EMILIN-1 (EMILIN1)

Homo sapiens — UniProt Q9Y6C2

Gene: EMILIN1Homo sapiensSwissProt reviewed

About EMILIN-1

EMILIN-1 (EMILIN1) is a protein from Homo sapiens identified by UniProt accession Q9Y6C2, 1016 residues long. MolForge cross-references it against 0 known binders and 163 disease associations.

Target properties

Protein nameEMILIN-1
UniProt accessionQ9Y6C2
GeneEMILIN1
OrganismHomo sapiens
Length1016 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 (163)

Diseases linked to this target (Open Targets).

  • neuronopathy, distal hereditary motor, autosomal dominant 10 · score 0.54
  • EMILIN-1-related connective tissue disease · score 0.37
  • genetic disorder · score 0.19
  • Familial prostate cancer · score 0.11
  • prostate cancer · score 0.11
  • prostate carcinoma · score 0.11
  • cortical surface area measurement · score 0.10
  • leukocyte count · score 0.09
  • neoplasm · score 0.09
  • Von Willebrand disease · score 0.09

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y6C2-F1alphafoldPREDICTED62.90—

Amino-acid sequence (1016 residues)

MAPRTLWSCY LCCLLTAAAG AASYPPRGFS LYTGSSGALS PGGPQAQIAP RPASRHRNWC AYVVTRTVSC VLEDGVETYV KYQPCAWGQP QCPQSIMYRR FLRPRYRVAY KTVTDMEWRC CQGYGGDDCA ESPAPALGPA SSTPRPLARP ARPNLSGSSA GSPLSGLGGE GPGESEKVQQ LEEQVQSLTK ELQGLRGVLQ GLSGRLAEDV QRAVETAFNG RQQPADAAAR PGVHETLNEI QHQLQLLDTR VSTHDQELGH LNNHHGGSSS SGGSRAPAPA SAPPGPSEEL LRQLEQRLQE SCSVCLAGLD GFRRQQQEDR ERLRAMEKLL ASVEERQRHL AGLAVGRRPP QECCSPELGR RLAELERRLD VVAGSVTVLS GRRGTELGGA AGQGGHPPGY TSLASRLSRL EDRFNSTLGP SEEQEESWPG APGGLSHWLP AARGRLEQLG GLLANVSGEL GGRLDLLEEQ VAGAMQACGQ LCSGAPGEQD SQVSEILSAL ERRVLDSEGQ LRLVGSGLHT VEAAGEARQA TLEGLQEVVG RLQDRVDAQD ETAAEFTLRL NLTAARLGQL EGLLQAHGDE GCGACGGVQE ELGRLRDGVE RCSCPLLPPR GPGAGPGVGG PSRGPLDGFS VFGGSSGSAL QALQGELSEV ILSFSSLNDS LNELQTTVEG QGADLADLGA TKDRIISEIN RLQQEATEHA TESEERFRGL EEGQAQAGQC PSLEGRLGRL EGVCERLDTV AGGLQGLREG LSRHVAGLWA GLRETNTTSQ MQAALLEKLV GGQAGLGRRL GALNSSLQLL EDRLHQLSLK DLTGPAGEAG PPGPPGLQGP PGPAGPPGSP GKDGQEGPIG PPGPQGEQGV EGAPAAPVPQ VAFSAALSLP RSEPGTVPFD RVLLNDGGYY DPETGVFTAP LAGRYLLSAV LTGHRHEKVE AVLSRSNQGV ARVDSGGYEP EGLENKPVAE SQPSPGTLGV FSLILPLQAG DTVCVDLVMG QLAHSEEPLT IFSGALLYGD PELEHA

Explore EMILIN-1 with MolForge

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Quick facts

UniProtQ9Y6C2
GeneEMILIN1
OrganismHomo sapiens
Length1016
Binders0
Diseases163
View on UniProt