Function
Processes
Occupies the Csy ribonucleoprotein complex and prevents productive R-loop formation. Inhibitory occupancy is stoichiometric; no universal molar-excess threshold is asserted.
Proteins encoded by bacteriophages, archaeal viruses, prophages and other mobile genetic elements suppress host CRISPR-Cas immunity through alternative mechanisms. These include blocking effector assembly or target recognition, sequestering an effector subunit or disabling its nuclease, modifying Cas proteins, cleaving guide RNA, and degrading an immune second messenger. A mobile element may combine several inhibitors, but these are not compulsory sequential steps. Optional anti-CRISPR-associated regulators control inhibitor expression. The examples span bacterial and archaeal hosts; plasmid and conjugative-element inhibitors need not have a viral origin.
The participant taxon envelope includes viral proteins and proteins deposited under bacterial genomes, including prophages and nonviral mobile elements. Hosts are bacteria or archaea as specified for each experimental system; heterologous human-cell editing assays do not extend the native host range. Inhibitory occupancy depends on affinity, concentration, binding stoichiometry and timing: a stoichiometric blocker does not universally require molar excess. Catalytic turnover can permit substoichiometric inhibition in vitro without establishing effective native expression. Families are sampled by tested members; conserved membership alone does not establish all targets or native counterdefense. Host CRISPR functions are described separately in MODULE:crispr_cas_adaptive_immunity. Host self-regulatory ring nucleases and unrelated anti-defense mechanisms remain outside the functional boundary.
knowledge_gaps[0] · provenance
(0/1)knowledge_gaps[1] · provenance
(0/1)knowledge_gaps[2] · provenance
(0/1)✗ none found
No MODULE:anti_crispr_suppression deep-research report alongside the module YAML.
✓ every leaf node grounds to a representative protein.
✓ every declared conforms_to bundle matches its template motif.
10 gene-function check(s) reflected in core functions · 0 conflict(s) · 13 evidence or coverage gap(s) (23 comparison(s))
Retained noncore functions are reported separately; they do not require promotion to core functions. Support from representative genes does not establish conservation across the whole family. Missing reviews or identifiers leave a claim unverified.
| Annoton | Participant | Function | Assessment |
|---|---|---|---|
| acrif8_csy_blocker | ZF40_0031 / acrIF8 (Pectobacterium phage ZF40) UniProtKB:H9C181 Family Representative |
ribonucleoprotein complex binding GO:0043021 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrif2_csy_blocker | orf30 / gp30 (Pseudomonas phage D3112) UniProtKB:Q6TM72 Family Representative |
nucleic acid mimicry-based competitive inhibitor activity No function ID |
No Function Id
A gene review exists, but this function lacks a GO identifier. Free-text chemistry is not automatically compared. |
| acriia4_dna_mimic | acrIIA4 (Listeria monocytogenes prophage) UniProtKB:A0A247D711 Family Representative |
DNA mimicry-based competitive occlusion of the Cas9 PAM-recognition site No function ID |
No Function Id
A gene review exists, but this function lacks a GO identifier. Free-text chemistry is not automatically compared. |
| acriic2_assembly_inhibitor | acrIIC2 (Neisseria meningitidis) UniProtKB:A0A425B3G2 Gene |
Cas9 ribonucleoprotein assembly inhibitor activity GO:0140721 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrif3_cas3_sequestration | JBD5_035 / acrIF3 (Pseudomonas phage JBD5) UniProtKB:L7P7R7 Family Representative |
protein sequestering activity GO:0140311 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acriic1_hnh_blocker | acrIIC1 (Neisseria meningitidis prophage) UniProtKB:A0A2D0TCG3 Family Representative |
nuclease inhibitor activity GO:0140721 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrid1_cas10d_sequesterer | acrID1 / gp02 (Sulfolobus islandicus rod-shaped virus 3) UniProtKB:A0A1B3SN05 Gene |
protein sequestering activity GO:0140311 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrvia1_cas13a_blocker | acrVIA1 (Listeria seeligeri phage phiLS46 gp2) UniProtKB:A0A6P3CWF5 Gene |
Cas13a target-RNA recognition inhibitor activity GO:0140721 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrva1_crrna_nuclease | acrVA1 (Moraxella bovoculi) UniProtKB:A0A5H1ZR47 Family Representative |
