1 , the sumoylation-deficient mutant of PLAGL2
is acetylated at a lower level than its wild-type counte
2 Furthermore, we determined that protein VII
is acetylated at alternative residues late during infect
3 The hematopoietic transcription factor GATA1
is acetylated at conserved lysines that are required for
4 Barley starches
were acetylated at different catalyst levels (11%, 17%,
5 allowing for the Asf1-H3K14ac/H4 complex to
be acetylated at H3K56 by Rtt109-Vps75.
6 factor alpha-induced protein 2 (TNFAIP2) to
be acetylated at histone H4.
7 In vitro, Cdt1 can
be acetylated at its N terminus by the lysine acetyltran
8 MSH2
is acetylated at its C terminus, and histone deacetylase
9 Here, we show that NAT1
is acetylated at K(100) and K(188) and that changes in p
10 Here we report that PNKP
is acetylated at K142 (AcK142) by p300 constitutively bu
11 We found that YAP
is acetylated at K265 by CBP (CREB-binding protein)/P300
12 In yeast, Hsp90 mutants that cannot
be acetylated at K294 have reduced viability and chapero
13 PML
is acetylated at K487 and its deacetylation by SIRT1 pro
14 Here, we report that MSH2 can
be acetylated at Lys-73 near the N terminus.
15 ctrometric analysis, we determined that Htz1
is acetylated at Lys 3, Lys 8, Lys 10, and Lys 14 within
16 n acetylated Rch1 peptide, we show that Rch1
was acetylated at Lys22 in vivo and that CBP or p300 cou
17 In addition, histone H3
is acetylated at Lys9 and Lys14, and the T(H)2-specific
18 KRAS can
be acetylated at lysine 104 (K104), and an acetylation-m
19 PHF5A, a component of U2 snRNPs, can
be acetylated at lysine 29 in response to multiple cellu
20 Here, we report that PGK1
is acetylated at lysine 220 (K220), which inhibits PGK1
21 Mouse p53
is acetylated at lysine 317 by PCAF and at multiple lysi
22 Newly synthesized histone H4
is acetylated at lysine 5 and 12 (H4K5,12) by histone ac
23 Here we show that ACLY
is acetylated at lysine residues 540, 546, and 554 (3K).
24 indicated that in SIRT3-deficient cells OPA1
was acetylated at lysine 926 and 931 residues.
25 In this study, we discovered that FUS
was acetylated at lysine-315/316 (K315/K316) and lysine-
26 XPA can
be acetylated at lysines 63 and 67.
27 ng cells to high glutamine concentration, GS
is acetylated at lysines 11 and 14, yielding a degron th
28 karyotic cells, newly synthesized histone H4
is acetylated at lysines 5 and 12, a transient modificat
29 Histone H4 can
be acetylated at N-terminal lysines K5, K8, K12, and K16
30 glucosyl residues and the mannosyl residues
were acetylated at O-2 and O-3.
31 of the thermosome, proteosome and ribosome,
are acetylated at the N-terminus.
32 Histone H3 at immediate-early promoters
is acetylated at the start of infection, while it is ini
33 P-43 expressed in either PC12 or COS-1 cells
was acetylated at the N-terminal methionine.
34 H3-K4 is methylated, and histones H3 and H4
are acetylated at this promoter.