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. Author manuscript; available in PMC: 2018 Aug 9.
Published in final edited form as: J Am Chem Soc. 2017 Jul 25;139(31):10617–10620. doi: 10.1021/jacs.7b05495

Table 1.

Efficiency of DPC formation by 5fC within NCPs.

5fC position and base pair histone H4 mutants in NCP DPC% at equilibriuma
5fC89-G WTb 20.1 ± 0.7
Del 1-20c 4.2 ± 0.2
K5, 8, 12, 16, 20Rd 14.7 ± 4.1
CapNe 6.7 ± 0.2
CapN-K5, 8, 12, 16, 20Rf 3.3 ± 0.2
5fC89-A WT 16.6 ± 4.6
5fC89-T WT 21.4 ± 0.7
5fC74-G WT 3.2 ± 0.1
5fC3-G WT 3.6 ± 0.1
5fC45-G WT 14.8 ± 0.3
a

Yields are averages ± standard deviations of at least three experiments.

b

Wild type histone H4.

c

Histone H4 without the N-terminal 1-20 amino acids.

d

H4 with Lys 5, 8, 12, 16, 20 to Argmutations.

e

H4 with capped N terminal by thiazolidine (see Scheme 1).

f

H4 with both capped N terminal and Lys 5, 8, 12, 16, 20 to Arg mutations.