Nicolin-1 (NICN1)

Homo sapiens — UniProt Q9BSH3

Gene: NICN1Homo sapiensSwissProt reviewed

About Nicolin-1

Nicolin-1 (NICN1) is a protein from Homo sapiens identified by UniProt accession Q9BSH3, 213 residues long. MolForge cross-references it against 0 known binders and 89 disease associations.

Target properties

Protein nameNicolin-1
UniProt accessionQ9BSH3
GeneNICN1
OrganismHomo sapiens
Length213 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 (89)

Diseases linked to this target (Open Targets).

  • glycine encephalopathy · score 0.56
  • Neurodevelopmental delay · score 0.34
  • Alzheimer disease · score 0.30
  • neurodegenerative disease · score 0.30
  • multiple sclerosis · score 0.30
  • lysosomal storage disease · score 0.30
  • Parkinson disease · score 0.30
  • genetic disorder · score 0.16
  • Red cell distribution width · score 0.12
  • osteoporosis · score 0.09

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9BSH3-F1alphafoldPREDICTED79.71—

Amino-acid sequence (213 residues)

MSRVLVPCHV KGSVALQVGD VRTSQGRPGV LVIDVTFPSV APFELQEITF KNYYTAFLSI RVRQYTSAHT PAKWVTCLRD YCLMPDPHSE EGAQEYVSLF KHQMLCDMAR ISELRLILRQ PSPLWLSFTV EELQIYQQGP KSPSVTFPKW LSHPVPCEQP ALLREGLPDP SRVSSEVQQM WALTEMIRAS HTSARIGRFD VDGCYDLNLL SYT

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Quick facts

UniProtQ9BSH3
GeneNICN1
OrganismHomo sapiens
Length213
Binders0
Diseases89
View on UniProt