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Table 1 Transcription factors predicted to interact with phosphoproteins found in MS experiments

From: New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells

BARD1

BRCA1 associated RING domain 1

BMI1

BMI1 polycomb ring finger oncogene

CBX3

Chromobox homolog 3

CTNNB1

Catenin (cadherin-associated protein), beta 1, 88 kDa

HIC1

Hypermethylated in cancer 1

HMGA1

High mobility group AT-hook 1

HNF4A

Hepatocyte nuclear factor 4, alpha

ID3

Inhibitor of DNA binding 3, dominant negative helix-loop-helix protein

KDM5B

Lysine (K)-specific demethylase 5B

MAZ

MYC-associated zinc finger protein (purine-binding transcription factor)

MTA1

Metastasis associated 1

MYC

v-myc myelocytomatosis viral oncogene homolog (avian)

NFATC1

Nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1

NFKB1

Nuclear factor of kappa light polypeptide gene enhancer in B-cells 1

PPP1R13L

Protein phosphatase 1, regulatory (inhibitor) subunit 13 like

SIAH2

Seven in absentia homolog 2 (Drosophila)

SMAD3

SMAD family member 3

SOX4

SRY (sex determining region Y)-box 4

SP1

Sp1 transcription factor

SREBF1

Sterol regulatory element binding transcription factor 1

TFDP1

Transcription factor Dp-1

TGFB1I1

Transforming growth factor beta 1 induced transcript 1

TLE1

Transducin-like enhancer of split 1 (E(sp1) homolog, Drosophila)

YAP1

Yes-associated protein 1

CBX4

Chromobox homolog 4

E2F4

E2F transcription factor 4, p107/p130-binding

  1. Predicted network of interaction for phosphoproteins found using Ingenuity Pathway Analysis. The list of phosphoproteins found were subjected to Ingenuity Pathway Analysis (IPA) to investigate problable protein interactions for each cellular compartment. Proteins described to be transcription factors were selected to investigate the activation of osteblast related genes by quantitative real-time PCR.