Figure 3.
A BioD model of structures and functional elements controlling the G1/S transition
of the cell cycle [6,10,11,12,13,14]. Key molecular players are represented by binding sites, phosphorylation sites and
kinase sites whose occupancies and activities interact to control the cell cycle.
The critical synthesis and degradation kinetics of cyclin D1 are represented by an
'identity' link to the nuclear cyclin D1 icon in the 'process' modeled in Figure 4. Additional inputs to the model (TGF-β stimulation and DNA damage) and outputs (G1/S
transition) are included as unmodeled processes. CAK, cyclin-activating kinase; DP,
DRTF1-polypeptide; DRTF, differentiation-regulated transcription factor; E2F, E2F
transcription factor; TK, thymidine kinase; TS,thymidylate synthetase; POL, DNA polymerase.
Cook et al. Genome Biology 2001 2:research0012.1 doi:10.1186/gb-2001-2-4-research0012 |