RNA endonuclease activity GO:0004521 |
Annotation Supported
A retained annotation or curated replacement supports this function, but core_functions does not yet reflect it. |
| acriii1_ring_nuclease | orf114 / gp29 / AcrIII-1 (Sulfolobus islandicus rod-shaped virus 1) UniProtKB:Q8QL27 Gene |
cyclic oligoadenylate ring nuclease activity No function ID |
No Function Id
A gene review exists, but this function lacks a GO identifier. Free-text chemistry is not automatically compared. |
| acrva5_cas12a_acetyltransferase | acrVA5 / AAX07_09540 (Moraxella bovoculi) UniProtKB:A0A0U2B867 Gene |
Cas12a lysine acetyltransferase activity GO:0061733 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| aca2_repressor | ZF40_0030 / aca2 (Pectobacterium phage ZF40) UniProtKB:H9C180 Family Representative |
DNA-binding transcription repressor activity GO:0001217 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| aca2_translation_repressor | ZF40_0030 / aca2 (Pectobacterium phage ZF40) UniProtKB:H9C180 Family Representative |
RNA binding GO:0003723 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| aca2_translation_repressor:required_function | ZF40_0030 / aca2 (Pectobacterium phage ZF40) UniProtKB:H9C180 Family Representative |
DNA-binding transcription repressor activity GO:0001217 |
Core Supported
The GO molecular function is reflected in core_functions (exact term or a reviewed subclass). |
| acrif8_csy_blocker | AcrF8 (AcrIF8) anti-CRISPR family InterPro:IPR057730 Family |
ribonucleoprotein complex binding GO:0043021 |
Family Review Missing
No supported structured family review is available for InterPro:IPR057730. |
| acrif2_csy_blocker | AcrF2 anti-CRISPR family InterPro:IPR057728 Family |
nucleic acid mimicry-based competitive inhibitor activity No function ID |
No Function Id
The family function has no GO identifier for comparison; prose is not matched. |
| acriia4_dna_mimic | AcrIIA4-like anti-CRISPR family InterPro:IPR056215 Family |
DNA mimicry-based competitive occlusion of the Cas9 PAM-recognition site No function ID |
No Function Id
The family function has no GO identifier for comparison; prose is not matched. |
| acrif3_cas3_sequestration | AcrF3-like Cas3 inhibitor family InterPro:IPR049085 Family |
protein sequestering activity GO:0140311 |
Family Review Missing
No supported structured family review is available for InterPro:IPR049085. |
| acriic1_hnh_blocker | AcrIIC1 anti-CRISPR family InterPro:IPR064626 Family |
nuclease inhibitor activity GO:0140721 |
Family Review Missing
No supported structured family review is available for InterPro:IPR064626. |
| acrva1_crrna_nuclease | AcrVA1-like anti-CRISPR family InterPro:IPR064663 Family |
RNA endonuclease activity GO:0004521 |
Family Review Missing
No supported structured family review is available for InterPro:IPR064663. |
| aca2_repressor | Aca2/YdiL-like anti-CRISPR-associated repressor family InterPro:IPR015060 Family |
DNA-binding transcription repressor activity GO:0001217 |
Family Review Missing
No supported structured family review is available for InterPro:IPR015060. |
| aca2_translation_repressor | Aca2/YdiL-like anti-CRISPR-associated repressor family InterPro:IPR015060 Family |
RNA binding GO:0003723 |
Family Review Missing
No supported structured family review is available for InterPro:IPR015060. |
| aca2_translation_repressor:required_function | Aca2/YdiL-like anti-CRISPR-associated repressor family InterPro:IPR015060 Family |
DNA-binding transcription repressor activity GO:0001217 |
Family Review Missing
No supported structured family review is available for InterPro:IPR015060. |
11 complete review(s) · 2 with deep research · 0 missing review · 11 reviewed but lacking deep research
| Gene | Review | Complete | Deep research |
|---|---|---|---|
| 114 Q8QL27 | ✓ | 3/4 | ✗ |
| aca2 H9C180 | ✓ | ✓ | ✓ |
| AcrF8 H9C181 | ✓ | ✓ | ✓ |
| acrID1 A0A1B3SN05 | ✓ | ✓ | ✗ |
| acrIF3 L7P7R7 | ✓ | ✓ | ✗ |
| acrIIA2 A0A059T5F6 | ✓ | ✓ | ✗ |
| acrIIA4 A0A247D711 | ✓ | ✓ | ✗ |
| acrIIC1 A0A2D0TCG3 | ✓ | ✓ | ✗ |
| acrIIC2 A0A425B3G2 | ✓ | ✓ | ✗ |
| acrVA1 A0A5H1ZR47 | ✓ | ✓ | ✗ |
| acrVA5 A0A0U2B867 | ✓ | 0/0 | ✗ |
| acrVIA1 A0A6P3CWF5 | ✓ | ✓ | ✗ |
| orf30 Q6TM72 | ✓ | ✓ | ✗ |
A realization uses a compatible inhibitor and susceptible host target. These variants are alternatives that may coexist, not an obligate series; the AcrIII-1 branch additionally requires a permissive expression context.
