View original ARBA rule on UniProt
Assigns EC 1.2.1.75 in the recommended name (displayed as "malonyl CoA reductase (malonate semialdehyde-forming)") to archaeal proteins matching CATH FunFam 3.40.50.720:FF:000411. The FunFam contains both malonyl-CoA reductases and their aspartate-semialdehyde dehydrogenase paralogs, and the rule has no condition that separates them.
Condition-set counts describe the sets recorded in this review, which may omit the full rule.
No domain overlap table is shown: the cached overlap analysis for this version of the review is not available.
Run just analyze-rule ARBA00067001 and re-render to add it.
The rule is right for about half of the proteins it annotates. Of 38 rule-annotated archaeal entries (UniProt, 2026-10-15), 17 match the MCR-type CDD models and are malonyl-CoA reductases, 17 match the archaeal/fungal ASD-type models and are aspartate-semialdehyde dehydrogenases, and 4 match neither. In each genome both paralogs receive the malonyl-CoA reductase annotation. Gene reviews in this repository document both sides: Msed_0709 (the real M. sedula MCR, curated in Swiss-Prot and not rule-annotated) and Msed_1700 (its ASD paralog, misannotated by this rule).
The single condition (FunFam plus Archaea) does not separate the neofunctionalized MCR from the ancestral ASD. The CDD subfamily models separate them cleanly in all 34 classified entries, so adding them as conditions fixes the rule without losing any MCR. NCBIfam TIGR00978 cannot be used: every MCR and ASD in this set carries it.
Incorrect count = entries matching only the ASD-type CDD models (classify_rule_matches.py). The 4 entries with no CDD model are counted neither correct nor incorrect; each comes from a species whose other entry is ASD-type, so they are probably MCRs. The two reviewed MCRs (A4YEN2, Q96YK1) carry curated, not rule, annotation.
Single condition set: CATH FunFam 3.40.50.720:FF:000411 (named "Aspartate-semialdehyde dehydrogenase") AND taxon Archaea. In Sulfolobales the FunFam covers both paralogs of the aspartate-semialdehyde dehydrogenase family: the malonyl-CoA reductase (MCR) of the 3-hydroxypropionate/4-hydroxybutyrate CO2-fixation cycle and the true aspartate-semialdehyde dehydrogenase (ASD) of aspartate-family amino acid synthesis.
The rule is minimal (one domain condition plus taxon). The problem is that it is not specific enough, which ParsimonyEnum does not capture; see annotation_assessments.
The MCR activity is well established for the MCR-type members (purified M. sedula and S. tokodaii enzymes). The literature also establishes that Sulfolobales carry a separate asd paralog in the aspartate-family gene cluster, which this rule annotates as MCR.
Only one domain condition, so there is no overlap to assess.
Restricting to Archaea is reasonable: the crenarchaeal MCR is unrelated to the Chloroflexus enzyme. The error is in the domain condition, not the taxon.
Archaeal MCR evolved by duplication of the aspartate-semialdehyde dehydrogenase gene; the two paralogs coexist in Sulfolobales genomes at different loci, with asd in the aspartate-family amino acid cluster.
17 of 38 rule-annotated archaeal entries are ASD-type by CDD models; TIGR00978 does not separate the paralogs.
id: ARBA00067001
description: Assigns EC 1.2.1.75 in the recommended name (displayed as "malonyl CoA
reductase (malonate semialdehyde-forming)") to archaeal proteins matching CATH FunFam
3.40.50.720:FF:000411. The FunFam contains both malonyl-CoA reductases and their
aspartate-semialdehyde dehydrogenase paralogs, and the rule has no condition that
separates them.
status: COMPLETE
rule_type: ARBA
rule:
rule_id: ARBA00067001
condition_sets:
- number: 1
conditions:
- condition_type: FUNFAM
value: 3.40.50.720:FF:000411
curie: CATH.FunFam:3.40.50.720:FF:000411
label: Aspartate-semialdehyde dehydrogenase
negated: false
- condition_type: TAXON
value: Archaea
curie: NCBITaxon:2157
label: Archaea
negated: false
notes: 'Single condition set: CATH FunFam 3.40.50.720:FF:000411 (named "Aspartate-semialdehyde
dehydrogenase") AND taxon Archaea. In Sulfolobales the FunFam covers both paralogs
of the aspartate-semialdehyde dehydrogenase family: the malonyl-CoA reductase
(MCR) of the 3-hydroxypropionate/4-hydroxybutyrate CO2-fixation cycle and the
true aspartate-semialdehyde dehydrogenase (ASD) of aspartate-family amino acid
synthesis.'
go_annotations: []
protein_name_annotations:
- name_type: RECOMMENDED
ec_numbers:
- 1.2.1.75
catalytic_activity_annotations: []
reviewed_protein_count: 0
unreviewed_protein_count: 38
created_date: '2025-03-21'
modified_date: '2025-03-21'
retrieved_date: '2026-11-10'
source_condition_set_count: 1
entries:
- id: 3.40.50.720:FF:000411
type: FUNFAM
label: Aspartate-semialdehyde dehydrogenase
appears_in_condition_sets:
- 1
review_summary: 'The rule is right for about half of the proteins it annotates. Of
38 rule-annotated archaeal entries (UniProt, 2026-10-15), 17 match the MCR-type
CDD models and are malonyl-CoA reductases, 17 match the archaeal/fungal ASD-type
models and are aspartate-semialdehyde dehydrogenases, and 4 match neither. In each
genome both paralogs receive the malonyl-CoA reductase annotation. Gene reviews
in this repository document both sides: Msed_0709 (the real M. sedula MCR, curated
in Swiss-Prot and not rule-annotated) and Msed_1700 (its ASD paralog, misannotated
by this rule).'
