id: pn_mapping_set:mitochondrial_proteostasis
label: Mitochondrial proteostasis PN mappings
references:
- proteostasis-workbook-2024
- proteostasis-ms1
notes: >-
  Curated PN-to-GO mappings for mitochondrial proteostasis transport and chaperone entries.
subject_curations:
- subject_code: Mitochondrial proteostasis
  subject_level: branch
  curation_status: no_mapping
  rationale: Reviewed as a top-level PN branch. This is a systems/taxonomy umbrella, not a
    direct GO assertion; narrower child curations carry any propagating GO mappings.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone
  subject_level: class
  curation_status: no_mapping
  rationale: >-
    This PN class is too heterogeneous for a single safe GO mapping. In the
    workbook it mixes HSP70, HSP60, and HSP90 systems, small
    intermembrane-space chaperones, membrane-protein chaperones, and other
    mitochondrial-specific factors.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
  notes: >-
    Gene-level projection exposed the problem with earlier propagation to GO
    mitochondrial intermembrane space chaperone complex: it incorrectly
    pulled in mixed mitochondrial-chaperone genes such as HSPA9, HSPD1,
    TRAP1, PHB1, and PHB2. Keep the class explicit and unmapped rather than
    forcing a misleading umbrella GO target.
- subject_code: Mitochondrial proteostasis|Folding enzyme
  subject_level: class
  curation_status: no_mapping
  rationale: Reviewed as a broad PN category rather than a specific GO class. The member
    genes span multiple activities, complexes, or contexts, so propagation from this node
    would overstate the shared biology; use narrower child or gene-level curations.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Membrane protein folding
  subject_level: class
  curation_status: no_mapping
  rationale: Reviewed as a broad PN category rather than a specific GO class. The member
    genes span multiple activities, complexes, or contexts, so propagation from this node
    would overstate the shared biology; use narrower child or gene-level curations.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Mitochondrial protein maturation
  subject_level: class
  curation_status: mapped
  target_term:
    id: GO:0034982
    label: mitochondrial protein processing
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN class groups maturation steps for mitochondrial proteins. The GO
    mitochondrial protein processing term captures the shared process-level semantics.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein degradation
  subject_level: class
  curation_status: mapped
  target_term:
    id: GO:0035694
    label: mitochondrial protein catabolic process
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN class groups mitochondrial protein-degradation pathways. GO
    mitochondrial protein catabolic process is the conservative shared target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Protein transport
  subject_level: class
  curation_status: mapped
  target_term:
    id: GO:0015031
    label: protein transport
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    The PN mitochondrial Protein transport class groups protein-targeting and
    import pathways into mitochondria. GO protein transport is the appropriate
    propagation target, while the source class remains mitochondria-specific
    and broader than any single GO transport subtype.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|Chaperone for complex III and LETM1
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a contextual PN bucket. The label is useful for curator triage, but
    no direct GO mapping is appropriate because propagation would add a process, activity,
    or localization not shared cleanly by all members.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP100 disaggregase
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0140545
    label: ATP-dependent protein disaggregase activity
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group denotes mitochondrial HSP100/LON-family disaggregase activity.
    The GO ATP-dependent protein disaggregase activity term is the closest
    molecular-function target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP60 system
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a broad PN category rather than a specific GO class. The member
    genes span multiple activities, complexes, or contexts, so propagation from this node
    would overstate the shared biology; use narrower child or gene-level curations.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP70 system
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a broad PN category rather than a specific GO class. The member
    genes span multiple activities, complexes, or contexts, so propagation from this node
    would overstate the shared biology; use narrower child or gene-level curations.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP90 system
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a broad PN category rather than a specific GO class. The member
    genes span multiple activities, complexes, or contexts, so propagation from this node
    would overstate the shared biology; use narrower child or gene-level curations.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|Membrane protein chaperone
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a contextual PN bucket. The label is useful for curator triage, but
    no direct GO mapping is appropriate because propagation would add a process, activity,
    or localization not shared cleanly by all members.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Chaperone|Small intermembrane space chaperone
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0042719
    label: mitochondrial intermembrane space chaperone complex
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group captures the small intermembrane-space chaperone system
    that stabilizes imported proteins in the mitochondrial intermembrane
    space. The GO cellular-component term for the mitochondrial intermembrane
    space chaperone complex is an appropriate propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|small HSP
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0044183
    label: protein folding chaperone
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group denotes mitochondrial small heat-shock chaperones. Protein
    folding chaperone is the appropriate shared molecular-function term.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
  - file:human/HSPB2/HSPB2-ai-review.yaml
  - file:human/HSPB3/HSPB3-ai-review.yaml
  - file:human/HSPB8/HSPB8-ai-review.yaml
  notes: >-
    The members projected here from proteostasis batch 5 (HSPB2, HSPB3, HSPB8)
    are ATP-independent small-HSP holdases whose gene-level core MF is GO:0051082
    (unfolded protein binding); the broad GO:0044183 is retained as the shared
    propagation target. Caveat on PN placement: gene-level review localizes these
    sHSPs primarily to the cytosol/sarcomere (HSPB2/HSPB3 muscle, HSPB8 CASA),
    so the "mitochondrial" branch context should be treated as PN systems
    metadata rather than evidence of a mitochondrial-matrix chaperone role; the
    chaperone/holdase MF mapping itself is compartment-agnostic and holds.
