Descriptions

Lmo0526 belongs to the TipA class of transcription factors, which constitutes minimal autoregulated multidrug resistance (MDR) against diverse antibiotics. Autoinhibitory mechanism in SkgA has been identified by structural analysis. Due to the structural similarity of Lmo0526 to SkgA, Lmo0526 could also possess an autoinhibitory mechanism. In the case of SkgA, upon binding of antibiotics to the TipAS domain within SkgA, SkgA is able to induce transcription of genes involved in multidrug resistance such as efflux pumps and antibiotics sequester proteins. The autoinhibition mechanism involves the a6–a7 region of the TipAS domain, which, in the unliganded state, interacts with the DNA-binding domain to stabilize the dimeric interface and hinder promoter DNA binding. This interaction prevents transcriptional activation by sterically blocking DNA access to the DNA-binding domain.

Autoinhibitory domains (AIDs)

Target domain

3-73 (MerR-type HTH domain)

Relief mechanism

Ligand binding

Assay

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

2 structures for Q8Y9K1

Entry ID Method Resolution Chain Position Source
3QAO X-ray 187 A A 1-246 PDB
AF-Q8Y9K1-F1 Predicted AlphaFoldDB

No variants for Q8Y9K1

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for Q8Y9K1

1 associated diseases with Q8Y9K1

[MIM: 616532]: Encephalopathy, acute, infection-induced, 7, herpes-specific (IIAE7)

A rare complication of human herpesvirus 1 (HHV-1) infection, occurring in only a small minority of HHV-1 infected individuals. It is characterized by hemorrhagic necrosis of parts of the temporal and frontal lobes. Onset is over several days and involves fever, headache, seizures, stupor, and often coma, frequently with a fatal outcome. {ECO:0000269|PubMed:26216125}. Note=Disease susceptibility is associated with variants affecting the gene represented in this entry.

Without disease ID
  • A rare complication of human herpesvirus 1 (HHV-1) infection, occurring in only a small minority of HHV-1 infected individuals. It is characterized by hemorrhagic necrosis of parts of the temporal and frontal lobes. Onset is over several days and involves fever, headache, seizures, stupor, and often coma, frequently with a fatal outcome. {ECO:0000269|PubMed:26216125}. Note=Disease susceptibility is associated with variants affecting the gene represented in this entry.

3 regional properties for Q8Y9K1

Type Name Position InterPro Accession
domain Interferon regulatory factor, DNA-binding domain 1 - 112 IPR001346
domain Interferon regulatory factor-3 201 - 380 IPR019471
conserved_site Interferon regulatory factor, conserved site 26 - 58 IPR019817

Functions

Description
EC Number
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

No GO annotations of cellular component

Name Definition
No GO annotations for cellular component

2 GO annotations of molecular function

Name Definition
DNA binding Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid).
DNA-binding transcription factor activity A transcription regulator activity that modulates transcription of gene sets via selective and non-covalent binding to a specific double-stranded genomic DNA sequence (sometimes referred to as a motif) within a cis-regulatory region. Regulatory regions include promoters (proximal and distal) and enhancers. Genes are transcriptional units, and include bacterial operons.

No GO annotations of biological process

Name Definition
No GO annotations for biological process

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MQIKELAELT GVSVRTLHHY DKIGLLVPQK DDWNGYRIYS EKDVDKLQQI LFFKELDFPL
70 80 90 100 110 120
KKIQQILDDP LFDKNVALDM QRHLLIEKKQ RIETMLATLD LTIKNEKGEI TMTNKEKFTG
130 140 150 160 170 180
FDFSSNPYEE EARKLWGDKV VEKANEKVNN MSEKEQLTLK ESFDAEFRHL ASVRKLTPES
190 200 210 220 230 240
EEAQLEIDHF FHYLNDTHGN IYSLEAFASL GEMYVNDERF TKNIDQFGDG LSQFLQEAMT
IYAKNK