UniProt ID | DPOG1_HUMAN | |
---|---|---|
UniProt AC | P54098 | |
Protein Name | DNA polymerase subunit gamma-1 | |
Gene Name | POLG | |
Organism | Homo sapiens (Human). | |
Sequence Length | 1239 | |
Subcellular Localization | Mitochondrion . Mitochondrion matrix, mitochondrion nucleoid . | |
Protein Description | Involved in the replication of mitochondrial DNA. Associates with mitochondrial DNA.. | |
Protein Sequence | MSRLLWRKVAGATVGPGPVPAPGRWVSSSVPASDPSDGQRRRQQQQQQQQQQQQQPQQPQVLSSEGGQLRHNPLDIQMLSRGLHEQIFGQGGEMPGEAAVRRSVEHLQKHGLWGQPAVPLPDVELRLPPLYGDNLDQHFRLLAQKQSLPYLEAANLLLQAQLPPKPPAWAWAEGWTRYGPEGEAVPVAIPEERALVFDVEVCLAEGTCPTLAVAISPSAWYSWCSQRLVEERYSWTSQLSPADLIPLEVPTGASSPTQRDWQEQLVVGHNVSFDRAHIREQYLIQGSRMRFLDTMSMHMAISGLSSFQRSLWIAAKQGKHKVQPPTKQGQKSQRKARRGPAISSWDWLDISSVNSLAEVHRLYVGGPPLEKEPRELFVKGTMKDIRENFQDLMQYCAQDVWATHEVFQQQLPLFLERCPHPVTLAGMLEMGVSYLPVNQNWERYLAEAQGTYEELQREMKKSLMDLANDACQLLSGERYKEDPWLWDLEWDLQEFKQKKAKKVKKEPATASKLPIEGAGAPGDPMDQEDLGPCSEEEEFQQDVMARACLQKLKGTTELLPKRPQHLPGHPGWYRKLCPRLDDPAWTPGPSLLSLQMRVTPKLMALTWDGFPLHYSERHGWGYLVPGRRDNLAKLPTGTTLESAGVVCPYRAIESLYRKHCLEQGKQQLMPQEAGLAEEFLLTDNSAIWQTVEELDYLEVEAEAKMENLRAAVPGQPLALTARGGPKDTQPSYHHGNGPYNDVDIPGCWFFKLPHKDGNSCNVGSPFAKDFLPKMEDGTLQAGPGGASGPRALEINKMISFWRNAHKRISSQMVVWLPRSALPRAVIRHPDYDEEGLYGAILPQVVTAGTITRRAVEPTWLTASNARPDRVGSELKAMVQAPPGYTLVGADVDSQELWIAAVLGDAHFAGMHGCTAFGWMTLQGRKSRGTDLHSKTATTVGISREHAKIFNYGRIYGAGQPFAERLLMQFNHRLTQQEAAEKAQQMYAATKGLRWYRLSDEGEWLVRELNLPVDRTEGGWISLQDLRKVQRETARKSQWKKWEVVAERAWKGGTESEMFNKLESIATSDIPRTPVLGCCISRALEPSAVQEEFMTSRVNWVVQSSAVDYLHLMLVAMKWLFEEFAIDGRFCISIHDEVRYLVREEDRYRAALALQITNLLTRCMFAYKLGLNDLPQSVAFFSAVDIDRCLRKEVTMDCKTPSNPTGMERRYGIPQGEALDIYQIIELTKGSLEKRSQPGP | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
|
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
80 | Phosphorylation | PLDIQMLSRGLHEQI HHHHHHHHHHHHHHH | 20.96 | 24114839 | |
109 | Ubiquitination | RSVEHLQKHGLWGQP HHHHHHHHCCCCCCC | 46.10 | - | |
296 | Phosphorylation | MRFLDTMSMHMAISG HHHHHHHHHHHHHHC | 13.97 | - | |
316 | Ubiquitination | RSLWIAAKQGKHKVQ HHHHHHHHCCCCCCC | 51.03 | - | |
321 | Ubiquitination | AAKQGKHKVQPPTKQ HHHCCCCCCCCCCCC | 46.15 | - | |
326 | Phosphorylation | KHKVQPPTKQGQKSQ CCCCCCCCCCCHHHH | 42.56 | 22210691 | |
327 | Ubiquitination | HKVQPPTKQGQKSQR CCCCCCCCCCHHHHH | 59.20 | - | |
371 | Ubiquitination | VGGPPLEKEPRELFV CCCCCCCCCCHHHHC | 79.35 | - | |
379 | Ubiquitination | EPRELFVKGTMKDIR CCHHHHCCCCHHHHH | 41.13 | - | |
383 | Ubiquitination | LFVKGTMKDIRENFQ HHCCCCHHHHHHHHH | 50.25 | - | |
433 | Phosphorylation | GMLEMGVSYLPVNQN HHHHCCCCEEECCCC | 18.41 | - | |
475 | Phosphorylation | NDACQLLSGERYKED HHHHHHHCCCCCCCC | 47.39 | 29759185 | |
479 | Phosphorylation | QLLSGERYKEDPWLW HHHCCCCCCCCCCHH | 17.90 | 22673903 | |
551 | Ubiquitination | MARACLQKLKGTTEL HHHHHHHHHCCCCCC | 38.94 | - | |
553 | Ubiquitination | RACLQKLKGTTELLP HHHHHHHCCCCCCCC | 62.34 | - | |
