NCBI Home Page NCBI Site Search page NCBI Guide that lists and describes the NCBI resources
Conserved domains on  [gi|74225569|dbj|BAE21635|]
View 

unnamed protein product [Mus musculus]

Protein Classification

yippee-like protein( domain architecture ID 41214)

yippee-like protein may contain zinc-finger-like, metal-binding domain; similar to the C-terminal domain of retinoic acid-inducible gene (RIG)-I-like receptors

Gene Ontology:  GO:0046872
PubMed:  15556292

Graphical summary

 Zoom to residue level

show extra options »

Show site features     Horizontal zoom: ×

List of domain hits

Name Accession Description Interval E-value
RLR_C_like super family cl13152
C-terminal domain of Retinoic acid-inducible gene (RIG)-I-like Receptors, Cereblon (CRBN), and ...
20-110 3.17e-05

C-terminal domain of Retinoic acid-inducible gene (RIG)-I-like Receptors, Cereblon (CRBN), and similar protein domains; Retinoic acid-inducible gene (RIG)-I-like Receptors (RLRs) are cytoplasmic RNA receptors that recognize non-self RNA and act as molecular sensors to detect viral pathogens. They play crucial roles in innate antiviral responses, including the production of proinflammatory cytokines and type I interferon. There are three RLRs in vertebrates, RIG-I, LGP2, and MDA5. They are characterized by a central DExD/H-box helicase domain and a C-terminal domain, both of which are responsible for binding viral RNA. Cereblon is part of an E3 ubiquitin ligase complex, together with damaged DNA binding protein 1 (DDB1), CUL4A and ROC1. Cereblon interacts directly with DDB1, although the C-terminal domain characterized here does not contribute to that interaction. The C-terminal domain of Cereblon was shown to contain the binding site for thalidomide and its analogs, a class of teratogenic drugs that exhibit an antiproliferative effect on myelomas. Mutations in CRBN, some of which map onto the C-terminal domain, were associated with autosomal recessive mental retardation, which may have to do with interactions between CRBN and ion channels in the brain. RLRs and Cereblon contain a common conserved zinc binding site in their C-terminal domains.


The actual alignment was detected with superfamily member pfam03226:

Pssm-ID: 472430  Cd Length: 99  Bit Score: 39.61  E-value: 3.17e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 74225569    20 TYSCIHCRAHLANHDELISksfQGSQGRAYLFNSVvnvgcgpaeERVLLTGLHAVAD-----------IYCENCKTTLGW 88
Cdd:pfam03226   2 VFQCKRCNTILGDSLALVS---SGRELNTIVLKKV---------TRNVVVGKELVTSesgfddctyspLFCAGCGAVLGR 69
                          90       100
                  ....*....|....*....|..
gi 74225569    89 KYEHAFEsSQKYKEGKFIIELA 110
Cdd:pfam03226  70 KYRSTPE-ELDYKRGLFCLETD 90
 
Name Accession Description Interval E-value
Yippee-Mis18 pfam03226
Yippee zinc-binding/DNA-binding /Mis18, centromere assembly; This family includes both ...
20-110 3.17e-05

Yippee zinc-binding/DNA-binding /Mis18, centromere assembly; This family includes both Yippee-type proteins and Mis18 kinetochore proteins. Yippee are putative zinc-binding/DNA-binding proteins. Mis18 are proteins involved in the priming of centromeres for recruiting CENP-A. Mis18-alpha and beta form part of a small complex with Mis18-binding protein. Mis18-alpha is found to interact with DNA de-methylases through a Leu-rich region located at its carboxyl terminus. This entry also includes the CULT domain proteins such as Cereblon.


Pssm-ID: 427204  Cd Length: 99  Bit Score: 39.61  E-value: 3.17e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 74225569    20 TYSCIHCRAHLANHDELISksfQGSQGRAYLFNSVvnvgcgpaeERVLLTGLHAVAD-----------IYCENCKTTLGW 88
Cdd:pfam03226   2 VFQCKRCNTILGDSLALVS---SGRELNTIVLKKV---------TRNVVVGKELVTSesgfddctyspLFCAGCGAVLGR 69
                          90       100
                  ....*....|....*....|..
gi 74225569    89 KYEHAFEsSQKYKEGKFIIELA 110
Cdd:pfam03226  70 KYRSTPE-ELDYKRGLFCLETD 90
 
Name Accession Description Interval E-value
Yippee-Mis18 pfam03226
Yippee zinc-binding/DNA-binding /Mis18, centromere assembly; This family includes both ...
20-110 3.17e-05

Yippee zinc-binding/DNA-binding /Mis18, centromere assembly; This family includes both Yippee-type proteins and Mis18 kinetochore proteins. Yippee are putative zinc-binding/DNA-binding proteins. Mis18 are proteins involved in the priming of centromeres for recruiting CENP-A. Mis18-alpha and beta form part of a small complex with Mis18-binding protein. Mis18-alpha is found to interact with DNA de-methylases through a Leu-rich region located at its carboxyl terminus. This entry also includes the CULT domain proteins such as Cereblon.


Pssm-ID: 427204  Cd Length: 99  Bit Score: 39.61  E-value: 3.17e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 74225569    20 TYSCIHCRAHLANHDELISksfQGSQGRAYLFNSVvnvgcgpaeERVLLTGLHAVAD-----------IYCENCKTTLGW 88
Cdd:pfam03226   2 VFQCKRCNTILGDSLALVS---SGRELNTIVLKKV---------TRNVVVGKELVTSesgfddctyspLFCAGCGAVLGR 69
                          90       100
                  ....*....|....*....|..
gi 74225569    89 KYEHAFEsSQKYKEGKFIIELA 110
Cdd:pfam03226  70 KYRSTPE-ELDYKRGLFCLETD 90
 
Blast search parameters
Data Source: Precalculated data, version = cdd.v.3.21
Preset Options:Database: CDSEARCH/cdd   Low complexity filter: no  Composition Based Adjustment: yes   E-value threshold: 0.01

References:

  • Wang J et al. (2023), "The conserved domain database in 2023", Nucleic Acids Res.51(D)384-8.
  • Lu S et al. (2020), "The conserved domain database in 2020", Nucleic Acids Res.48(D)265-8.
  • Marchler-Bauer A et al. (2017), "CDD/SPARCLE: functional classification of proteins via subfamily domain architectures.", Nucleic Acids Res.45(D)200-3.
Help | Disclaimer | Write to the Help Desk
NCBI | NLM | NIH