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Protein : FBpp0073488 D. melanogaster

Primary Accession  ? Q9VYL1 Organism . Name  Drosophila melanogaster
MD5 Checksum  f65e74f1740115ca9e02a14143bebc97 UniProt Accession  Q9VYL1
UniProt Name  Q9VYL1_DROME GenBank Identifier  AAF48181
Is UniProt Canonical  true Is Fragment  false
Length  572 Molecular Weight  64317
Name  Folylpolyglutamate synthase Secondary Identifier  FBpp0073488

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0030407 CG2543 CG2543 FlyBase D. melanogaster


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


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0 Components

2 Cross References

Source . Name

Subject . Primary Identifier
Dm.13446 UniGene FBpp0073488
NP_572814.1 RefSeq FBpp0073488

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
X 12506515 12509367 1

23 Pathways

Identifier Name
112201 Metabolism
93230 Metabolism of folate and pterines
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
IPR001645 Folylpolyglutamate synthetase Folylpolyglutamate_synth Family
IPR018109 Folylpolyglutamate synthetase, conserved site Folylpolyglutamate_synth_CS Conserved_site
IPR004101 Mur ligase, C-terminal Mur_ligase_C Domain
IPR013221 Mur ligase, central Mur_ligase_cen Domain
IPR023600 Folylpolyglutamate synthase, eukaryota Folylpolyglutamate_synth_euk Family

1 Transcripts

DB identifier Gene
FBtr0073655 CG2543