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1IIQ
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BU of 1iiq by Molmil
CRYSTAL STRUCTURE OF HIV-1 PROTEASE COMPLEXED WITH A HYDROXYETHYLAMINE PEPTIDOMIMETIC INHIBITOR
分子名称: GLYCEROL, N-{(2R,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-4-phenylbutyl}-L-phenylalanyl-L-glutaminyl-L-phenylalaninamide, PROTEASE RETROPEPSIN
著者Dohnalek, J, Hasek, J, Duskova, J, Petrokova, H, Hradilek, M, Soucek, M, Konvalinka, J, Brynda, J, Sedlacek, J, Fabry, M.
登録日2001-04-24
公開日2002-04-12
最終更新日2024-03-13
実験手法X-RAY DIFFRACTION (1.83 Å)
主引用文献Hydroxyethylamine isostere of an HIV-1 protease inhibitor prefers its amine to the hydroxy group in binding to catalytic aspartates. A synchrotron study of HIV-1 protease in complex with a peptidomimetic inhibitor.
J.Med.Chem., 45, 2002
2N3A
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BU of 2n3a by Molmil
Solution structure of LEDGF/p75 IBD in complex with POGZ peptide (1389-1404)
分子名称: PC4 and SFRS1-interacting protein, Pogo transposable element with ZNF domain
著者Tesina, P, Cermakova, K, Horejsi, M, Prochazkova, K, Fabry, M, Sharma, S, Christ, F, Demeulemeester, J, Debyser, Z, De Rijck, J, Veverka, V, Rezacova, P.
登録日2015-05-26
公開日2015-08-19
最終更新日2024-05-01
実験手法SOLUTION NMR
主引用文献Multiple cellular proteins interact with LEDGF/p75 through a conserved unstructured consensus motif.
Nat Commun, 6, 2015
2HKH
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BU of 2hkh by Molmil
Crystal structure of the Fab M75
分子名称: GLYCEROL, Immunoglobulin Heavy chain Fab fragment, Immunoglobulin Light chain Fab fragment
著者Kral, V, Mader, P, Stouracova, R, Fabry, M, Sedlacek, J, Brynda, J.
登録日2006-07-04
公開日2007-11-13
最終更新日2023-08-30
実験手法X-RAY DIFFRACTION (2.1 Å)
主引用文献Stabilization of antibody structure upon association to a human carbonic anhydrase IX epitope studied by X-ray crystallography, microcalorimetry, and molecular dynamics simulations.
Proteins, 71, 2008
2HKF
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BU of 2hkf by Molmil
Crystal structure of the Complex Fab M75- Peptide
分子名称: Carbonic anhydrase 9, Immunoglobulin Heavy chain Fab fragment, Immunoglobulin Light chain Fab fragment
著者Kral, V, Mader, P, Stouracova, R, Fabry, M, Horejsi, M, Brynda, J.
登録日2006-07-04
公開日2007-11-13
最終更新日2011-07-13
実験手法X-RAY DIFFRACTION (2.01 Å)
主引用文献Stabilization of antibody structure upon association to a human carbonic anhydrase IX epitope studied by X-ray crystallography, microcalorimetry, and molecular dynamics simulations.
Proteins, 71, 2008
1NH0
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BU of 1nh0 by Molmil
1.03 A structure of HIV-1 protease: inhibitor binding inside and outside the active site
分子名称: BETA-MERCAPTOETHANOL, PROTEASE RETROPEPSIN, SULFATE ION, ...
著者Brynda, J, Rezacova, P, Fabry, M, Horejsi, M, Hradilek, M, Soucek, M, Konvalinka, J, Sedlacek, J.