AcrIF8 uses protein and guide-RNA contacts to inhibit the tested type I-F complex.
Occupies the Csy ribonucleoprotein complex and prevents productive R-loop formation. Inhibitory occupancy is stoichiometric; no universal molar-excess threshold is asserted.
DNA mimicry can inhibit distinct class 1 surveillance systems, with effector-specific susceptibility.
Prevents target-DNA engagement by susceptible surveillance complexes; type I-F and selected type I-C activity are compatible with one inhibitor.
A DNA mimic blocks target recognition and access to a nuclease pocket in RNA-loaded SpyCas9.
Inhibits productive target binding by susceptible RNA-loaded Cas9; this is a time- and effector-dependent mechanism, not universal reversal of already bound Cas9.
The LP-101 representative is an ortholog-based example of a separately characterized DNA-mimic family.
A distinct AcrIIA2 family converges on Cas9 target-site occlusion. Sequence identity and target specificity must be checked for individual orthologs.
Binding apo-Cas9 prevents effector ribonucleoprotein assembly, an alternative to attacking an assembled effector.
Acts before a functional Cas9–guide complex forms; it need not first block target-DNA recognition.
In the tested type I-F system a separate nuclease-helicase is sequestered. This does not describe all class 1 effector architectures.
AcrIF3 binds the type I-F Cas2/3 nuclease-helicase and prevents productive recruitment to the target-bound Csy complex. DNA recognition can remain intact.
A catalytic-domain inhibitor can preserve target occupancy while inhibiting cleavage.
Suppresses cleavage by susceptible Cas9 proteins; broad activity across tested orthologs is not universal inhibition of all Cas9 enzymes.
A viral inhibitor disrupts subtype I-D effector assembly by trapping Cas10d in a nonfunctional oligomer.
Sequesters a large subunit whose HD nuclease and polymerase-like architecture differ from the separate type I-F Cas2/3 recruitment target. The completed target-bound effector complex resists inhibition under the tested conditions.
Type VI-A counterdefense inhibits an RNA-targeting immune effector rather than a DNA nuclease.
Prevents both target-RNA recognition and activation of collateral RNA cleavage in the susceptible Cas13a system. Native specificity and the phiLS46 sequence distinguish it from unrelated proteins sharing an AcrVIA name.
Guide cleavage and PAM-pocket interference inhibit susceptible Cas12a complexes through overlapping mechanisms.
Truncates the targeting region of Cas12a-bound crRNA and can act under substoichiometric assay conditions. The retained 5-prime fragment means the product is not simply apo-Cas12a; irreversibility in every assay context is not asserted.
cA4 degradation can dampen the cA4-dependent accessory-defense branch of type III systems. It does not abolish every type III activity: direct RNA cleavage, Cas10 nuclease activity and other cyclic-oligonucleotide specificities are distinct.
Established cA4 chemistry provides a conditional suppression capability. Its contribution during native viral infection remains disputed, so no unconditional GO:0098672 process assertion is attached to this representative.
Catalytic transfer of an acetyl group blocks target recognition without requiring permanent occupancy of the effector.
Covalently modifies a Cas protein instead of destroying it. Inhibition depends on the susceptible lysine and can be reversed enzymatically; GNAT-like fold membership does not establish anti-CRISPR function.
The ZF40 acrIF8–aca2 locus couples inhibitor expression to a regulator that represses its own operon at transcriptional and translational levels. The loop regulates expression rather than sensing whether Cas inhibition has succeeded. Other loci may lack Aca2 or use distinct regulators.
Controls the abundance of the ZF40 AcrIF8 inhibitor through negative feedback on its shared operon. Aca2 is not itself a Cas inhibitor and need not sense successful immune suppression.
RNA recognition limits translation from the regulated transcript; this mode complements promoter repression in the characterized Aca2 system.