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Protein : FBpp0075903 D. melanogaster

Primary Accession  ? Q9VTI0 Organism . Name  Drosophila melanogaster
MD5 Checksum  258738e8f668caad2d48a571aead3f73 UniProt Accession  Q9VTI0
UniProt Name  Q9VTI0_DROME GenBank Identifier  AAF50068
Is UniProt Canonical  true Is Fragment  false
Length  349 Molecular Weight  39370
Name  Methylenetetrahydrofolate reductase Secondary Identifier  FBpp0075903

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Genomics

1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0036157 CG7560 CG7560 FlyBase D. melanogaster

Proteins

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

Interactions

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Other

2 Synonyms

0 Components

2 Cross References

Identifier
Source . Name

Subject . Primary Identifier
NP_648462.1 RefSeq FBpp0075903
Dm.13614 UniGene FBpp0075903

3 Data Sets

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

1 Ec Numbers

Identifier Description
1.5.1.20  

1 Locations


Located On . Primary Identifier
Start End Strand
3L 11418282 11419459 1

23 Pathways

Identifier Name
112201 Metabolism
93230 Metabolism of folate and pterines
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
IPR029041 FAD-linked oxidoreductase-like FAD-linked_oxidoreductase-like Domain
IPR003171 Methylenetetrahydrofolate reductase Mehydrof_redctse Family

1 Transcripts

DB identifier Gene
FBtr0076173 CG7560