Protein profile

PA2654

chemotaxis transducer

Genome: NC_002516.2

Gene: PA2654 tlpQ Structure source: Experimental + AlphaFold UniProt Q9I0I4
Amino acids 714
Annotations 4
Features 26
PDB binders 7
Druggability 0.837

Overview

Basic information about this protein and its source genome.

Accession
PA2654
Gene
PA2654 tlpQ
Status
annotated
Amino acids
714
Structure source
Experimental + AlphaFold

Target profile

Computed evidence for target prioritization.

Human off-target
No hit
Gut microbiome off-target
hit
Essential (DEG)
N
Localization
CytoplasmicMembrane

Selected Druggability evidence

Selected Druggability is the FPocket score chosen for ranking using the curated structure priority. The 3D viewer may show a different loaded structure, so its visible pockets can differ.

FPocket 0.837
Structure
Pocket

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

4 GO

Gene Ontology (GO)

4
  • GO:0005886 The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
  • GO:0006935 The directed movement of a motile cell or organism, or the directed growth of a cell guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).
  • GO:0007165 The cellular process in which a signal is conveyed to trigger a change in the activity or state of a cell. Signal transduction begins with reception of a signal (e.g. a ligand binding to a receptor or receptor activation by a stimulus such as light), or for signal transduction in the absence of ligand, signal-withdrawal or the activity of a constitutively active receptor. Signal transduction ends with regulation of a downstream cellular process, e.g. regulation of transcription or regulation of a metabolic process. Signal transduction covers signaling from receptors located on the surface of the cell and signaling via molecules located within the cell. For signaling between cells, signal transduction is restricted to events at and within the receiving cell.
  • GO:0016020 A lipid bilayer along with all the proteins and protein complexes embedded in it and attached to it.

Sequence Features

Domain/signature hits from InterPro and related databases.

26 records
Show feature table
Start End DB Term Name
91 240 Gene3D G3DSA:3.30.450.20 PAS domain
14 713 PANTHER PTHR32089 METHYL-ACCEPTING CHEMOTAXIS PROTEIN MCPB
383 714 FunFam G3DSA:1.10.287.950:FF:000001 Methyl-accepting chemotaxis sensory transducer
381 433 Pfam PF00672 HAMP domain
381 433 InterPro IPR003660 HAMP domain
381 714 Phobius NON_CYTOPLASMIC_DOMAIN Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region.
430 714 Gene3D G3DSA:1.10.287.950 -
442 678 ProSiteProfiles PS50111 Bacterial chemotaxis sensory transducers domain profile.
442 678 InterPro IPR004089 Methyl-accepting chemotaxis protein (MCP) signalling domain
383 437 ProSiteProfiles PS50885 HAMP domain profile.
383 437 InterPro IPR003660 HAMP domain
383 437 SMART SM00304 HAMP_11
452 713 SMART SM00283 MA_2
452 713 InterPro IPR004089 Methyl-accepting chemotaxis protein (MCP) signalling domain
12 33 Phobius TRANSMEMBRANE Region of a membrane-bound protein predicted to be embedded in the membrane.
90 242 CDD cd12913 PDC1_MCP_like
386 432 CDD cd06225 HAMP
471 678 CDD cd11386 MCP_signal
34 359 Phobius CYTOPLASMIC_DOMAIN Region of a membrane-bound protein predicted to be outside the membrane, in the cytoplasm.
405 713 SUPERFAMILY SSF58104 Methyl-accepting chemotaxis protein (MCP) signaling domain
12 34 TMHMM TMhelix Region of a membrane-bound protein predicted to be embedded in the membrane.
1 11 Phobius NON_CYTOPLASMIC_DOMAIN Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region.
360 380 Phobius TRANSMEMBRANE Region of a membrane-bound protein predicted to be embedded in the membrane.
382 429 Gene3D G3DSA:1.10.8.500 HAMP domain in histidine kinase
525 681 Pfam PF00015 Methyl-accepting chemotaxis protein (MCP) signalling domain
525 681 InterPro IPR004089 Methyl-accepting chemotaxis protein (MCP) signalling domain

3D Structure

Selected loaded structure. Experimental PDB entries may cover only a portion of the sequence; predicted models typically cover the full protein.

3D visualization script Full viewer

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Structural evidence

1 + 1

Experimental PDB entries and predicted models. Click Switch to display a different structure in the viewer.

Entry Method Resolution Chain Coverage Links Status
PDB 6FU4
X-ray 2.45 Å A,B,C,D
45.5% 36-360
Viewing
AlphaFold PA2654
AlphaFold full sequence Loaded
Pocket details FPocket · P2Rank — toggle visibility and zoom from here, or open full viewer

Pockets (FPOCKET)

Showing top-ranked FPocket candidates by druggability. Druggability is color-coded: high (0.7 or higher), medium (0.4 to 0.69), low (below 0.4).

FPOCKET Sticks Spheres Surfaces Druggability Labels Zoom Positions
3 0.837
2 0.339
1 0.205

Pockets (P2RANK)

Showing top-ranked P2Rank candidates by probability. Probability is color-coded per P2Rank calibration: high (≥ 0.5), medium (0.2 – 0.49), low (< 0.2).

P2RANK Sticks Spheres Surfaces Score Probability Labels Zoom Positions
1 3.9 0.153
2 3.57 0.132

Ligand evidence

Ligands grouped by evidence source. PDB ligands keep the source crystal visible, and loaded crystals can be opened directly in the structure viewer.

57 records

Highest-confidence structural evidence: ligands co-crystallized with this exact protein. If the source PDB is loaded in TPW, use Open crystal to inspect it in the structure viewer.

Show only:
Ligand Source crystal MW · LogP · TPSA Lipinski PAINS SMILES
HSM 111.1 Da LogP -0.09 TPSA 54.7 ✓ Ro5 ✓ Clean c1c(nc[nH]1)CCN

PDB and ChEMBL records on this protein are shown in full. ChEMBL records from similar proteins are capped at the top 100 per protein (by pchembl) and ZINC at the top 50 (Tanimoto ≥ 0.5). ADME columns are descriptor-based screening flags, not experimental toxicity results.