| UniProt ID | TIM16_HUMAN | |
|---|---|---|
| UniProt AC | Q9Y3D7 | |
| Protein Name | Mitochondrial import inner membrane translocase subunit TIM16 | |
| Gene Name | PAM16 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 125 | |
| Subcellular Localization |
Mitochondrion inner membrane Peripheral membrane protein Matrix side . |
|
| Protein Description | Regulates ATP-dependent protein translocation into the mitochondrial matrix. Inhibits DNAJC19 stimulation of HSPA9/Mortalin ATPase activity.. | |
| Protein Sequence | MAKYLAQIIVMGVQVVGRAFARALRQEFAASRAAADARGRAGHRSAAASNLSGLSLQEAQQILNVSKLSPEEVQKNYEHLFKVNDKSVGGSFYLQSKVVRAKERLDEELKIQAQEDREKGQMPHT | |
| 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 |
|---|---|---|---|---|---|
| 4 | Phosphorylation | ----MAKYLAQIIVM ----CHHHHHHHHHH | 9.57 | - | |
| 45 | Phosphorylation | RGRAGHRSAAASNLS HCCHHHHHHHHHCCC | 19.31 | 26434776 | |
| 49 | Phosphorylation | GHRSAAASNLSGLSL HHHHHHHHCCCCCCH | 33.31 | 30177828 | |
| 52 | Phosphorylation | SAAASNLSGLSLQEA HHHHHCCCCCCHHHH | 41.77 | 30177828 | |
| 55 | Phosphorylation | ASNLSGLSLQEAQQI HHCCCCCCHHHHHHH | 31.37 | 30177828 | |
| 66 | Phosphorylation | AQQILNVSKLSPEEV HHHHHCHHCCCHHHH | 27.14 | 23663014 | |
| 69 | Phosphorylation | ILNVSKLSPEEVQKN HHCHHCCCHHHHHHH | 33.72 | 25849741 | |
| 75 | Acetylation | LSPEEVQKNYEHLFK CCHHHHHHHHHHHHC | 67.67 | 27452117 | |
| 77 | Phosphorylation | PEEVQKNYEHLFKVN HHHHHHHHHHHHCCC | 16.26 | - | |
| 82 | Ubiquitination | KNYEHLFKVNDKSVG HHHHHHHCCCCCCCC | 46.63 | 22817900 | |
| 86 | Ubiquitination | HLFKVNDKSVGGSFY HHHCCCCCCCCCCHH | 41.66 | 33845483 | |
| 87 | Phosphorylation | LFKVNDKSVGGSFYL HHCCCCCCCCCCHHH | 28.94 | 24247654 | |
| 91 | Phosphorylation | NDKSVGGSFYLQSKV CCCCCCCCHHHHHHH | 12.56 | - | |
| 119 | Ubiquitination | QAQEDREKGQMPHT- HHHHHHHCCCCCCC- | 56.17 | 24816145 |
| 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 TIM16_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of TIM16_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 TIM16_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| FEZ1_HUMAN | FEZ1 | physical | 16169070 | |
| TIM14_HUMAN | DNAJC19 | physical | 20053669 | |
| TIM14_YEAST | PAM18 | physical | 20053669 | |
| FEZ1_HUMAN | FEZ1 | physical | 21900206 | |
| MOFA1_HUMAN | MRFAP1 | physical | 21900206 | |
| GPM6A_HUMAN | GPM6A | physical | 21900206 | |
| CEP70_HUMAN | CEP70 | physical | 21900206 | |
| BL1S2_HUMAN | BLOC1S2 | physical | 21900206 | |
| DNM3B_HUMAN | DNMT3B | physical | 21900206 | |
| PGRC1_HUMAN | PGRMC1 | physical | 21900206 | |
| DJC15_HUMAN | DNAJC15 | physical | 23263864 | |
| TIM16_HUMAN | PAM16 | physical | 23263864 | |
| TI17A_HUMAN | TIMM17A | physical | 23263864 | |
| TI17B_HUMAN | TIMM17B | physical | 23263864 | |
| TIM44_HUMAN | TIMM44 | physical | 22031295 | |
| MARC1_HUMAN | MARC1 | physical | 27173435 | |
| TFB2M_HUMAN | TFB2M | physical | 27173435 | |
| MCATL_HUMAN | SLC25A29 | physical | 27173435 |
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| There are no disease associations of PTM sites. | ||||||
| OMIM Disease | ||||||
| 613320 | Spondylometaphyseal dysplasia, Megarbane-Dagher-Melike type (SMDMDM) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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