Properdin (CFP)

Homo sapiens — UniProt P27918

Gene: CFPHomo sapiensSwissProt reviewed

About Properdin

Properdin (CFP) is a protein from Homo sapiens identified by UniProt accession P27918, 469 residues long. MolForge cross-references it against 0 known binders and 313 disease associations.

Target properties

Protein nameProperdin
UniProt accessionP27918
GeneCFP
OrganismHomo sapiens
Length469 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 (313)

Diseases linked to this target (Open Targets).

  • Properdin deficiency · score 0.70
  • properdin deficiency, X-linked · score 0.69
  • neurodegenerative disease · score 0.29
  • head and neck squamous cell carcinoma · score 0.22
  • gastric adenocarcinoma · score 0.20
  • genetic disorder · score 0.18
  • breast adenocarcinoma · score 0.15
  • esophageal cancer · score 0.15
  • glioblastoma multiforme · score 0.13
  • urinary bladder cancer · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P27918-F1alphafoldPREDICTED83.30—

Amino-acid sequence (469 residues)

MITEGAQAPR LLLPPLLLLL TLPATGSDPV LCFTQYEESS GKCKGLLGGG VSVEDCCLNT AFAYQKRSGG LCQPCRSPRW SLWSTWAPCS VTCSEGSQLR YRRCVGWNGQ CSGKVAPGTL EWQLQACEDQ QCCPEMGGWS GWGPWEPCSV TCSKGTRTRR RACNHPAPKC GGHCPGQAQE SEACDTQQVC PTHGAWATWG PWTPCSASCH GGPHEPKETR SRKCSAPEPS QKPPGKPCPG LAYEQRRCTG LPPCPVAGGW GPWGPVSPCP VTCGLGQTME QRTCNHPVPQ HGGPFCAGDA TRTHICNTAV PCPVDGEWDS WGEWSPCIRR NMKSISCQEI PGQQSRGRTC RGRKFDGHRC AGQQQDIRHC YSIQHCPLKG SWSEWSTWGL CMPPCGPNPT RARQRLCTPL LPKYPPTVSM VEGQGEKNVT FWGRPLPRCE ELQGQKLVVE EKRPCLHVPA CKDPEEEEL

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Quick facts

UniProtP27918
GeneCFP
OrganismHomo sapiens
Length469
Binders0
Diseases313
View on UniProt