about
Covalent modifications of the catalytic tyrosine in octahaem cytochrome c nitrite reductase and their effect on the enzyme activityExpression, purification, crystallization and preliminary crystallographic analysis of a thermostable DNA ligase from the archaeonThermococcus sibiricusElucidation of the crystal structure of Coriolopsis caperata laccase: restoration of the structure and activity of the native enzyme from the T2-depleted form by copper ionsConcerted action of two subunits of the functional dimer of Shewanella oneidensis MR-1 uridine phosphorylase derived from a comparison of the C212S mutant and the wild-type enzymeCrystal structures of the two epimers from the unusual thermal C6-epimerization of 5-oxo-1,2,3,5,5a,6,7,9b-octa-hydro-7,9a-ep-oxy-pyrrolo-[2,1-a]iso-indole-6-carb-oxy-lic acid, 5a(RS),6(SR),7(RS),9a(SR),9b(SR) and 5a(RS),6(RS),7(RS),9a(SR),9b(SR)Crystal structures of (5RS)-(Z)-4-[5-(furan-2-yl)-3-phenyl-4,5-di-hydro-1H-pyrazol-1-yl]-4-oxobut-2-enoic acid and (5RS)-(Z)-4-[5-(furan-2-yl)-3-(thio-phen-2-yl)-4,5-di-hydro-1H-pyrazol-1-yl]-4-oxobut-2-enoic acid.Crystal structures of ethyl {2-[4-(4-iso-propyl-phen-yl)thia-zol-2-yl]phen-yl}carbamate and ethyl {2-[4-(3-nitro-phen-yl)thia-zol-2-yl]phen-yl}carbamate.Crystal structures of N-[(4-phenyl-thia-zol-2-yl)carbamo-thio-yl]benzamide and N-{[4-(4-bromo-phen-yl)thia-zol-2-yl]carbamo-thio-yl}benzamide from synchrotron X-ray diffraction.The synthesis and crystal structure of 2-(chloro-selan-yl)pyridine 1-oxide: the first monomeric organoselenenyl chloride stabilized by an intra-molecular secondary Se⋯O inter-action.Ring-expansion synthesis and crystal structure of dimethyl 4-ethyl-1,4,5,6,7,8-hexa-hydro-azonino[5,6-b]indole-2,3-di-carboxyl-ate.Inter-action between maleic acid and N-R-furfuryl-amines: crystal structure of 2-methyl-N-[(5-phenyl-furan-2-yl)meth-yl]propan-2-aminium (2Z)-3-carb-oxy-acrylate and N-[(5-iodo-furan-2-yl)meth-yl]-2-methyl-propan-2-aminium (2Z)-3-carb-oxy-prop-2-enoFormamidinium iodide: crystal structure and phase transitionsIncorporation of copper ions into crystals of T2 copper-depleted laccase from Botrytis aclada.Effect of the L499M mutation of the ascomycetous Botrytis aclada laccase on redox potential and catalytic properties.Identification of the ligand in the structure of the protein with unknown function STM4435 from Salmonella typhimurium.Characterization of the size and orientation of Na and Cl(2) nanocrystals in electron irradiated NaCl crystals by means of synchrotron radiation.Unusual Tri-, Hexa-, and Nonanuclear Cu(II) Cage Methylsilsesquioxanes: Synthesis, Structures, and Catalytic Activity in Oxidations with Peroxides.Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.Solid-State Reactions of Eicosaborate [B20 H18 ]2- Salts and Complexes.Tuning linkage isomerism and magnetic properties of bi- and tri-metallic cage silsesquioxanes by cation and solvent effects.Cage-like Fe,Na-Germsesquioxanes: Structure, Magnetism, and Catalytic Activity.Exploitation of knowledge databases in the synthesis of zinc(II) malonates with photo-sensitive and photo-insensitive N,N'-containing linkers.Synthesis, crystal structure and catalytic activity in reductive amination of di-chlorido-(η6-p-cymene)(2'-di-cyclo-hexyl-phosphanyl-2,6-di-meth-oxy-biphen-yl-κP)ruthenium(II).Design of new anti-Alzheimer drugs: ring-expansion synthesis and synchrotron X-ray diffraction study of dimethyl 4-ethyl-11-fluoro-1,4,5,6,7,8-hexa-hydro-azonino[5,6-b]indole-2,3-di-carboxyl-ate.Optical readout of controlled monomer-dimer self-assemblyIMDAV reaction between phenyl-maleic anhydride and thien-yl(fur-yl)allyl-amines: synthesis and mol-ecular structure of (3a,4,4a,7a)-5-oxothieno- and (3a,4,4a,7a)-5-oxofuro[2,3-]iso-indole-4-carb-oxy-lic acidsHigh-Cluster (Cu9) Cage Silsesquioxanes: Synthesis, Structure, and Catalytic Activity[A new approach for study of structural and functional properties of proteins with unknown functions]Crystal structures of (E)-5-(4-methyl-phen-yl)-1-(pyridin-2-yl)pent-2-en-4-yn-1-one and [3,4-bis(phenyl-ethyn-yl)cyclo-butane-1,2-di-yl]bis-(pyridin-2-yl-methanone)Revision of the Regioselectivity of the Beirut Reaction of Monosubstituted Benzofuroxans with Benzoylacetonitrile. 