登録日2002-12-18
公開日2004-04-13
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (1.03 Å)
主引用文献A Phenylnorstatine Inhibitor Binding to HIV-1 Protease: Geometry, Protonation, and Subsite-Pocket Interactions Analyzed at Atomic Resolution
J.Med.Chem., 47, 2004
1JP5
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BU of 1jp5 by Molmil
Crystal structure of the single-chain Fv fragment 1696 in complex with the epitope peptide corresponding to N-terminus of HIV-1 protease
分子名称: epitope peptide corresponding to N-terminus of HIV-1 protease, single-chain Fv fragment 1696
著者Rezacova, P, Lescar, J, Brynda, J, Fabry, M, Horejsi, M, Sedlacek, J, Bentley, G.A.
登録日2001-08-01
公開日2001-10-12
最終更新日2023-08-16
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structural basis of HIV-1 and HIV-2 protease inhibition by a monoclonal antibody.
Structure, 9, 2001
1U8G
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Crystal structure of a HIV-1 Protease in complex with peptidomimetic inhibitor KI2-PHE-GLU-GLU-NH2
分子名称: PROTEASE RETROPEPSIN, peptidomimetic inhibitor KI2-PHE-GLU-GLU-NH2
著者Brynda, J, Rezacova, P, Fabry, M, Horejsi, M, Hradilek, M, Soucek, R, Stouracova, R, Konvalinka, J, Sedlacek, J.
登録日2004-08-06
公開日2004-11-02
最終更新日2018-02-14
実験手法X-RAY DIFFRACTION (2.201 Å)
主引用文献Inhibitor binding at the protein interface in crystals of a HIV-1 protease complex.
Acta Crystallogr.,Sect.D, 60, 2004
1N4X
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Structure of scFv 1696 at acidic pH
分子名称: CHLORIDE ION, immunoglobulin heavy chain variable region, immunoglobulin kappa chain variable region
著者Lescar, J, Brynda, J, Fabry, M, Horejsi, M, Rezacova, P, Sedlacek, J, Bentley, G.A.
登録日2002-11-02
公開日2003-06-10
最終更新日2022-12-21
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Structure of a single-chain Fv fragment of an antibody that inhibits the HIV-1 and HIV-2 proteases.
Acta Crystallogr.,Sect.D, 59, 2003
1RL8
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BU of 1rl8 by Molmil
Crystal structure of the complex of resistant strain of hiv-1 protease(v82a mutant) with ritonavir
分子名称: RITONAVIR, protease RETROPEPSIN
著者Rezacova, P, Brynda, J, Sedlacek, J, Konvalinka, J, Fabry, M, Horejsi, M.
登録日2003-11-25
公開日2005-04-19
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystal structure of the complex of resistant strain of hiv-1 protease(v82a mutant) with ritonavir
To be Published, 2005
1SVZ
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BU of 1svz by Molmil
Crystal structure of the single-chain Fv fragment 1696 in complex with the epitope peptide corresponding to N-terminus of HIV-2 protease
分子名称: epitope peptide corresponding to N-terminus of HIV-2 protease, single-chain Fv fragment 1696
著者Rezacova, P, Brynda, J, Lescar, J, Bentley, G.A, Fabry, M, Horejsi, M, Sedlacek, J.
登録日2004-03-30
公開日2005-03-01
最終更新日2023-08-23
実験手法X-RAY DIFFRACTION (1.89 Å)
主引用文献Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide
J.Struct.Biol., 149, 2005
1FQX
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BU of 1fqx by Molmil
CRYSTAL STRUCTURE OF THE COMPLEX OF HIV-1 PROTEASE WITH A PEPTIDOMIMETIC INHIBITOR
分子名称: N-{(2S,3S)-3-[(tert-butoxycarbonyl)amino]-2-hydroxy-4-phenylbutyl}-L-phenylalanyl-L-alpha-glutamyl-L-phenylalaninamide, PROTEASE RETROPEPSIN
著者Dohnalek, J, Hasek, J, Duskova, J, Petrokova, H, Hradilek, M, Soucek, M, Konvalinka, J, Brynda, J, Sedlacek, J, Fabry, M.
