KpKP13 Protein target profile

putative acyltransferase

Accession: KP13_02104

Gene: AHE46104.1 3D evidence: AlphaFold DB model + ColabFold model UniProt A0A0H3GNB3
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Length 572
Pocket druggability (P2Rank · AlphaFold DB model) 0.868
Functional annotation 1 EC 3 GO
Target summary

Promising target candidate with multiple supporting evidence streams.

Automated synthesis of the evidence currently loaded. Review the underlying records before prioritizing this protein.

Main supporting evidence

Independent pocket support: P2Rank + FPocket Both predictors report a high-scoring binding site (P2Rank 0.87, FPocket 0.96). Use the 3D pocket comparison to verify whether they identify the same site. No similar human protein detected The current BLAST sequence screen did not find a significant human match, lowering apparent off-target risk. Core gene across strains Marked as conserved by both pan-genome tools: Roary and CoreCruncher. Strong predicted binding pocket FPocket selected-pocket score 0.96. This is a computational pocket signal, not binding validation. Review the complete evidence below

Risks to review

Microbiome similarity 60 of 4744 screened genomes (1.3%) have a significant similarity hit. This target also has a predicted binding pocket (P2Rank 0.87) — check the ligand evidence before deprioritizing on off-target risk alone.

Evidence gaps

No metabolic context No SBML/network-derived reaction evidence is loaded for this protein. No ligand evidence No experimental PDB ligands, measured ChEMBL bioactivity, or proposed ZINC compound records are available.
Terms and data sources used on this page

PDB: experimentally determined structures from the Protein Data Bank. These are the strongest structural evidence, but may cover only part of the protein.

AlphaFold DB model: a precomputed predicted structure downloaded from AlphaFold Database/UniProt, not an experiment performed here.

ColabFold model: a predicted structure generated for this workspace; interpret it with coverage and confidence.

pLDDT: confidence score for predicted structures. High values support local geometry; low values mean the region should not drive pocket interpretation.

FPocket / P2Rank: software tools that predict possible ligand-binding pockets on a 3D structure. They are useful screening signals, not experimental validation.

Druggability: a pocket-based estimate of whether a small molecule could bind productively. It does not mean a drug already exists.

PDB ligand: a compound observed in an experimental structure. Direct same-protein records are stronger than homolog-transferred records.

ChEMBL: a public database of measured compound bioactivity. Direct entries are stronger than entries transferred from similar proteins.

ZINC: a purchasable-compound database. Here it marks proposed candidates from chemical similarity, not measured binders.

LigQ / LigQ_2: an internal Target pipeline step that gathers PDB, ChEMBL, and ZINC ligand evidence for each protein.

Off-target: sequence similarity to proteins we prefer not to hit, such as human proteins or beneficial gut microbiome proteins.

DEG: Database of Essential Genes. A match suggests the protein resembles genes known to be essential in other organisms.

Roary / CoreCruncher: pan-genome tools used to decide whether a gene is core across analyzed strains or accessory/strain-specific.

EC / GO: functional annotations: EC describes enzyme reactions; GO describes biological process, molecular function, or cellular component.

KEGG pathway: a curated metabolic route label used here to group reactions imported from the metabolic model.

Chokepoint: a metabolic reaction that is the only producer or consumer of a metabolite in the imported model.

Prioritization evidence

Selectivity, essentiality, structural confidence, conservation, and predicted binding-site evidence.

Off-target risk

Human off-target
No hit
Gut microbiome similarity
1.3% of screened genomes Lower prevalence suggests narrower overlap with the screened gut microbiome.

Essentiality

Essential (DEG)
N
DEG identity (%)
0.0 Higher values support similarity to known essential genes.

Structure confidence

ColabFold pLDDT
90.65 0-100 confidence; >70 supports local structural interpretation.

Binding-site evidence

AlphaFold DB / UniProt model

P2Rank's binding-site probability is the primary druggability signal shown across the app; FPocket's druggability score is shown alongside it for comparison. Both estimate small-molecule pocket quality after applying the curated structure priority — neither is experimental binding evidence. The 3D viewer may show a different loaded structure, so visible pockets can differ.

Druggability (P2Rank) 0.868
Structure A0A0H3GNB3
Pocket Pocket 1
Druggability (FPocket) 0.96
Structure A0A0H3GNB3
Pocket Pocket 18
ColabFold model
P2Rank 0.884 · Pocket 1
FPocket 0.539 · Pocket 6
Core conservation Conserved core gene
Roary core
CoreCruncher core
Gut microbiome 60 / 4744 genomes with a hit
Prevalence 1.3%

Sequence

Primary amino-acid sequence viewer.

MFSLDNVLDDLWPQARPAPWQKKLLKKLFYEEEFQQFADRHRHLKGLDTVEQVLEYLNIRCAIPAHDLEQIPEYGPLVIIANHPTGTLDGLALLYAVSRVRRDVKVVTNRMLTHLEPLSSLFIPVDNIHGRTAKAALQQMDQQLQAGGVLIFFPAGEVSRLTRRGIRDKKWHSGFIKLAAKYRAPLLPAWINARNSALFYASTLVSDNLPLLLLMQQMFRRRNSSLPVRIGQQIPWSSWFDAQSSARELTGRCYQHLEQLRKGLPGRFKTESAIARPEDRALLKRELHKAECLGRTADGKVIYLWQRNGQEDAPLLRELGRLREIAFRAVGEGSGKRRDIDGYDDDYLHLILWDEEDLEIVGAYRFMPTAIQLAKRGLEGIYSYSLFHYDGRMDDVLQHGIELGRSFIQPRYWGRRGLDYLWSGIGAYLARYPHYRYLFGPVSISGGLPPAARDLLVAFYRMWFPATHPLAESRRPYPASLPDVLAQFGGEDYNDDLARLKSLLGNLGCAIPPLYKQYSEVCEPGGVQFIDFGSDPDFNNCVDGLVLVDLTYLKANRYQRYIGAHLGAQKSA

Functional annotations

Enzyme classification and Gene Ontology terms linked to this protein.

