Target Information

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Target General Information
Drugs and Modes of Action
Drug Binding Sites of Target
Different Human System Profiles of Target
Chemical Structure based Activity Landscape of Target
Drug Property Profile of Target
Co-Targets
Target Poor or Non Binders
Target Regulators
Target Profiles in Patients
Target Affiliated Biological Pathways
Target-Related Models and Studies
References
Drug Binding Sites of Target  Top
Ligand Name: N-(4-Methylthiazol-2-yl)acetamide Ligand Info
Structure Description Crystal structure of a low occupancy fragment candidate (N-(4-Methyl-1,3-thiazol-2-yl)propanamide) bound adjacent to the ubiquitin binding pocket of the HDAC6 zinc-finger domain PDB:5B8D
Method X-ray diffraction Resolution 1.05 Å Mutation No [33]
PDB Sequence
PLPWCPHLVA
1118
VCPIPAAGLD
1128
VTQPCGDCGT
1138
IQENWVCLSC
1148
YQVYCGRYIN
1158

GHMLQHHGNS
1168
GHPLVLSYID
1178
LSAWCYYCQA
1188
YVHHQALLDV
1198
KNIAHQNKFG
1208
Residue
Distance (Å)
GLU1141
3.592
ASN1142
3.322
TRP1143
3.350
GLY1154
4.971
SER1175
2.710
Residue
Distance (Å)
TYR1176
4.350
ILE1177
3.899
ASP1178
2.802
SER1180
4.205
TYR1189
3.684
Ligand Name: 6-Methyl-5-[(4-Propan-2-Ylphenyl)amino]-2~{h}-1,2,4-Triazin-3-One Ligand Info
Structure Description Crystal structure of a low occupancy fragment candidate (5-[(4-Isopropylphenyl)amino]-6-methyl-1,2,4-triazin-3(2H)-one) bound in the ubiquitin binding pocket of the HDAC6 zinc-finger domain PDB:5KH9
Method X-ray diffraction Resolution 1.07 Å Mutation No [33]
PDB Sequence
PLPWCPHLVA
1118
VCPIPAAGLD
1128
VTQPCGDCGT
1138
IQENWVCLSC
1148
YQVYCGRYIN
1158

GHMLQHHGNS
1168
GHPLVLSYID
1178
LSAWCYYCQA
1188
YVHHQALLDV
1198
KNIAHQNKFG
1208
Residue
Distance (Å)
TRP1143
3.677
ARG1155
3.374
Residue
Distance (Å)
TRP1182
3.385
TYR1189
2.975
Click to View More Binding Site Information of This Target with Different Ligands
Different Human System Profiles of Target  Top
Human Similarity Proteins of target is determined by comparing the sequence similarity of all human proteins with the target based on BLAST. The similarity proteins for a target are defined as the proteins with E-value < 0.005 and outside the protein families of the target.
A target that has fewer human similarity proteins outside its family is commonly regarded to possess a greater capacity to avoid undesired interactions and thus increase the possibility of finding successful drugs (Brief Bioinform, 21: 649-662, 2020).
Human Tissue Distribution of target is determined from a proteomics study that quantified more than 12,000 genes across 32 normal human tissues. Tissue Specificity (TS) score was used to define the enrichment of target across tissues.
The distribution of targets among different tissues or organs need to be taken into consideration when assessing the target druggability, as it is generally accepted that the wider the target distribution, the greater the concern over potential adverse effects (Nat Rev Drug Discov, 20: 64-81, 2021).
Human Pathway Affiliation of target is determined by the life-essential pathways provided on KEGG database. The target-affiliated pathways were defined based on the following two criteria (a) the pathways of the studied target should be life-essential for both healthy individuals and patients, and (b) the studied target should occupy an upstream position in the pathways and therefore had the ability to regulate biological function.
Targets involved in a fewer pathways have greater likelihood to be successfully developed, while those associated with more human pathways increase the chance of undesirable interferences with other human processes (Pharmacol Rev, 58: 259-279, 2006).
Biological Network Descriptors of target is determined based on a human protein-protein interactions (PPI) network consisting of 9,309 proteins and 52,713 PPIs, which were with a high confidence score of ≥ 0.95 collected from STRING database.
The network properties of targets based on protein-protein interactions (PPIs) have been widely adopted for the assessment of target’s druggability. Proteins with high node degree tend to have a high impact on network function through multiple interactions, while proteins with high betweenness centrality are regarded to be central for communication in interaction networks and regulate the flow of signaling information (Front Pharmacol, 9, 1245, 2018; Curr Opin Struct Biol. 44:134-142, 2017).
Human Similarity Proteins
Human Tissue Distribution
Human Pathway Affiliation
Biological Network Descriptors
There is no similarity protein (E value < 0.005) for this target
Note: If a protein has TS (tissue specficity) scores at least in one tissue >= 2.5, this protein is called tissue-enriched (including tissue-enriched-but-not-specific and tissue-specific). In the plots, the vertical lines are at thresholds 2.5 and 4.
 Download Picture         KEGG Link      
KEGG Pathway Pathway ID Affiliated Target Pathway Map
Neutrophil extracellular trap formation hsa04613 Affiliated Target
  Class: Organismal Systems => Immune system Pathway Hierarchy
Degree 20 Degree centrality 2.15E-03 Betweenness centrality 3.83E-03
Closeness centrality 2.54E-01 Radiality 1.44E+01 Clustering coefficient 8.95E-02
Neighborhood connectivity 5.04E+01 Topological coefficient 6.77E-02 Eccentricity 11
Download Click to Download the Full PPI Network of This Target

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