PEX14

Synonyms: PEX14, PTS1 receptor-docking protein, Peroxisomal membrane anchor protein PEX14, Peroxisomal membrane protein PEX14, Peroxin-14

ID psp01265
Organism Homo sapiens
Length 377
Source UniProt: O75381

PS Record in Articles

No phase separation records for this protein in the article.

This entry is just use for illustrate the sequence variants relationship.

Protein Sequence

Sequence Variants

ID Name Remain region Mutation sites Ref seq
psp01265 PEX14 1-377 -
psp00671 PEX14 CTD (226-377) 226-377 -
psp04806 PEX14 CC-CTD (139-377) 139-377 -
psp05120 PEX14 CC (139-225) 139-225 -
psp00592 PEX14 CC-CTD-CS1 139-377 R227D, D263R, E298K, R351E, E359R, R365E, E373R
psp00915 PEX14 CC-CTD F229A 139-377 F229A
psp01226 PEX14 CC-CTD RKA17 139-377 R226A, R227A, K237A, K246A, K278A, K306A, R310A, K319A, R320A, K323A, R347A, R350A, R351A, K363A, R365A, R366A, R376A
psp01831 PEX14 CC-CTD W241A 139-377 W241A
psp02087 PEX14 CC-CTD WFYA 139-377 F229A, W241A, Y290A
psp02194 PEX14 CC-CTD-CS3 139-377 E279R, R310E, E348R, R376E
psp03041 PEX14 CC-CTD WFA 139-377 F229A, W241A
psp03873 PEX14 CC-CTD EQDN9 139-377 F229A, W241A, Y290A, D325N, E326Q, E327Q, D328N, E329Q, E330Q, D331N, D332N, D333N
psp04449 PEX14 CC-CTD-CS2 139-377 R226E, R227D, K246E, D263R, E298R, E316R, E326R, E329K, E330R, D338R, R350E, R351E, R365E, R366D
psp04860 PEX14 CC-CTD Y290A 139-377 Y290A
psp00201 PEX14 CC-CTD Flag - -
psp03722 PEX14-CC G3BP1 - -
psp04294 PEX14-CC TDP43 - -

Orthologs and Paralogs

No orthologs or paralogs found for this protein in the database.

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