FBP26/YJL155C Summary Help

Standard Name FBP26
Systematic Name YJL155C
Feature Type ORF, Verified
Description Fructose-2,6-bisphosphatase, required for glucose metabolism; protein abundance increases in response to DNA replication stress (1, 2)
Name Description Fructose BisPhosphatase
Chromosomal Location
ChrX:130643 to 129285 | ORF Map | GBrowse
Note: this feature is encoded on the Crick strand.
Gbrowse
Gene Ontology Annotations All FBP26 GO evidence and references
  View Computational GO annotations for FBP26
Molecular Function
Manually curated
Biological Process
Manually curated
Cellular Component
High-throughput
Regulators 105 genes
Resources
Classical genetics
null
Large-scale survey
null
Resources
49 total interaction(s) for 42 unique genes/features.
Physical Interactions
  • Affinity Capture-MS: 8
  • Affinity Capture-RNA: 1
  • Affinity Capture-Western: 1
  • Two-hybrid: 4

Genetic Interactions
  • Negative Genetic: 19
  • Positive Genetic: 14
  • Synthetic Growth Defect: 2

Resources
Expression Summary
histogram
Resources
Length (a.a.) 452
Molecular Weight (Da) 52,594
Isoelectric Point (pI) 6.79
Localization
Phosphorylation PhosphoGRID | PhosphoPep Database
Structure
Homologs
sequence information
ChrX:130643 to 129285 | ORF Map | GBrowse
Note: this feature is encoded on the Crick strand.
SGD ORF map
Last Update Coordinates: 2011-02-03 | Sequence: 1996-07-31
Subfeature details
Relative
Coordinates
Chromosomal
Coordinates
Most Recent Updates
Coordinates Sequence
CDS 1..1359 130643..129285 2011-02-03 1996-07-31
Retrieve sequences
Analyze Sequence
S288C only
S288C vs. other species
S288C vs. other strains
Resources
External Links All Associated Seq | E.C. | Entrez Gene | Entrez RefSeq Protein | MIPS | Search all NCBI (Entrez) | UniProtKB
Primary SGDIDS000003691
References cited on this page View Complete Literature Guide for FBP26
1) Paravicini G and Kretschmer M  (1992) The yeast FBP26 gene codes for a fructose-2,6-bisphosphatase. Biochemistry 31(31):7126-33
2) Tkach JM, et al.  (2012) Dissecting DNA damage response pathways by analysing protein localization and abundance changes during DNA replication stress. Nat Cell Biol 14(9):966-76