Erlin-2 (ERLIN2)

Homo sapiens — UniProt O94905

Gene: ERLIN2Homo sapiensSwissProt reviewed

About Erlin-2

Erlin-2 (ERLIN2) is a protein from Homo sapiens identified by UniProt accession O94905, 339 residues long. MolForge cross-references it against 0 known binders and 83 disease associations.

Target properties

Protein nameErlin-2
UniProt accessionO94905
GeneERLIN2
OrganismHomo sapiens
Length339 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (83)

Diseases linked to this target (Open Targets).

  • Autosomal recessive spastic paraplegia type 18 · score 0.74
  • hereditary spastic paraplegia 18 · score 0.71
  • hereditary spastic paraplegia · score 0.63
  • cancer · score 0.59
  • bone development disease · score 0.56
  • Spastic paraplegia · score 0.54
  • Neurodegeneration · score 0.46
  • cystic fibrosis · score 0.46
  • Intellectual disability · score 0.37
  • juvenile primary lateral sclerosis · score 0.37

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-O94905-F1alphafoldPREDICTED85.13—

Amino-acid sequence (339 residues)

MAQLGAVVAV ASSFFCASLF SAVHKIEEGH IGVYYRGGAL LTSTSGPGFH LMLPFITSYK SVQTTLQTDE VKNVPCGTSG GVMIYFDRIE VVNFLVPNAV YDIVKNYTAD YDKALIFNKI HHELNQFCSV HTLQEVYIEL FDQIDENLKL ALQQDLTSMA PGLVIQAVRV TKPNIPEAIR RNYELMESEK TKLLIAAQKQ KVVEKEAETE RKKALIEAEK VAQVAEITYG QKVMEKETEK KISEIEDAAF LAREKAKADA ECYTAMKIAE ANKLKLTPEY LQLMKYKAIA SNSKIYFGKD IPNMFMDSAG SVSKQFEGLA DKLSFGLEDE PLETATKEN

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Quick facts

UniProtO94905
GeneERLIN2
OrganismHomo sapiens
Length339
Binders0
Diseases83
View on UniProt