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Protein : FBpp0081245 D. melanogaster

Primary Accession  ? Q7KSW3 Organism . Name  Drosophila melanogaster
MD5 Checksum  e05dec87a0dc15608b12ae87dc835593 UniProt Accession  Q7KSW3
UniProt Name  Q7KSW3_DROME GenBank Identifier  AAN13381
Is UniProt Canonical  true Is Fragment  false
Length  237 Molecular Weight  26787
Name  CG31472, isoform B Secondary Identifier  FBpp0081245

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0051472 CG31472 CG31472 FlyBase D. melanogaster


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


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2 Synonyms

0 Components

2 Cross References

Source . Name

Subject . Primary Identifier
NP_731187.1 RefSeq FBpp0081245
Dm.20783 UniGene FBpp0081245

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
TrEMBL data set
Reactome data set  

1 Ec Numbers

Identifier Description  

1 Locations

Located On . Primary Identifier
Start End Strand
3R 3636478 3637255 1

23 Pathways

Identifier Name
112201 Metabolism
133634 Vitamins B6 activation to pyridoxal phosphate
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

5 Protein Domains

DB identifier Name Short Name Type
IPR000659 Pyridoxamine 5'-phosphate oxidase Pyridox_Oxase Family
IPR019740 Pyridoxamine 5'-phosphate oxidase, conserved site Pyridox_Oxase_CS Conserved_site
IPR011576 Pyridoxamine 5'-phosphate oxidase-like, FMN-binding domain Pyridox_Oxase_FMN-bd Domain
IPR019576 Pyridoxine 5'-phosphate oxidase, dimerisation, C-terminal Pyridoxamine_oxidase_dimer_C Domain
IPR012349 FMN-binding split barrel Split_barrel_FMN-bd Domain

1 Transcripts

DB identifier Gene
FBtr0081748 CG31472