UniProt ID | DEFM_HUMAN | |
---|---|---|
UniProt AC | Q9HBH1 | |
Protein Name | Peptide deformylase, mitochondrial | |
Gene Name | ||
Organism | Homo sapiens (Human). | |
Sequence Length | 243 | |
Subcellular Localization | Mitochondrion . | |
Protein Description | Removes the formyl group from the N-terminal Met of newly synthesized proteins.. | |
Protein Sequence | MARLWGALSLWPLWAAVPWGGAAAVGVRACSSTAAPDGVEGPALRRSYWRHLRRLVLGPPEPPFSHVCQVGDPVLRGVAAPVERAQLGGPELQRLTQRLVQVMRRRRCVGLSAPQLGVPRQVLALELPEALCRECPPRQRALRQMEPFPLRVFVNPSLRVLDSRLVTFPEGCESVAGFLACVPRFQAVQISGLDPNGEQVVWQASGWAARIIQHEMDHLQGCLFIDKMDSRTFTNVYWMKVND | |
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 |
---|---|---|---|---|---|
112 | Phosphorylation | RRRCVGLSAPQLGVP HCCCCCCCCCCCCCC | 31.79 | 21964256 | |
227 | Acetylation | QGCLFIDKMDSRTFT CCCEEEEECCCCCEE | 39.53 | 25038526 | |
240 | Ubiquitination | FTNVYWMKVND---- EEEEEEEEECC---- | 24.60 | - |
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 DEFM_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of DEFM_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 DEFM_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
MYO5B_HUMAN | MYO5B | physical | 27173435 |
Kegg Drug | ||||||
---|---|---|---|---|---|---|
DrugBank | ||||||
There are no disease associations of PTM sites. |
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