2002
DOI: 10.1016/s0022-2836(02)00615-0
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The N-terminal Basic Domain of Human Parvulin hPar14 is Responsible for the Entry to the Nucleus and High-affinity DNA-binding

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Cited by 32 publications
(57 citation statements)
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“…NMR spectra were processed using the standard Bruker software XWINNMR. Analysis and visual representation of two-dimensional spectra were performed using the NDEE program package (SpinUp Inc., Dortmund, Germany) and three-dimensional spectra were analyzed with the program Aurelia (Bruker) on O2 and Octane workstations (Silicon Graphics Inc. NMR Titration Analysis-Titration analysis was done by fitting chemical shift data to a quadratic equation as described in detail in a previous study (19). Chemical shift differences were calculated using Equation 6 (20).…”
Section: Methodsmentioning
confidence: 99%
“…NMR spectra were processed using the standard Bruker software XWINNMR. Analysis and visual representation of two-dimensional spectra were performed using the NDEE program package (SpinUp Inc., Dortmund, Germany) and three-dimensional spectra were analyzed with the program Aurelia (Bruker) on O2 and Octane workstations (Silicon Graphics Inc. NMR Titration Analysis-Titration analysis was done by fitting chemical shift data to a quadratic equation as described in detail in a previous study (19). Chemical shift differences were calculated using Equation 6 (20).…”
Section: Methodsmentioning
confidence: 99%
“…The influence of this PTM on the structure and function of hPar14 remains elusive. Phosphorylation does not seem to be the only PTM of Par14/17 (Figure 7 below), as a putative acetylation motif in the N-terminus of the protein (Surmacz et al, 2002) was also described. Acetylation within this motif at position Lys 6 and Lys 11 is reported by PhosphositePlus (Hornbeck et al, 2015).…”
Section: The Cellular Function Of Hpar14 Is Regulated By Ptmmentioning
confidence: 99%
“…In early protein sequence based analyses conserved DNA binding motifs were identified in Par14 Surmacz et al, 2002). In consequence, Surmacz and coworkers demonstrated the binding of Par14 to bent A-tract motifs of double strand DNA oligonucleotides as well as to DNA-sepharose in vitro.…”
Section: The Cellular Function Of Hpar14 Is Regulated By Ptmmentioning
confidence: 99%
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