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Protein : FBpp0112362 D. melanogaster

Primary Accession  ? A8DYC9 Organism . Name  Drosophila melanogaster
MD5 Checksum  a1d6e671d58a73447f55e140e15e124b UniProt Accession  A8DYC9
UniProt Name  A8DYC9_DROME GenBank Identifier  ABV53790
Is UniProt Canonical  true Is Fragment  false
Length  450 Molecular Weight  49921
Name  CG33156, isoform F Secondary Identifier  FBpp0112362

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0053156 CG33156 CG33156 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_001097302.1 RefSeq FBpp0112362
Dm.11518 UniGene FBpp0112362

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
2R 9436115 9440666 -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

4 Protein Domains

DB identifier Name Short Name Type
IPR016064 ATP-NAD kinase-like domain ATP-NAD_kinase_PpnK-typ Domain
IPR017438 Inorganic polyphosphate/ATP-NAD kinase, domain 1 ATP-NAD_kinase_dom_1 Domain
IPR017437 ATP-NAD kinase, PpnK-type, all-beta ATP-NAD_kinase_PpnK-typ_all-b Domain
IPR002504 Inorganic polyphosphate/ATP-NAD kinase PolyP/ATP_NADK Family

1 Transcripts

DB identifier Gene
FBtr0113450 CG33156