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Protein : FBpp0073676 D. melanogaster

Primary Accession  ? Q9VYA0 Organism . Name  Drosophila melanogaster
MD5 Checksum  8e50e4d34518953ed40c9787035cd62e UniProt Accession  Q9VYA0
UniProt Name  NADE_DROME GenBank Identifier  AAN09333
Is UniProt Canonical  true Is Fragment  false
Length  787 Molecular Weight  87615
Name  Probable glutamine-dependent NAD(+) synthetase Secondary Identifier  FBpp0073676

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Uni Prot Comments Displayer

Protein Sequence Displayer


1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0030512 CG9940 CG9940 FlyBase D. melanogaster


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


Cytoscape Network Displayer



0 Components

3 Cross References

Source . Name

Subject . Primary Identifier
Dm.4895 UniGene FBpp0073676
NP_572913.1 RefSeq FBpp0073676
NP_727727.1 RefSeq FBpp0073676

3 Data Sets

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

1 Ec Numbers

Identifier Description  

3 Locations

Located On . Primary Identifier
Start End Strand
X 13579845 13582436 -1
X 13579845 13582436 -1
X 13579845 13582436 -1

23 Pathways

Identifier Name
112201 Metabolism
28199 Nicotinate metabolism
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
IPR014729 Rossmann-like alpha/beta/alpha sandwich fold Rossmann-like_a/b/a_fold Domain
IPR003010 Carbon-nitrogen hydrolase C-N_Hydrolase Domain
IPR022310 NAD/GMP synthase NAD/GMP_synthase Domain
IPR014445 Glutamine-dependent NAD(+) synthetase Gln-dep_NAD_synthase Family
IPR003694 NAD(+) synthetase NAD_synthase Family

3 Transcripts

DB identifier Gene
FBtr0073844 CG9940
FBtr0073845 CG9940
FBtr0343352 CG9940