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  1. 3041
    “…At frog motor nerve terminals, repetitive Ca(2+) entries slowly prime and subsequently activate the mechanism of CICR via ryanodine receptors and asynchronous exocytosis of transmitters. …”
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    Functional Coupling of Ca(2+) Channels to Ryanodine Receptors at Presynaptic Terminals: Amplification of Exocytosis and Plasticity
  2. 3042
    “…TWINKLE is not an active primase in vitro and the functional role of the N-terminal region has remained elusive. In this report, we demonstrate that the N-terminal part of TWINKLE is required for efficient binding to single-stranded DNA. …”
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    The N-terminal domain of TWINKLE contributes to single-stranded DNA binding and DNA helicase activities
  3. 3043
    Publicado 1992
    “…The targeting signal of trypanosome phosphoglycerate kinase resides in the COOH- terminal hexapeptide, NRWSSL; a basic amino acid is not required. …”
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    Glycosome assembly in trypanosomes: variations in the acceptable degeneracy of a COOH-terminal microbody targeting signal
  4. 3044
    Publicado 1991
    “…The beta epitope is represented in a synthetic peptide (PII) modeled after the 30 COOH- terminal residues of peripherin, as seen by comparative immunoblotting assays. …”
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    A potential role for the COOH-terminal domain in the lateral packing of type III intermediate filaments
  5. 3045
    Publicado 1994
    “…Recent findings have also revealed that the NH2-terminal domain of ezrin is associated with the plasma membrane and the COOH-terminal domain with the cytoskeleton (Algrain, M., O. …”
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    Ezrin has a COOH-terminal actin-binding site that is conserved in the ezrin protein family
  6. 3046
    por Killoran, Michael P., Keck, James L.
    Publicado 2008
    “…The RecQ helicase from Deinococcus radiodurans (DrRecQ) is unusual among RecQ family members in that it has evolved to utilize three ‘Helicase and RNaseD C-terminal’ (HRDC) domains to regulate its activity. …”
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    Structure and function of the regulatory C-terminal HRDC domain from Deinococcus radiodurans RecQ
  7. 3047
    “…Several amino acid substitutions conferring hyperactivity, including E449K, were localized to one face of a predicted coiled-coil motif in the C-terminal domain. This work shows that a motif in the C-terminal domain of ϕC31 integrase controls the formation of the synaptic interface in both integration and excision, possibly through a direct role in protein–protein interactions.…”
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    A motif in the C-terminal domain of ϕC31 integrase controls the directionality of recombination
  8. 3048
    “…We studied the effects of phosphorylation on the secondary structure of the DNA-bound H1 carboxy-terminal domain (CTD), which contains most of the phosphorylation sites of the molecule. …”
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    Phosphorylation of the carboxy-terminal domain of histone H1: effects on secondary structure and DNA condensation
  9. 3049
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    A comparison of the performance and clinical utility of mid-molecular and C-terminal parathyroid hormone assays
  10. 3050
    “…Using the yeast two-hybrid screening method, two small GTPases, AtRabD1 and AtRabC2a, were identified as factors that interact with the C-terminal tail region of MYA2. Both recombinant AtRabs tagged with His bound to the recombinant C-terminal tail region of MYA2 tagged with GST in a GTP-dependent manner. …”
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    An isoform of Arabidopsis myosin XI interacts with small GTPases in its C-terminal tail region
  11. 3051
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    Effect of asymmetric terminal structures of short RNA duplexes on the RNA interference activity and strand selection
  12. 3052
    “…Moreover, introduction of the MESNA/diMESNA redox couple in the cleavage buffer allowed simultaneous on-column refolding of Ribonuclease A and intein-mediated cleavage to yield Ribonuclease A with a C-terminal MESNA-thioester. The C-terminal thioester was shown to be active in native chemical ligation. …”
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    One-step refolding and purification of disulfide-containing proteins with a C-terminal MESNA thioester
  13. 3053
    “…Further analysis revealed that MNAR inhibited transactivation by the ligand-independent activation function (AF)1 but potentiated the COOH-terminal AF2 domain. The effect of MNAR was independent of c-Src activity, demonstrated by inhibitors and c-Src knockdown studies. …”
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    MNAR functionally interacts with both NH(2)- and COOH-terminal GR domains to modulate transactivation
  14. 3054
    “…Therefore AZT mitochondrial toxicity is likely due to a mechanism that does not involve strand termination of mtDNA replication.…”
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    An Analysis of Enzyme Kinetics Data for Mitochondrial DNA Strand Termination by Nucleoside Reverse Transcription Inhibitors
  15. 3055
    “…BACKGROUND: Members of the eukaryote/archaea specific eRF1 and eRF3 protein families have central roles in translation termination. They are also central to various mRNA surveillance mechanisms, together with the eRF1 paralogue Dom34p and the eRF3 paralogues Hbs1p and Ski7p. …”
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    Evolution of nonstop, no-go and nonsense-mediated mRNA decay and their termination factor-derived components
  16. 3056
    “…Upon Ets1 induction in differentiating cells of stratified squamous epithelium, these mice exhibited dramatic changes in epithelial organization including increased proliferation and blocked terminal differentiation. The phenotype was completely reversed when Ets1 expression was suppressed. …”
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    Ets1 Induces Dysplastic Changes When Expressed in Terminally-Differentiating Squamous Epidermal Cells
  17. 3057
    “…[Image: see text] The carboxyl-terminal domain (CTD, residues 146−231) of the HIV-1 capsid (CA) protein plays an important role in the CA−CA dimerization and viral assembly of the human immunodeficiency virus type 1. …”
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    Mutational Analysis and Allosteric Effects in the HIV-1 Capsid Protein Carboxyl-Terminal Dimerization Domain
  18. 3058
    “…[Image: see text] The BARD1 N-terminal RING domain binds BRCA1 while the BARD1 C-terminal ankyrin and tandem BRCT repeat domains bind CstF-50 to modulate mRNA processing and RNAP II stability in response to DNA damage. …”
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    The BARD1 C-Terminal Domain Structure and Interactions with Polyadenylation Factor CstF-50
  19. 3059
    “…If LDAg binding to clathrin is essential to HDV life cycle, a clathrin box sequence at the C-terminus of LDAg should be conserved across all HDV. However, the C-terminal sequence of LDAg is variable among 43 HDV isolates. …”
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    The C-terminal sequence of the large hepatitis delta antigen is variable but retains the ability to bind clathrin
  20. 3060
    “…On the other hand, the CbfA and CbfB proteins have completely different carboxy-terminal domains, suggesting that the plasticity of such domains may have contributed to the adaptation of the CbfA-like transcription factors to the rapid genome evolution in the dictyostelid clade. …”
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    The Carboxy-Terminal Domain of Dictyostelium C-Module-Binding Factor Is an Independent Gene Regulatory Entity
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