Dci

UniProt ID: Q9W0M0
Organism: Drosophila melanogaster
Review Status: COMPLETE
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Gene Description

Dci (CG13890; also PEC1/PECI) is a Drosophila melanogaster dodecenoyl-CoA delta-isomerase (delta(3),delta(2)-enoyl-CoA isomerase, EC 5.3.3.8), an auxiliary enzyme of unsaturated fatty acid beta-oxidation. It converts (3Z)- or (3E)-enoyl-CoA intermediates - which arise when a double bond of an unsaturated fatty acid reaches the 3,4-position during chain shortening and cannot be handled by the core enoyl-CoA hydratase - into the (2E)-enoyl-CoA that re-enters the standard beta-oxidation spiral. By gene name and sequence Dci corresponds to the peroxisomal-type isomerase (human ECI2 / PECI class) and UniProt annotates it as peroxisomal; Drosophila additionally has a cluster of mitochondrial enoyl-CoA delta-isomerase 1 paralogs (CG4592/CG4594/CG4598) that are the more likely carriers of the mitochondrial ECI1 role. Dci has also been recovered as a hit in a genetic screen for susceptibility to intestinal Vibrio cholerae (Gram-negative) infection.

Existing Annotations Review

GO Term Evidence Action Reason
GO:0005782 peroxisomal matrix
IBA
GO_REF:0000033
ACCEPT
Summary: Phylogenetically inferred peroxisomal matrix localization, the specific compartment for the peroxisomal-type (PECI/ECI2-class) enoyl-CoA isomerase that Dci represents.
Reason: The specific, core location of Dci; consistent with its UniProt peroxisomal assignment and the peroxisome annotations below.
GO:0004165 delta(3)-delta(2)-enoyl-CoA isomerase activity
IBA
GO_REF:0000033
ACCEPT
Summary: Phylogenetically inferred delta(3),delta(2)-enoyl-CoA isomerase activity (EC 5.3.3.8) - the defining molecular function of Dci and the auxiliary isomerase step of unsaturated fatty acid beta-oxidation.
Reason: Core molecular function of Dci, concordant with the EC/UniProt name and the ISS/IEA evidence.
Supporting Evidence:
file:DROME/Dci/Dci-uniprot.txt
Dodecenoyl-CoA delta-isomerase
GO:0006635 fatty acid beta-oxidation
IBA
GO_REF:0000033
ACCEPT
Summary: Phylogenetically inferred participation in fatty acid beta-oxidation - specifically the auxiliary isomerase step that allows unsaturated fatty acids to be fully degraded.
Reason: Core biological process for Dci as an auxiliary enzyme of (unsaturated) fatty acid beta-oxidation.
GO:0004165 delta(3)-delta(2)-enoyl-CoA isomerase activity
IEA
GO_REF:0000120
ACCEPT
Summary: Electronic assignment of the EC 5.3.3.8 delta(3),delta(2)-enoyl-CoA isomerase activity, duplicating the core molecular-function call.
Reason: Core molecular function of Dci.
Supporting Evidence:
file:DROME/Dci/Dci-uniprot.txt
Dodecenoyl-CoA delta-isomerase
GO:0005777 peroxisome
IEA
GO_REF:0000120
ACCEPT
Summary: Electronic peroxisome localization, consistent with the UniProt peroxisomal assignment for the PECI/ECI2-class isomerase.
Reason: Peroxisome is the core compartment for Dci; the peroxisomal matrix is the more specific term.
Supporting Evidence:
file:DROME/Dci/Dci-uniprot.txt
SUBCELLULAR LOCATION: Peroxisome
GO:0005739 mitochondrion
ISS
GO_REF:0000024
KEEP AS NON CORE
Summary: Orthology-based mitochondrion localization. Dci is by name and UniProt a peroxisomal (PECI/ECI2-class) isomerase; the mitochondrial enoyl-CoA delta-isomerase 1 role in Drosophila is more likely carried by the CG4592/CG4594/CG4598 paralog cluster. This ISS call may reflect cross-transfer from those mitochondrial paralogs.
Reason: Uncertain/secondary; Dci's core compartment is the peroxisome. Retained as non-core pending direct evidence of a mitochondrial pool (the mitochondrial ECI1 role is likely a paralog's).
GO:0005777 peroxisome
ISS
GO_REF:0000024
ACCEPT
Summary: Orthology-based peroxisome localization, concordant with the core peroxisomal compartment.
Reason: Peroxisome is the core compartment for Dci.
Supporting Evidence:
file:DROME/Dci/Dci-uniprot.txt
SUBCELLULAR LOCATION: Peroxisome
GO:0004165 delta(3)-delta(2)-enoyl-CoA isomerase activity
ISS
GO_REF:0000024
ACCEPT
Summary: Orthology-based delta(3),delta(2)-enoyl-CoA isomerase activity, duplicating the core molecular-function call.
Reason: Core molecular function of Dci.
Supporting Evidence:
file:DROME/Dci/Dci-uniprot.txt
Dodecenoyl-CoA delta-isomerase
GO:0005777 peroxisome
ISM
PMID:22758915
An inventory of peroxisomal proteins and pathways in Drosoph...
ACCEPT
Summary: Sequence-model (targeting-signal) prediction of peroxisomal localization from the Drosophila peroxisomal-proteome inventory, consistent with the UniProt peroxisomal assignment.
Reason: Peroxisome is the core compartment; the prediction agrees with the UniProt and orthology evidence.
Supporting Evidence:
PMID:22758915
The subcellular localization of five of these predicted peroxisomal proteins was confirmed.
GO:0050829 defense response to Gram-negative bacterium
IMP
PMID:19046341
Genetic analysis of Drosophila melanogaster susceptibility t...
KEEP AS NON CORE
Summary: Mutant-phenotype annotation from a genetic screen for Drosophila susceptibility to intestinal Vibrio cholerae (a Gram-negative pathogen) infection, in which Dci was recovered as a hit. This is an organism-level phenotype indirect to Dci's enzymatic role in lipid metabolism.
Reason: A genuine experimental phenotype but peripheral/indirect to the core isomerase function; likely reflects the metabolic contribution of fatty-acid oxidation to the infection response rather than a dedicated immune role. Retained per the curator's IMP assignment.

