InnateDB Protein
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IDBP-107428.7
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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SPRTN
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Protein Name
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chromosome 1 open reading frame 124
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000295050
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InnateDB Gene
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IDBG-107422 (SPRTN)
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Protein Structure
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Function |
Regulator of UV-induced DNA damage response: acts as a 'reader' of ubiquitinated PCNA that enhances RAD18-mediated PCNA ubiquitination and translesion DNA synthesis (TLS). Recruited to sites of UV damage and interacts with ubiquitinated PCNA and RAD18, the E3 ubiquitin ligase that monoubiquitinates PCNA. Facilitates chromatin association of RAD18 and is required for efficient PCNA monoubiquitination, promoting a feed-forward loop to enhance PCNA ubiquitination and translesion DNA synthesis. Acts as a regulator of TLS by recruiting VCP/p97 to sites of DNA damage, possibly leading to extraction of DNA polymerase eta (POLH) by VCP/p97 to prevent excessive translesion DNA synthesis and limit the incidence of mutations induced by DNA damage. {ECO:0000269PubMed:22681887, ECO:0000269PubMed:22894931, ECO:0000269PubMed:22902628, ECO:0000269PubMed:22987070, ECO:0000269PubMed:23042605, ECO:0000269PubMed:23042607}.
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Subcellular Localization |
Nucleus. Chromosome. Note=Localizes to sites of UV damage via the PIP-box. Recruited to stalled relication forks at sites of replication stress.
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Disease Associations |
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 91 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
91
[view]
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Protein-Protein |
90
[view]
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Protein-DNA |
1
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR006640
Domain of unknown function SprT-like
IPR006642
Zinc finger, Rad18-type putative
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PFAM |
PF10263
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PRINTS |
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PIRSF |
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SMART |
SM00731
SM00734
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TIGRFAMs |
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Modification |
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SwissProt |
Q9H040
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PhosphoSite |
PhosphoSite-Q9H040
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TrEMBL |
L8E708
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UniProt Splice Variant |
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Entrez Gene |
83932
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UniGene |
Hs.623990
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RefSeq |
NP_114407
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HUGO |
HGNC:25356
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OMIM |
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CCDS |
CCDS1594
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HPRD |
13164
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IMGT |
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EMBL |
AK027317
AK027613
AL117352
AL512744
AY358611
BC015740
BC068478
CH471098
HF583533
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GenPept |
AAH15740
AAH68478
AAQ88974
BAB55037
BAB55232
CAC21670
CCQ43030
EAW69956
EAW69958
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