- subject_code: Mitochondrial proteostasis|Folding enzyme|Peptidyl-prolyl isomerases
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0003755
    label: peptidyl-prolyl cis-trans isomerase activity
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group is the mitochondrial peptidyl-prolyl isomerase branch. The
    matching GO molecular-function term is appropriate for propagation.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Folding enzyme|Protein disulfide isomerases
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0160203
    label: mitochondrial disulfide relay system
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group contains CHCHD4/GFER mitochondrial disulfide-relay factors. The
    GO mitochondrial disulfide relay system process captures the shared mitochondrial
    folding chemistry better than a generic PDI label.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Membrane protein folding|Insertase for helical proteins into the
    outer
    membrane
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0045040
    label: protein insertion into mitochondrial outer membrane
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group covers the machinery that inserts helical membrane proteins
    into the mitochondrial outer membrane. The corresponding GO process term
    protein insertion into mitochondrial outer membrane is an appropriate
    propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Membrane protein folding|MICOS complex
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0061617
    label: MICOS complex
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group denotes MICOS-complex components. The GO MICOS complex
    cellular-component term is the direct target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Membrane protein folding|Sorting and assembly
    machinery outer membrane
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0005741
    label: mitochondrial outer membrane
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group denotes the SAM outer-membrane assembly system. The GO
    mitochondrial outer membrane cellular-component term is a conservative
    propagation target for this assembly-focused bucket.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Mitochondrial protein maturation|Methionine
    deformylation
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0042586
    label: peptide deformylase activity
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN group captures mitochondrial N-terminal methionine deformylation. The
    shared catalytic activity is peptide deformylase activity.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Mitochondrial protein maturation|Processing peptidase
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0017087
    label: mitochondrial processing peptidase complex
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group captures the mitochondrial processing peptidase machinery
    that removes targeting presequences from imported mitochondrial proteins.
    The GO cellular-component term for the mitochondrial processing
    peptidase complex is the best supported propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein
    degradation|Degradation of mitochondrial membrane proteins that fail targeting
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a narrower taxonomy bucket that is already covered by a curated
    parent mapping or by gene-level annotations. No additional direct GO mapping is
    appropriate from this node.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Organelle-specific protein degradation|Intermembrane space protease
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0005758
    label: mitochondrial intermembrane space
  mapping_scope: ok_for_propagation_to_go
  representative_genes:
  - NLN
  - ATP23
  - HTRA2
  rationale: >-
    This PN group captures proteases assigned specifically to the
    mitochondrial intermembrane space. The source bucket is compartmental and
    mechanistic rather than a single shared enzymatic GO class, so the
    mitochondrial intermembrane space cellular-component term is the
    conservative propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein degradation|Matrix
    protease
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0005759
    label: mitochondrial matrix
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group identifies matrix-local protease systems. The source is a
    compartmental proteostasis bucket, so the mitochondrial matrix
    cellular-component term is the conservative propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein degradation|Vms
    pathway
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a narrower taxonomy bucket that is already covered by a curated
    parent mapping or by gene-level annotations. No additional direct GO mapping is
    appropriate from this node.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein degradation|mitoCPR
    pathway
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a narrower taxonomy bucket that is already covered by a curated
    parent mapping or by gene-level annotations. No additional direct GO mapping is
    appropriate from this node.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Organelle-specific protein degradation|mitoTAD
    pathway
  subject_level: group
  curation_status: no_mapping
  rationale: Reviewed as a narrower taxonomy bucket that is already covered by a curated
    parent mapping or by gene-level annotations. No additional direct GO mapping is
