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. 2007 Dec 15;36(3):793–802. doi: 10.1093/nar/gkm1093

Table 1.

Identified Pol I phosphopeptides and –sites and corresponding amino acids in the Pol I homology model

Subunit Phosphopeptide 3D-localization

Position Sequencea Phosphosite Amino acid in homology modelb
A190 352–366 ADSFFMDVLVVPPTR S354 Rpb1 W234
684–689 DSFFTR S685 Rpb1 T539
935–955 GSNVNVSQIMCLLGQQALEGR S936 or S941c Rpb1 S754/A759
A43 207–212 FSFGNR S208 N/D
213–228 SLGHWVDSNGEPIDGK S220 A43 S220
242–264 VVSVDGTLISDADEEGNGYNSSR S262 or S263c N/D
278–289 IVFDDEVSIENK S285 N/D
A34.5 7–31 DYVSDSDSDDEVISNEFSIPDGFKK S10/S12/S14 N/D
ABC23 98–119 ALQISMNAPVFVDLEGETDPLR S102 ABC23 S102
AC19 21–46 HIQEEEEQDVDMTGDEEQEEEPDREK T33 Rpb11 A3
49–77 LLTQATSEDGTSASFQIVEEDHTLGNALR T51 or T54 or S55c Rpb11 I21/D24/T25

aPhosphoserines/-threonines are presented as bold, underlined characters.

bSome phosphosites could not be localized in the Pol I homology model due to weak homology of the respective protein regions to Pol II, missing homologous subunits or deletions in the A43/14 crystal structure.

cThree phosphopeptides could be identified due to the specific mass shift after chemical derivatization and a partial MS/MS spectrum, but the phosphorylation site could not be unambiguously assigned. The remaining possible serines and threonines are shown in bold, italic letters in the peptide sequence.