Binding

Binding

• Antigen binding
  • SLC7A9: solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
• Carbohydrate binding
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • FGFR1: fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
  • GAA: glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II)
  • GALK1: galactokinase 1
  • LPL: lipoprotein lipase
  • TNXB: tenascin XB
• Chromatin binding
  • APTX: aprataxin
  • ERCC6: excision repair cross-complementing rodent repair deficiency, complementation group 6
  • FOXC2: forkhead box C2 (MFH-1, mesenchyme forkhead 1)
  • NSD1: nuclear receptor binding SET domain protein 1
  • SMC1A: structural maintenance of chromosomes 1A
  • TP53: tumor protein p53
• Cofactor binding
  • AGXT: alanine-glyoxylate aminotransferase
  • GRHPR: glyoxylate reductase/hydroxypyruvate reductase
  • MTRR: 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
  • PPOX: protoporphyrinogen oxidase
• Hormone binding
  • AR: androgen receptor (dihydrotestosterone receptor; testicular feminization; spinal and bulbar muscular atrophy; Kennedy disease)
• Ion binding
• Lipid binding
  • ABCA1: ATP-binding cassette, sub-family A (ABC1), member 1
  • APOB: apolipoprotein B (including Ag(x) antigen)
  • APOE: apolipoprotein E
  • AR: androgen receptor (dihydrotestosterone receptor; testicular feminization; spinal and bulbar muscular atrophy; Kennedy disease)
  • NPC2: Niemann-Pick disease, type C2
  • PSAP: prosaposin (variant Gaucher disease and variant metachromatic leukodystrophy)
• Molecular adaptor activity
  • SH3BP2: SH3-domain binding protein 2
• Neurotransmitter binding
  • DRD3: dopamine receptor D3
• Nucleic acid binding
• Nucleotide binding
• Oxygen binding
  • CYP1B1: cytochrome P450, family 1, subfamily B, polypeptide 1
  • HBB: hemoglobin, beta
• Pattern binding
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • FGFR1: fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
  • LPL: lipoprotein lipase
  • NOD2: nucleotide-binding oligomerization domain containing 2
  • TNXB: tenascin XB
• Peptide binding
  • ANG: angiogenin, ribonuclease, RNase A family, 5
  • SLC7A9: solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
• Protein binding
• Tetrapyrrole binding
  • CYP1B1: cytochrome P450, family 1, subfamily B, polypeptide 1
• Vitamin binding
  • AGXT: alanine-glyoxylate aminotransferase
  • MCCC1: methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)
  • PC: pyruvate carboxylase
  • PCCA: propionyl Coenzyme A carboxylase, alpha polypeptide
  • TTPA: tocopherol (alpha) transfer protein

Source: Gene Ontology Consortium (June 2008).