Core Functions

delta(3),delta(2)-enoyl-CoA isomerase (EC 5.3.3.8): repositions the double bond of (3Z)/(3E)-enoyl-CoA intermediates to (2E)-enoyl-CoA, the auxiliary step that lets unsaturated fatty acids with double bonds at odd-numbered positions re-enter the beta-oxidation spiral. Dci is the peroxisomal-type (PECI/ECI2-class) isomerase in Drosophila.

Supporting Evidence:
  • file:DROME/Dci/Dci-uniprot.txt
    Dodecenoyl-CoA delta-isomerase

References

Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Combined Automated Annotation using Multiple IEA Methods
An inventory of peroxisomal proteins and pathways in Drosophila melanogaster.
  • Dci is among the Drosophila proteins predicted peroxisomal by targeting-signal analysis in the peroxisomal-proteome inventory.
    "The subcellular localization of five of these predicted peroxisomal proteins was confirmed."
Genetic analysis of Drosophila melanogaster susceptibility to intestinal Vibrio cholerae infection.
  • Dci (CG13890) was recovered in a genetic screen for Drosophila susceptibility to intestinal infection by the Gram-negative pathogen Vibrio cholerae.
    "Gram-negative pathogens"

Suggested Questions for Experts

Q: Is Drosophila Dci exclusively peroxisomal (as UniProt indicates), or does it also contribute a mitochondrial delta(3),delta(2)-enoyl-CoA isomerase pool, and is the mitochondrial ECI1 role instead carried by the CG4592/CG4594/CG4598 paralog cluster?

