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Protein : FBpp0076348 D. melanogaster

Primary Accession  ? Q9VSL2 Organism . Name  Drosophila melanogaster
MD5 Checksum  f94ed46209fcf12ce0b8631408c5e181 UniProt Accession  Q9VSL2
UniProt Name  Q9VSL2_DROME GenBank Identifier  AAF50406
Is UniProt Canonical  true Is Fragment  false
Length  241 Molecular Weight  27722
Name  RE55344p Secondary Identifier  FBpp0076348

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Genomics

1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0035904 CG6776 GstO3 Glutathione S transferase O3 FlyBase D. melanogaster

Proteins

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

Interactions

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Other

3 Synonyms

0 Components

2 Cross References

Identifier
Source . Name

Subject . Primary Identifier
Dm.5905 UniGene FBpp0076348
NP_648234.1 RefSeq FBpp0076348

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
TrEMBL data set http://www.ebi.ac.uk/trembl/
Reactome data set  

4 Ec Numbers

Identifier Description
2.5.1.18  
1.8.5.1  
1.5.4.1  
2.8.-.-  

1 Locations


Located On . Primary Identifier
Start End Strand
3L 8512054 8513306 1

29 Pathways

Identifier Name
112201 Metabolism
109448 Sulfur amino acid metabolism
78106 Biological oxidations
86268 Amino acid and derivative metabolism
102710 Phase II conjugation
97782 Glutathione conjugation
98722 Glutathione synthesis and recycling
96904 Metabolism of vitamins and cofactors
99870 Metabolism of water-soluble vitamins and cofactors
108418 Vitamin C (ascorbate) metabolism
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

4 Protein Domains

DB identifier Name Short Name Type
IPR010987 Glutathione S-transferase, C-terminal-like Glutathione-S-Trfase_C-like Domain
IPR004045 Glutathione S-transferase, N-terminal Glutathione_S-Trfase_N Domain
IPR005442 Glutathione S-transferase, omega-class GST_omega Family
IPR012336 Thioredoxin-like fold Thioredoxin-like_fold Domain

1 Transcripts

DB identifier Gene
FBtr0076622 GstO3