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ADH4 and RPL35
Number of citations of the paper that reports this interaction (PMID
21988832
)
14
Data Source:
BioGRID
(two hybrid)
ADH4
RPL35
Gene Name
alcohol dehydrogenase 4 (class II), pi polypeptide
ribosomal protein L35
Image
Gene Ontology Annotations
Cellular Component
Cytosol
Nucleolus
Cytoplasm
Cytosol
Membrane
Cytosolic Large Ribosomal Subunit
Molecular Function
NADPH:quinone Reductase Activity
Alcohol Dehydrogenase (NAD) Activity
Alcohol Dehydrogenase Activity, Zinc-dependent
Alditol:NADP+ 1-oxidoreductase Activity
Retinol Dehydrogenase Activity
All-trans Retinal Binding
Zinc Ion Binding
Oxidoreductase Activity, Acting On The Aldehyde Or Oxo Group Of Donors, NAD Or NADP As Acceptor
Benzaldehyde Dehydrogenase Activity
Retinol Binding
Ethanol Binding
NAD Binding
MRNA Binding
Structural Constituent Of Ribosome
Poly(A) RNA Binding
Biological Process
Retinoid Metabolic Process
Alcohol Metabolic Process
Ethanol Oxidation
Cellular Aldehyde Metabolic Process
Xenobiotic Metabolic Process
Retinol Metabolic Process
Small Molecule Metabolic Process
Alcohol Catabolic Process
Quinone Metabolic Process
Nuclear-transcribed MRNA Catabolic Process, Nonsense-mediated Decay
Translation
Translational Initiation
Translational Elongation
Translational Termination
SRP-dependent Cotranslational Protein Targeting To Membrane
Gene Expression
Viral Process
Viral Life Cycle
Viral Transcription
Cellular Protein Metabolic Process
Pathways
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
Metabolic disorders of biological oxidation enzymes
Ethanol oxidation
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)
Biological oxidations
RA biosynthesis pathway
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)
Signaling by Retinoic Acid
Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
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)
Defective MAOA causes Brunner syndrome (BRUNS)
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Nonsense-Mediated Decay (NMD)
Translation
SRP-dependent cotranslational protein targeting to membrane
Eukaryotic Translation Termination
Peptide chain elongation
Influenza Infection
Viral mRNA Translation
L13a-mediated translational silencing of Ceruloplasmin expression
Influenza Life Cycle
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
Influenza Viral RNA Transcription and Replication
GTP hydrolysis and joining of the 60S ribosomal subunit
Eukaryotic Translation Initiation
Formation of a pool of free 40S subunits
Eukaryotic Translation Elongation
Cap-dependent Translation Initiation
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Drugs
NADH
Nicotinamide-Adenine-Dinucleotide
Cyclohexylformamide
Diseases
GWAS
Alcohol dependence (
23456092
)
Esophageal cancer (alcohol interaction) (
22960999
)
Protein-Protein Interactions
2 interactors:
APP
RPL35
7 interactors:
ACTN2
ADH4
CDKN1A
LAMC3
MAX
SGSM3
TUBB2B
Entrez ID
127
11224
HPRD ID
00068
10200
Ensembl ID
ENSG00000198099
ENSG00000136942
Uniprot IDs
P08319
P42766
PDB IDs
3COS
3J3B
Enriched GO Terms of Interacting Partners
?
Synaptic Growth At Neuromuscular Junction
Collateral Sprouting In Absence Of Injury
Collateral Sprouting
Axon Midline Choice Point Recognition
Smooth Endoplasmic Reticulum Calcium Ion Homeostasis
Axon Choice Point Recognition
MRNA Metabolic Process
Neuron Remodeling
Cellular Copper Ion Homeostasis
Copper Ion Homeostasis
Suckling Behavior
Positive Regulation Of G2/M Transition Of Mitotic Cell Cycle
Neuron Maturation
MRNA Polyadenylation
Regulation Of Epidermal Growth Factor-activated Receptor Activity
Mating Behavior
Endoplasmic Reticulum Calcium Ion Homeostasis
RNA Polyadenylation
Neuron Recognition
Nucleotide-binding Domain, Leucine Rich Repeat Containing Receptor Signaling Pathway
Ionotropic Glutamate Receptor Signaling Pathway
Regulation Of G2/M Transition Of Mitotic Cell Cycle
Regulation Of Cell Cycle G2/M Phase Transition
Intracellular Transport
Axon Cargo Transport
Mating
Neuromuscular Junction Development
Positive Regulation Of Mitotic Cell Cycle Phase Transition
Neuron Apoptotic Process
Positive Regulation Of Cell Cycle Phase Transition
Regulation Of Protein Tyrosine Kinase Activity
Visual Learning
Glutamate Receptor Signaling Pathway
Visual Behavior
Neuron Death
Platelet Degranulation
Regulation Of Epidermal Growth Factor Receptor Signaling Pathway
Neuromuscular Process Controlling Balance
Synapse Assembly
MRNA 3'-end Processing
Regulation Of ERBB Signaling Pathway
Associative Learning
Developmental Cell Growth
Establishment Of Localization In Cell
Viral Transcription
Regulation Of Synapse Structure Or Activity
Nuclear-transcribed MRNA Catabolic Process, Nonsense-mediated Decay
SRP-dependent Cotranslational Protein Targeting To Membrane
Feeding Behavior
Cotranslational Protein Targeting To Membrane
Tagcloud
?
actors
adh3
adhs
conjunctiva
conjunctival
cornea
corneal
crabp1
crabp2
crabps
crbp
crbp1
crbps
cyp26
dehydrogenases
dependant
dhrs4
dhrs9
exhaustive
histochemistry
keratocytes
ocular
raldh1
raldh3
raldhs
retinol
rodh4
rxrs
sdr
Tagcloud (Difference)
?
actors
adh3
adhs
conjunctiva
conjunctival
cornea
corneal
crabp1
crabp2
crabps
crbp
crbp1
crbps
cyp26
dehydrogenases
dependant
dhrs4
dhrs9
exhaustive
histochemistry
keratocytes
ocular
raldh1
raldh3
raldhs
retinol
rodh4
rxrs
sdr
Tagcloud (Intersection)
?