WO2002002758A3 - Crystallization and structure of staphylococcus aureus peptide deformylase - Google Patents

Crystallization and structure of staphylococcus aureus peptide deformylase Download PDF

Info

Publication number
WO2002002758A3
WO2002002758A3 PCT/US2001/020777 US0120777W WO0202758A3 WO 2002002758 A3 WO2002002758 A3 WO 2002002758A3 US 0120777 W US0120777 W US 0120777W WO 0202758 A3 WO0202758 A3 WO 0202758A3
Authority
WO
WIPO (PCT)
Prior art keywords
staphylococcus aureus
peptide deformylase
crystallization
aureus peptide
ray crystal
Prior art date
Application number
PCT/US2001/020777
Other languages
French (fr)
Other versions
WO2002002758A2 (en
Inventor
Eric T Baldwin
Melissa S Harris
Original Assignee
Upjohn Co
Eric T Baldwin
Melissa S Harris
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Upjohn Co, Eric T Baldwin, Melissa S Harris filed Critical Upjohn Co
Priority to AU71647/01A priority Critical patent/AU7164701A/en
Publication of WO2002002758A2 publication Critical patent/WO2002002758A2/en
Publication of WO2002002758A3 publication Critical patent/WO2002002758A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/78Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • C12N9/80Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in linear amides (3.5.1)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2299/00Coordinates from 3D structures of peptides, e.g. proteins or enzymes

Abstract

Staphylococcus aureus peptide deformylase has been crystallized, and the three-dimensional x-ray crystal structure has been solved to 1.9 Å resolution. The x-ray crystal structure is useful for solving the structure of other molecules or molecular complexes, and designing modifiers of peptide deformylase activity.
PCT/US2001/020777 2000-06-30 2001-06-29 Crystallization and structure of staphylococcus aureus peptide deformylase WO2002002758A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU71647/01A AU7164701A (en) 2000-06-30 2001-06-29 Crystallization and structure of staphylococcus aureus peptide deformylase

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US21555000P 2000-06-30 2000-06-30
US60/215,550 2000-06-30

Publications (2)

Publication Number Publication Date
WO2002002758A2 WO2002002758A2 (en) 2002-01-10
WO2002002758A3 true WO2002002758A3 (en) 2002-08-29

Family

ID=22803414

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2001/020777 WO2002002758A2 (en) 2000-06-30 2001-06-29 Crystallization and structure of staphylococcus aureus peptide deformylase

Country Status (2)

Country Link
AU (1) AU7164701A (en)
WO (1) WO2002002758A2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0879879A2 (en) * 1997-05-21 1998-11-25 Smithkline Beecham Corporation Polypeptide deformylase 1 (Def1)

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0879879A2 (en) * 1997-05-21 1998-11-25 Smithkline Beecham Corporation Polypeptide deformylase 1 (Def1)

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
CHEN DAWN Z ET AL: "Actinonin, a naturally occurring antibacterial agent, is a potent deformylase inhibitor.", BIOCHEMISTRY, vol. 39, no. 6, 15 February 2000 (2000-02-15), pages 1256 - 1262, XP002202852, ISSN: 0006-2960 *
GREER J: "PROTEIN STRUCTURE AND FUNCTION BY COMPARATIVE MODEL BUILDING", ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, NEW YORK ACADEMY OF SCIENCES, NEW YORK, NY, US, vol. 439, 1985, pages 44 - 63, XP001053165, ISSN: 0077-8923 *
HAO BING ET AL: "Structural basis for the design of antibiotics targeting peptide deformylase.", BIOCHEMISTRY, vol. 38, no. 15, 13 April 1999 (1999-04-13), pages 4712 - 4719, XP002202851, ISSN: 0006-2960 *
HUNTINGTON KRISTI M ET AL: "Synthesis and antibacterial activity of peptide deformylase inhibitors.", BIOCHEMISTRY, vol. 39, no. 15, 18 April 2000 (2000-04-18), pages 4543 - 4551, XP002202850, ISSN: 0006-2960 *
JANCARIK J ET AL: "SPARSE MATRIX SAMPLING: A SCREENING METHOD FOR CRYSTALLIZATION OF PROTEINS", JOURNAL OF APPLIED CRYSTALLOGRAPHY, COPENHAGEN, DK, vol. 24, 1991, pages 409 - 411, XP001053042, ISSN: 0021-8898 *
KUNTZ I D ET AL: "STRUCTURE-BASED MOLECULAR DESIGN", ACCOUNTS OF CHEMICAL RESEARCH, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, vol. 27, no. 5, May 1994 (1994-05-01), pages 117 - 123, XP000885741, ISSN: 0001-4842 *

