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<SDOBI lang="en"><B000><eptags><B001EP>ATBECHDEDKESFRGBGRITLILUNLSEMCPTIE......FI....CY..TR................................................</B001EP><B003EP>*</B003EP><B005EP>J</B005EP><B007EP>DIM360 Ver 2.15 (14 Jul 2008) -  2999001/0</B007EP></eptags></B000><B100><B110>1283872</B110><B120><B121>CORRECTED EUROPEAN PATENT SPECIFICATION</B121></B120><B130>B8</B130><B132EP>B1</B132EP><B140><date>20091216</date></B140><B150><B151>W1</B151><B153>73</B153><B155><B1551>de</B1551><B1552>Bibliographie</B1552><B1551>en</B1551><B1552>Bibliography</B1552><B1551>fr</B1551><B1552>Bibliographie</B1552></B155></B150><B190>EP</B190></B100><B200><B210>01930379.1</B210><B220><date>20010507</date></B220><B240><B241><date>20021118</date></B241><B242><date>20051114</date></B242></B240><B250>en</B250><B251EP>en</B251EP><B260>en</B260></B200><B300><B310>0001698</B310><B320><date>20000505</date></B320><B330><ctry>SE</ctry></B330></B300><B400><B405><date>20091216</date><bnum>200951</bnum></B405><B430><date>20030219</date><bnum>200308</bnum></B430><B450><date>20091007</date><bnum>200941</bnum></B450><B452EP><date>20081230</date></B452EP><B480><date>20091216</date><bnum>200951</bnum></B480></B400><B500><B510EP><classification-ipcr sequence="1"><text>C12N   9/10        20060101AFI20020219BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C07K   1/10        20060101ALI20020219BHEP        </text></classification-ipcr><classification-ipcr sequence="3"><text>C07K  14/00        20060101ALI20020219BHEP        </text></classification-ipcr></B510EP><B540><B541>de</B541><B542>KATALYTISCH AKTIVE PEPTIDE</B542><B541>en</B541><B542>CATALYTICALLY ACTIVE PEPTIDES</B542><B541>fr</B541><B542>PEPTIDES D'ACTION CATALYTIQUE</B542></B540><B560><B561><text>WO-A1-00/32623</text></B561><B561><text>WO-A1-97/43302</text></B561><B562><text>DATABASE SWISSPROT [Online] 01 February 1996 XP002948862 Database accession no. P48330</text></B562><B562><text>DATABASE GENBANK [Online] HOLDINGBOGALET VID GOTEBORGS UNIVERSITET 'Acyl transfer with stabilised transition complex using catalyst with catalytic imidazole (e.g. histidine) function', XP002948863 Database accession no. W33375 &amp; WO 97 43302 A1 20 November 1997</text></B562><B562><text>DATABASE GENBANK [Online] A+ SCIENCE INVEST AB 'Improved method for siteselective glycosylation', XP002948864 Database accession no. W87914 &amp; WO 98 55501 A1 10 December 1998</text></B562><B562><text>THOR J. BORGFORD ET AL.: 'Site directed mutagenesis reveals transition-state stabilization as a general catalytic mechanism for aminoacyl-tRNA' BIOCHEMISTRY vol. 26, 1987, pages 7246 - 7249, XP000917994</text></B562><B562><text>KERSTIN S. BROO ET AL.: 'Cooperative nucleophilic and general-acid catalysis by the HisH+-His pair and arginine transition state binding in catalysis of ester hydrolysis reactions by designed helix-loop-helix motifs' J. AM. CHEM. SOC. vol. 120, 1998, pages 4063 - 4068, XP002948865</text></B562><B562><text>JUN LI ET AL.: 'Conversion of serine-114 to cysteine -114 and the role of the active site nucleophile in acyl transfer by myristoyl-ACP thioesterase from vibrio harveyi' BIOCHEMISTRY vol. 35, 1996, pages 9967 - 9973, XP002948866</text></B562><B562><text>DATABASE [Online] 01 October 1994 Retrieved from NCBI Database accession no. P37722</text></B562></B560></B500><B700><B720><B721><snm>BALTZER, Lars</snm><adr><str>Förtroligheten 23</str><city>S-412 70 Göteborg</city><ctry>SE</ctry></adr></B721></B720><B730><B731><snm>Modpro AB</snm><iid>10355480</iid><irf>P7423EP00/HAM</irf><adr><str>Box 561</str><city>751 22 Uppsala</city><ctry>SE</ctry></adr></B731></B730><B740><B741><snm>Lindgren, Anders</snm><sfx>et al</sfx><iid>00069824</iid><adr><str>BRANN AB 
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