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Protein : FBpp0079989 D. melanogaster

Primary Accession  ? Q9VK64 Organism . Name  Drosophila melanogaster
MD5 Checksum  1f4c3e53a4a5964f0265ae7df985718c UniProt Accession  Q9VK64
UniProt Name  Q9VK64_DROME GenBank Identifier  AAF53215
Is UniProt Canonical  true Is Fragment  false
Length  432 Molecular Weight  47776
Name  CG17036, isoform B Secondary Identifier  FBpp0079989

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Genomics

1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0032449 CG17036 CG17036 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
NP_609584.1 RefSeq FBpp0079989
Dm.18082 UniGene FBpp0079989

3 Data Sets

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

0 Ec Numbers

2 Locations


Located On . Primary Identifier
Start End Strand
2L 12699155 12700514 -1
2L 12699155 12700514 -1

24 Pathways

Identifier Name
112201 Metabolism
93230 Metabolism of folate and pterines
77753 Vitamin B1 (thiamin) 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

2 Protein Domains

DB identifier Name Short Name Type
IPR016196 Major facilitator superfamily domain, general substrate transporter MFS_dom_general_subst_transpt Domain
IPR002666 Reduced folate carrier Folate_carrier Family

2 Transcripts

DB identifier Gene
FBtr0080408 CG17036
FBtr0340545 CG17036