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. Author manuscript; available in PMC: 2016 Dec 1.
Published in final edited form as: Proteomics Clin Appl. 2015 Dec;9(11-12):1035–1052. doi: 10.1002/prca.201500106

Table 2.

Characterization of HLA-B*35;01-restricted self peptides presented during active infection

Protein Peptide sequencesa Prior Reportsb Interferon Responsivec Cnd DPIe # Hitsf Oncogene statusg VACVh
AHSA1 SPEELYRVF 3.6857 1,3 4
AIM1 LPDNSLKVF 4 2.2947 3 2 candidate KVF7DGYi
APEH VPFKQGMEY 1 2
ARHGEF18 LPSGVGPEY 1 2.3883 1 2
ARPC4 KPVEGYDISF 3.4382 3 4
ATP5F1 VPVPPLPEY 1 2.4713 3 7
ATP6V1B2 HPIPDLTGY 2 1 2
BLMH KPLFNMEDKI 2.1907 1 1
CANX APPSSPKVTY 1 2.5506 3 1
CAPN1 LPIKDGKLVF 2.2217 3 1
CCT4 HPTIISESF [1] 2.2973 1 2 H1Y;I5F;S8T
CTNNA1 NPVQALSEF 2.6248 1 3
DDOST FPDKPITQY 1 2.8022 1,2 7
DDX21 SPPKDVESY 2.4713 3 2
DDX50 SPPQDVESY 2.8877 2,3 5
DEK FPFEKGSVQY 2 2.6723 1,3 3 known
DNAJC13 LPVARFLKY 1 2.0127 3 1
EEF1G FPAGKVPAF 2.6279 1,3 5
EEF2 LPSPVTAQKY 3 3 4
LPVNESFGF 2.275 1 3
EFHD2 NPYTEFKEF 2.7636 3 1
ERH NPNSPSITY [2] 3.0901 1,2,3 15
FH MPTPVIKAF 2 2.8021 1 6 known*
FLNA VPASLPVEF 2 2.0951 3 2 candidate
GLS DPRLKECMDM 16 2.1995 1 1
GOT2 LPIGGLAEF 2.1101 1 5
HDGF FPYEESKEKF 1 3 5
HPRT1 IPDKFVVGY 3.1871 1,3 7
HSPA8 IPTKQTQTF 1 2.4455 3 2 TQ6NF
K4R;Q5K; Q7R
QPGVLIQVY 2.2033 3 1
ILF2 KPAPDETSF 2.1768 1 1
ISOC1 IPVIVTEQY 1 2.4097 1 2
LGALS3 FPFESGKPF 2.2508 1 1
LTA4H VPYEKGFAL 4 2.4068 3 3
MPI RPVEEIVTF 1 2.4651 3 4 candidate
MTHFD1 TPVPGGVGPM 1 2.5411 1 3
MYO1C APVGGHILSY 2.3905 3 2
MYO1G DPIGGHIHSY 2.6728 3 4
NARG1 TPLEEAIKF 2.0495 1 1 candidate
NDUFS2 LPYFDRLDY 2.1946 3 1
NIT2 IPEEDAGKLY 2.7275 1 1
NONO RPSGKGIVEF 1 2.4937 2,3 7
NUP210 FPAPAKAVVY 7 2.0796 3 2 known
PABPC1 VPNPVINPY 2 3.4778 1,2 2 candidate
PDCD6IP FPQPPQQSY 2.1958 1 1 candidate
PLEC1 LPTEEQRVY 2.171 3 2
PPA2 EPMNPIKQY 2.9655 3 1
PRPF8 SPIPFPPLSY 2 2.7818 1,3 17
PSMD7 LPINHQIIY 2.6684 3 2 candidate
RAD23A FPVAGQKLIY 2.7215 3 2
RAD23B FPEGLVIQAY 1 2.2462 1 1
RPL15 RPVPKGATY 3 2.725 3 2
RPN1 APDELHYTY 2.1773 1,3 2
SFRS2IP LPADVQNYY 2.6707 1 2 known
SLC25A6 IPKEQGVLSF 7 2.2361 1 1
SPTBN1 YPNVNIHNF 1 2.5082 3 2
SRRM2 SPRVPLSAY 2.2579 3 2
STIP1 NPFNMPNLY 2.2604 1 1
SYNCRIP DPYYGYEDF 1 3.1554 3 3 candidate
SYTL3 RPDGTLNSF 2.1761 1 1 G4S;T5E; F9S
TMOD3 IPIPTLKDF 1 2.6011 1 3
TMPO TPFKGGTLF 2 2.7071 1,3 8
FPEISTRPPL 2.6193 3 6
TOP2A LPVKGFRSY 2 2.2794 1 1
TUBB3 YPDRIMNTF 1 2.6326 3 1
UBE2L3 YPFKPPKITF 2.0431 1 1
VCP YPVEHPDKF 2.9714 1 4
a

Potential peptides were determined to be derived from proteins encoded by the HeLa genome.

b

Prior reports according to immune epitope data base (IEDB; www.iedb.org); blank, this study

c

Number of entries reporting type I interferon responsiveness for the protein

d

Correlation coefficient represents the number of peak identities determined between the theoretically and experimentally derived spectra for a given parent ion normalized to the charge state of the peptide

e

Days post infection of HeLa cultures with VACV at which the peptide was identified

f

Total number of times a given peptide sequence was identified by mass spectrometry

g

Peptides derived from proteins that represent known or potential oncogenes

*

indicates mutated self peptide

h

Amino acid substitutions compared with VACV proteome. Only amino acid substitutions from sequences >66% identical are annotated. Blank, no significant homology

i

Amino acid changes for homologous VACV epitopes; blank, no significant homology