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Protein : FBpp0077198 D. melanogaster

Primary Accession  ? Q9VQW0 Organism . Name  Drosophila melanogaster
MD5 Checksum  bb394e427750b8d2e20e285d47fa71fa UniProt Accession  Q9VQW0
UniProt Name  Q9VQW0_DROME GenBank Identifier  AAF51052
Is UniProt Canonical  true Is Fragment  false
Length  758 Molecular Weight  84356
Name  CG31773 Secondary Identifier  FBpp0077198

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0051773 CG31773 CG31773 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_722953.1 RefSeq FBpp0077198
Dm.33697 UniGene FBpp0077198

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
2L 3911907 3914180 -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

2 Protein Domains

DB identifier Name Short Name Type
IPR001645 Folylpolyglutamate synthetase Folylpolyglutamate_synth Family
IPR013221 Mur ligase, central Mur_ligase_cen Domain

1 Transcripts

DB identifier Gene
FBtr0077509 CG31773