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  1. ...tryptophan and tyrosine in proteins, Biochemistry 6(7), 1948-1954. 71. Chen, B. K., Saksela, K., Andino, R., and Baltimore, D. (1994) Distinct modes of human immunodeficiency virus type 1 proviral latency revealed by superinfection of nonproductively infected cell lines with recombinant luciferase-e ~~~
  2. ...-ray crystallographic structures of the S. pombe (36), maize (37), mouse (38), rat and human (39) SR enzymes are available. Mammalian SR has a type II eliminase fold reminiscent of the classical PLP-dependent enzyme, tryptophan synthase. Accordingly, it is perhaps not surprising that the enzyme catalyzes both the ~~~
  3. ...phosphoribosyltransferase (QPRTase) is not encoded in its genome, Caenorhabditis elegans are reported to lack a de novo NAD biosynthetic pathway. However, all the genes of the kynurenine pathway required for quinolinic acid (QA) production from tryptophan are present. Thus, we investigated the presence ofde novo NAD ~~~
  4. ...tryptophan ~~~
  5. ...), and thus requires the supplementation of choline or ethanolamine to synthesize PC or PE by the Kennedy pathway (1, 2). Studies with cells lacking Cho1 have revealed that PS is required for protein kinase C function (23, 24), tryptophan transport (25), vacuole function and morphogenesis (26), and directing ~~~
  6. ...tryptophan ~~~
  7. ...proteins. A replacement of Thr-22 or Gly-25 with a highly hydrophobic isoleucine or valine residue, respectively, evidently resulted in much higher export of the corresponding reporter variants compared with substitutions by less hydrophobic amino acids, i.e. alanine or tryptophan, as indicated by faster ~~~
  8. ...in the proper folding of P450 21A2 variants is the proper incorporation of the heme prosthetic group. An approximate index of heme incorporation is provided by theA417/A280 ratio of the purified variants, in that only one of the 12 variants examined involved a change in tryptophan (which would lower A280) (see ~~~
  9. ...of CrSEPT is the most unusual to have been reported to date. The first three strands of the central -sheet are longer than those found in the majority of other septin structures (Fig. 3B), enabling two tryptophan residues from strands 2 and 3 (Trp163 and Trp-173, respectively) to make contact with helix ~~~
  10. ..., from 510 to 450 nm, further indicating ANS complexation by the polysaccharide. In fact, as observed for tryptophan in proteins (25), fluorescent chromophoresmay change their emissionmaximumas a function of the polarity of the environment they experience. We speculate that the ANS-EpolC1576 interaction ~~~
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