6-Substituted quinoxaline-2-carbonitrile 1,4- dioxides: Structural Characterization and Estimation of Anticancer Activity and HypoxiaMethylammonium Polyiodides: Remarkable Phase Diversity of the Simplest and Low-Melting Alkylammonium Polyiodide SystemPeculiarities of supramolecular organization of cyclic ketones with vinylacetylene fragmentsTowards the surface hydroxyl species in CeO2 nanoparticlesImidazol-5-one as an Acceptor in Donor-Acceptor Cyclopropanes: Cycloaddition with AldehydesTuning the Molecular and Cationic Affinity in a Series of Multifunctional Metal-Organic Frameworks Based on Dodecanuclear Zn(II) Carboxylate WheelsRedox-mediated formation of plutonium oxide nanoparticlesThree-component reaction between isatoic anhydride, amine and meth-yl-subs-tituted furyl-acryl-alde-hydes: crystal structures of 3-benzyl-2-[(E)-2-(5-methylfuran-2-yl)vin-yl]-2,3-di-hydro-quinazolin-4(1H)-one, 3-benzyl-2-[(E)-2-(furan-2-yl)-1-methyl
P50
Q27676913-915F3F62-1155-4A29-985D-C73BF516BD35Q27677005-D4574B8B-FDFA-4576-8E27-4C5B3EAADEE7Q27700111-2BE84CD7-2D10-4FE0-91B6-91CD31C3100AQ27704052-510BE3F7-A9B5-46B1-82A5-B35203206278Q37311229-40AFA1D0-0DDD-49CD-A325-40B5DFC8CA35Q37394175-963D3F86-4166-4C5E-8785-F0A6746B2EF1Q37432493-730C98AC-5A64-4CD2-9298-A209A8B6C5EEQ37432507-E0CDBD54-F588-4D9F-ADB9-BDDF3E4B5A83Q37473489-193BF275-FC28-46AA-8E86-27DB0CEBC21AQ37695254-6E569DF6-07AE-488F-88A3-E6BE77926CE9Q37739508-5086F275-928D-4671-871B-BEE38DA87D41Q37739517-95FD8562-8FBC-4B2F-9208-EF10B37BD0F0Q40254725-06ED09DB-ADF1-4447-BD19-271533D5012FQ41766777-7CCF36F8-AF85-41DF-B00A-77DAA3A40FF9Q43680519-B4AE6ED8-6712-4B2A-9B75-321BD6EB1A3BQ47283300-69860012-143E-46D3-9625-FF56130073B4Q48104041-DCE09F51-8B5F-45E3-ABEA-ED7F34C33DBAQ48116287-34DA4962-883B-46DD-9BAB-6FCF3D536087Q48133829-9C49B82C-65BC-40B7-AE58-55262CA78033Q50022399-554C5158-5E1A-43CE-B8CC-ADE56EBD2E16Q51038146-479329E9-712B-4DE9-AA66-5B26012FF69EQ54933512-BFDCA247-4AC2-4B5E-8F17-65D6E55D91FEQ54950172-D3B6BA80-E1D6-4151-93E0-A285D65A92C2Q55322321-B6143F6F-B48C-496D-85C8-CF5B9B4AC929Q57456780-C79764C5-E4B2-44AB-AABE-DBF5091B7C9CQ57493825-7FFFEA19-C42C-4D56-AED2-AF6BF6EFB99DQ61771043-2A4EACF4-3461-43D1-B4E6-255E2C8E2604Q84571143-4C95DA87-7C31-4AA0-A837-037252C2A0B0Q89768825-56633709-0C0C-4669-82F3-9EFE2004D7D4Q89905756-DC31A731-1BB4-46D8-B35D-07D57F209079Q90065211-55017DE4-2EEF-4592-9229-08B701BF4A46Q90268681-B37C3E04-7560-4C18-9D0C-E8043C7E33A2Q90294622-2233B446-4EB6-4CED-BECD-38EB5CA55230Q90420532-B0CC6F46-2A76-4AF5-8029-EA9248FA6033Q90482053-F0FE1E3D-2CF3-41F1-B4B3-DB42449E2095Q90606426-4643E07E-75AF-4445-B3C9-8BF80FE2E895Q90991936-6DF98D3A-24DF-49A8-B05C-996F304DA9A1
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Pavel Dorovatovskii
@en
Pavel Dorovatovskii
@nl
Pavel V Dorovatovskii
@ast
Pavel V Dorovatovskii
@es
Pavel V Dorovatovskii
@sl
Pawel Wladimirowitsch Dorowatowski
@de
Павел Владимирович Дороватовский
@ru
type
label
Pavel Dorovatovskii
@en
Pavel Dorovatovskii
@nl
Pavel V Dorovatovskii
@ast
Pavel V Dorovatovskii
@es
Pavel V Dorovatovskii
@sl
Pawel Wladimirowitsch Dorowatowski
@de
Павел Владимирович Дороватовский
@ru
altLabel
Pavel Dorovatovskiy
@en
Pavel Dorovatovsky
@en
Pavel V Dorovatovskii
@en
Pavel Vladimirovich Dorovatovsky
@en
Pawel Dorowatowski
@de
Павел Дороватовский
@en
prefLabel
Pavel Dorovatovskii
@en
Pavel Dorovatovskii
@nl
Pavel V Dorovatovskii
@ast
Pavel V Dorovatovskii
@es
Pavel V Dorovatovskii
@sl
Pawel Wladimirowitsch Dorowatowski
@de
Павел Владимирович Дороватовский
@ru
P1053
F-7723-2014
P106
P21
P31
P3829
P496
0000-0002-2978-3614