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Protein : FBpp0076826 D. melanogaster

Primary Accession  ? Q9VRP4 Organism . Name  Drosophila melanogaster
MD5 Checksum  81566a7aa4448aa75dbad6b8fc83a29a UniProt Accession  Q9VRP4
UniProt Name  Q9VRP4_DROME GenBank Identifier  AAF50749
Is UniProt Canonical  true Is Fragment  false
Length  518 Molecular Weight  57641
Name  Bifunctional phosphopantetheine adenylyltransferase-Dephospho-CoA kinase Secondary Identifier  FBpp0076826

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Genomics

1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0035632 CG10575 Ppat-Dpck Bifunctional Phosphopantetheine adenylyltransferase - Dephospho-CoA kinase FlyBase D. melanogaster

Proteins

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

Interactions

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Other

0 Components

2 Cross References

Identifier
Source . Name

Subject . Primary Identifier
Dm.21607 UniGene FBpp0076826
NP_647985.1 RefSeq FBpp0076826

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
TrEMBL data set http://www.ebi.ac.uk/trembl/
Reactome data set  

2 Ec Numbers

Identifier Description
2.7.1.24  
2.7.7.3  

1 Locations


Located On . Primary Identifier
Start End Strand
3L 5760239 5761859 -1

24 Pathways

Identifier Name
112201 Metabolism
30509 Vitamin B5 (pantothenate) metabolism
98290 Coenzyme A biosynthesis
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
IPR027417 P-loop containing nucleoside triphosphate hydrolase P-loop_NTPase Domain
IPR014729 Rossmann-like alpha/beta/alpha sandwich fold Rossmann-like_a/b/a_fold Domain
IPR004821 Cytidyltransferase-like domain Cyt_trans-like Domain
IPR001977 Dephospho-CoA kinase Depp_CoAkinase Family

1 Transcripts

DB identifier Gene
FBtr0077120 Ppat-Dpck