Q5XIP4
Gene name |
Ubqlnl |
Protein name |
Ubiquilin-like protein |
Names |
|
Species |
Rattus norvegicus (Rat) |
KEGG Pathway |
rno:293287 |
EC number |
|
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
1 structures for Q5XIP4
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q5XIP4-F1 | Predicted | AlphaFoldDB |
No variants for Q5XIP4
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q5XIP4 | |||||
No associated diseases with Q5XIP4
1 regional properties for Q5XIP4
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Ubiquitin-like domain | 31 - 105 | IPR000626 |
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| polyubiquitin modification-dependent protein binding | Binding to a protein upon poly-ubiquitination of the target protein. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| ubiquitin-dependent protein catabolic process | The chemical reactions and pathways resulting in the breakdown of a protein or peptide by hydrolysis of its peptide bonds, initiated by the covalent attachment of a ubiquitin group, or multiple ubiquitin groups, to the protein. |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MPHIISRSPR | MPQSRHPAGV | PADGNIPPGV | IRVIVKTPGN | QNVFTVAEDT | SVRQFKEQLS |
| 70 | 80 | 90 | 100 | 110 | 120 |
| SHFKCQMEQL | VLVSMGRLLK | DHDTLSQRGI | TDGHTIHVVI | KSKHGSRSLT | HSFRNLLTNN |
| 130 | 140 | 150 | 160 | 170 | 180 |
| PCHQDRNPKG | NSSTVCQSAG | MSETKVESSI | LMEPDASKVC | TQDPEVGSPE | QIEQMLETLC |
| 190 | 200 | 210 | 220 | 230 | 240 |
| VQRLLSNMFF | MHQLPPEHPD | MQDLIQQNPE | VSHLLDNSEI | LCQTLELARH | LAIIQEIMQI |
| 250 | 260 | 270 | 280 | 290 | 300 |
| QQPAQNPEHT | LNPQPYLGLE | TIPNGNIVLG | QGYDNFNDHM | LNGVHVHDLL | EDDSFTALLA |
| 310 | 320 | 330 | 340 | 350 | 360 |
| EQVLEQVQTP | SLCQPPPQEQ | WGQLSSSQVI | FANSCGFLTT | PTEANLNTTN | NASRENPAIA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| ATQGQSNVCA | VQQPTEIPSL | CTIPVIQEPR | EGDKDTTIPQ | GSSAQWLEED | LQQSEEQSSS |
| 430 | 440 | 450 | 460 | 470 | 480 |
| QITRSMIQLL | RTHPHMAAEM | LLLLNPPQLN | EQWRQQTATP | LQSSQLSDLL | LALANPKTSQ |
| 490 | 500 | 510 | 520 | 530 | 540 |
| ALLQIEHGLQ | LLATEAPALL | PYIEPYLWGL | GWLIPSSCDY | LDTVPWTWNV | QDTVEPQCPE |
| 550 | 560 | 570 | 580 | 590 | 600 |
| SCHKSGTVLQ | REQPLSGDSS | HSLQAPEVRF | SKEMECLQAM | GFVNYNANLQ | ALIATDGDTN |
| 610 | |||||
| AAIHKLKASQ | GF |