Q9UHD2

Background

Protein Name
Serine/threonine-protein kinase TBK1
Gene Name
TBK1
Organism
Homo sapiens

Annotations

Function
Serine/threonine kinase that plays an essential role in regulating inflammatory responses to foreign agents. Following activation of toll-like receptors by viral or bacterial components, associates with TRAF3 and TANK and phosphorylates interferon regulatory factors (IRFs) IRF3 and IRF7 as well as DDX3X. This activity allows subsequent homodimerization and nuclear translocation of the IRFs leading to transcriptional activation of pro-inflammatory and antiviral genes including IFNA and IFNB. In order to establish such an antiviral state, TBK1 form several different complexes whose composition depends on the type of cell and cellular stimuli. Thus, several scaffolding molecules including FADD, TRADD, MAVS, AZI2, TANK or TBKBP1/SINTBAD can be recruited to the TBK1-containing-complexes. Under particular conditions, functions as a NF-kappa-B effector by phosphorylating NF-kappa-B inhibitor alpha/NFKBIA, IKBKB or RELA to translocate NF-Kappa-B to the nucleus. Restricts bacterial proliferation by phosphorylating the autophagy receptor OPTN/Optineurin on 'Ser-177', thus enhancing LC3 binding affinity and antibacterial autophagy. Phosphorylates and activates AKT1. Seems to play a role in energy balance regulation by sustaining a state of chronic, low-grade inflammation in obesity, wich leads to a negative impact on insulin sensitivity. Attenuates retroviral budding by phosphorylating the endosomal sorting complex required for transport-I (ESCRT-I) subunit VPS37C. Phosphorylates Borna disease virus (BDV) P protein.

Mapping Statistics

Site Maximum Consensus Site Population Minimum Consensus Site Population Median Consensus Site Population
MPP 16 9 12.0
DFG 22 3 5.0
PIF 20 2 13.0
DRS 4 4 4.0
EDI 14 14 14.0
MT3 19 2 10.5
AAS 22 2 17.0
CMP 23 2 6.5
PDIG 22 2 8.5
ATP 27 4 16.0

Mapping Results

PDB ID Maximum Consensus Site Population
MPP site DFG site PIF site DRS site DEF site EDI site MT3 site AAS site LBP site CMP site PDIG site ATP site PMP site
Total Druggable Structures per Site 1 1 3 0 0 0 2 2 0 2 2 5 0
4IM2 10 0 13 0 0 0 6 0 0 0 11 0 0
4IWO 16 0 14 0 0 0 19 0 0 0 11 13 0
4IM0 12 0 20 0 0 0 13 0 0 0 17 0 0
4EUU 14 0 5 0 0 14 12 0 0 0 22 21 0
4EUT 9 5 20 4 0 0 13 20 0 5 0 27 0
4IW0 10 0 2 0 0 0 8 0 0 14 14 21 0
4IWP 14 0 16 0 0 0 19 0 0 23 2 16 0
AFQ9UHD2 0 22 0 0 0 0 0 0 0 0 0 0 0
4IWQ 13 0 0 0 0 0 13 0 0 22 0 23 0
4IM3 12 0 0 0 0 0 0 22 0 0 0 0 0