dbHDPLS[Database of Human Disease Protein-Ligand Structure]
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PDB ID Protein name Function Keywords Disease Keywords Ligands Drug molecular
121PGTPase HRas Oncogene ProteinDisease mutation Proto-oncogeneMG GCP
12CACarbonic anhydrase 2 Lyase(Oxo-Acid)Disease mutation OsteopetrosisHG ZN
1A00Hemoglobin subunit alpha Oxygen TransportDisease mutation Hereditary hemolytic anemiaHEM
1A01Hemoglobin subunit alpha Oxygen TransportDisease mutation Hereditary hemolytic anemiaHEM
1A07Hemoglobin subunit alpha Complex (Transferase/Peptide)Disease mutation Hereditary hemolytic anemiaACE DIP PTRPTR (experimental)
1A08Hemoglobin subunit alpha Complex (Transferase/Peptide)Disease mutation Hereditary hemolytic anemiaACE DIP FTY
1A09Prothrombin Complex (Transferase/Peptide)Disease mutation ThrombophiliaACE DIP PTH
1A0UProthrombin Oxygen TransportDisease mutation ThrombophiliaHEM
1A0ZProthrombin Oxygen TransportDisease mutation ThrombophiliaHEM
1A1AHemoglobin subunit alpha Complex (Transferase/Peptide)Disease mutation Hereditary hemolytic anemiaACE DIP PTH
1A1BHemoglobin subunit alpha Complex (Transferase/Peptide)Disease mutation Hereditary hemolytic anemiaACE DIP PTRPTR (experimental)
1A1CCarbonic anhydrase 2 Complex (Transferase/Peptide)Disease mutation OsteopetrosisACE DIX PTRPTR (experimental)
1A1EProthrombin Complex (Transferase/Peptide)Disease mutation ThrombophiliaACE DIY PTRPTR (experimental)
1A2CC-1-tetrahydrofolate synthase, cytoplasmic Hydrolase/Hydrolase InhibitorDisease mutationNA 34H OAR PRJ TYS
1A31Prothrombin Isomerase/DnaDisease mutation Thrombophilia5IU PTRPTR 5IU (experimental)
1A35Estrogen receptor Isomerase/DnaDisease mutationBRUBRU (experimental)
1A3BProthrombin Hydrolase/Hydrolase InhibitorDisease mutation ThrombophiliaT29
1A3EProthrombin Hydrolase/Hydrolase InhibitorDisease mutation ThrombophiliaT16
1A3NAdenosylhomocysteinase Oxygen TransportDisease mutationHEM
1A3OPlasminogen activator inhibitor 1 Oxygen TransportHEM
1A42Serotransferrin LyaseDisease mutationHG ZN BZUBZU (approved)
1A46Serotransferrin Hydrolase/Hydrolase InhibitorDisease mutationNA 00K TYS
1A4IHemoglobin subunit alpha OxidoreductaseDisease mutation Hereditary hemolytic anemiaNDPNDP (experimental)
1A4WProthrombin Hydrolase/Hydrolase InhibitorDisease mutation ThrombophiliaNA QWE TYS
1A52Prothrombin ReceptorDisease mutation ThrombophiliaAU EST
1A5GHemoglobin subunit alpha Hydrolase/Hydrolase InhibitorDisease mutation Hereditary hemolytic anemiaNA 00L TYS
1A5HHemoglobin subunit alpha HydrolaseDisease mutation Hereditary hemolytic anemiaBBABBA (experimental)
1A61Prothrombin Hydrolase/Hydrolase InhibitorDisease mutation ThrombophiliaNA 00N TYS
1A7AProthrombin HydrolaseDisease mutation ThrombophiliaADC MSE NADADC (experimental)
1A7CProthrombin Hydrolase Inhibitor/PeptideDisease mutation ThrombophiliaACE NAG NH2 RIPNAG (approved)
1A8EGTPase HRas Iron TransportDisease mutation Proto-oncogeneFE CO3
1A8FFibroblast growth factor receptor 1 Iron TransportCraniosynostosis Disease mutation Dwarfism Holoprosencephaly Kallmann syndrome Mental retardation Hypogonadotropic hypogonadismFE CO3
1A9WProthrombin Oxygen TransportDisease mutation ThrombophiliaCMO HEM
1ABIProthrombin Hydrolase/Hydrolase InhibitorDisease mutation ThrombophiliaDPN HMRDPN (experimental)
1ABJProthrombin Hydrolase/Hydrolase InhibitorDisease mutation Thrombophilia0G60G6 (experimental)
1ABWIg gamma-1 chain C regionOxygen TransportHEM LEU METLEU MET (approved)
1ABYHemoglobin subunit alpha Oxygen TransportDisease mutation Hereditary hemolytic anemiaCYN HEM
1AD5Low-density lipoprotein receptor Tyrosine-Protein KinaseDisease mutationCA ANP PTRANP PTR (experimental)
1AD8Interleukin-6 Hydrolase/Hydrolase InhibitorNA MDL TYS
1AE8Carbonic anhydrase 2 Hydrolase/Hydrolase InhibitorDisease mutation OsteopetrosisAZL NAG TYSNAG (approved)
1AFEAnnexin A5 Hydrolase/Hydrolase InhibitorALZ NAG TYSNAG (approved)
1AGPAnnexin A5 Oncogene ProteinMG GNP
1AGWSuperoxide dismutase [Mn], mitochondrial Protein KinaseSU2SU2 (experimental)
1AHTSuperoxide dismutase [Mn], mitochondrial Hydrolase/Hydrolase InhibitorAPA TYSAPA (experimental)
1AI8N(4)-(beta-N-acetylglucosaminyl)-L-asparaginaseBlood Coagulation/Hydrolase InhibitorDisease mutationT42 TYS
1AIXN(4)-(beta-N-acetylglucosaminyl)-L-asparaginaseBlood Coagulation/Hydrolase InhibitorDisease mutationT19 TYS
1AJ7Ig gamma-1 chain C regionImmunoglobulinNPENPE (experimental)
1AJ9Cathepsin K Oxygen TransportDisease mutationCMO HEM PO4
1AJJCathepsin K ReceptorDisease mutationCA SO4
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