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Protein : FBpp0079295 D. melanogaster

Primary Accession  ? Q9VLJ8 Organism . Name  Drosophila melanogaster
MD5 Checksum  ebb7706ad6322cf5f7ac7e508ac4662d UniProt Accession  Q9VLJ8
UniProt Name  MOCS3_DROME GenBank Identifier  AGB92792
Is UniProt Canonical  true Is Fragment  false
Length  453 Molecular Weight  50239
Name  Adenylyltransferase and sulfurtransferase MOCS3 Secondary Identifier  FBpp0079295

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0032054 CG13090 CG13090 FlyBase D. melanogaster


Protein --> Gene + chromosomal location and length of the gene.


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0 Components

4 Cross References

Source . Name

Subject . Primary Identifier
NP_609240.2 RefSeq FBpp0079295
NP_001260255.1 RefSeq FBpp0079295
Dm.5113 UniGene FBpp0079295
NP_001260256.1 RefSeq FBpp0079295

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
Swiss-Prot data set
Reactome data set  

2 Ec Numbers

Identifier Description  

3 Locations

Located On . Primary Identifier
Start End Strand
2L 8517667 8519025 1
2L 8517667 8519025 1
2L 8517667 8519025 1

23 Pathways

Identifier Name
112201 Metabolism
134278 Molybdenum cofactor biosynthesis
96904 Metabolism of vitamins and cofactors
99870 Metabolism of water-soluble vitamins and cofactors
172141 Defective HLCS causes multiple carboxylase deficiency
170704 Defective BTD causes biotidinase deficiency
170877 Defective MMAA causes methylmalonic aciduria type cblA
171816 Defective MUT causes methylmalonic aciduria mut type
170863 Defective CD320 causes methylmalonic aciduria
170480 Defects in biotin (Btn) metabolism
170427 Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
170479 Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
170421 Defective MMAB causes methylmalonic aciduria type cblB
172030 Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
172052 Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
172351 Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
171186 Defective GIF causes intrinsic factor deficiency
172253 Defective CUBN causes hereditary megaloblastic anemia 1
172121 Defective TCN2 causes hereditary megaloblastic anemia
172488 Defects in cobalamin (B12) metabolism
172146 Defective AMN causes hereditary megaloblastic anemia 1
170642 Defects in vitamin and cofactor metabolism
118381 Disease

6 Protein Domains

DB identifier Name Short Name Type
IPR016040 NAD(P)-binding domain NAD(P)-bd_dom Domain
IPR028885 Adenylyltransferase and sulfurtransferase MOCS3/Uba4 MOCS3/Uba4 Family
IPR007901 MoeZ/MoeB MoeZ_MoeB Domain
IPR009036 Molybdenum cofactor biosynthesis, MoeB Molybdenum_cofac_synth_MoeB Domain
IPR001763 Rhodanese-like domain Rhodanese-like_dom Domain
IPR000594 UBA/THIF-type NAD/FAD binding fold ThiF_NAD_FAD-bd Domain

3 Transcripts

DB identifier Gene
FBtr0333414 CG13090
FBtr0079683 CG13090
FBtr0333413 CG13090