modENCODE |  Help |  blog

Protein : FBpp0070792 D. melanogaster

Primary Accession  ? Q9W457 Organism . Name  Drosophila melanogaster
MD5 Checksum  a69af1a6676775f8558641d4e127fcc6 UniProt Accession  Q9W457
UniProt Name  Q9W457_DROME GenBank Identifier  AAF46101
Is UniProt Canonical  true Is Fragment  false
Length  537 Molecular Weight  58801
Name  Serine hydroxymethyltransferase Secondary Identifier  FBpp0070792

Publication Counts Displayer

Uni Prot Comments Displayer

Protein Sequence Displayer

Genomics

1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0029823 CG3011 CG3011 FlyBase D. melanogaster

Proteins

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

Interactions

Cytoscape Network Displayer

 

Other

2 Synonyms

0 Components

2 Cross References

Identifier
Source . Name

Subject . Primary Identifier
NP_572278.1 RefSeq FBpp0070792
Dm.11053 UniGene FBpp0070792

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
2.1.2.1  

1 Locations


Located On . Primary Identifier
Start End Strand
X 5807233 5810502 -1

25 Pathways

Identifier Name
112201 Metabolism
93230 Metabolism of folate and pterines
86268 Amino acid and derivative metabolism
97653 Carnitine synthesis
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

5 Protein Domains

DB identifier Name Short Name Type
IPR015424 Pyridoxal phosphate-dependent transferase PyrdxlP-dep_Trfase Domain
IPR015421 Pyridoxal phosphate-dependent transferase, major region, subdomain 1 PyrdxlP-dep_Trfase_major_sub1 Domain
IPR015422 Pyridoxal phosphate-dependent transferase, major region, subdomain 2 PyrdxlP-dep_Trfase_major_sub2 Domain
IPR001085 Serine hydroxymethyltransferase Ser_HO-MeTrfase Family
IPR019798 Serine hydroxymethyltransferase, pyridoxal phosphate binding site Ser_HO-MeTrfase_PLP_BS Binding_site

1 Transcripts

DB identifier Gene
FBtr0070827 CG3011