Table 1 Selection of frequently reported molecules that mediate the PTMs of the p53 protein under homeostatic and stress conditions.

From: DNA damage response revisited: the p53 family and its regulators provide endless cancer therapy opportunities

Protein

Type

PTM

Effect on p53

Deletion phenotype in mice

MDM2

E3 ubiquitin ligase, RING-type

Ubiquitination

Nuclear export, degradation

Embryonic lethal

Pirh2

E3 ubiquitin ligase, RING-type

Ubiquitination

Degradation

Viable

Cop1

E3 ubiquitin ligase, RING-type

Ubiquitination

Degradation

Embryonic lethal

UBE4B

E3/E4 ubiquitin ligase, U-box type

Ubiquitination

Degradation

Embryonic lethal

CHIP

E3 ubiquitin ligase, U-box type

Ubiquitination

Degradation

Viable, aging

Trim24

E3 ubiquitin ligase, RING-type

Ubiquitination

Degradation

Viable

USP7

Deubiquitinating enzyme

Deubiquitination

Stabilization, degradation

Embryonic lethal

ATM

Kinase

Phosphorylation

Stabilization

Viable, acutely radiosensitive

ATR

Kinase

Phosphorylation

Stabilization

Embryonic lethal

CHK1

Kinase

Phosphorylation

Stabilization

Embryonic lethal

CHK2

Kinase

Phosphorylation

Stabilization

Viable

DNA-PK

Kinase

Phosphorylation

Stabilization

Viable

WIP1

Phosphatase

Dephosphorylation

Destabilization

Viable, cancer resistant