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. Author manuscript; available in PMC: 2008 Nov 1.
Published in final edited form as: Mol Biochem Parasitol. 2007 Jul 17;156(1):41–50. doi: 10.1016/j.molbiopara.2007.07.005

Table 3.

Summary of Histone Modifications in Bloodstream Forms

Histone N-terminus Acetyl Lysine Methyl Lysine
H2A A1me1 (60%)a,b K4 (1%)a none
A1aca K115b
K119b
K120b
K122b
K125b
K128b
H2B A1me1 (60%)a,b K4 (1%)a none
A1me2b K12b
K16b
H3 S1acb K23b K32me3b
K76me1, K76me2, K76me3b
H4 A1me1 (60%)a,b K2 (2%)a,b K2me2b
K4 (73%)a,b K17me1 (4%), K17me2 (8%), K17me3 (9%)a,b
K5 (7%)a,b
K10 (7%)a,b K18me1 (6%), K18me2 (4%), K18me3 (18%)a,b
K14 (1%)a
a

PTMs observed by Edman degradation. The levels of acetylation and methylation, shown in parenthesis, were quantified by comparison to known standards.

b

PTMs observed by tandem MS

Kme1, Kme2, and Kme3 refer to mono-, di-, and tri-methyl lysine, respectively; Aac, Ame1, and Ame2 refer to acetyl, monomethyl, and dimethyl alanine, respectively; Sac refers to acetyl serine.