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Protein : FBpp0079874 D. melanogaster

Primary Accession  ? Q9VKD3 Organism . Name  Drosophila melanogaster
MD5 Checksum  a30ecd18fd91702c98940874ba57d2fa UniProt Accession  Q9VKD3
UniProt Name  NFS1_DROME GenBank Identifier  AAF53143
Is UniProt Canonical  true Is Fragment  false
Length  462 Molecular Weight  51074
Name  Probable cysteine desulfurase, mitochondrial Secondary Identifier  FBpp0079874

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0032393 CG12264 CG12264 FlyBase D. melanogaster


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


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3 Synonyms

0 Components

2 Cross References

Source . Name

Subject . Primary Identifier
Dm.21103 UniGene FBpp0079874
NP_609533.1 RefSeq FBpp0079874

3 Data Sets

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

1 Ec Numbers

Identifier Description  

1 Locations

Located On . Primary Identifier
Start End Strand
2L 11999725 12001168 1

25 Pathways

Identifier Name
112201 Metabolism
134278 Molybdenum cofactor biosynthesis
158952 Electron Transport from NADPH to Ferredoxin
157153 Mitochondrial Iron-Sulfur Cluster Biogenesis
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

7 Protein Domains

DB identifier Name Short Name Type
IPR015424 Pyridoxal phosphate-dependent transferase PyrdxlP-dep_Trfase Domain
IPR015421 Pyridoxal phosphate-dependent transferase, major region, subdomain 1 PyrdxlP-dep_Trfase_major_sub1 Domain
IPR015422 Pyridoxal phosphate-dependent transferase, major region, subdomain 2 PyrdxlP-dep_Trfase_major_sub2 Domain
IPR000192 Aminotransferase, class V/Cysteine desulfurase Aminotrans_V/Cys_dSase Domain
IPR016454 Cysteine desulfurase, NifS Cysteine_dSase_NifS Family
IPR020578 Aminotransferase class-V pyridoxal-phosphate binding site Aminotrans_V_PyrdxlP_BS Binding_site
IPR010240 Cysteine desulfurase Cys_deSase Family

1 Transcripts

DB identifier Gene
FBtr0080290 CG12264