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ZBTB26 and CYP2W1
Number of citations of the paper that reports this interaction (PMID
21988832
)
14
Data Source:
BioGRID
(two hybrid)
ZBTB26
CYP2W1
Gene Name
zinc finger and BTB domain containing 26
cytochrome P450, family 2, subfamily W, polypeptide 1
Image
No pdb structure
No pdb structure
Gene Ontology Annotations
Cellular Component
Cellular_component
Nucleoplasm
Cytoplasm
Cytoplasm
Endoplasmic Reticulum Lumen
Endoplasmic Reticulum Membrane
Cell Surface
Intracellular Membrane-bounded Organelle
Molecular Function
Molecular_function
DNA Binding
Metal Ion Binding
Iron Ion Binding
Steroid Hydroxylase Activity
Oxidoreductase Activity, Acting On Paired Donors, With Incorporation Or Reduction Of Molecular Oxygen, Reduced Flavin Or Flavoprotein As One Donor, And Incorporation Of One Atom Of Oxygen
Oxygen Binding
Heme Binding
Biological Process
Transcription, DNA-templated
Regulation Of Transcription, DNA-templated
Biological_process
Organic Acid Metabolic Process
Xenobiotic Metabolic Process
Exogenous Drug Catabolic Process
Aflatoxin B1 Metabolic Process
Small Molecule Metabolic Process
Oxidation-reduction Process
Pathways
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
Metabolic disorders of biological oxidation enzymes
Phase 1 - Functionalization of compounds
Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
Cytochrome P450 - arranged by substrate type
Biological oxidations
Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
Defective FMO3 causes Trimethylaminuria (TMAU)
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)
Miscellaneous substrates
Defective CYP1B1 causes Glaucoma
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)
Xenobiotics
Defective MAOA causes Brunner syndrome (BRUNS)
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs
Diseases
GWAS
Protein-Protein Interactions
8 interactors:
CYP2W1
EIF6
GIPC2
PBK
SUMO1
SUMO1P1
UBE2I
ZBTB6
2 interactors:
CYB5A
ZBTB26
Entrez ID
57684
54905
HPRD ID
15692
07901
Ensembl ID
ENSG00000171448
ENSG00000073067
Uniprot IDs
Q9HCK0
Q8TAV3
PDB IDs
Enriched GO Terms of Interacting Partners
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Protein Sumoylation
Aflatoxin B1 Metabolic Process
Positive Regulation Of SUMO Transferase Activity
Regulation Of Proteasomal Ubiquitin-dependent Protein Catabolic Process
PML Body Organization
Regulation Of Proteasomal Protein Catabolic Process
Post-translational Protein Modification
Mature Ribosome Assembly
Protein Localization To Nuclear Pore
Protein Localization To Nuclear Envelope
Peptidyl-lysine Modification
Ribosomal Subunit Export From Nucleus
Positive Regulation Of Intracellular Steroid Hormone Receptor Signaling Pathway
Mitotic Nuclear Division
Regulation Of Sequence-specific DNA Binding Transcription Factor Activity
Toxin Metabolic Process
Regulation Of Protein Catabolic Process
Exogenous Drug Catabolic Process
Regulation Of Interferon-gamma-mediated Signaling Pathway
Drug Catabolic Process
Regulation Of Response To Interferon-gamma
Ribosomal Large Subunit Biogenesis
Organelle Organization
Tagcloud
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Tagcloud (Difference)
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Tagcloud (Intersection)
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