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Protein : FBpp0086807 D. melanogaster

Primary Accession  ? Q8SZX5 Organism . Name  Drosophila melanogaster
MD5 Checksum  47314ad7e858baefa91befc2d513ff3f UniProt Accession  Q8SZX5
UniProt Name  Q8SZX5_DROME GenBank Identifier  AAM68590
Is UniProt Canonical  true Is Fragment  false
Length  420 Molecular Weight  46827
Name  MIP19477p Secondary Identifier  FBpp0086807

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0033853 CG6145 CG6145 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_725315.1 RefSeq FBpp0086807
Dm.1981 UniGene FBpp0086807

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 9425270 9426793 -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
FBtr0087687 CG6145