Endoglin (ENG)

Homo sapiens — UniProt P17813

Gene: ENGHomo sapiensSwissProt reviewed

About Endoglin

Endoglin (ENG) is a protein from Homo sapiens identified by UniProt accession P17813, 658 residues long. MolForge cross-references it against 0 known binders and 682 disease associations.

Target properties

Protein nameEndoglin
UniProt accessionP17813
GeneENG
OrganismHomo sapiens
Length658 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 (682)

Diseases linked to this target (Open Targets).

  • telangiectasia, hereditary hemorrhagic, type 1 · score 0.85
  • hereditary hemorrhagic telangiectasia · score 0.80
  • vascular disease · score 0.60
  • arteriovenous hemangioma/malformation · score 0.59
  • congenital anomaly of the great arteries · score 0.57
  • Abnormality of the cardiovascular system · score 0.56
  • Abnormality of the vasculature · score 0.55
  • congenital anomaly of cardiovascular system · score 0.55
  • heritable pulmonary arterial hypertension · score 0.47
  • pulmonary hypertension, primary, 1 · score 0.46

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P17813-F1alphafoldPREDICTED80.05—

Amino-acid sequence (658 residues)

MDRGTLPLAV ALLLASCSLS PTSLAETVHC DLQPVGPERG EVTYTTSQVS KGCVAQAPNA ILEVHVLFLE FPTGPSQLEL TLQASKQNGT WPREVLLVLS VNSSVFLHLQ ALGIPLHLAY NSSLVTFQEP PGVNTTELPS FPKTQILEWA AERGPITSAA ELNDPQSILL RLGQAQGSLS FCMLEASQDM GRTLEWRPRT PALVRGCHLE GVAGHKEAHI LRVLPGHSAG PRTVTVKVEL SCAPGDLDAV LILQGPPYVS WLIDANHNMQ IWTTGEYSFK IFPEKNIRGF KLPDTPQGLL GEARMLNASI VASFVELPLA SIVSLHASSC GGRLQTSPAP IQTTPPKDTC SPELLMSLIQ TKCADDAMTL VLKKELVAHL KCTITGLTFW DPSCEAEDRG DKFVLRSAYS SCGMQVSASM ISNEAVVNIL SSSSPQRKKV HCLNMDSLSF QLGLYLSPHF LQASNTIEPG QQSFVQVRVS PSVSEFLLQL DSCHLDLGPE GGTVELIQGR AAKGNCVSLL SPSPEGDPRF SFLLHFYTVP IPKTGTLSCT VALRPKTGSQ DQEVHRTVFM RLNIISPDLS GCTSKGLVLP AVLGITFGAF LIGALLTAAL WYIYSHTRSP SKREPVVAVA APASSESSST NHSIGSTQST PCSTSSMA

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Quick facts

UniProtP17813
GeneENG
OrganismHomo sapiens
Length658
Binders0
Diseases682
View on UniProt