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Journal Abstract Search

106 related items for PubMed ID: 8103452

  • 1. Sweet potato beta-amylase. Primary structure and identification of the active-site glutamyl residue.
    Toda H, Nitta Y, Asanami S, Kim JP, Sakiyama F.
    Eur J Biochem; 1993 Aug 15; 216(1):25-38. PubMed ID: 8103452
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  • 2. Identification of glutamic acid 186 affinity-labeled by 2,3-epoxypropyl alpha-D-glucopyranoside in soybean beta-amylase.
    Nitta Y, Isoda Y, Toda H, Sakiyama F.
    J Biochem; 1989 Apr 15; 105(4):573-6. PubMed ID: 2474529
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  • 3. Crystallization, molecular replacement solution, and refinement of tetrameric beta-amylase from sweet potato.
    Cheong CG, Eom SH, Chang C, Shin DH, Song HK, Min K, Moon JH, Kim KK, Hwang KY, Suh SW.
    Proteins; 1995 Feb 15; 21(2):105-17. PubMed ID: 7777485
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  • 4. Molecular cloning and expression in Escherichia coli of cDNA encoding the subunit of sweet potato beta-amylase.
    Yoshida N, Nakamura K.
    J Biochem; 1991 Aug 15; 110(2):196-201. PubMed ID: 1837016
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  • 5. PCR cloning and sequencing of the beta-amylase cDNA from barley.
    Yoshigi N, Okada Y, Sahara H, Koshino S.
    J Biochem; 1994 Jan 15; 115(1):47-51. PubMed ID: 8188635
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  • 6. Affinity labeling of soybean beta-amylase with 2',3'-epoxypropyl alpha-D-glucopyranoside.
    Isoda Y, Nitta Y.
    J Biochem; 1986 Jun 15; 99(6):1631-7. PubMed ID: 2427503
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  • 9. Cloning of the beta-amylase gene from Bacillus cereus and characteristics of the primary structure of the enzyme.
    Nanmori T, Nagai M, Shimizu Y, Shinke R, Mikami B.
    Appl Environ Microbiol; 1993 Feb 15; 59(2):623-7. PubMed ID: 8434930
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  • 13. Identification of a glutamate residue at the active site of xylanase A from Schizophyllum commune.
    Bray MR, Clarke AJ.
    Eur J Biochem; 1994 Feb 01; 219(3):821-7. PubMed ID: 7906649
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  • 17. Characterization of a cDNA encoding a novel DNA-binding protein, SPF1, that recognizes SP8 sequences in the 5' upstream regions of genes coding for sporamin and beta-amylase from sweet potato.
    Ishiguro S, Nakamura K.
    Mol Gen Genet; 1994 Sep 28; 244(6):563-71. PubMed ID: 7969025
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  • 19. Removal of the four C-terminal glycine-rich repeats enhances the thermostability and substrate binding affinity of barley beta-amylase.
    Ma YF, Eglinton JK, Evans DE, Logue SJ, Langridge P.
    Biochemistry; 2000 Nov 07; 39(44):13350-5. PubMed ID: 11063571
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