登録日2000-09-07
公開日2001-03-14
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献A distinct binding mode of a hydroxyethylamine isostere inhibitor of HIV-1 protease.
Acta Crystallogr.,Sect.D, 57, 2001
8C25
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purine nucleoside phosphorylase in complex with JS-375
分子名称: CHLORIDE ION, GLYCEROL, Purine nucleoside phosphorylase, ...
著者Djukic, S, Pachl, P, Rezacova, P.
登録日2022-12-21
公開日2023-05-31
最終更新日2023-10-11
実験手法X-RAY DIFFRACTION (1.56 Å)
主引用文献Design, Synthesis, Biological Evaluation, and Crystallographic Study of Novel Purine Nucleoside Phosphorylase Inhibitors.
J.Med.Chem., 66, 2023
8R3G
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Central glycolytic genes regulator (CggR) bound to DNA operator
分子名称: Central glycolytic genes regulator, operator DNA
著者Skerlova, J, Soltysova, M, Rezacova, P, Skubnik, K.
登録日2023-11-09
公開日2024-06-19
最終更新日2024-07-17
実験手法ELECTRON MICROSCOPY (4.4 Å)
主引用文献Structural characterization of two prototypical repressors of SorC family reveals tetrameric assemblies on DNA and mechanism of function.
Nucleic Acids Res., 52, 2024
8R6T
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BU of 8r6t by Molmil
NMR solution structure of thyropin IrThy-Cd from the hard tick Ixodes ricinus
分子名称: Putative two thyropin protein (Fragment)
著者Srb, P, Veverka, V, Matouskova, Z, Orsaghova, K, Mares, M.
登録日2023-11-23
公開日2024-02-28
最終更新日2024-03-06
実験手法SOLUTION NMR
主引用文献An Unusual Two-Domain Thyropin from Tick Saliva: NMR Solution Structure and Highly Selective Inhibition of Cysteine Cathepsins Modulated by Glycosaminoglycans.
Int J Mol Sci, 25, 2024
8R7Y
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Deoxyribonucleoside regulator DeoR in complex with the DNA operator
分子名称: Deoxyribonucleoside regulator, OL18 DNA operator, strand 1, ...
著者Pachl, P, Soltysova, M, Rezacova, P.
登録日2023-11-27
公開日2024-06-19
最終更新日2024-07-17
実験手法X-RAY DIFFRACTION (3.7 Å)
主引用文献Structural characterization of two prototypical repressors of SorC family reveals tetrameric assemblies on DNA and mechanism of function.
Nucleic Acids Res., 52, 2024
2HRP
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BU of 2hrp by Molmil
ANTIGEN-ANTIBODY COMPLEX
分子名称: HIV-1 PROTEASE PEPTIDE, MONOCLONAL ANTIBODY F11.2.32
著者Lescar, J, Bentley, G.A.
登録日1996-12-27
公開日1997-12-31
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2.2 Å)
主引用文献Three-dimensional structure of an Fab-peptide complex: structural basis of HIV-1 protease inhibition by a monoclonal antibody.
J.Mol.Biol., 267, 1997
6RVA
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BU of 6rva by Molmil
STRUCTURE OF [ASP58]-IGF-I ANALOGUE
分子名称: Insulin-like growth factor I
著者Jiracek, J, Zakova, L, Socha, O.
登録日2019-05-31
公開日2019-10-02
最終更新日2023-06-14
実験手法SOLUTION NMR
主引用文献Mutations at hypothetical binding site 2 in insulin and insulin-like growth factors 1 and 2 result in receptor- and hormone-specific responses.
J.Biol.Chem., 294, 2019
7OYK
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BU of 7oyk by Molmil
DNA-binding domain of CggR in complex with the DNA operator
分子名称: 1,2-ETHANEDIOL, CALCIUM ION, Central glycolytic genes regulator, ...
著者Novakova, M, Rezacova, P, Skerlova, J, Brynda, J.