action: MODIFY
action_rationale: 'The single condition (FunFam plus Archaea) does not separate the
neofunctionalized MCR from the ancestral ASD. The CDD subfamily models separate
them cleanly in all 34 classified entries, so adding them as conditions fixes the
rule without losing any MCR. NCBIfam TIGR00978 cannot be used: every MCR and ASD
in this set carries it.'
suggested_modifications:
- Implemented as the curated replacement rule rules/curated/CR-0004.yaml (FunFam AND MCR-type CDD model AND Archaea)
- Require an MCR-type CDD model (cd23940 ASADH_C_MCR or cd24150 ASADH_MCR_N) in the
condition set
- Alternatively add the archaeal/fungal ASD-type CDD models (cd18130, cd02315) as
negative conditions
- Re-check the 4 entries with neither model (A0A8D5U5J5, A0AAT9GNW8, A0AAX4L5L8, Q4J6D4)
after the change
- ARBA00052213 (catalytic activity RHEA:26446) has the identical condition set and
should be fixed in the same way
parsimony:
assessment: ACCEPTABLE
notes: The rule is minimal (one domain condition plus taxon). The problem is that
it is not specific enough, which ParsimonyEnum does not capture; see annotation_assessments.
literature_support:
assessment: MODERATE
notes: The MCR activity is well established for the MCR-type members (purified M.
sedula and S. tokodaii enzymes). The literature also establishes that Sulfolobales
carry a separate asd paralog in the aspartate-family gene cluster, which this
rule annotates as MCR.
supported_by:
- reference_id: PMID:23325803
supporting_text: The two paralogous MCR and ASD enzymes show ∼40% amino acid sequence
identity in the same organism, and their genes mcr and asd have different chromosomal
locations.
- reference_id: PMID:23325803
supporting_text: The asd gene clusters together with threonine synthase, aspartokinase,
and ornithine carbamoyltransferase, among other genes, which is in line with
its role in the biosynthesis of amino acids of the aspartate family.
condition_overlap:
assessment: NONE
notes: Only one domain condition, so there is no overlap to assess.
supported_by: []
taxonomic_scope:
assessment: APPROPRIATE
notes: 'Restricting to Archaea is reasonable: the crenarchaeal MCR is unrelated
to the Chloroflexus enzyme. The error is in the domain condition, not the taxon.'
supported_by: []
annotation_assessments:
- annotation_kind: EC_NUMBER
value: EC:1.2.1.75
label: EC 1.2.1.75 in the recommended name (displayed as "malonyl CoA reductase
(malonate semialdehyde-forming)")
assessment: PARTIALLY_CORRECT
matched_protein_count: 38
incorrect_protein_count: 17
correct_examples:
- A0A031LU45
- A0A1W6JXP6
- A0A2U9IBW6
- A0A2U9IQ94
- A0A4D8S1H1
- A0A510DRG8
- A0A650CK04
- A0A650CYF4
- A0A6A9QEN3
- A0A6A9QJK8
- A0A6N0NWX1
- A0A8F5BTZ9
- A0AAQ4CTM4
- F0NCD9
- F4BA03
- Q97WN3
- W7KXV3
incorrect_examples:
- A0A2U9IP35
- A0A4D8S3J4
- A0A510DUH8
- A0A650CGS8
- A0A650CNP6
- A0A6A9QII6
- A0A8D5U8A4
- A0A8F5BX26
- A0AAQ4CPM1
- A0AAT9GTT2
- A0AAX4L0T0
- A4YHF3
- F0NEZ2
- Q4J8Z0
- Q971Y6
- Q97ZL8
- W7KWJ9
gene_reviews:
- genes/METS5/Msed_1700/Msed_1700-ai-review.yaml
- genes/METS5/Msed_0709/Msed_0709-ai-review.yaml
discriminating_features:
- CDD:cd23940
- CDD:cd24150
- CDD:cd18130
- CDD:cd02315
notes: Incorrect count = entries matching only the ASD-type CDD models (classify_rule_matches.py).
The 4 entries with no CDD model are counted neither correct nor incorrect; each
comes from a species whose other entry is ASD-type, so they are probably MCRs.
The two reviewed MCRs (A4YEN2, Q96YK1) carry curated, not rule, annotation.
supported_by:
- reference_id: file:rules/arba/ARBA00067001/RESULTS.md
supporting_text: 'Every species with an ASD-type entry also has a second entry
that is MCR-type or
unclassified, so in effect the rules name both paralogs of each genome "malonyl-CoA
reductase".'
- reference_id: file:rules/arba/ARBA00067001/RESULTS.md
supporting_text: 'NCBIfam TIGR00978 (asd_EA) is present on all 19 MCR-type and
all 17 ASD-type entries, so
it cannot separate them. The CDD models do, with no entry matching both.'
confidence: 0.5
references:
- id: PMID:23325803
title: Structural basis for a bispecific NADP+ and CoA binding site in an archaeal
malonyl-coenzyme A reductase.
findings:
- statement: Archaeal MCR evolved by duplication of the aspartate-semialdehyde dehydrogenase
gene; the two paralogs coexist in Sulfolobales genomes at different loci, with
asd in the aspartate-family amino acid cluster.
- id: file:rules/arba/ARBA00067001/RESULTS.md
title: 'ARBA00067001 / ARBA00052213: which proteins do they annotate?'
findings:
- statement: 17 of 38 rule-annotated archaeal entries are ASD-type by CDD models;
TIGR00978 does not separate the paralogs.
supported_by:
- reference_id: file:rules/arba/ARBA00067001/RESULTS.md
supporting_text: 'Every species with an ASD-type entry also has a second entry that
is MCR-type or
unclassified, so in effect the rules name both paralogs of each genome "malonyl-CoA
reductase".'