UniProt ID | FP100_HUMAN | |
---|---|---|
UniProt AC | Q0VG06 | |
Protein Name | Fanconi anemia core complex-associated protein 100 {ECO:0000303|PubMed:17396147, ECO:0000312|HGNC:HGNC:26171} | |
Gene Name | FAAP100 {ECO:0000303|PubMed:17396147, ECO:0000312|HGNC:HGNC:26171} | |
Organism | Homo sapiens (Human). | |
Sequence Length | 881 | |
Subcellular Localization | Nucleus . | |
Protein Description | Plays a role in Fanconi anemia-associated DNA damage response network. Regulates FANCD2 monoubiquitination and the stability of the FA core complex. Induces chromosomal instability as well as hypersensitivity to DNA cross-linking agents, when repressed.. | |
Protein Sequence | MAGAAPRVRYLAGFCCPLGGLAAGKPRVLCHEAEVFLSTGSELVYVYDQEGGLLTAAFRFPDQVWHLELLAPRRLLYALCARRGLYCLSLDHPGRSRSTSQDDRDSEDGDQPSPVIPVDPDACILPDAALCAFTLLDSVLVTLVQGPARWKMQLFEQPCPGEDPRPGGQIGEVELSSYTPPAGVPGKPAAPHFLPVLCSVSPSGSRVPHDLLGGSGGFTLEDALFGLLFGADATLLQSPVVLCGLPDGQLCCVILKALVTSRSAPGDPNALVKILHHLEEPVIFIGALKTEPQAAEAAENFLPDEDVHCDCLVAFGHHGRMLAIKASWDESGKLVPELREYCLPGPVLCAACGGGGRVYHSTPSDLCVVDLSRGSTPLGPEQPEEGPGGLPPMLCPASLNICSVVSLSASPRTHEGGTKLLALSAKGRLMTCSLDLDSEMPGPARMTTESAGQKIKELLSGIGNISERVSFLKKAVDQRNKALTSLNEAMNVSCALLSSGTGPRPISCTTSTTWSRLQTQDVLMATCVLENSSSFSLDQGWTLCIQVLTSSCALDLDSACSAITYTIPVDQLGPGARREVTLPLGPGENGGLDLPVTVSCTLFYSLREVVGGALAPSDSEDPFLDECPSDVLPEQEGVCLPLSRHTVDMLQCLRFPGLAPPHTRAPSPLGPTRDPVATFLETCREPGSQPAGPASLRAEYLPPSVASIKVSAELLRAALKDGHSGVPLCCATLQWLLAENAAVDVVRARALSSIQGVAPDGANVHLIVREVAMTDLCPAGPIQAVEIQVESSSLADICRAHHAVVGRMQTMVTEQATQGSSAPDLRVQYLRQIHANHETLLREVQTLRDRLCTEDEASSCATAQRLLQVYRQLRHPSLILL | |
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 |
---|---|---|---|---|---|
25 | Ubiquitination | LGGLAAGKPRVLCHE CCHHHCCCCEEEEEE | 25.56 | - | |
333 | Ubiquitination | ASWDESGKLVPELRE EEECCCCCCCHHHHH | 56.44 | - | |
426 | Ubiquitination | KLLALSAKGRLMTCS EEEEEECCCCEEEEE | 40.98 | - | |
431 | Phosphorylation | SAKGRLMTCSLDLDS ECCCCEEEEECCCCC | 11.97 | 28348404 | |
433 | Phosphorylation | KGRLMTCSLDLDSEM CCCEEEEECCCCCCC | 18.76 | 28348404 | |
438 | Phosphorylation | TCSLDLDSEMPGPAR EEECCCCCCCCCCCC | 42.99 | 28348404 | |
454 | Ubiquitination | TTESAGQKIKELLSG CCHHHHHHHHHHHHC | 55.62 | - | |
456 | Ubiquitination | ESAGQKIKELLSGIG HHHHHHHHHHHHCCC | 49.71 | - | |
470 | Phosphorylation | GNISERVSFLKKAVD CCHHHHHHHHHHHHH | 30.96 | 24719451 | |
605 | Phosphorylation | VSCTLFYSLREVVGG EEEEEEECHHHHHCC | 17.39 | 24719451 | |
667 | Phosphorylation | PPHTRAPSPLGPTRD CCCCCCCCCCCCCCC | 31.60 | 30266825 | |
672 | Phosphorylation | APSPLGPTRDPVATF CCCCCCCCCCHHHHH | 46.00 | 22617229 | |
678 | Phosphorylation | PTRDPVATFLETCRE CCCCHHHHHHHHHCC | 29.05 | 28450419 | |
682 | Phosphorylation | PVATFLETCREPGSQ HHHHHHHHHCCCCCC | 21.00 | 29978859 | |
688 | Phosphorylation | ETCREPGSQPAGPAS HHHCCCCCCCCCCCH | 43.64 | 26552605 | |
695 | Phosphorylation | SQPAGPASLRAEYLP CCCCCCCHHCHHHCC | 22.86 | 26552605 | |
810 | Phosphorylation | AVVGRMQTMVTEQAT HHHHHHHHHHHHHHH | 12.31 | 24043423 | |
813 | Phosphorylation | GRMQTMVTEQATQGS HHHHHHHHHHHHCCC | 16.14 | 24043423 | |
817 | Phosphorylation | TMVTEQATQGSSAPD HHHHHHHHCCCCCCH | 32.91 | 24043423 | |
820 | Phosphorylation | TEQATQGSSAPDLRV HHHHHCCCCCCHHHH | 17.32 | 24043423 | |
821 | Phosphorylation | EQATQGSSAPDLRVQ HHHHCCCCCCHHHHH | 51.12 | 24043423 | |
846 | Phosphorylation | TLLREVQTLRDRLCT HHHHHHHHHHHHHCC | 29.01 | 24043423 | |
877 | Phosphorylation | YRQLRHPSLILL--- HHHHHCCCCCCC--- | 23.16 | 27251275 |
Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
---|---|---|---|---|---|---|
Oops, there are no upstream regulatory protein records of FP100_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of FP100_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 FP100_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
FANCA_HUMAN | FANCA | physical | 17396147 | |
FANCB_HUMAN | FANCB | physical | 17396147 | |
FANCL_HUMAN | FANCL | physical | 17396147 | |
FANCM_HUMAN | FANCM | physical | 17396147 | |
A4_HUMAN | APP | physical | 21832049 | |
FANCM_HUMAN | FANCM | physical | 22343915 | |
BLM_HUMAN | BLM | physical | 22343915 | |
FANCA_HUMAN | FANCA | physical | 22343915 | |
TOP3A_HUMAN | TOP3A | physical | 22343915 | |
FANCB_HUMAN | FANCB | physical | 22343915 | |
RMI1_HUMAN | RMI1 | physical | 22343915 | |
FANCC_HUMAN | FANCC | physical | 22343915 | |
FANCG_HUMAN | FANCG | physical | 22343915 | |
FANCE_HUMAN | FANCE | physical | 22343915 | |
FANCL_HUMAN | FANCL | physical | 22343915 | |
FANCF_HUMAN | FANCF | physical | 22343915 | |
FAP24_HUMAN | C19orf40 | physical | 22343915 | |
FAP20_HUMAN | C1orf86 | physical | 22343915 | |
RMI2_HUMAN | RMI2 | physical | 22343915 | |
CENPS_HUMAN | APITD1 | physical | 22343915 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
There are no disease associations of PTM sites. | ||||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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