1 EC 3 GO

Subcellular localization

Localization
Cytoplasmic

Enzyme Commission (EC)

1

Gene Ontology (GO)

3
  • GO:0016746 Catalysis of the transfer of an acyl group from one compound (donor) to another (acceptor).
  • GO:0043810 Catalysis of the reaction: (3R)-3-hydroxyacyl-[acyl-carrier protein] + L-ornithine = lyso-ornithine lipid + [acyl-carrier protein]. The enzyme, found in bacteria, catalyzes the first step in the biosynthesis of ornithine lipids.
  • GO:0006629 The chemical reactions and pathways involving lipids, compounds soluble in an organic solvent but not, or sparingly, in an aqueous solvent. Includes fatty acids; neutral fats, other fatty-acid esters, and soaps; long-chain (fatty) alcohols and waxes; sphingoids and other long-chain bases; glycolipids, phospholipids and sphingolipids; and carotenes, polyprenols, sterols, terpenes and other isoprenoids.

Sequence domains and features

Domain and signature matches imported from InterPro and related databases.

12 records
Show feature table
Start End DB Term Name
269 566 PANTHER PTHR37323 GCN5-RELATED N-ACETYLTRANSFERASE
310 483 SUPERFAMILY SSF55729 Acyl-CoA N-acyltransferases (Nat)
310 483 InterPro IPR016181 Acyl-CoA N-acyltransferase
40 262 SUPERFAMILY SSF69593 Glycerol-3-phosphate (1)-acyltransferase
322 422 Pfam PF13444 Acetyltransferase (GNAT) domain
54 256 CDD cd07986 LPLAT_ACT14924-like
54 256 InterPro IPR045746 Putative acyltransferase ACT14924-like, acyltransferase domain
303 445 Gene3D G3DSA:3.40.630.30 -
29 247 Pfam PF19576 Acyltransferase
29 247 InterPro IPR045746 Putative acyltransferase ACT14924-like, acyltransferase domain
77 194 SMART SM00563 plsc_2
77 194 InterPro IPR002123 Phospholipid/glycerol acyltransferase

3D structure

Selected loaded structure. Experimental PDB entries may cover only a portion of the sequence; AlphaFold DB and ColabFold models typically cover the full protein but remain computational predictions.

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Pocket score High Medium Low
How colors and pocket overlays are used
Uniform protein color marks the displayed model as a single molecular object.
Experimental PDB structures may be colored by chain to distinguish subunits or copies present in the file.
Pocket colors and alpha spheres are evidence overlays for predicted binding cavities; they are not alternative protein chains.
'Alpha spheres' is FPocket's own cavity-shape geometry, imported when available and aligned with the loaded structure.
'Pocket atoms'/'Predicted site atoms' show the pocket's residue atoms instead: P2Rank reports residues rather than alpha spheres, and FPocket falls back to this when alpha-sphere geometry is unavailable or doesn't align.
'No pocket geometry' means neither alpha spheres nor residue-position data could be found for that pocket; the layer just highlights the same residues as 'Nearby residues'.
Pocket details Inspect a specific pocket, or open the full viewer

Binding pockets · P2Rank

Druggability (P2Rank): high ≥ 0.5 · medium 0.2–0.49 · low < 0.2

Pocket 1 P2Rank #1
0.868
Likely same site as FPocket 18 2.6 Å 24 shared residues 89% of smaller site
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Surrounding area
Pocket 2 P2Rank #2
0.763
Likely same site as FPocket 6 2.1 Å 22 shared residues 88% of smaller site
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Surrounding area
Pocket 3 P2Rank #3
0.617
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Surrounding area
Pocket 4 P2Rank #4
0.406
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Surrounding area
Pocket 5 P2Rank #5
0.262
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Surrounding area

Binding pockets · FPocket

Druggability (FPocket): high ≥ 0.7 · medium 0.4–0.69 · low < 0.4

Pocket 1 FPocket #18
0.96 Unusual size
Likely same site as P2Rank 1 2.6 Å 24 shared residues 89% of smaller site
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Surrounding area
Pocket 2 FPocket #6
0.888 Unusual size
Likely same site as P2Rank 2 2.1 Å 22 shared residues 88% of smaller site
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Surrounding area
All structural evidence 0 experimental · 2 predicted

Structural evidence

0 + 2

Experimental PDB entries plus predicted AlphaFold DB or ColabFold models. Click Switch to display a different loaded structure in the viewer.

Entry Method Resolution Chain Coverage Links Status
AlphaFold DB AF_A0A0H3GNB3
AlphaFold DB — — full sequence — Viewing
ColabFold KP13_02104
ColabFold — — full sequence — Loaded

Cross-references

External database identifiers for this protein, its structures, ligands, and metabolic reactions.

Sequence

UniProt A0A0H3GNB3