UniProt ID | MFRN2_HUMAN | |
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UniProt AC | Q96A46 | |
Protein Name | Mitoferrin-2 | |
Gene Name | SLC25A28 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 364 | |
Subcellular Localization |
Mitochondrion inner membrane Multi-pass membrane protein . Isoform 1 and isoform 2 are both localized in the mitochondrion. |
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Protein Description | Mitochondrial iron transporter that mediates iron uptake. Probably required for heme synthesis of hemoproteins and Fe-S cluster assembly in non-erythroid cells. The iron delivered into the mitochondria, presumably as Fe(2+), is then probably delivered to ferrochelatase to catalyze Fe(2+) incorporation into protoprophyrin IX to make heme (By similarity).. | |
Protein Sequence | MELEGRGAGGVAGGPAAGPGRSPGESALLDGWLQRGVGRGAGGGEAGACRPPVRQDPDSGPDYEALPAGATVTTHMVAGAVAGILEHCVMYPIDCVKTRMQSLQPDPAARYRNVLEALWRIIRTEGLWRPMRGLNVTATGAGPAHALYFACYEKLKKTLSDVIHPGGNSHIANGAAGCVATLLHDAAMNPAEVVKQRMQMYNSPYHRVTDCVRAVWQNEGAGAFYRSYTTQLTMNVPFQAIHFMTYEFLQEHFNPQRRYNPSSHVLSGACAGAVAAAATTPLDVCKTLLNTQESLALNSHITGHITGMASAFRTVYQVGGVTAYFRGVQARVIYQIPSTAIAWSVYEFFKYLITKRQEEWRAGK | |
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 |
---|---|---|---|---|---|
6 | Methylation | --MELEGRGAGGVAG --CCCCCCCCCCCCC | 23.55 | 115917073 | |
22 | Phosphorylation | PAAGPGRSPGESALL CCCCCCCCCCHHHCH | 43.08 | 22199227 | |
26 | Phosphorylation | PGRSPGESALLDGWL CCCCCCHHHCHHHHH | 30.08 | 22199227 | |
39 | Methylation | WLQRGVGRGAGGGEA HHHCCCCCCCCCCCC | 29.40 | 54559367 | |
334 | Phosphorylation | GVQARVIYQIPSTAI CEEEEEEEECCCHHH | 9.49 | 22817900 | |
346 | Phosphorylation | TAIAWSVYEFFKYLI HHHHHHHHHHHHHHH | 11.08 | 22817900 | |
351 | Phosphorylation | SVYEFFKYLITKRQE HHHHHHHHHHHHHHH | 9.74 | 22817900 |
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 MFRN2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of MFRN2_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 MFRN2_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
Oops, there are no PPI records of MFRN2_HUMAN !! |
Kegg Disease | ||||||
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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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