CYB5A and CYP17A1

Number of citations of the paper that reports this interaction (PMID 9601054)
2

Data Source:
HPRD (in vitro)

		CYB5A	CYP17A1
Gene Name		cytochrome b5 type A (microsomal)	cytochrome P450, family 17, subfamily A, polypeptide 1
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Gene Ontology Annotations	Cellular Component	Mitochondrial Outer Membrane Endoplasmic Reticulum Membrane Membrane Integral Component Of Membrane Extracellular Vesicular Exosome	Mitochondrion Endoplasmic Reticulum Endoplasmic Reticulum Membrane Axon Neuronal Cell Body
	Molecular Function	Aldo-keto Reductase (NADP) Activity Cytochrome-c Oxidase Activity Enzyme Binding Heme Binding Metal Ion Binding	Steroid 17-alpha-monooxygenase Activity Iron Ion Binding Oxygen Binding Heme Binding 17-alpha-hydroxyprogesterone Aldolase Activity
	Biological Process	Vitamin Metabolic Process Water-soluble Vitamin Metabolic Process L-ascorbic Acid Metabolic Process Small Molecule Metabolic Process Response To Cadmium Ion Oxidation-reduction Process Hydrogen Ion Transmembrane Transport	Steroid Biosynthetic Process Androgen Biosynthetic Process Glucocorticoid Biosynthetic Process Xenobiotic Metabolic Process Sex Differentiation Steroid Metabolic Process Response To Herbicide Response To Acetate Response To Ionizing Radiation Sterol Metabolic Process Response To Insecticide Biphenyl Metabolic Process Dibenzo-p-dioxin Metabolic Process Phenol-containing Compound Metabolic Process Phthalate Metabolic Process Hippocampus Development Adrenal Gland Development Ovulation Response To Nutrient Levels Response To Retinoic Acid Leydig Cell Differentiation Response To Cytokine Hormone Biosynthetic Process Progesterone Metabolic Process Response To Drug Small Molecule Metabolic Process Response To Steroid Hormone Response To CAMP Response To Methylmercury Oxidation-reduction Process Response To Fungicide Cellular Response To Lipopolysaccharide Cellular Response To Antibiotic Cellular Response To Gonadotropin Stimulus Positive Regulation Of Steroid Hormone Biosynthetic Process
Pathways		Metabolism of vitamins and cofactors Defective CD320 causes methylmalonic aciduria Defective GIF causes intrinsic factor deficiency Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF Defective HLCS causes multiple carboxylase deficiency Defective MMAB causes methylmalonic aciduria type cblB Defective BTD causes biotidinase deficiency Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC Defective MTR causes methylmalonic aciduria and homocystinuria type cblG Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD Vitamin C (ascorbate) metabolism Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE Defective MMAA causes methylmalonic aciduria type cblA Defective CUBN causes hereditary megaloblastic anemia 1 Defective AMN causes hereditary megaloblastic anemia 1 Defective MUT causes methylmalonic aciduria mut type Metabolism of water-soluble vitamins and cofactors Defects in biotin (Btn) metabolism Defective TCN2 causes hereditary megaloblastic anemia Defects in cobalamin (B12) metabolism Defects in vitamin and cofactor metabolism	Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B) Metabolism of lipids and lipoproteins Glucocorticoid biosynthesis Metabolic disorders of biological oxidation enzymes Androgen biosynthesis Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A) Phase 1 - Functionalization of compounds Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56) Cytochrome P450 - arranged by substrate type Endogenous sterols Biological oxidations Defective FMO3 causes Trimethylaminuria (TMAU) Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR) Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX) Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4) Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Defective CYP1B1 causes Glaucoma Metabolism of steroid hormones and vitamin D Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5) Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Defective CYP19A1 causes Aromatase excess syndrome (AEXS) Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5) Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Defective MAOA causes Brunner syndrome (BRUNS) Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs		Heme Dimethyl Propionate Ester Heme	NADH Progesterone Abiraterone
Diseases
