5VGB


Conserved Protein Domain Family
AcrIIC1

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cd22213: AcrIIC1 
Click on image for an interactive view with Cn3D
Anti-CRISPR type II subtype C1
AcrIIC1 was discovered via a guilt-by association (GBA) approach, which was based on the strong co-occurrence and clustering of acr and anti-CRISPR associated (aca) genes through proximity and homology searches. Subsequent structural and biochemical work has shown that AcrIIC1 is a broad-spectrum type II-C anti-CRISPR, inhibiting divergent Cas9 orthologs both in vitro and in vivo. AcrIIC1 interacts directly with the Cas9 HNH domain and blocks DNA cleavage via trapping it on its DNA target in a catalytically inactivated state. Type IIC CRISPR-Cas systems are the simplest of the type II systems, employing only three Cas proteins, Cas9, Cas1, and Cas2. Almost all type II Acrs characterized to date directly interact with the Cas9 endonuclease, although by distinct mechanisms. The type II CRISPR/Cas subtype has a distinct crRNA-guided surveillance complex encoded by cas9 (formerly csn1), cas1, cas2, and csn2 (for type IIA) or cas4 (for type IIB) genes, all located in a single transcriptional unit directly upstream of the CRISPR locus. Cleavage of the DNA target in type II systems is carried out by Cas9 which is an RNA-guided double-stranded DNase with two independent nuclease domains, HNH and RuvC. Due to the reliance of the type II system on a single protein for function, Cas9 homologs derived from different subtypes and species have been utilized for numerous gene editing applications. CRISPR-Cas immune systems are used by certain prokaryotes and archaea to resist the invasion of foreign nucleic acids such as phages or plasmids. Anti-CRISPRs are small proteins which are the natural inhibitors for CRISPR-Cas systems; encoded on bacterial and archaeal viruses, they allow the virus to evade host CRISPR-Cas systems. The CRISPR-Cas-mediated adaptive immune response can be divided into three steps, including the acquisition of spacer derived from invading nucleic acids, crRNA processing, and target degradation. Theoretically, Acr proteins could suppress any step to disrupt the CRISPR-Cas system. Acr proteins are diverse with no common sequence or structural motif, and they inhibit a wide range of CRISPR-Cas systems with various inhibition mechanisms. CRISPR-Cas systems are divided into two classes (1 and 2) and six types (class 1: types I, III and IV; class 2: types II, V and VI). Class 2 systems employ a single multi-domain effector Cas9 protein complex that performs target recognition and cleavage. Acr families are named for their type and subtype which are numbered sequentially as they are discovered.
Links
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Statistics
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PSSM-Id: 439322
Aligned: 15 rows
Threshold Bit Score: 88.1686
Created: 13-Oct-2021
Updated: 17-Oct-2022
Structure
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Program:
Drawing:
Aligned Rows:
 
Cas9 binding
Conserved site includes 20 residues -Click on image for an interactive view with Cn3D
Feature 1:Cas9 binding site [polypeptide binding site]
Evidence:
  • Structure:5VGB: Bacteriophage AcrIIC1 in complex with Neisseria meningitidis Cas9; contact at 4A.
  • Comment:AcrIIC1 interacts directly with the HNH domain of Cas9 and blocks DNA cleavage by trapping it on its DNA target in a catalytically inactivated state.

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1         #    #      ####                  #   #  #       ####                          
5VGB_B         4 KTYKIGKNAG---YDGCGLCLAAISENEAIKVKYLRDICPDYDg------DDKAEDwlr--wgtDSRVKAAALEMEQ-YA 71  Neisseria menin...
WP_094837751   1 MIYSIPESLQd-sHDGEEWAIATILGGRVVALRYLADVAPDLEli----ePAIKEW--------LASNPIELRELQA-LG 66  Bordetella geno...
WP_094837162   1 MIYPIPESLQd-sHDGDEWAIGALLGGRVVALRYISDIAPHIAle----aQPITEW--------LHSDPLELRELHA-LG 66  Bordetella geno...
WP_019939893   5 TTFPLPDNLAr-eRIETGWALAAISGNQIAAVREFRRLSPQVAqhlpigaEQAAEVirr--wldTLPASSVVDELQQ-LG 80  Bordetella sp. ...
WP_126708169   2 NTYPIPESLAg-sYRGDGWALAATLNGQVVAIRYISEIAPGIAeq----lEGPHASlfvkqwlgTLEAMSVVRELQA-LG 75  Candidimonas sp...
WP_086014401   2 NVFKVPQSLAd-kYHGAGYALAATVAGQLVDIVYLADMLPDFGg-----qDGPTRAdaqt-aidEPVLAPTVRHLQA-LG 73  Verminephrobact...
WP_028357638   3 EVFKLKPELVt--YKGCGWALACIKDGEIIDLTYVRDLGIEEYde---nfDGLEPEiiyydvvaSQACKEVAYRYEE-MG 76  Brackiella oedi...
OGS91742       3 NILKIPDALEs-kYHGCGIAIASVTGGQIVNLVYLRDVLEEFDd------EDGAALpal---ldDARLGPTVRLLQS-TG 71  Gallionellales ...
ADV01251      50 NVYPIPETLAa-kYHGAGHALAAVTGGQIVDLVYIEDALLDYDa------DAPGALaaa---idDQRLAPTVRRLQA-LG 118 Alicycliphilus ...
WP_066156305   3 EHYNLAGTAVedqYKGAGYAFLVVENGEFTKLIYENPECPPVAk------DLSEDEil----klFIENSVDFYELEKnKG 72  Bacillus krulwi...
Feature 1             #       #### # #
5VGB_B        72 YTSVGMA------SCWEFVEL 86  Neisseria meningitidis
WP_094837751  67 PVSVGVVgvqgfdQRWRLTEW 87  Bordetella genomosp. 4
WP_094837162  67 PVGVGLVg----tDGIALKWL 83  Bordetella genomosp. 4
WP_019939893  81 RITVGMC------HEGQFLEC 95  Bordetella sp. FB-8
WP_126708169  76 KVSLGMC------RNWEFLEQ 90  Candidimonas sp. SYP-B2681
WP_086014401  74 SVHMGML------SGWAFVEL 88  Verminephrobacter eiseniae
WP_028357638  77 EFTFGLC------SCWEFNVM 91  Brackiella oedipodis
OGS91742      72 DVFVGMC------SCWEFVEL 86  Gallionellales bacterium GWA2_59_43
ADV01251     119 QVSAGMC------GAWEFVEL 133 Alicycliphilus denitrificans BC
WP_066156305  73 KIYSGMC------SCFQFVLP 87  Bacillus krulwichiae

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