Neuromedin-B (NMB)

Homo sapiens — UniProt P08949

Gene: NMBHomo sapiensSwissProt reviewed

About Neuromedin-B

Neuromedin-B (NMB) is a protein from Homo sapiens identified by UniProt accession P08949, 121 residues long. MolForge cross-references it against 0 known binders and 99 disease associations.

Target properties

Protein nameNeuromedin-B
UniProt accessionP08949
GeneNMB
OrganismHomo sapiens
Length121 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 (99)

Diseases linked to this target (Open Targets).

  • schizophrenia · score 0.28
  • bipolar disorder · score 0.26
  • anorexia nervosa · score 0.24
  • autism spectrum disorder · score 0.22
  • dilated cardiomyopathy · score 0.22
  • aspartate aminotransferase measurement · score 0.20
  • bipolar I disorder · score 0.20
  • creatinine measurement · score 0.20
  • Tourette syndrome · score 0.18
  • unipolar depression · score 0.18

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P08949-F1alphafoldPREDICTED67.93—

Amino-acid sequence (121 residues)

MARRAGGARM FGSLLLFALL AAGVAPLSWD LPEPRSRASK IRVHSRGNLW ATGHFMGKKS LEPSSPSPLG TAPHTSLRDQ RLQLSHDLLG ILLLKKALGV SLSRPAPQIQ YRRLLVQILQ K

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Quick facts

UniProtP08949
GeneNMB
OrganismHomo sapiens
Length121
Binders0
Diseases99
View on UniProt