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IID00880
UniprotQ9HCU8
ProteinDNA polymerase delta subunit 4
GenePOLD4
OrganismHomo sapiens
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
Network xml rdf
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
107
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 1-19 Hetero hexamer : IID00022Complex
 Evidence X-RAY 6hvo F Reference
       Region 6hvo F 1-2 disorder
       Region 6hvo F 3-15 order
       Region 6hvo F 16-19 disorder
 Evidence X-RAY 6hvo E Reference
       Region 6hvo E 1-2 disorder
       Region 6hvo E 3-14 order
       Region 6hvo E 15-19 disorder
 Evidence X-RAY 6hvo D Reference
       Region 6hvo D 1-3 disorder
       Region 6hvo D 4-15 order
       Region 6hvo D 16-19 disorder
SeqProS possible 3-15 PIP box motif Hetero hexamer : IID00022Complex
       Region 6hvo D 4-15 order
       Region 6hvo E 3-14 order
       Region 6hvo F 3-15 order
 
Prediction
NeProc
Disorder 1-40
Order 41-107
ProS 5-21,34-40
AlphaFold
Disorder 1-1,17-38
Order 2-16,39-107
Pfam Hmmer
PF04081 1-103 3e-67
SEG 31-51
Function
Function in SwissProt
As a component of the tetrameric DNA polymerase delta complex (Pol-delta4), plays a role in high fidelity genome replication and repair. Within this complex, increases the rate of DNA synthesis and decreases fidelity by regulating POLD1 polymerase and proofreading 3' to 5' exonuclease activity (PubMed:16510448, PubMed:19074196, PubMed:20334433). Pol-delta4 participates in Okazaki fragment processing, through both the short flap pathway, as well as a nick translation system (PubMed:24035200). Under conditions of DNA replication stress, required for the repair of broken replication forks through break-induced replication (BIR), a mechanism that may induce segmental genomic duplications of up to 200 kb (PubMed:24310611). Involved in Pol-delta4 translesion synthesis (TLS) of templates carrying O6-methylguanine or abasic sites (PubMed:19074196). Its degradation in response to DNA damage is required for the inhibition of fork progression and cell survival (PubMed:24022480).
Biological Process
See also
Diagram with PDB data
XPA/ERCC1Solution structure of a ERCC1-XPA heterodimer