UniProt ID | FOXD3_HUMAN | |
---|---|---|
UniProt AC | Q9UJU5 | |
Protein Name | Forkhead box protein D3 | |
Gene Name | FOXD3 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 478 | |
Subcellular Localization | Nucleus . | |
Protein Description | Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promotes development of neural crest cells from neural tube progenitors. Restricts neural progenitor cells to the neural crest lineage while suppressing interneuron differentiation. Required for maintenance of pluripotent cells in the pre-implantation and peri-implantation stages of embryogenesis.. | |
Protein Sequence | MTLSGGGSASDMSGQTVLTAEDVDIDVVGEGDDGLEEKDSDAGCDSPAGPPELRLDEADEVPPAAPHHGQPQPPHQQPLTLPKEAAGAGAGPGGDVGAPEADGCKGGVGGEEGGASGGGPGAGSGSAGGLAPSKPKNSLVKPPYSYIALITMAILQSPQKKLTLSGICEFISNRFPYYREKFPAWQNSIRHNLSLNDCFVKIPREPGNPGKGNYWTLDPQSEDMFDNGSFLRRRKRFKRHQQEHLREQTALMMQSFGAYSLAAAAGAAGPYGRPYGLHPAAAAGAYSHPAAAAAAAAAAALQYPYALPPVAPVLPPAVPLLPSGELGRKAAAFGSQLGPGLQLQLNSLGAAAAAAGTAGAAGTTASLIKSEPSARPSFSIENIIGGGPAAPGGSAVGAGVAGGTGGSGGGSTAQSFLRPPGTVQSAALMATHQPLSLSRTTATIAPILSVPLSGQFLQPAASAAAAAAAAAQAKWPAQ | |
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 |
---|---|---|---|---|---|
40 | Phosphorylation | DGLEEKDSDAGCDSP CCCCCCCCCCCCCCC | 40.19 | 25850435 | |
46 | Phosphorylation | DSDAGCDSPAGPPEL CCCCCCCCCCCCCCC | 22.26 | 29255136 | |
146 | Phosphorylation | LVKPPYSYIALITMA CCCCCHHHHHHHHHH | 5.60 | - | |
213 | N-linked_Glycosylation | PGNPGKGNYWTLDPQ CCCCCCCCCCCCCCC | 32.43 | - | |
213 | N-linked_Glycosylation | PGNPGKGNYWTLDPQ CCCCCCCCCCCCCCC | 32.43 | 19349973 | |
214 | Phosphorylation | GNPGKGNYWTLDPQS CCCCCCCCCCCCCCC | 14.40 | - | |
229 | Phosphorylation | EDMFDNGSFLRRRKR HHHCCCCHHHHHHHH | 27.62 | - | |
335 | Phosphorylation | RKAAAFGSQLGPGLQ HHHHHHHHCCCCCHH | 18.77 | 22210691 | |
347 | Phosphorylation | GLQLQLNSLGAAAAA CHHHHHHHHHHHHHH | 36.45 | 22210691 | |
366 | Phosphorylation | GAAGTTASLIKSEPS CCCCHHHHHHHCCCC | 28.65 | 24719451 | |
436 | Phosphorylation | MATHQPLSLSRTTAT HHHCCCCCCCCCCCC | 30.86 | 24719451 | |
438 | Phosphorylation | THQPLSLSRTTATIA HCCCCCCCCCCCCCC | 24.97 | 17081983 |
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 FOXD3_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of FOXD3_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 FOXD3_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
PO5F1_HUMAN | POU5F1 | physical | 11891324 | |
FOXD1_HUMAN | FOXD1 | physical | 25609649 | |
HXD13_HUMAN | HOXD13 | physical | 25609649 | |
2ABD_HUMAN | PPP2R2D | physical | 25609649 | |
CUX1_HUMAN | CUX1 | physical | 25609649 | |
CASP_HUMAN | CUX1 | physical | 25609649 | |
TOP2A_HUMAN | TOP2A | physical | 25609649 | |
TOP2B_HUMAN | TOP2B | physical | 25609649 | |
DNLI3_HUMAN | LIG3 | physical | 25609649 | |
VRK3_HUMAN | VRK3 | physical | 25609649 | |
UBIP1_HUMAN | UBP1 | physical | 25609649 | |
ML12B_HUMAN | MYL12B | physical | 25609649 | |
SATB1_HUMAN | SATB1 | physical | 25609649 | |
XRCC1_HUMAN | XRCC1 | physical | 25609649 | |
NC2A_HUMAN | DRAP1 | physical | 25609649 | |
HXB9_HUMAN | HOXB9 | physical | 25609649 | |
MYL9_HUMAN | MYL9 | physical | 25609649 | |
SATB2_HUMAN | SATB2 | physical | 25609649 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
607836 | Autoimmune disease 1 (AIS1) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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