| UniProt ID | IFT43_HUMAN | |
|---|---|---|
| UniProt AC | Q96FT9 | |
| Protein Name | Intraflagellar transport protein 43 homolog | |
| Gene Name | IFT43 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 208 | |
| Subcellular Localization | Cytoplasm, cytoskeleton . Cell projection, cilium . Associated with microtubules. | |
| Protein Description | Component of IFT complex A (IFT-A) involved in retrograde ciliary transport along microtubules from the ciliary tip to the base.. | |
| Protein Sequence | MEDLLDLDEELRYSLATSRAKMGRRAQQESAQAENHLNGKNSSLTLTGETSSAKLPRCRQGGWAGDSVKASKFRRKASEEIEDFRLRPQSLNGSDYGGDIPIIPDLEEVQEEDFVLQVAAPPSIQIKRVMTYRDLDNDLMKYSAIQTLDGEIDLKLLTKVLAPEHEVREDDVGWDWDHLFTEVSSEVLTEWDPLQTEKEDPAGQARHT | |
| 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 |
|---|---|---|---|---|---|
| 1 | Acetylation | -------MEDLLDLD -------CCHHHCCC | 9.02 | 22814378 | |
| 13 | Phosphorylation | DLDEELRYSLATSRA CCCHHHHHHHHHHHH | 22.21 | 28796482 | |
| 14 | Phosphorylation | LDEELRYSLATSRAK CCHHHHHHHHHHHHH | 12.70 | 28796482 | |
| 43 | Phosphorylation | HLNGKNSSLTLTGET HHCCCCCCEEEECCC | 34.46 | 28857561 | |
| 43 (in isoform 2) | Phosphorylation | - | 34.46 | 27251275 | |
| 51 | Phosphorylation | LTLTGETSSAKLPRC EEEECCCCCCCCCCC | 24.81 | 28555341 | |
| 67 | Phosphorylation | QGGWAGDSVKASKFR CCCCCCHHHHHHHHH | 25.30 | 23401153 | |
| 67 (in isoform 2) | Phosphorylation | - | 25.30 | 27251275 | |
| 69 | Ubiquitination | GWAGDSVKASKFRRK CCCCHHHHHHHHHHH | 51.39 | - | |
| 71 | Phosphorylation | AGDSVKASKFRRKAS CCHHHHHHHHHHHHH | 26.98 | 26074081 | |
| 76 | Ubiquitination | KASKFRRKASEEIED HHHHHHHHHHHHHHH | 52.59 | - | |
| 78 | Phosphorylation | SKFRRKASEEIEDFR HHHHHHHHHHHHHHC | 38.50 | 29255136 | |
| 131 | Phosphorylation | IQIKRVMTYRDLDND EEEEEEEEHHHCCCH | 16.73 | - | |
| 132 | Phosphorylation | QIKRVMTYRDLDNDL EEEEEEEHHHCCCHH | 5.52 | - | |
| 147 (in isoform 2) | Phosphorylation | - | 22.24 | 27642862 | |
| 159 | Ubiquitination | IDLKLLTKVLAPEHE CCHHHHHHHHCCCCC | 34.91 | 21890473 | |
| 159 (in isoform 1) | Ubiquitination | - | 34.91 | 21890473 | |
| 159 | Ubiquitination | IDLKLLTKVLAPEHE CCHHHHHHHHCCCCC | 34.91 | 21890473 | |
| 164 (in isoform 2) | Ubiquitination | - | 47.26 | 21890473 |
| 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 IFT43_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of IFT43_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 IFT43_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| IF122_HUMAN | IFT122 | physical | 28514442 | |
| TT21B_HUMAN | TTC21B | physical | 28514442 | |
| WDR35_HUMAN | WDR35 | physical | 28514442 | |
| CK074_HUMAN | C11orf74 | physical | 28514442 | |
| WDR19_HUMAN | WDR19 | physical | 28514442 | |
| IF140_HUMAN | IFT140 | physical | 28514442 | |
| TULP3_HUMAN | TULP3 | physical | 28514442 | |
| TYK2_HUMAN | TYK2 | physical | 28514442 | |
| SENP8_HUMAN | SENP8 | physical | 28514442 | |
| BBS1_HUMAN | BBS1 | physical | 28514442 | |
| TCAL1_HUMAN | TCEAL1 | physical | 28514442 | |
| UBP11_HUMAN | USP11 | physical | 28514442 | |
| MYO9B_HUMAN | MYO9B | physical | 28514442 | |
| UBP7_HUMAN | USP7 | physical | 28514442 | |
| TT21B_HUMAN | TTC21B | physical | 27173435 |
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| There are no disease associations of PTM sites. | ||||||
| OMIM Disease | ||||||
| 614099 | Cranioectodermal dysplasia 3 (CED3) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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