Pyruvate carboxylase, mitochondrial (PC)

Homo sapiens — UniProt P11498

Gene: PCHomo sapiensSwissProt reviewed

About Pyruvate carboxylase, mitochondrial

Pyruvate carboxylase, mitochondrial (PC) is a protein from Homo sapiens identified by UniProt accession P11498, 1178 residues long. MolForge cross-references it against 0 known binders and 144 disease associations.

Target properties

Protein namePyruvate carboxylase, mitochondrial
UniProt accessionP11498
GenePC
OrganismHomo sapiens
Length1178 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 (144)

Diseases linked to this target (Open Targets).

  • pyruvate carboxylase deficiency disease · score 0.82
  • Congenital lactic acidosis · score 0.42
  • pyruvate carboxylase deficiency, infantile form · score 0.37
  • pyruvate carboxylase deficiency, severe neonatal type · score 0.37
  • pyruvate carboxylase deficiency, benign type · score 0.37
  • Global developmental delay · score 0.34
  • urate measurement · score 0.22
  • genetic disorder · score 0.19
  • low grade glioma · score 0.18
  • thyroid gland adenocarcinoma · score 0.18

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P11498-F1alphafoldPREDICTED90.39—

Amino-acid sequence (1178 residues)

MLKFRTVHGG LRLLGIRRTS TAPAASPNVR RLEYKPIKKV MVANRGEIAI RVFRACTELG IRTVAIYSEQ DTGQMHRQKA DEAYLIGRGL APVQAYLHIP DIIKVAKENN VDAVHPGYGF LSERADFAQA CQDAGVRFIG PSPEVVRKMG DKVEARAIAI AAGVPVVPGT DAPITSLHEA HEFSNTYGFP IIFKAAYGGG GRGMRVVHSY EELEENYTRA YSEALAAFGN GALFVEKFIE KPRHIEVQIL GDQYGNILHL YERDCSIQRR HQKVVEIAPA AHLDPQLRTR LTSDSVKLAK QVGYENAGTV EFLVDRHGKH YFIEVNSRLQ VEHTVTEEIT DVDLVHAQIH VAEGRSLPDL GLRQENIRIN GCAIQCRVTT EDPARSFQPD TGRIEVFRSG EGMGIRLDNA SAFQGAVISP HYDSLLVKVI AHGKDHPTAA TKMSRALAEF RVRGVKTNIA FLQNVLNNQQ FLAGTVDTQF IDENPELFQL RPAQNRAQKL LHYLGHVMVN GPTTPIPVKA SPSPTDPVVP AVPIGPPPAG FRDILLREGP EGFARAVRNH PGLLLMDTTF RDAHQSLLAT RVRTHDLKKI APYVAHNFSK LFSMENWGGA TFDVAMRFLY ECPWRRLQEL RELIPNIPFQ MLLRGANAVG YTNYPDNVVF KFCEVAKENG MDVFRVFDSL NYLPNMLLGM EAAGSAGGVV EAAISYTGDV ADPSRTKYSL QYYMGLAEEL VRAGTHILCI KDMAGLLKPT ACTMLVSSLR DRFPDLPLHI HTHDTSGAGV AAMLACAQAG ADVVDVAADS MSGMTSQPSM GALVACTRGT PLDTEVPMER VFDYSEYWEG ARGLYAAFDC TATMKSGNSD VYENEIPGGQ YTNLHFQAHS MGLGSKFKEV KKAYVEANQM LGDLIKVTPS SKIVGDLAQF MVQNGLSRAE AEAQAEELSF PRSVVEFLQG YIGVPHGGFP EPFRSKVLKD LPRVEGRPGA SLPPLDLQAL EKELVDRHGE EVTPEDVLSA AMYPDVFAHF KDFTATFGPL DSLNTRLFLQ GPKIAEEFEV ELERGKTLHI KALAVSDLNR AGQRQVFFEL NGQLRSILVK DTQAMKEMHF HPKALKDVKG QIGAPMPGKV IDIKVVAGAK VAKGQPLCVL SAMKMETVVT SPMEGTVRKV HVTKDMTLEG DDLILEIE

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Quick facts

UniProtP11498
GenePC
OrganismHomo sapiens
Length1178
Binders0
Diseases144
View on UniProt