| UniProt ID | PHX2A_HUMAN | |
|---|---|---|
| UniProt AC | O14813 | |
| Protein Name | Paired mesoderm homeobox protein 2A | |
| Gene Name | PHOX2A | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 284 | |
| Subcellular Localization | Nucleus . | |
| Protein Description | May be involved in regulating the specificity of expression of the catecholamine biosynthetic genes. Acts as a transcription activator/factor. Could maintain the noradrenergic phenotype.. | |
| Protein Sequence | MDYSYLNSYDSCVAAMEASAYGDFGACSQPGGFQYSPLRPAFPAAGPPCPALGSSNCALGALRDHQPAPYSAVPYKFFPEPSGLHEKRKQRRIRTTFTSAQLKELERVFAETHYPDIYTREELALKIDLTEARVQVWFQNRRAKFRKQERAASAKGAAGAAGAKKGEARCSSEDDDSKESTCSPTPDSTASLPPPPAPGLASPRLSPSPLPVALGSGPGPGPGPQPLKGALWAGVAGGGGGGPGAGAAELLKAWQPAESGPGPFSGVLSSFHRKPGPALKTNLF | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
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* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 54 | Phosphorylation | PPCPALGSSNCALGA CCCCCCCCCCCHHHH | 21.16 | 27732954 | |
| 55 | Phosphorylation | PCPALGSSNCALGAL CCCCCCCCCCHHHHH | 33.84 | 27732954 | |
| 76 | Ubiquitination | PYSAVPYKFFPEPSG CCCCCCCCCCCCCCC | 34.16 | 23503661 | |
| 87 | Ubiquitination | EPSGLHEKRKQRRIR CCCCHHHHHHHHHHH | 54.90 | 23503661 | |
| 89 | Ubiquitination | SGLHEKRKQRRIRTT CCHHHHHHHHHHHHH | 60.26 | 23503661 | |
| 103 | Ubiquitination | TFTSAQLKELERVFA HHCHHHHHHHHHHHH | 48.44 | 23503661 | |
| 153 | Phosphorylation | RKQERAASAKGAAGA HHHHHHHHHHHHHHH | 29.54 | 22817900 | |
| 155 | Acetylation | QERAASAKGAAGAAG HHHHHHHHHHHHHHH | 46.73 | 12436251 | |
| 155 | Ubiquitination | QERAASAKGAAGAAG HHHHHHHHHHHHHHH | 46.73 | 23503661 | |
| 171 | Phosphorylation | KKGEARCSSEDDDSK CCCCCCCCCCCCCCC | 31.07 | 30177828 | |
| 172 | Phosphorylation | KGEARCSSEDDDSKE CCCCCCCCCCCCCCC | 48.98 | 30177828 | |
| 180 | Phosphorylation | EDDDSKESTCSPTPD CCCCCCCCCCCCCCC | 38.15 | 27732954 | |
| 181 | Phosphorylation | DDDSKESTCSPTPDS CCCCCCCCCCCCCCC | 20.35 | 27732954 | |
| 183 | Phosphorylation | DSKESTCSPTPDSTA CCCCCCCCCCCCCCC | 31.71 | 27732954 | |
| 185 | Phosphorylation | KESTCSPTPDSTASL CCCCCCCCCCCCCCC | 24.35 | 27732954 | |
| 188 | Phosphorylation | TCSPTPDSTASLPPP CCCCCCCCCCCCCCC | 27.38 | 27732954 | |
| 189 | Phosphorylation | CSPTPDSTASLPPPP CCCCCCCCCCCCCCC | 27.87 | 27732954 | |
| 191 | Phosphorylation | PTPDSTASLPPPPAP CCCCCCCCCCCCCCC | 41.31 | 27732954 | |
| 202 | Phosphorylation | PPAPGLASPRLSPSP CCCCCCCCCCCCCCC | 18.65 | 27732954 | |
| 206 | Phosphorylation | GLASPRLSPSPLPVA CCCCCCCCCCCCCCC | 25.31 | 29900121 | |
| 208 | Phosphorylation | ASPRLSPSPLPVALG CCCCCCCCCCCCCCC | 35.38 | 24117733 | |
| 216 | Phosphorylation | PLPVALGSGPGPGPG CCCCCCCCCCCCCCC | 42.54 | 27732954 | |
| 269 | Phosphorylation | GPFSGVLSSFHRKPG CCCCCHHHHHCCCCC | 28.66 | 24117733 | |
| 270 | Phosphorylation | PFSGVLSSFHRKPGP CCCCHHHHHCCCCCC | 22.40 | 24117733 |
| Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
|---|---|---|---|---|---|---|
| 153 | S | Phosphorylation | Kinase | PRKACA | P17612 | GPS |
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of PHX2A_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 PHX2A_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| HAND2_HUMAN | HAND2 | physical | 14506227 | |
| JUN_HUMAN | JUN | physical | 14506227 | |
| PHX2A_HUMAN | PHOX2A | physical | 10644760 | |
| SP1_HUMAN | SP1 | physical | 17344216 |
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| There are no disease associations of PTM sites. | ||||||
| OMIM Disease | ||||||
| 602078 | Fibrosis of extraocular muscles, congenital, 2 (CFEOM2) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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