Nodal homolog (NODAL)

Homo sapiens — UniProt Q96S42

Gene: NODALHomo sapiensSwissProt reviewed

About Nodal homolog

Nodal homolog (NODAL) is a protein from Homo sapiens identified by UniProt accession Q96S42, 347 residues long. MolForge cross-references it against 0 known binders and 167 disease associations.

Target properties

Protein nameNodal homolog
UniProt accessionQ96S42
GeneNODAL
OrganismHomo sapiens
Length347 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 (167)

Diseases linked to this target (Open Targets).

  • heterotaxy, visceral, 5, autosomal · score 0.76
  • visceral heterotaxy · score 0.68
  • Heterotaxia · score 0.64
  • Situs inversus totalis · score 0.44
  • congenital heart disease · score 0.38
  • Abnormal heart morphology · score 0.37
  • semilobar holoprosencephaly · score 0.37
  • midline interhemispheric variant of holoprosencephaly · score 0.37
  • septopreoptic holoprosencephaly · score 0.37
  • microform holoprosencephaly · score 0.37

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96S42-F1alphafoldPREDICTED75.46—

Amino-acid sequence (347 residues)

MHAHCLPFLL HAWWALLQAG AATVATALLR TRGQPSSPSP LAYMLSLYRD PLPRADIIRS LQAEDVAVDG QNWTFAFDFS FLSQQEDLAW AELRLQLSSP VDLPTEGSLA IEIFHQPKPD TEQASDSCLE RFQMDLFTVT LSQVTFSLGS MVLEVTRPLS KWLKHPGALE KQMSRVAGEC WPRPPTPPAT NVLLMLYSNL SQEQRQLGGS TLLWEAESSW RAQEGQLSWE WGKRHRRHHL PDRSQLCRKV KFQVDFNLIG WGSWIIYPKQ YNAYRCEGEC PNPVGEEFHP TNHAYIQSLL KRYQPHRVPS TCCAPVKTKP LSMLYVDNGR VLLDHHKDMI VEECGCL

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Quick facts

UniProtQ96S42
GeneNODAL
OrganismHomo sapiens
Length347
Binders0
Diseases167
View on UniProt