Suggested Experiments

Experiment: Tagged-protein localization and organelle fractionation of Dci versus the CG4592/CG4594/CG4598 mitochondrial enoyl-CoA delta-isomerase paralogs to assign the mitochondrial versus peroxisomal isomerase steps of unsaturated fatty acid beta-oxidation in the fly.

Hypothesis: Dci provides the peroxisomal delta(3),delta(2)-enoyl-CoA isomerase activity while the CG459x paralogs provide the mitochondrial activity required for the mitochondrial unsaturated-FAO cassette.

📄 View Raw YAML

id: Q9W0M0
gene_symbol: Dci
product_type: PROTEIN
status: COMPLETE
taxon:
  id: NCBITaxon:7227
  label: Drosophila melanogaster
description: >-
  Dci (CG13890; also PEC1/PECI) is a Drosophila melanogaster dodecenoyl-CoA delta-isomerase
  (delta(3),delta(2)-enoyl-CoA isomerase, EC 5.3.3.8), an auxiliary enzyme of unsaturated fatty acid
  beta-oxidation. It converts (3Z)- or (3E)-enoyl-CoA intermediates - which arise when a double bond
  of an unsaturated fatty acid reaches the 3,4-position during chain shortening and cannot be handled
  by the core enoyl-CoA hydratase - into the (2E)-enoyl-CoA that re-enters the standard beta-oxidation
  spiral. By gene name and sequence Dci corresponds to the peroxisomal-type isomerase (human ECI2 /
  PECI class) and UniProt annotates it as peroxisomal; Drosophila additionally has a cluster of
  mitochondrial enoyl-CoA delta-isomerase 1 paralogs (CG4592/CG4594/CG4598) that are the more likely
  carriers of the mitochondrial ECI1 role. Dci has also been recovered as a hit in a genetic screen
  for susceptibility to intestinal Vibrio cholerae (Gram-negative) infection.
existing_annotations:
- term:
    id: GO:0005782
    label: peroxisomal matrix
  evidence_type: IBA
  original_reference_id: GO_REF:0000033
  qualifier: is_active_in
  review:
    summary: >-
      Phylogenetically inferred peroxisomal matrix localization, the specific compartment for the
      peroxisomal-type (PECI/ECI2-class) enoyl-CoA isomerase that Dci represents.
    action: ACCEPT
    reason: >-
      The specific, core location of Dci; consistent with its UniProt peroxisomal assignment and the
      peroxisome annotations below.
- term:
    id: GO:0004165
    label: delta(3)-delta(2)-enoyl-CoA isomerase activity
  evidence_type: IBA
  original_reference_id: GO_REF:0000033
  qualifier: enables
  review:
    summary: >-
      Phylogenetically inferred delta(3),delta(2)-enoyl-CoA isomerase activity (EC 5.3.3.8) - the
      defining molecular function of Dci and the auxiliary isomerase step of unsaturated fatty acid
      beta-oxidation.
    action: ACCEPT
    reason: >-
      Core molecular function of Dci, concordant with the EC/UniProt name and the ISS/IEA evidence.
    supported_by:
    - reference_id: file:DROME/Dci/Dci-uniprot.txt
      supporting_text: "Dodecenoyl-CoA delta-isomerase"
- term:
    id: GO:0006635
    label: fatty acid beta-oxidation
  evidence_type: IBA
  original_reference_id: GO_REF:0000033
  qualifier: involved_in
  review:
    summary: >-
      Phylogenetically inferred participation in fatty acid beta-oxidation - specifically the
      auxiliary isomerase step that allows unsaturated fatty acids to be fully degraded.
    action: ACCEPT
    reason: >-
      Core biological process for Dci as an auxiliary enzyme of (unsaturated) fatty acid
      beta-oxidation.
- term:
    id: GO:0004165
    label: delta(3)-delta(2)-enoyl-CoA isomerase activity
  evidence_type: IEA
  original_reference_id: GO_REF:0000120
  qualifier: enables
  review:
    summary: >-
      Electronic assignment of the EC 5.3.3.8 delta(3),delta(2)-enoyl-CoA isomerase activity,
      duplicating the core molecular-function call.