    appropriate from this node.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Protein transport|Cytosolic mitochondria import stimulation factor
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0015031
    label: protein transport
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group captures cytosolic factors that stimulate mitochondrial
    import before TOM/TIM route commitment. The source is broader than a
    specific matrix-import pathway, so the conservative propagation target is
    GO protein transport.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Protein transport|Inner membrane import
  subject_level: group
  curation_status: context_only
  target_term:
    id: GO:0044743
    label: protein transmembrane import into intracellular organelle
  mapping_scope: too_broad_to_propagate
  rationale: >-
    In `4.3.11`, inner-membrane import is a group that covers TIM22,
    TIM17/23, PAM-associated matrix import, and related inner-membrane sorting
    routes. The source is useful context for mitochondrial protein import, but
    protein insertion into mitochondrial inner membrane is too specific for all
    descendants because reviewed TIM23/PAM components include matrix-import
    motor and gatekeeper roles. Propagation should come from narrower child
    nodes such as TIM22 complex, TIM23 complex, or OXA1L-mediated insertion.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
  - file:human/PAM16/PAM16-ai-review.yaml
  - file:human/TIMM44/TIMM44-ai-review.yaml
- subject_code: Mitochondrial proteostasis|Protein transport|Outer membrane import
  subject_level: group
  curation_status: mapped
  target_term:
    id: GO:0045040
    label: protein insertion into mitochondrial outer membrane
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN group covers the outer-membrane entry route for mitochondrial
    protein import. The matching GO process protein insertion into
    mitochondrial outer membrane is the best conservative propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP60 system|HSP10
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0044183
    label: protein folding chaperone
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN type denotes mitochondrial HSP10/HSPE co-chaperonins. The shared GO
    function is protein folding chaperone.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP60 system|HSP60
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0140662
    label: ATP-dependent protein folding chaperone
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    The mitochondrial HSP60 PN category corresponds to canonical chaperonins
    that carry out ATP-dependent protein folding. The source label denotes the
    family/system member type rather than the GO molecular-function class
    itself, so propagation scope is the better fit.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Protein transport|Inner membrane import|For
    assembly of inner membrane complexes
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0032977
    label: membrane insertase activity
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN leaf is represented by OXA1L, the mitochondrial inner-membrane
    insertase for assembly of membrane complexes. Membrane insertase activity is the
    best-supported molecular-function target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Protein transport|Inner membrane import|TIMM17/23
    complex
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0005744
    label: TIM23 mitochondrial import inner membrane translocase complex
  mapping_scope: ok_for_propagation_to_go
  rationale: This PN type denotes TIMM17/23 import-complex components. The GO TIM23
    mitochondrial import inner membrane translocase complex term is the direct
    cellular-component target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Protein transport|Inner membrane import|TIMM22 complex
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0042721
    label: TIM22 mitochondrial import inner membrane insertion complex
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN type captures TIMM22-complex components responsible for a
    specific inner-membrane import route. The GO cellular-component term for
    the TIM22 insertion complex is an appropriate propagation target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: >-
    Mitochondrial proteostasis|Protein transport|Outer membrane import|TOMM complex
  subject_level: type
  curation_status: mapped
  target_term:
    id: GO:0005742
    label: mitochondrial outer membrane translocase complex
  mapping_scope: ok_for_propagation_to_go
  rationale: >-
    This PN subtype denotes TOMM-complex component membership for outer-
    membrane import. The source is a component-role category that maps
    naturally to the GO cellular-component term for the mitochondrial outer
    membrane translocase complex.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
- subject_code: Mitochondrial proteostasis|Chaperone|HSP70 system|HSP70 nucleotide exchange
    factor|GRPE subtype
  subject_level: subtype
  curation_status: mapped
  target_term:
    id: GO:0001405
    label: PAM complex, Tim23 associated import motor
  mapping_scope: ok_for_propagation_to_go
  rationale: This mitochondrial GRPE subtype is represented by GRPEL1/GRPEL2, PAM
    import-motor nucleotide-exchange factors. The GO PAM complex term is the direct
    complex-membership target.
  references:
  - proteostasis-workbook-2024
  - proteostasis-ms1
