Dvl2 ∆93-267

ID psp03045
Organism Mus musculus
Length 561

PS Record in Articles

Reference (Pubmed ID) In vitro results In vivo results
36342472 - Negative

Protein Sequence

Sequence Variants

ID Name Remain region Mutation sites Ref seq
psp02415 DVL2 1-736 -
psp03045 Dvl2 ∆93-267 1-92, 268-736 -
psp00067 Dvl2 ∆507-736 1-506 -
psp00118 DVL2 DIX (1-114) 1-114 -
psp00133 DVL2 ΔDEP 1-418, 522-736 -
psp00452 DVL2 1-418+CFR 1-418, 679-736 -
psp00540 DVL2 ΔDEP ΔCD2 1-418, 522-698 -
psp01865 DVL2 ΔDEP ΔLCR3 1-418, 522-612, 654-736 -
psp01958 Dvl2 ∆355-414 1-354, 415-736 -
psp01988 Dvl2 D1 1-140, 260-736 -
psp02543 DVL2 ΔDEP ΔLCR2 1-418, 522-571, 607-736 -
psp02853 Dvl2 ∆DIX 1-10, 94-736 -
psp02943 DVL2 ΔCFR 1-678 -
psp03168 DVL2 ΔDEP ΔLCR1 1-418, 522-551, 570-736 -
psp03345 DVL2 ΔDEP ΔLCR4 1-418, 522-678, 693-736 -
psp03932 DVL2 ΔDEP ΔCD1 1-418, 522-525, 539-736 -
psp03954 DVL2 1-418 1-418 -
psp04124 DVL2 1-418+CD2 1-418, 699-736 -
psp04920 DVL2 1-418+LCR4 1-418, 679-692 -
psp05111 DVL2 ΔDEP ΔCFR 1-418, 522-678 -
psp05178 Dvl2 dRE 1-159, 168-209, 216-234, 241-736 -
psp02779 DVL2 ΔDEP FF-AA 1-418, 522-736 F731A, F732A
psp04222 DVL2 ΔDEP VV-AA 1-418, 522-736 V682A, V683A

Orthologs and Paralogs

ID Name Organism Length
psp03059 DVL2 Homo sapiens 736
psp02913 GST-Dvl2 Synthetic 954
psp03143 DVL2 D1TDP43 Synthetic 765
psp00871 DVL2 ΔDEP (421-502) Homo sapiens 654
psp01433 DVL2 ΔPDZ (263-352) Homo sapiens 646
psp03312 DVL2 ΔCT (515-736) Homo sapiens 514
psp04858 DVL2 ΔIDR1 (94-252) Homo sapiens 577
psp04875 DVL2 ΔDIX (1-93) Homo sapiens 643

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

Colered by pLDDT:
Very high (pLDDT > 90)
Confident (90 > pLDDT > 70)
Low (70 > pLDDT > 50)
Very low (pLDDT < 50)

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