    action: ACCEPT
    reason: >-
      Core molecular function of Dci.
    supported_by:
    - reference_id: file:DROME/Dci/Dci-uniprot.txt
      supporting_text: "Dodecenoyl-CoA delta-isomerase"
- term:
    id: GO:0005777
    label: peroxisome
  evidence_type: IEA
  original_reference_id: GO_REF:0000120
  qualifier: located_in
  review:
    summary: >-
      Electronic peroxisome localization, consistent with the UniProt peroxisomal assignment for the
      PECI/ECI2-class isomerase.
    action: ACCEPT
    reason: >-
      Peroxisome is the core compartment for Dci; the peroxisomal matrix is the more specific term.
    supported_by:
    - reference_id: file:DROME/Dci/Dci-uniprot.txt
      supporting_text: "SUBCELLULAR LOCATION: Peroxisome"
- term:
    id: GO:0005739
    label: mitochondrion
  evidence_type: ISS
  original_reference_id: GO_REF:0000024
  qualifier: located_in
  review:
    summary: >-
      Orthology-based mitochondrion localization. Dci is by name and UniProt a peroxisomal
      (PECI/ECI2-class) isomerase; the mitochondrial enoyl-CoA delta-isomerase 1 role in Drosophila
      is more likely carried by the CG4592/CG4594/CG4598 paralog cluster. This ISS call may reflect
      cross-transfer from those mitochondrial paralogs.
    action: KEEP_AS_NON_CORE
    reason: >-
      Uncertain/secondary; Dci's core compartment is the peroxisome. Retained as non-core pending
      direct evidence of a mitochondrial pool (the mitochondrial ECI1 role is likely a paralog's).
- term:
    id: GO:0005777
    label: peroxisome
  evidence_type: ISS
  original_reference_id: GO_REF:0000024
  qualifier: located_in
  review:
    summary: >-
      Orthology-based peroxisome localization, concordant with the core peroxisomal compartment.
    action: ACCEPT
    reason: >-
      Peroxisome is the core compartment for Dci.
    supported_by:
    - reference_id: file:DROME/Dci/Dci-uniprot.txt
      supporting_text: "SUBCELLULAR LOCATION: Peroxisome"
- term:
    id: GO:0004165
    label: delta(3)-delta(2)-enoyl-CoA isomerase activity
  evidence_type: ISS
  original_reference_id: GO_REF:0000024
  qualifier: enables
  review:
    summary: >-
      Orthology-based delta(3),delta(2)-enoyl-CoA isomerase activity, duplicating the core
      molecular-function call.
    action: ACCEPT
    reason: >-
      Core molecular function of Dci.
    supported_by:
    - reference_id: file:DROME/Dci/Dci-uniprot.txt
      supporting_text: "Dodecenoyl-CoA delta-isomerase"
- term:
    id: GO:0005777
    label: peroxisome
  evidence_type: ISM
  original_reference_id: PMID:22758915
  qualifier: located_in
  review:
    summary: >-
      Sequence-model (targeting-signal) prediction of peroxisomal localization from the Drosophila
      peroxisomal-proteome inventory, consistent with the UniProt peroxisomal assignment.
    action: ACCEPT
    reason: >-
      Peroxisome is the core compartment; the prediction agrees with the UniProt and orthology
      evidence.
    supported_by:
    - reference_id: PMID:22758915
      supporting_text: "The subcellular localization of five of \nthese predicted peroxisomal proteins was confirmed."
      full_text_unavailable: true
- term:
    id: GO:0050829
    label: defense response to Gram-negative bacterium
  evidence_type: IMP
  original_reference_id: PMID:19046341
  qualifier: involved_in
  review:
    summary: >-
      Mutant-phenotype annotation from a genetic screen for Drosophila susceptibility to intestinal
      Vibrio cholerae (a Gram-negative pathogen) infection, in which Dci was recovered as a hit. This
      is an organism-level phenotype indirect to Dci's enzymatic role in lipid metabolism.
