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Protein : FBpp0288674 D. melanogaster
Primary Accession  ? B7Z0X1 Organism . Name  Drosophila melanogaster
MD5 Checksum  b76e4af31641fb64cff88933f2f43a1f UniProt Accession  B7Z0X1
UniProt Name  B7Z0X1_DROME GenBank Identifier  ACL82894
Is UniProt Canonical  true Is Fragment  false
Length  467 Molecular Weight  50984
Name  Serine hydroxymethyltransferase Secondary Identifier  FBpp0288674
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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

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Other

2 Synonyms

0 Components

2 Cross References

Identifier
Source . Name
Subject . Primary Identifier
Dm.11053 UniGene FBpp0288674
NP_001138162.1 RefSeq FBpp0288674

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 5808810 -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
FBtr0290235 CG3011




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