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Article title matches

  1. Category:Non-homologues end joining (57 bytes)
    1: List of pages with the keyword Non-homologues end joining

Page text matches

  1. 2lun (2,935 bytes)
    11: ...volutionarily conserved protein with thousands of homologues in all kingdoms of life. It has been suggested th...
  2. 1hg3 (4,880 bytes)
    24: ... in higher oligomeric forms than their mesophilic homologues. Triosephosphate isomerase (TIM) is one of the mo...
  3. 3zj0 (3,907 bytes)
    14: ...tained via the use of the structures of bacterial homologues. However, the molecular basis of AT activity of O...
  4. 2v25 (5,378 bytes)
    24: ...ignments and phylogenetic analyses revealed PEB1a homologues in some Gram-positive bacteria. The alignments su...
  5. 2cfz (5,650 bytes)
    24: ...es such as SDS as a sole carbon or sulfur source. Homologues of SdsA1 are found in many pathogenic and some no...
  6. 2cfu (5,731 bytes)
    24: ...es such as SDS as a sole carbon or sulfur source. Homologues of SdsA1 are found in many pathogenic and some no...
  7. 3a0k (5,020 bytes)
    24: ...el and assembles into tetramers as do many of its homologues. The CRLI carbohydrate binding site was predicted...
  8. 2bgj (5,056 bytes)
    24: ...0 s(-)(1)) as is true for most of its prokaryotic homologues. To identify the mechanistic basis for the slow t...
  9. 2bgi (5,314 bytes)
    24: ...0 s(-)(1)) as is true for most of its prokaryotic homologues. To identify the mechanistic basis for the slow t...
  10. 1o6y (5,205 bytes)
    24: ...d. Moreover, these kinases could be classified as homologues of those belonging to the well characterized supe...
  11. 2iux (7,592 bytes)
    26: ...y than subdomain I in the structures of three ACE homologues. Crystallizable glycosylation mutants open up new...
  12. 2iul (7,115 bytes)
    26: ...y than subdomain I in the structures of three ACE homologues. Crystallizable glycosylation mutants open up new...
  13. 1gyt (4,785 bytes)
    24: ... is exclusively intramolecular. In contrast, PepA homologues from other species have no known DNA-binding acti...
  14. 1gmz (5,623 bytes)
    24: ...ake venoms are rich sources of phospholipase A(2) homologues, both active calcium-binding Asp49 enzymes and es...
  15. 2ivn (4,986 bytes)
    24: ...elomeres maintenance complex KEOPS in yeast. Kae1 homologues are encoded by all sequenced genomes in the three...
  16. 2ivo (4,855 bytes)
    24: ...elomeres maintenance complex KEOPS in yeast. Kae1 homologues are encoded by all sequenced genomes in the three...
  17. 2ivp (4,916 bytes)
    24: ...elomeres maintenance complex KEOPS in yeast. Kae1 homologues are encoded by all sequenced genomes in the three...
  18. 1e1f (5,354 bytes)
    24: ...etween the two maize isoenzymes and their sorghum homologues, ZMGlu1 was produced in Escherichia coli, purifie...
  19. 1e1e (5,100 bytes)
    23: ...etween the two maize isoenzymes and their sorghum homologues, ZMGlu1 was produced in Escherichia coli, purifie...
  20. 2v1o (5,540 bytes)
    24: ...l-CoA thioesterase 7 (Acot7). Whereas prokaryotic homologues possess a single thioesterase domain, mammalian A...

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