Protein profile

PA2129

chaperone CupA2

Genome: NC_002516.2

Gene: cupA2 PA2129 Structure source: AlphaFold UniProt Q9I1Y6
Amino acids 248
Annotations 8
Features 31
PDB binders 3
Druggability 0.845

Overview

Basic information about this protein and its source genome.

Accession
PA2129
Gene
cupA2 PA2129
Status
annotated
Amino acids
248
Structure source
AlphaFold

Target profile

Computed evidence for target prioritization.

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

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 0.845
Structure
Pocket

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

8 GO

Gene Ontology (GO)

8
  • GO:0097311 A structure lying external to bacterial cells. A biofilm is an aggregate of surface-associated bacteria, and the biofilm matrix is the envelope of polymeric substances that surrounds the bacteria.
  • GO:0030288 The region between the inner (cytoplasmic or plasma) membrane and outer membrane of organisms with two membranes such as Gram negative bacteria. These periplasmic spaces are relatively thick and contain a thin peptidoglycan layer (PGL), also referred to as a thin cell wall.
  • GO:0044183 Binding to a protein or a protein-containing complex to assist the protein folding process.
  • GO:0007155 The attachment of a cell, either to another cell or to an underlying substrate such as the extracellular matrix, via cell adhesion molecules.
  • GO:0071555 A process that results in the assembly, arrangement of constituent parts, or disassembly of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis.
  • GO:0071453 Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus reflecting the presence, absence, or concentration of oxygen.
  • GO:0043711 A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a pilus, a short filamentous structure on a bacterial cell, flagella-like in structure and generally present in many copies.
  • GO:0061077 OBSOLETE. The process of inhibiting aggregation and assisting in the covalent and noncovalent assembly of single chain polypeptides or multisubunit complexes into the correct tertiary structure that is dependent on interaction with a chaperone.

Sequence Features

Domain/signature hits from InterPro and related databases.

31 records
Show feature table
Start End DB Term Name
1 27 SignalP_GRAM_NEGATIVE SignalP-noTM SignalP-noTM
154 246 SUPERFAMILY SSF49584 Periplasmic chaperone C-domain
154 246 InterPro IPR036316 Pili assembly chaperone, C-terminal domain superfamily
1 27 Phobius SIGNAL_PEPTIDE Signal peptide region
1 10 Phobius SIGNAL_PEPTIDE_N_REGION N-terminal region of a signal peptide.
1 25 SignalP_GRAM_POSITIVE SignalP-TM SignalP-TM
28 248 Phobius NON_CYTOPLASMIC_DOMAIN Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region.
176 240 Pfam PF02753 Pili assembly chaperone PapD, C-terminal domain
176 240 InterPro IPR016148 Pili assembly chaperone, C-terminal
152 244 Gene3D G3DSA:2.60.40.10 Immunoglobulins
152 244 InterPro IPR013783 Immunoglobulin-like fold
11 22 Phobius SIGNAL_PEPTIDE_H_REGION Hydrophobic region of a signal peptide.
132 147 PRINTS PR00969 Pili chaperone signature
132 147 InterPro IPR001829 Pili assembly chaperone, bacterial
106 123 PRINTS PR00969 Pili chaperone signature
106 123 InterPro IPR001829 Pili assembly chaperone, bacterial
171 186 PRINTS PR00969 Pili chaperone signature
171 186 InterPro IPR001829 Pili assembly chaperone, bacterial
78 99 PRINTS PR00969 Pili chaperone signature
78 99 InterPro IPR001829 Pili assembly chaperone, bacterial
29 38 PRINTS PR00969 Pili chaperone signature
29 38 InterPro IPR001829 Pili assembly chaperone, bacterial
24 150 SUPERFAMILY SSF49354 PapD-like
24 150 InterPro IPR008962 PapD-like superfamily
29 148 FunFam G3DSA:2.60.40.10:FF:000458 Molecular chaperone FimC
3 243 PANTHER PTHR30251 PILUS ASSEMBLY CHAPERONE
29 148 Gene3D G3DSA:2.60.40.10 Immunoglobulins
29 148 InterPro IPR013783 Immunoglobulin-like fold
29 150 Pfam PF00345 Pili and flagellar-assembly chaperone, PapD N-terminal domain
29 150 InterPro IPR016147 Pili assembly chaperone, N-terminal
23 27 Phobius SIGNAL_PEPTIDE_C_REGION C-terminal region of a signal peptide.

3D Structure

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

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Structural evidence

0 + 1

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

Entry Method Resolution Chain Coverage Links Status
AlphaFold PA2129
AlphaFold full sequence Viewing
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
2 0.845
1 0.361

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.

3 records

Structural evidence inferred from similar proteins. The source crystal indicates where the ligand was observed; the UniProt column identifies the homologous protein carrying that ligand.

Show only:
Ligand Source crystal UniProt (homolog) MW · LogP · TPSA Lipinski PAINS SMILES
EC2 P15319 453.6 Da LogP 5.94 TPSA 59.3 1 viol. ✓ Clean c1ccc(cc1)[C@@H]2[C@H](N3C(=O)C=C(C(=C3S2)C4CC4…
EC5 P15319 471.6 Da LogP 5.90 TPSA 79.5 1 viol. ✓ Clean c1ccc(cc1)C[C@@H](C(=O)O)N2C(=O)C=C(C(=C2SO)C3C…
XC2 P15319 476.6 Da LogP 4.03 TPSA 71.8 ✓ Ro5 ✓ Clean c1ccc2c(c1)cccc2CC3=C(C(=O)N4[C@@H](CSC4=C3C5CC…

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.