UBQLN2 450-624 V564Q
Protein Sequence
Sequence Variants
| ID | Name | Remain region | Mutation sites | Ref seq |
|---|---|---|---|---|
| psp00678 | UBQLN2 | 1-624 | - | ✓ |
| psp05022 | UBQLN2 450-624 V564Q | 450-624 | V564Q | |
| psp00633 | UBQLN2 430-624 | 430-624 | - | |
| psp00725 | UBQLN2 ΔUBL | 107-624 | - | |
| psp01052 | UBQLN2 ΔUBA | 1-576 | - | |
| psp01403 | UBQLN2 575-624 | 575-624 | - | |
| psp01686 | UBQLN2 Δ378-486 | 1-378, 487-624 | - | |
| psp02503 | UBQLN2 ΔUBLΔUBA | 109-576 | - | |
| psp02635 | UBQLN2 450-624 | 450-624 | - | |
| psp02881 | UBQLN2 ΔUBA | 1-575 | - | |
| psp03346 | UBQLN2 ΔPXX | 1-490, 538-624 | - | |
| psp03892 | UBQLN2 ΔUBA | 1-576, 621-624 | - | |
| psp04200 | UBQLN2 487-624 | 487-624 | - | |
| psp04962 | UBQLN2 1-106 | 1-106 | - | |
| psp05050 | UBQLN2 ΔUBL | 109-624 | - | |
| psp05086 | UBQLN2 (379-624) | 379-624 | - | |
| psp00943 | UBQLN2 (P497H) | - | P497H | |
| psp01563 | UBQLN2 A282V | - | A282V | |
| psp03204 | UBQLN2 P497S | - | P497S | |
| psp04765 | UBQLN2 P506T | - | P506T | |
| psp00031 | UBQLN2 450-624 V564R | 450-624 | V564R | |
| psp00596 | UBQLN2 450-624 P506R | 450-624 | P506R | |
| psp00960 | UBQLN2 450-624 P506E | 450-624 | P506E | |
| psp01003 | UBQLN2 (450-624) T487I | 450-624 | T487I | |
| psp01103 | UBQLN2 (450-624) P506T | 450-624 | P506T | |
| psp01314 | UBQLN2 450-624 V564L | 450-624 | V564L | |
| psp01399 | UBQLN2 450-624 V538Q | 450-624 | V538Q | |
| psp01485 | UBQLN2 450-624 P497G | 450-624 | P497G | |
| psp01617 | UBQLN2 450-624 V538G | 450-624 | V538G | |
| psp01648 | UBQLN2 450-624 V564G | 450-624 | V564G | |
| psp01720 | UBQLN2 450-624 P497R | 450-624 | P497R | |
| psp01834 | UBQLN2 450-624 V564E | 450-624 | V564E | |
| psp02002 | UBQLN2 (450-624) P497L | 450-624 | P497L | |
| psp02036 | UBQLN2 (450-624) P497S | 450-624 | P497S | |
| psp02048 | UBQLN2 (450-624) P525S | 450-624 | P525S | |
| psp02217 | UBQLN2 450-624 P497Q | 450-624 | P497Q | |
| psp02270 | UBQLN2 450-624 P497E | 450-624 | P497E | |
| psp02424 | UBQLN2 450-624 P506Q | 450-624 | P506Q | |
| psp03323 | UBQLN2 450-624 V538W | 450-624 | V538W | |
| psp03425 | UBQLN2 450-624 V538E | 450-624 | V538E | |
| psp03586 | UBQLN2 450-624 V538L | 450-624 | V538L | |
| psp03635 | UBQLN2 450-624 V538R | 450-624 | V538R | |
| psp03771 | UBQLN2 450-624 P525G | 450-624 | P525G | |
| psp03830 | UBQLN2 450-624 P525L | 450-624 | P525L | |
| psp03874 | UBQLN2 450-624 P525Q | 450-624 | P525Q | |
| psp03981 | UBQLN2 ΔUBL P506T | 107-624 | P506T | |
| psp04258 | UBQLN2 450-624 P497W | 450-624 | P497W | |
| psp04322 | UBQLN2 450-624 P506W | 450-624 | P506W | |
| psp04398 | UBQLN2 450-624 P525W | 450-624 | P525W | |
| psp04408 | UBQLN2 ΔUBA P506T | 1-575 | P506T | |
| psp04701 | UBQLN2 450-624 P506G | 450-624 | P506G | |
| psp04792 | UBQLN2 450-624 V564W | 450-624 | V564W | |
| psp04802 | UBQLN2 450-624 P525E | 450-624 | P525E | |
| psp04929 | UBQLN2 450-624 P506L | 450-624 | P506L | |
| psp05033 | UBQLN2 450-624 P525R | 450-624 | P525R |
Orthologs and Paralogs
| ID | Name | Organism | Length |
|---|---|---|---|
| psp03543 | UBQLN4 | Homo sapiens | 601 |
| psp01732 | UBQLN1 | Homo sapiens | 589 |
| psp03659 | UBQLN1 438-589 | Homo sapiens | 152 |
| psp00113 | UBQLN4 444-601 | Homo sapiens | 158 |
Biophysical Features
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IDR (Intrinsically Disordered Region) was predicted by Mobidb-lite 4.0, please refer to: MobiDB-lite 4.0: faster prediction of intrinsic protein disorder and structural compactness.
Pi-Pi interaction was predicted by PScore, please refer to: Pi-Pi contacts are an overlooked protein feature relevant to phase separation.
PLAAC and PrD. like were both predicted by PLAAC, please refer to: PLAAC: a web and command-line application to identify proteins with prion-like amino acid composition.
LCR (Low Complexity Region) was predicted by SEG, please refer to: Statistics of local complexity in amino acid sequences and sequence databases.
NCPR (Net Charge Per Residue), FCR (Fraction of Charged Residues) and hydrophobicity were both computated by CIDER, please refer to: CIDER: Resources to Analyze Sequence-Ensemble Relationships of Intrinsically Disordered Proteins.
Polarity was computated by ProtScale, please refer to: ProtScale.
SASA (Solvent-Accessible Surface Area) was computated by BioPython based on the predicted structure, please refer to: Bio.PDB.SASA module.
Protein Structure
Protein structure was predicted by Chai-1, which also produces predicted local distance difference test (pLDDT) score between 0 and 100.
For pLDDT, please refer to: pLDDT: Understanding local confidence