| UniProt ID | FDXA1_HUMAN | |
|---|---|---|
| UniProt AC | Q9BRP7 | |
| Protein Name | Ferredoxin-fold anticodon-binding domain-containing protein 1 | |
| Gene Name | FDXACB1 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 624 | |
| Subcellular Localization | ||
| Protein Description | ||
| Protein Sequence | MAPRRLLLVGEGNFSFAAALSETLDQSTQLTATCLQRPAELARDPLAWENLQCLRERGIDVRFGVDCTQLADVFELHEREFDQIYFIFPHCGRKAGVAKNRELLAKFFQSCADVLAEEGEVHVALCRGQGGTPADKPQREWHNSWQVVAMAALGGLILSDVYPFSCKAVAGYKCTGYRSQDKSFHVEGALNHIFTRSLPFEGSQPRIFRIKLGNQWFSFPEPEALVGKLNRGFLEAPSCHPIKTINEKLIAELGKVFPLKRLKCSYPLLPQEGTSVLPFWNCDFLSAAFWISLHEDNSNSESLTGGTSQDVEDFLVSFSELSLLKNPGRDGKEEACEGTCGQAKICLRPSLLVHVQDVIEVPDFLSGSLHILSGPVFQKCHILPFTMPAFHETLFILGVNQNLKDGCLQSLLDHLKGILDSLLTQTLPESSKLSSLVKFVLQSNGKDYMIRVKTHNFSPDCTEDLIIGSVITSATSVIHKDQCFVFVSMNLDLLAMLVWCISDWRMLWTFDNRFLKNFVPGKIEPFKSHSLYPPCYVHDVSFWIDQKKGFDELEFHTVARAVSQDTIISIQFLSRFQHPKTQQVSLCYRLTYQTCDKALTQQQVASMQSQFRKEIQQHLYVIPR | |
| 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 |
|---|---|---|---|---|---|
| 99 | Acetylation | GRKAGVAKNRELLAK CCCCCHHHCHHHHHH | 54.88 | 24848129 | |
| 173 | Ubiquitination | CKAVAGYKCTGYRSQ CCEEECCCCCCEECC | 25.14 | 29967540 | |
| 243 | Ubiquitination | APSCHPIKTINEKLI CCCCCCCCCCCHHHH | 48.04 | - | |
| 248 | Ubiquitination | PIKTINEKLIAELGK CCCCCCHHHHHHHCC | 40.48 | 29967540 | |
| 322 | Phosphorylation | LVSFSELSLLKNPGR HHCHHHHHCCCCCCC | 27.83 | 24719451 | |
| 373 | Phosphorylation | SGSLHILSGPVFQKC CCCEEEECCCHHHCC | 40.21 | 24719451 | |
| 410 | Phosphorylation | LKDGCLQSLLDHLKG CCCCHHHHHHHHHHH | 20.25 | 25159151 | |
| 421 | Phosphorylation | HLKGILDSLLTQTLP HHHHHHHHHHHHCCC | 23.10 | 20230923 | |
| 424 | Phosphorylation | GILDSLLTQTLPESS HHHHHHHHHCCCCHH | 25.46 | 20230923 | |
| 426 | Phosphorylation | LDSLLTQTLPESSKL HHHHHHHCCCCHHCH | 38.76 | 26074081 | |
| 430 | Phosphorylation | LTQTLPESSKLSSLV HHHCCCCHHCHHHHH | 30.73 | 26074081 | |
| 431 | Phosphorylation | TQTLPESSKLSSLVK HHCCCCHHCHHHHHH | 35.63 | 20230923 | |
| 434 | Phosphorylation | LPESSKLSSLVKFVL CCCHHCHHHHHHHHH | 25.93 | 26074081 | |
| 435 | Phosphorylation | PESSKLSSLVKFVLQ CCHHCHHHHHHHHHH | 47.84 | 26074081 | |
| 464 | Ubiquitination | FSPDCTEDLIIGSVI CCCCCCCCCCHHCHH | 25.64 | - | |
| 522 | Ubiquitination | LKNFVPGKIEPFKSH HHHCCCCCCCCCCCC | 37.51 | 29967540 | |
| 581 | Phosphorylation | SRFQHPKTQQVSLCY HHCCCCCCCCEEEEH | 28.78 | - | |
| 585 | Phosphorylation | HPKTQQVSLCYRLTY CCCCCCEEEEHHHHH | 14.37 | - | |
| 588 | Phosphorylation | TQQVSLCYRLTYQTC CCCEEEEHHHHHHHH | 17.60 | 21214269 | |
| 613 | Ubiquitination | SMQSQFRKEIQQHLY HHHHHHHHHHHHHHE | 61.53 | - |
| 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 FDXA1_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of FDXA1_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 FDXA1_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| RMXL2_HUMAN | RBMXL2 | physical | 22939629 | |
| HERC4_HUMAN | HERC4 | physical | 28514442 | |
| RMXL1_HUMAN | RBMXL1 | physical | 28514442 |
| 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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