| UniProt ID | PEX10_HUMAN | |
|---|---|---|
| UniProt AC | O60683 | |
| Protein Name | Peroxisome biogenesis factor 10 | |
| Gene Name | PEX10 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 326 | |
| Subcellular Localization |
Peroxisome membrane Peripheral membrane protein . |
|
| Protein Description | Somewhat implicated in the biogenesis of peroxisomes.. | |
| Protein Sequence | MAPAAASPPEVIRAAQKDEYYRGGLRSAAGGALHSLAGARKWLEWRKEVELLSDVAYFGLTTLAGYQTLGEEYVSIIQVDPSRIHVPSSLRRGVLVTLHAVLPYLLDKALLPLEQELQADPDSGRPLQGSLGPGGRGCSGARRWMRHHTATLTEQQRRALLRAVFVLRQGLACLQRLHVAWFYIHGVFYHLAKRLTGITYLRVRSLPGEDLRARVSYRLLGVISLLHLVLSMGLQLYGFRQRQRARKEWRLHRGLSHRRASLEERAVSRNPLCTLCLEERRHPTATPCGHLFCWECITAWCSSKAECPLCREKFPPQKLIYLRHYR | |
| 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 |
|---|---|---|---|---|---|
| 7 | Phosphorylation | -MAPAAASPPEVIRA -CCCCCCCCHHHHHH | 35.94 | 29255136 | |
| 17 | Ubiquitination | EVIRAAQKDEYYRGG HHHHHHHCCHHHHHC | 48.04 | - | |
| 17 (in isoform 2) | Ubiquitination | - | 48.04 | - | |
| 27 | Phosphorylation | YYRGGLRSAAGGALH HHHHCHHHHHHHHHH | 27.75 | 24719451 | |
| 89 | Phosphorylation | SRIHVPSSLRRGVLV HHCCCCCHHHHCCCH | 21.59 | 17081983 | |
| 136 | Methylation | GSLGPGGRGCSGARR CCCCCCCCCCHHHHH | 49.19 | 115487031 | |
| 149 | Phosphorylation | RRWMRHHTATLTEQQ HHHHHHHCCCCCHHH | 18.40 | 30576142 | |
| 153 | Phosphorylation | RHHTATLTEQQRRAL HHHCCCCCHHHHHHH | 27.65 | 30576142 | |
| 196 | Phosphorylation | YHLAKRLTGITYLRV HHHHHHHHCCEEEEE | 30.48 | 22210691 | |
| 199 | Phosphorylation | AKRLTGITYLRVRSL HHHHHCCEEEEEECC | 20.18 | 22210691 | |
| 200 | Phosphorylation | KRLTGITYLRVRSLP HHHHCCEEEEEECCC | 7.21 | 22210691 | |
| 216 | Phosphorylation | EDLRARVSYRLLGVI HHHHHHHHHHHHHHH | 10.05 | 23828894 | |
| 261 | Phosphorylation | GLSHRRASLEERAVS HHCHHHHCHHHHHHH | 34.21 | 27794612 | |
| 281 | Phosphorylation | TLCLEERRHPTATPC HHHHHCCCCCCCCCC | 43.34 | 24719451 | |
| 321 | Phosphorylation | FPPQKLIYLRHYR-- CCCCCEEEEEECC-- | 14.23 | - |
| 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 PEX10_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of PEX10_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 PEX10_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| PEX12_HUMAN | PEX12 | physical | 10837480 | |
| PEX10_HUMAN | PEX10 | physical | 10837480 | |
| PEX5_HUMAN | PEX5 | physical | 10837480 | |
| PEX12_HUMAN | PEX12 | physical | 12096124 | |
| PEX19_HUMAN | PEX19 | physical | 12096124 | |
| PEX10_HUMAN | PEX10 | physical | 22493164 |
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| H00205 | Zellweger syndrome spectrum, including: Zellweger syndrome (ZS); Adrenoleukodystrophy, neonatal (NAL | |||||
| OMIM Disease | ||||||
| 614870 | Peroxisome biogenesis disorder complementation group 7 (PBD-CG7) | |||||
| 614870 | Peroxisome biogenesis disorder 6A (PBD6A) | |||||
| 614871 | Peroxisome biogenesis disorder 6B (PBD6B) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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