Skip to content
DraconiticResearch
Search Sources API
194,161 studies31 sourcesUpdated 29 min ago
Peer-reviewedCC BYJournal of Biological Chemistry

Crystal Structure of Imaginal Disc Growth Factor-2

Abstract

Imaginal disc growth factor-2 (IDGF-2) is a member of a recently described family of Drosophila melanogaster-soluble polypeptide growth factors that promote cell proliferation in imaginal discs. Although their precise mode of action has not been established, IDGFs cooperate with insulin in stimulating the growth of imaginal disc cells. We report the crystal structure of IDGF-2 at 1.3-A resolution. The structure shows the classical (betaalpha)(8) barrel-fold of family 18 glycosyl hydrolases, with an insertion of an alpha + beta domain similar to that of Serratia marcescens chitinases A and B. However, amino acid substitutions in the consensus catalytic sequence of chitinases give IDGF-2 a less negatively charged environment in its putative ligand-binding site and preclude the nucleophilic attack mechanism of chitin hydrolysis. Particularly important is the replacement of Glu by Gln at position 132, which has been shown to abolish enzymatic activity in chitinases. Nevertheless, a modest conservation of residues that participate in oligosaccharide recognition suggests that IDGF-2 could bind carbohydrates, assuming several conformational changes to open the partially occluded binding site. Thus, IDGFs may have evolved from chitinases to acquire new functions as growth factors, interacting with cell surface glycoproteins implicated in growth-promoting processes, such as the Drosophila insulin receptor.

Related

  1. Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII.
    Edvard Wigren, Jean-Marie Bourhis, Inari Kursula +2
    FEBS LettersPeer-reviewedLicence not statedFull text28 citedMolecular biology & gene regulationHAL
  2. Lactate signals through hepatic fibroblast growth factor 21 to facilitate exercise-induced lipid mobilization
    Moslem Hamidi, Rohollah Nikooie, Soheil Aminizadeh +1
    Scientific ReportsPeer-reviewedCC BY-NC-ND 4.0Full textMolecular biology & gene regulationCrossref
  3. Drosophila Heat Shock Factor (HSF) Regulates Developmental Growth by Maintaining the Basal Expression of HSP83/HSP90
    Jinghong J. Tang, Alicia Shipley, Roger P. White +3
    Development (Cambridge, England)Peer-reviewedLicence not statedFull textMolecular biology & gene regulationPMC
  4. Crystal structure of tyrosine-tRNA synthetase from Helicobacter pylori G27
    David Igbalajobi, Jason E. Taylor, Raymond Gao +11
    Acta Crystallographica Section F: Structural Biology CommunicationsPeer-reviewedCC BY 4.0Full textMolecular biology & gene regulationPMC
  5. Crystal Structure of Bacillus subtilis Cysteine Desulfurase SufS and Its Dynamic Interaction with Frataxin and Scaffold Protein SufU.
    Blauenburg B, Mielcarek A, Altegoer F +4
    PLoS ONEPeer-reviewedCC BYFull text33 citedStructural biologyGeneral biologyHAL
BibTeX
@article{varela2026crystal,
  title = {{Crystal Structure of Imaginal Disc Growth Factor-2}},
  author = {Paloma Varela and Andrea Llera and Roy Mariuzza and José Tormo},
  journal = {Journal of Biological Chemistry},
  year = {2026},
  month = sep,
  doi = {10.1074/jbc.m110502200},
  url = {https://hal.science/hal-05768145v1},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Crystal Structure of Imaginal Disc Growth Factor-2
AU  - Paloma Varela
AU  - Andrea Llera
AU  - Roy Mariuzza
AU  - José Tormo
PY  - 2026
DA  - 2026/09/28
JO  - Journal of Biological Chemistry
DO  - 10.1074/jbc.m110502200
UR  - https://hal.science/hal-05768145v1
AB  - Imaginal disc growth factor-2 (IDGF-2) is a member of a recently described family of Drosophila melanogaster-soluble polypeptide growth factors that promote cell proliferation in imaginal discs. Although their precise mode of action has not been established, IDGFs cooperate with insulin in stimulating the growth of imaginal disc cells. We report the crystal structure of IDGF-2 at 1.3-A resolution. The structure shows the classical (betaalpha)(8) barrel-fold of family 18 glycosyl hydrolases, with an insertion of an alpha + beta domain similar to that of Serratia marcescens chitinases A and B. However, amino acid substitutions in the consensus catalytic sequence of chitinases give IDGF-2 a less negatively charged environment in its putative ligand-binding site and preclude the nucleophilic attack mechanism of chitin hydrolysis. Particularly important is the replacement of Glu by Gln at position 132, which has been shown to abolish enzymatic activity in chitinases. Nevertheless, a modest conservation of residues that participate in oligosaccharide recognition suggests that IDGF-2 could bind carbohydrates, assuming several conformational changes to open the partially occluded binding site. Thus, IDGFs may have evolved from chitinases to acquire new functions as growth factors, interacting with cell surface glycoproteins implicated in growth-promoting processes, such as the Drosophila insulin receptor.
SN  - 0021-9258
SN  - 1083-351X
ER  -