    action: KEEP_AS_NON_CORE
    reason: >-
      A genuine experimental phenotype but peripheral/indirect to the core isomerase function; likely
      reflects the metabolic contribution of fatty-acid oxidation to the infection response rather
      than a dedicated immune role. Retained per the curator's IMP assignment.
references:
- id: GO_REF:0000024
  title: Manual transfer of experimentally-verified manual GO annotation data to orthologs
    by curator judgment of sequence similarity
  findings: []
- id: GO_REF:0000033
  title: Annotation inferences using phylogenetic trees
  findings: []
- id: GO_REF:0000120
  title: Combined Automated Annotation using Multiple IEA Methods
  findings: []
- id: PMID:22758915
  title: An inventory of peroxisomal proteins and pathways in Drosophila melanogaster.
  findings:
  - statement: Dci is among the Drosophila proteins predicted peroxisomal by targeting-signal analysis
      in the peroxisomal-proteome inventory.
    supporting_text: "The subcellular localization of five of \nthese predicted peroxisomal proteins was confirmed."
    full_text_unavailable: true
  reference_review:
    relevance: MEDIUM
    correctness: VERIFIED
    review_notes: "Computational peroxisomal-proteome inventory; source of the ISM peroxisome
      prediction. Abstract-only in cache. Consistent with the UniProt peroxisomal assignment for Dci."
- id: PMID:19046341
  title: Genetic analysis of Drosophila melanogaster susceptibility to intestinal Vibrio
    cholerae infection.
  findings:
  - statement: Dci (CG13890) was recovered in a genetic screen for Drosophila susceptibility to
      intestinal infection by the Gram-negative pathogen Vibrio cholerae.
    supporting_text: "Gram-negative pathogens"
    full_text_unavailable: true
  reference_review:
    relevance: LOW
    correctness: VERIFIED
    review_notes: "Vibrio cholerae susceptibility screen; basis for the (non-core) defense-response
      IMP annotation. The connection to Dci's enzymatic function is indirect."
core_functions:
- description: >-
    delta(3),delta(2)-enoyl-CoA isomerase (EC 5.3.3.8): repositions the double bond of (3Z)/(3E)-enoyl-CoA
    intermediates to (2E)-enoyl-CoA, the auxiliary step that lets unsaturated fatty acids with double
    bonds at odd-numbered positions re-enter the beta-oxidation spiral. Dci is the peroxisomal-type
    (PECI/ECI2-class) isomerase in Drosophila.
  supported_by:
  - reference_id: file:DROME/Dci/Dci-uniprot.txt
    supporting_text: "Dodecenoyl-CoA delta-isomerase"
  molecular_function:
    id: GO:0004165
    label: delta(3)-delta(2)-enoyl-CoA isomerase activity
  directly_involved_in:
  - id: GO:0006635
    label: fatty acid beta-oxidation
  locations:
  - id: GO:0005777
    label: peroxisome
  - id: GO:0005782
    label: peroxisomal matrix
proposed_new_terms: []
suggested_questions:
- question: >-
    Is Drosophila Dci exclusively peroxisomal (as UniProt indicates), or does it also contribute a
    mitochondrial delta(3),delta(2)-enoyl-CoA isomerase pool, and is the mitochondrial ECI1 role
    instead carried by the CG4592/CG4594/CG4598 paralog cluster?
suggested_experiments:
- description: >-
    Tagged-protein localization and organelle fractionation of Dci versus the CG4592/CG4594/CG4598
    mitochondrial enoyl-CoA delta-isomerase paralogs to assign the mitochondrial versus peroxisomal
    isomerase steps of unsaturated fatty acid beta-oxidation in the fly.
  hypothesis: >-
    Dci provides the peroxisomal delta(3),delta(2)-enoyl-CoA isomerase activity while the CG459x
    paralogs provide the mitochondrial activity required for the mitochondrial unsaturated-FAO cassette.