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Table 1 Proteins identified by LC-MS/MS, showing different expression levels in the different cell lines. Detailed information on peptides/proteins identification is reported in Additional File 2.

From: Proteome characterization of a human urothelial cell line resistant to the bladder carcinogen 4-aminobiphenyl

Spot #

Protein identified

Symbol

Swiss-Prot

pI Theor./Exp.b)

MW (kD) Theor./Exp.b)

#pept. c)

Cov% d)

Score e)

46

Programmed cell death 6-interacting protein

PDCD6IP

Q8WUM4

6.13/6

96/95

15

17

93.9

146

Calreticulin

CALR

P27797

4.3/4.3

48/60

36

62

187.0

206

Aldehyde dehydrogenase 1A3 a

ALDH1A3a

P47895

6.9/6.4

56/56

20

25

108.6

207

Aldehyde dehydrogenase 1A3 b

ALDH1A3b

P47895

6.9/7

56/56

19

28

123

349

Elongation factor Tu

TUFM

P49411

7.3/7.5

49/46

12

30

64.2

431

3-Hydroxyisobutyl Coenzyme A hydrolase

HIBCH

Q53GA8

8.4/7.4

43/43

16

  

463

Glyceraldehyde-3-phosphate dehydrogenase

GAPDH

P04406

8.6/8

36/37

10

27

57.1

479

Annexin A2

ANXA2

P07355

7.6/8.7

38/37

11

33

81.5

680

Transgelin-2

TAGLN2

P37802

8.4/5.8

22/21

3

19

25.1

744

Fatty acid-binding protein

FABP4

P15090

6.8/6

14/14

39

73

145.9

801

Lamin-A/C

LMNA

P02545

6.6/6.2

74/75

35

41

197.6

841

94 kDa glucose-regulated protein

GRP94

P14625

4.7/4.7

92/95

15

18

105.2

906

NADH-ubiquinone oxidoreductase 30 kDa subunit

NDUFS3

O75489

6.9/5

30/28

10

46

84.3

912

Triosephosphate isomerase

TPI

P60174

6.5/6

26/27

12

42

77.1

  1. a) Arbitrary label assigned to the different isoforms.
  2. b) Theor.: theoretical, data-based annotations; Exp.: experimental, from 2-D gels.
  3. c) # pept.: number of valid peptide matches found for the given protein
  4. d) Cov%: the percent ratio of all amino acids from valid peptide matches to the total number of amino acids in the protein.
  5. e) Score: the protein score is a function calculated from the individual normalized z-scores of validated peptides. Peptide z-score refers to the distribution of calculated scores compared to that of random peptide sequences in order to find the mean and variance http://www.phenyx-ms.com. Database redundancy is handled and solved by the Phenyx software. If a protein shares all its validated peptides with another one, it is considered a subset and will not appear in the best-scoring protein list. It appears in the protein Details panel under Subset for the principal and better scoring parameters. Therefore the entries reported (Swiss_Prot AC) refer exclusively to the best-scoring protein found by the search engine.