Overview
| Uniprot ID | Q9H171 |
| Protein Name | Z-DNA-binding protein 1 |
| Gene Name | ZBP1 |
| Organism | Homo sapiens |
Kla Sites from experimental identification
| Position |
Flanking peptide |
| 391 |
PITPSHSKLTPKLET |
Function
Key innate sensor that recognizes and binds Z-RNA structures, which are produced by a number of viruses, such as herpesvirus, orthomyxovirus or flavivirus, and triggers different forms of cell death (PubMed:32200799). ZBP1 acts as an essential mediator of pyroptosis, necroptosis and apoptosis (PANoptosis), an integral part of host defense against pathogens, by activating RIPK3, caspase-8 (CASP8), and the NLRP3 inflammasome (By similarity). Key activator of necroptosis, a programmed cell death process in response to death-inducing TNF family members, via its ability to bind Z-RNA: once activated upon Z-RNA-binding, ZBP1 interacts and stimulates RIPK3 kinase, which phosphorylates and activates MLKL, triggering execution of programmed necrosis (By similarity). In addition to TNF-induced necroptosis, necroptosis can also take place in the nucleus in response to orthomyxoviruses infection: ZBP1 recognizes and binds Z-RNA structures that are produced in infected nuclei by orthomyxoviruses, such as the influenza A virus (IAV), leading to ZBP1 activation, RIPK3 stimulation and subsequent MLKL phosphorylation, triggering disruption of the nuclear envelope and leakage of cellular DNA into the cytosol (PubMed:32200799). ZBP1-dependent cell death in response to IAV infection promotes interleukin-1 alpha (IL1A) induction in an NLRP3-inflammasome-independent manner: IL1A expression is required for the optimal interleukin-1 beta (IL1B) production, and together, these cytokines promote infiltration of inflammatory neutrophils to the lung, leading to the formation of neutrophil extracellular traps (By similarity). In addition to its direct role in driving necroptosis via its ability to sense Z-RNAs, also involved in PANoptosis triggered in response to bacterial infection: component of the AIM2 PANoptosome complex, a multiprotein complex that triggers PANoptosis (By similarity). Also acts as the apical sensor of fungal infection responsible for activating PANoptosis (By similarity). Involved in CASP8-mediated cell death via its interaction with RIPK1 but independently of its ability to sense Z-RNAs (By similarity). In some cell types, also able to restrict viral replication by promoting cell death-independent responses (By similarity). In response to Zika virus infection in neurons, promotes a cell death-independent pathway that restricts viral replication: together with RIPK3, promotes a death-independent transcriptional program that modifies the cellular metabolism via up-regulation expression of the enzyme ACOD1/IRG1 and production of the metabolite itaconate (By similarity). Itaconate inhibits the activity of succinate dehydrogenase, generating a metabolic state in neurons that suppresses replication of viral genomes (By similarity)
Protein Sequence
10
MAQAPADPGR
20
EGHLEQRILQ
30
VLTEAGSPVK
40
LAQLVKECQA
50
PKRELNQVLY
60
RMKKELKVSL
70
TSPATWCLGG
80
TDPEGEGPAE
90
LALSSPAERP
100
QQHAATIPET
110
PGPQFSQQRE
120
EDIYRFLKDN
130
GPQRALVIAQ
140
ALGMRTAKDV
150
NRDLYRMKSR
160
HLLDMDEQSK
170
AWTIYRPEDS
180
GRRAKSASII
190
YQHNPINMIC
200
QNGPNSWISI
210
ANSEAIQIGH
220
GNIITRQTVS
230
REDGSAGPRH
240
LPSMAPGDSS
250
TWGTLVDPWG
260
PQDIHMEQSI
270
LRRVQLGHSN
280
EMRLHGVPSE
290
GPAHIPPGSP
300
PVSATAAGPE
310
ASFEARIPSP
320
GTHPEGEAAQ
330
RIHMKSCFLE
340
DATIGNSNKM
350
SISPGVAGPG
360
GVAGSGEGEP
370
GEDAGRRPAD
380
TQSRSHFPRD
390
IGQPITPSHS
400
KLTPKLETMT
410
LGNRSHKAAE
420
GSHYVDEASH
EGSWWGGGI
Gene Ontology
| Classification |
GO ID |
Description |
| Cellular Component |
GO:0005737 |
cytoplasm |
| Cellular Component |
GO:0005829 |
cytosol |
| Cellular Component |
GO:0005634 |
nucleus |
| Molecular Function |
GO:0003677 |
DNA binding |
| Molecular Function |
GO:0003726 |
double-stranded RNA adenosine deaminase activity |
| Molecular Function |
GO:0003725 |
double-stranded RNA binding |
| Molecular Function |
GO:0042802 |
identical protein binding |
| Molecular Function |
GO:0003692 |
left-handed Z-DNA binding |
| Molecular Function |
GO:0003723 |
RNA binding |
| Biological Process |
GO:0002218 |
activation of innate immune response |
| Biological Process |
GO:0140374 |
antiviral innate immune response |
| Biological Process |
GO:0006915 |
apoptotic process |
| Biological Process |
GO:0050832 |
defense response to fungus |
| Biological Process |
GO:0051607 |
defense response to virus |
| Biological Process |
GO:0043065 |
positive regulation of apoptotic process |
| Biological Process |
GO:0050729 |
positive regulation of inflammatory response |
| Biological Process |
GO:0060545 |
positive regulation of necroptotic process |
| Biological Process |
GO:0060340 |
positive regulation of type I interferon-mediated signaling pathway |
| Biological Process |
GO:0070269 |
pyroptotic inflammatory response |
| Biological Process |
GO:0050727 |
regulation of inflammatory response |
| Biological Process |
GO:2000659 |
regulation of interleukin-1-mediated signaling pathway |
Reference
[1] Guo X, Ren X, Yan C, Huang H. Quantitative Proteomics Reveals the Role of Lysine Lactylation in Lenalidomide-Resistance in Multiple Myeloma Cells.. ACS Chem Biol 20(7):1728-1738. 2025 Jul 18. PMID: 40590393.