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Protein : FBpp0087856 D. melanogaster

Primary Accession  ? Q9U622 Organism . Name  Drosophila melanogaster
MD5 Checksum  aa3d161525ea426081e8e9fce2ffefd6 UniProt Accession  Q9U622
UniProt Name  Q9U622_DROME GenBank Identifier  AAF59140
Is UniProt Canonical  true Is Fragment  false
Length  491 Molecular Weight  54018
Name  Sugar transporter 2 Secondary Identifier  FBpp0087856

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0028562 CG17975 sut2 sugar transporter 2 FlyBase D. melanogaster


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


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0 Components

2 Cross References

Source . Name

Subject . Primary Identifier
NP_524732.1 RefSeq FBpp0087856
Dm.1638 UniGene FBpp0087856

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
TrEMBL data set
Reactome data set  

0 Ec Numbers

1 Locations

Located On . Primary Identifier
Start End Strand
2R 3974945 3976711 1

37 Pathways

Identifier Name
87602 Regulation of Insulin Secretion
89538 Integration of energy metabolism
106046 Carbohydrate metabolism
112201 Metabolism
96904 Metabolism of vitamins and cofactors
99870 Metabolism of water-soluble vitamins and cofactors
108418 Vitamin C (ascorbate) metabolism
113552 Developmental Biology
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
93479 Regulation of beta-cell development
97083 Regulation of gene expression in beta cells
84551 Transcriptional Regulation of White Adipocyte Differentiation
118381 Disease

4 Protein Domains

DB identifier Name Short Name Type
IPR020846 Major facilitator superfamily domain MFS_dom Domain
IPR016196 Major facilitator superfamily domain, general substrate transporter MFS_dom_general_subst_transpt Domain
IPR005828 General substrate transporter Sub_transporter Family
IPR003663 Sugar/inositol transporter Sugar/inositol_transpt Family

1 Transcripts

DB identifier Gene
FBtr0088778 sut2