-11-06
Method:X-RAY DIFFRACTION (1.95 Å)
Cite:Improving the second-order nonlinear optical response of fluorescent proteins: the symmetry argument.
J.Am.Chem.Soc., 135, 2013
1TA2
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BU of 1ta2 by Molmil
Crystal structure of thrombin in complex with compound 1
Descriptor: 1-(2-AMINO-3,3-DIPHENYL-PROPIONYL)-PYRROLIDINE-3-CARBOXYLIC ACID 2,5-DICHLORO-BENZYLAMIDE, Hirudin, thrombin
Authors:Tucker, T.J, Brady, S.F, Lumma, W.C, Lewis, S.D, Gardel, S.J, Naylor-Olsen, A.M, Yan, Y, Sisko, J.T, Stauffer, K.J, Lucas, B.Y, Lynch, J.J, Cook, J.J, Stranieri, M.T, Holahan, M.A, Lyle, E.A, Baskin, E.P, Chen, I.-W, Dancheck, K.B, Krueger, J.A, Cooper, C.M, Vacca, J.P.
Deposit date:2004-05-19
Release date:2004-06-08
Last modified:2017-10-11
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position
J.Med.Chem., 41, 1998
1TA6
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Crystal structure of thrombin in complex with compound 14b
Descriptor: 1-[2-AMINO-2-CYCLOHEXYL-ACETYL]-PYRROLIDINE-3-CARBOXYLIC ACID 5-CHLORO-2-(2-ETHYLCARBAMOYL-ETHOXY)-BENZYLAMIDE, Hirudin, thrombin
Authors:Tucker, T.J, Brady, S.F, Lumma, W.C, Lewis, S.D, Gardel, S.J, Naylor-Olsen, A.M, Yan, Y, Sisko, J.T, Stauffer, K.J, Lucas, B.Y, Lynch, J.J, Cook, J.J, Stranieri, M.T, Holahan, M.A, Lyle, E.A, Baskin, E.P, Chen, I.-W, Dancheck, K.B, Krueger, J.A, Cooper, C.M, Vacca, J.P.
Deposit date:2004-05-19
Release date:2004-06-08
Last modified:2017-10-11
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Design and synthesis of a series of potent and orally bioavailable noncovalent thrombin inhibitors that utilize nonbasic groups in the P1 position
J.Med.Chem., 41, 1998

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