Homo sapiens Gene: MOCS3
Summary
InnateDB Gene IDBG-81183.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MOCS3
Gene Name molybdenum cofactor synthesis 3
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000124217
Encoded Proteins
molybdenum cofactor synthesis 3
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Molybdenum cofactor (MoCo) is necessary for the function of all molybdoenzymes. The protein encoded by this gene adenylates and activates molybdopterin synthase, an enzyme required for biosynthesis of MoCo. This gene contains no introns. A pseudogene of this gene is present on chromosome 14. [provided by RefSeq, Nov 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:50958826-50963931
Strand Forward strand
Band q13.13
Transcripts
ENST00000244051 ENSP00000244051
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated
Total 8 [view]
Protein-Protein 7 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004792 thiosulfate sulfurtransferase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016779 nucleotidyltransferase activity
GO:0016783 sulfurtransferase activity
GO:0042292 URM1 activating enzyme activity
GO:0046872 metal ion binding
GO:0061604 molybdopterin-synthase sulfurtransferase activity
GO:0061605 molybdopterin-synthase adenylyltransferase activity
GO:0070733 protein adenylyltransferase activity
Biological Process
GO:0002098 tRNA wobble uridine modification
GO:0002143 tRNA wobble position uridine thiolation
GO:0006766 vitamin metabolic process
GO:0006767 water-soluble vitamin metabolic process
GO:0006777 Mo-molybdopterin cofactor biosynthetic process
GO:0018117 protein adenylylation
GO:0018192 enzyme active site formation via L-cysteine persulfide
GO:0032324 molybdopterin cofactor biosynthetic process
GO:0032447 protein urmylation
GO:0034227 tRNA thio-modification
GO:0044281 small molecule metabolic process
Cellular Component
GO:0005829 cytosol
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Molybdenum cofactor biosynthesis pathway
Defective HLCS causes multiple carboxylase deficiency pathway
Defective MUT causes methylmalonic aciduria mut type pathway
Defective MMAA causes methylmalonic aciduria type cblA pathway
Defective TCN2 causes hereditary megaloblastic anemia pathway
Metabolism of water-soluble vitamins and cofactors pathway
Defective AMN causes hereditary megaloblastic anemia 1 pathway
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG pathway
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF pathway
Defective CD320 causes methylmalonic aciduria pathway
Defects in cobalamin (B12) metabolism pathway
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC pathway
Defects in biotin (Btn) metabolism pathway
Defective BTD causes biotidinase deficiency pathway
Defective GIF causes intrinsic factor deficiency pathway
Defects in vitamin and cofactor metabolism pathway
Defective CUBN causes hereditary megaloblastic anemia 1 pathway
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD pathway
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE pathway
Metabolism pathway
Defective MMAB causes methylmalonic aciduria type cblB pathway
Disease pathway
Metabolism of vitamins and cofactors pathway
KEGG
Sulfur relay system pathway
INOH
PID NCI
Cross-References
SwissProt O95396
TrEMBL
UniProt Splice Variant
Entrez Gene 27304
UniGene Hs.159410
RefSeq NM_014484
HUGO HGNC:15765
OMIM 609277
CCDS CCDS13435
HPRD 10092
IMGT
EMBL AF102544 AL034553 BC015939
GenPept AAC72412 AAH15939 CAB53750
RNA Seq Atlas 27304