登録日2021-06-24
公開日2021-11-10
最終更新日2021-11-24
実験手法X-RAY DIFFRACTION (2.101 Å)
主引用文献Structural insight into DNA recognition by bacterial transcriptional regulators of the SorC/DeoR family.
Acta Crystallogr D Struct Biol, 77, 2021
1MF2
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BU of 1mf2 by Molmil
ANTI HIV1 PROTEASE FAB COMPLEX
分子名称: MONOCLONAL ANTIBODY F11.2.32
著者Lescar, J, Bentley, G.A.
登録日1996-12-27
公開日1997-12-31
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献Three-dimensional structure of an Fab-peptide complex: structural basis of HIV-1 protease inhibition by a monoclonal antibody.
J.Mol.Biol., 267, 1997
6EMR
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BU of 6emr by Molmil
Solution structure of the LEDGF/p75 IBD - IWS1 (aa 446-548) complex
分子名称: PC4 and SFRS1-interacting protein,Protein IWS1 homolog
著者Veverka, V.
登録日2017-10-03
公開日2018-07-25
最終更新日2024-06-19
実験手法SOLUTION NMR
主引用文献Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation.
Proc. Natl. Acad. Sci. U.S.A., 115, 2018
6EMP
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BU of 6emp by Molmil
Solution structure of the LEDGF/p75 IBD - POGZ (aa 1370-1404) complex
分子名称: PC4 and SFRS1-interacting protein,Pogo transposable element with ZNF domain
著者Veverka, V.
登録日2017-10-03
公開日2018-07-25
最終更新日2024-06-19
実験手法SOLUTION NMR
主引用文献Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation.
Proc. Natl. Acad. Sci. U.S.A., 115, 2018
6EMO
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BU of 6emo by Molmil
Solution structure of the LEDGF/p75 IBD - JPO2 (aa 1-32) complex
分子名称: PC4 and SFRS1-interacting protein,LEDGF/p75 IBD-JPO2 M1
著者Veverka, V.
登録日2017-10-03
公開日2018-07-25
最終更新日2024-06-19
実験手法SOLUTION NMR
主引用文献Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation.
Proc. Natl. Acad. Sci. U.S.A., 115, 2018
6EMQ
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Solution structure of the LEDGF/p75 IBD - MLL1 (aa 111-160) complex
分子名称: PC4 and SFRS1-interacting protein,Histone-lysine N-methyltransferase 2A
著者Veverka, V.
登録日2017-10-03
公開日2018-08-01
最終更新日2024-06-19
実験手法SOLUTION NMR
主引用文献Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation.
Proc. Natl. Acad. Sci. U.S.A., 115, 2018
3CMS
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BU of 3cms by Molmil
ENGINEERING ENZYME SUB-SITE SPECIFICITY: PREPARATION, KINETIC CHARACTERIZATION AND X-RAY ANALYSIS AT 2.0-ANGSTROMS RESOLUTION OF VAL111PHE SITE-MUTATED CALF CHYMOSIN
分子名称: CHYMOSIN B
著者Newman, M, Frazao, C, Shearer, A, Tickle, I.J, Blundell, T.L.
登録日1990-02-26
公開日1992-10-15
最終更新日2017-11-29
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Engineering enzyme subsite specificity: preparation, kinetic characterization, and X-ray analysis at 2.0-A resolution of Val111Phe site-mutated calf chymosin.
Biochemistry, 29, 1990
7BHY
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DNA-binding domain of DeoR in complex with the DNA operator
分子名称: DNA operator - strand 1, DNA operator - strand 2, Deoxyribonucleoside regulator, ...
著者Novakova, M, Rezacova, P, Skerlova, J, Brynda, J.
登録日2021-01-11
公開日2021-11-10
最終更新日2024-01-31
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Structural insight into DNA recognition by bacterial transcriptional regulators of the SorC/DeoR family.
Acta Crystallogr D Struct Biol, 77, 2021

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