Core component of multiple cullin-RING-based E3 ubiquitin- protein ligase complexes which mediate the ubiquitination of target proteins (PubMed:
14578910, PubMed:
15811626, PubMed:
15548678, PubMed:
15448697, PubMed:
14739464, PubMed:
16678110, PubMed:
17041588, PubMed:
24209620, PubMed:
30166453, PubMed:
33854232, PubMed:
33854239). As a scaffold protein may contribute to catalysis through positioning of the substrate and the ubiquitin-conjugating enzyme (PubMed:
14578910, PubMed:
15811626, PubMed:
15548678, PubMed:
15448697, PubMed:
14739464, PubMed:
16678110, PubMed:
17041588, PubMed:
24209620). The E3 ubiquitin- protein ligase activity of the complex is dependent on the neddylation of the cullin subunit and is inhibited by the association of the deneddylated cullin subunit with TIP120A/CAND1 (PubMed:
14578910, PubMed:
15811626, PubMed:
15548678, PubMed:
15448697, PubMed:
14739464, PubMed:
16678110, PubMed:
17041588, PubMed:
24209620). The functional specificity of the E3 ubiquitin-protein ligase complex depends on the variable substrate recognition component (PubMed:
14578910, PubMed:
15811626, PubMed:
15548678, PubMed:
15448697, PubMed:
14739464, PubMed:
16678110, PubMed:
17041588, PubMed:
24209620). DCX(DET1-COP1) directs ubiquitination of JUN (PubMed:
14739464). DCX(DDB2) directs ubiquitination of XPC (PubMed:
15811626). DCX(DDB2) ubiquitinates histones H3-H4 and is required for efficient histone deposition during replication-coupled (H3.1) and replication-independent (H3.3) nucleosome assembly, probably by facilitating the transfer of H3 from ASF1A/ASF1B to other chaperones involved in histone deposition (PubMed:
16678110, PubMed:
17041588, PubMed:
24209620). DCX(DTL) plays a role in PCNA-dependent polyubiquitination of CDT1 and MDM2-dependent ubiquitination of p53/TP53 in response to radiation-induced DNA damage and during DNA replication (PubMed:
14578910, PubMed:
15548678, PubMed:
15448697). DCX(DTL) directs autoubiquitination of DTL (PubMed:
23478445). In association with DDB1 and SKP2 probably is involved in ubiquitination of CDKN1B/p27kip (PubMed:
16537899). Is involved in ubiquitination of HOXA9 (PubMed:
14609952). The DDB1-CUL4A- DTL E3 ligase complex regulates the circadian clock function by mediating the ubiquitination and degradation of CRY1 (PubMed:
26431207). A number of DCX complexes (containing either TRPC4AP or DCAF12 as substrate-recognition component) are part of the DesCEND (destruction via C-end degrons) pathway, which recognizes a C-degron located at the extreme C terminus of target proteins, leading to their ubiquitination and degradation (PubMed:
29779948). The DCX(AMBRA1) complex is a master regulator of the transition from G1 to S cell phase by mediating ubiquitination of phosphorylated cyclin-D (CCND1, CCND2 and CCND3) (PubMed:
33854232, PubMed:
33854239). The DCX(AMBRA1) complex also acts as a regulator of Cul5-RING (CRL5) E3 ubiquitin-protein ligase complexes by mediating ubiquitination and degradation of Elongin-C (ELOC) component of CRL5 complexes (PubMed:
30166453). With CUL4B, contributes to ribosome biogenesis (PubMed:
26711351).