GWAS			Blood pressure ( 21572416 21909110) Coronary heart disease ( 21378990) Parkinson's disease ( 19915575) Prostate cancer ( 23535732) Systolic blood pressure ( 19430479 19430483 21909115)
Protein-Protein Interactions		15 interactors: CYB5R3 CYCS CYP17A1 CYP1A1 CYP1A2 CYP2A6 CYP2D6 CYP2E1 CYP2W1 CYP3A4 CYP4A11 CYP4F2 POR SCD UGT1A4	8 interactors: ATP5E BARX1 CDO1 CYB5A HSP90AB1 POR RPAIN TIGD7
Entrez ID		1528	1586
HPRD ID		08941	01944
Ensembl ID		ENSG00000166347	ENSG00000148795
Uniprot IDs		P00167	P05093 Q1HB44
PDB IDs		2I96	2C17 3RUK 3SWZ
Enriched GO Terms of Interacting Partners?		Xenobiotic Metabolic Process Cellular Response To Xenobiotic Stimulus Response To Xenobiotic Stimulus Drug Metabolic Process Epoxygenase P450 Pathway Oxidation-reduction Process Exogenous Drug Catabolic Process Organic Acid Metabolic Process Small Molecule Metabolic Process Drug Catabolic Process Arachidonic Acid Metabolic Process Carboxylic Acid Metabolic Process Fatty Acid Metabolic Process Icosanoid Metabolic Process Monocarboxylic Acid Metabolic Process Unsaturated Fatty Acid Metabolic Process Lipid Metabolic Process Long-chain Fatty Acid Metabolic Process Steroid Metabolic Process Monoterpenoid Metabolic Process Response To Drug Omega-hydroxylase P450 Pathway Catabolic Process Cellular Lipid Metabolic Process Demethylation Coumarin Metabolic Process Isoprenoid Metabolic Process Dibenzo-p-dioxin Metabolic Process Alkaloid Metabolic Process Toxin Metabolic Process Oxidative Demethylation Flavonoid Metabolic Process Vitamin Metabolic Process Alkaloid Catabolic Process Pressure Natriuresis Leukotriene B4 Catabolic Process Cellular Metabolic Process Cellular Response To Stimulus Porphyrin-containing Compound Metabolic Process Positive Regulation Of Steroid Hormone Biosynthetic Process Long-chain Fatty Acid Catabolic Process Response To Herbicide Heterocycle Metabolic Process Hydrogen Peroxide Biosynthetic Process Lipid Catabolic Process Cellular Ketone Metabolic Process Positive Regulation Of Hormone Biosynthetic Process Tetrapyrrole Metabolic Process Lipid Biosynthetic Process Vitamin D Metabolic Process	Cellular Organofluorine Metabolic Process Nitrate Catabolic Process Nitric Oxide Catabolic Process Oxidation-reduction Process Regulation Of Growth Plate Cartilage Chondrocyte Proliferation Taurine Biosynthetic Process Nitrate Metabolic Process L-cysteine Catabolic Process Hydrogen Ion Transmembrane Transport Proton Transport Positive Regulation Of Cholesterol Biosynthetic Process Taurine Metabolic Process Positive Regulation Of Cholesterol Metabolic Process Positive Regulation Of Steroid Hormone Biosynthetic Process Cysteine Metabolic Process Carboxylic Acid Metabolic Process Small Molecule Metabolic Process Cellular Metabolic Process Positive Regulation Of Hormone Biosynthetic Process Organic Acid Metabolic Process Positive Regulation Of Protein Import Into Nucleus, Translocation L-ascorbic Acid Metabolic Process Carnitine Metabolic Process Negative Regulation Of Proteolysis Sulfur Amino Acid Catabolic Process Serine Family Amino Acid Catabolic Process Cellular Response To Follicle-stimulating Hormone Stimulus Positive Regulation Of Cell Size Negative Regulation Of Protein Processing Mitochondrial ATP Synthesis Coupled Proton Transport Amino-acid Betaine Metabolic Process Regulation Of Protein Import Into Nucleus, Translocation Negative Regulation Of Lipase Activity Regulation Of Cholesterol Biosynthetic Process Transport Regulation Of Protein Processing
Tagcloud ?		administering anxa1 c4bpalpha cox2 cpla2alpha crip1 ctsl1 endorses eva1 gstp1 hgd il6st interferes levonorgestrel lng loc90133 maoa mifepristone ovulatory paep receptive receptivity s100a4 sat1 serpinb9 slc25a29 slc39a14 tgm2 unproven	acth adrenal adrenocortical adrenocorticotropin belongs biosynthesis camp confers cortisol dbhs exoribonuclease export facilitating glucocorticoid h295r isoforms nono p54nrb pde pde11a pde2a pde3a pde3b pde4a pde4d phosphodiesterase select splicing xrn2
Tagcloud (Difference) ?		administering anxa1 c4bpalpha cox2 cpla2alpha crip1 ctsl1 endorses eva1 gstp1 hgd il6st interferes levonorgestrel lng loc90133 maoa mifepristone ovulatory paep receptive receptivity s100a4 sat1 serpinb9 slc25a29 slc39a14 tgm2 unproven	acth adrenal adrenocortical adrenocorticotropin belongs biosynthesis camp confers cortisol dbhs exoribonuclease export facilitating glucocorticoid h295r isoforms nono p54nrb pde pde11a pde2a pde3a pde3b pde4a pde4d phosphodiesterase select splicing xrn2
Tagcloud (Intersection) ?