561 | Ubiquitination | GTTELLPKRPQHLPG CCCCCCCCCCCCCCC | 76.35 | - | |
606 | Phosphorylation | TPKLMALTWDGFPLH CCCCEEEEECCCCCC | 16.39 | 29759185 | |
614 | Phosphorylation | WDGFPLHYSERHGWG ECCCCCCCHHHCCCC | 21.65 | 29759185 | |
615 | Phosphorylation | DGFPLHYSERHGWGY CCCCCCCHHHCCCCE | 19.87 | 29759185 | |
622 | Phosphorylation | SERHGWGYLVPGRRD HHHCCCCEECCCCCC | 9.68 | 22468782 | |
633 | Ubiquitination | GRRDNLAKLPTGTTL CCCCCCCCCCCCCCH | 59.16 | - | |
658 | Ubiquitination | AIESLYRKHCLEQGK HHHHHHHHHHHHHHH | 25.72 | - | |
726 | Ubiquitination | LTARGGPKDTQPSYH EEECCCCCCCCCCCC | 76.35 | - | |
755 | Ubiquitination | WFFKLPHKDGNSCNV EEEECCCCCCCCCCC | 66.45 | - | |
768 | Ubiquitination | NVGSPFAKDFLPKME CCCCCCHHHHCHHCC | 49.76 | - | |
773 | Ubiquitination | FAKDFLPKMEDGTLQ CHHHHCHHCCCCCCC | 58.00 | - | |
796 | Ubiquitination | PRALEINKMISFWRN CHHHHHHHHHHHHHH | 43.18 | - | |
819 | Phosphorylation | MVVWLPRSALPRAVI EEEEEEHHHCCCHHH | 32.02 | 24719451 | |
831 | Phosphorylation | AVIRHPDYDEEGLYG HHHCCCCCCCCCCHH | 29.70 | 27642862 | |
934 | Ubiquitination | RGTDLHSKTATTVGI CCCCCCCCCCCCCCC | 31.28 | - | |
935 | Phosphorylation | GTDLHSKTATTVGIS CCCCCCCCCCCCCCC | 32.05 | 24114839 | |
947 | Ubiquitination | GISREHAKIFNYGRI CCCHHHHHHHCCCCC | 50.14 | - | |
981 | Ubiquitination | TQQEAAEKAQQMYAA HHHHHHHHHHHHHHH | 46.93 | 21906983 | |
990 | Ubiquitination | QQMYAATKGLRWYRL HHHHHHHCCCCEEEE | 51.74 | 21906983 | |
1014 | Methylation | ELNLPVDRTEGGWIS EECCCCCCCCCCEEE | 34.61 | 115488101 | |
1040 | Ubiquitination | ARKSQWKKWEVVAER HHHHHHHHHHHHHHH | 45.70 | - | |
1050 | Ubiquitination | VVAERAWKGGTESEM HHHHHHHCCCCHHHH | 46.61 | - | |
1060 | Ubiquitination | TESEMFNKLESIATS CHHHHHHHHHHHHCC | 42.22 | 21906983 | |
1191 | Ubiquitination | DIDRCLRKEVTMDCK CHHHHHHCEECCCCC | 43.52 | - | |
1194 | Phosphorylation | RCLRKEVTMDCKTPS HHHHCEECCCCCCCC | 14.37 | 26657352 | |
1198 | Ubiquitination | KEVTMDCKTPSNPTG CEECCCCCCCCCCCH | 60.24 | - | |
1221 | Phosphorylation | QGEALDIYQIIELTK CCCCCHHHHHHHHCC | 8.04 | - |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of DPOG1_HUMAN !! |
* Distance = the distance between SAP position and PTM sites.
Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of DPOG1_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
Oops, there are no PPI records of DPOG1_HUMAN !! |
Kegg Disease | ||||||
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There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
157640 | Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 1 (PEOA1) | |||||
258450 | Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB) | |||||
607459 | Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) | |||||
203700 | Mitochondrial DNA depletion syndrome 4A (MTDPS4A) | |||||
613662 | Mitochondrial DNA depletion syndrome 4B (MTDPS4B) | |||||
256000 | Leigh syndrome (LS) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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