Also Published As

Publication number Publication date
AU7164701A (en) 2002-01-14
WO2002002758A2 (en) 2002-01-10

Similar Documents

Publication Publication Date Title
CA2386690A1 (en) Pharmaceutical tramadol salts
AU2348988A (en) 4H-1-benzopyran-4-one derivative or its salt, processes for producing the same and pharmaceutical composition comprising the same as active ingredient
RU93050129A (en) NEW ERYTHROMYCIN DERIVATIVES, THE METHOD FOR THEIR PRODUCTION AND THE PHARMACEUTICAL COMPOSITION ON THE BASIS AND INTERMEDIATE SYNTHESIS COMPOUNDS
CA2148928A1 (en) Pharmacologically active pyridine derivatives and processes for the preparation thereof
CA2155322A1 (en) Crystalline Ceftiofur Free Acid
CA2218555A1 (en) Compositions and methods to prevent toxicity induced by nonsteroidal antiinflammatory drugs
RU93005350A (en) NEW SUBSTITUTED PHENYLIMIDAZOLIDINES, METHOD FOR THEIR PRODUCTION, THEIR USE AS MEDICINES AND INCLUDING THEIR PHARMACEUTICAL COMPOUNDS
RU93050124A (en) NEW DERIVATIVES OF ERYTHROMYCIN, THE METHOD OF THEIR PRODUCTION AND PHARMACEUTICAL COMPOSITION ON THEIR BASIS
CA2239174A1 (en) Novel compounds with analgesic effect
DE69919142D1 (en) BICYCLO [2.2.1] HEPTANESE AND RELATED COMPOUNDS
AU5574799A (en) Pyridyl ethers and thioethers as ligands for nicotinic acetylcholine receptor and its therapeutic application
IT1303249B1 (en) SOME N- (2-ARYL-PROPIONYL) -SULPHONAMIDS AND PHARMACEUTICAL PREPARATIONS THAT CONTAIN THEM.
DE69720666D1 (en) Crystalline powdery saccharides, their production and use
WO2001000566A3 (en) Substituted phenoxyacetic acids
CA2267309A1 (en) Use of 1-hydroxy-2-pyridones for the treatment of skin infections
KR937000160A (en) Inclusion compound of cyclodextrin and nimesulide
WO2002002758A3 (en) Crystallization and structure of staphylococcus aureus peptide deformylase
DE60035133D1 (en) PHARMACEUTICAL COMPOSITIONS WITH WOUND HEALING AND ANTI-COMPLEMENTARY EFFECT THAT CONTAIN A DEXTRANDERIVATE
CA2364258A1 (en) 3-cyclopropylmethoxy-4-difluoromethoxy-n-(3,5-dichloropyrid-4-yl)benzamide in the treatment of multiple sclerosis
DE60027268D1 (en) PYROGLUTAMINE ACID DERIVATIVES AND ASSOCIATED COMPOUNDS THAT REDUCE THE LEUKOCYTADHESION EVALUATED BY VLA-4
AU4937699A (en) Use of succinic acid or salts thereof for the treatment of diabetes mellitus andwound healing
WO2001011025A3 (en) Crystallization and structure determination of staphylococcus aureus thymidylate kinase
CA2192481A1 (en) Drug salts
WO2001077309A3 (en) Crystallization and structure determination of staphylococcus aureus thioredoxin reductase
AU2001284476A1 (en) Novel crystals of 1,3,4-oxadiazole derivative, process for producing the crystals and medicines containing the same as the active ingredient

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: JP