Protein profile

PA5567

tRNA modification GTPase TrmE

Genome: NC_002516.2

Gene: mnmE trmE PA5567 Structure source: AlphaFold UniProt Q9HT07
Amino acids 455
Annotations 10
Features 34
PDB binders 5
Druggability 0.569

Overview

Basic information about this protein and its source genome.

Accession
PA5567
Gene
mnmE trmE PA5567
Status
annotated
Amino acids
455
Structure source
AlphaFold

Target profile

Computed evidence for target prioritization.

Human off-target
hit
Human identity (%)
43.011
Human E-value
6.28e-15
Gut microbiome off-target
hit
Essential (DEG)
Y
Localization
Cytoplasmic

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 0.569
Structure
Pocket

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

1 EC 9 GO

Enzyme Commission (EC)

1

Gene Ontology (GO)

9
  • GO:0005737 The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
  • GO:0005829 The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
  • GO:0005525 Binding to GTP, guanosine triphosphate.
  • GO:0003924 Catalysis of the reaction: GTP + H2O = GDP + H+ + phosphate.
  • GO:0046872 Binding to a metal ion.
  • GO:0030488 The posttranscriptional addition of methyl groups to specific residues in a tRNA molecule.
  • GO:0002098 The process in which a uridine at position 34 of a tRNA is post-transcriptionally modified. The wobble nucleoside of the tRNA sequence (position 34) corresponds to the first position of the anticodon.
  • GO:0006400 The covalent alteration of one or more nucleotides within a tRNA molecule to produce a tRNA molecule with a sequence that differs from that coded genetically.
  • GO:0005515 Binding to a protein.

Sequence Features

Domain/signature hits from InterPro and related databases.

34 records
Show feature table
Start End DB Term Name
286 304 PRINTS PR00326 GTP1/OBG GTP-binding protein family signature
286 304 InterPro IPR006073 GTP binding domain
219 239 PRINTS PR00326 GTP1/OBG GTP-binding protein family signature
219 239 InterPro IPR006073 GTP binding domain
217 383 Gene3D G3DSA:3.40.50.300 -
217 383 InterPro IPR027417 P-loop containing nucleoside triphosphate hydrolase
123 452 Pfam PF12631 MnmE helical domain
123 452 InterPro IPR025867 MnmE, helical domain
7 455 PANTHER PTHR42714 TRNA MODIFICATION GTPASE GTPBP3
6 118 CDD cd14858 TrmE_N
6 118 InterPro IPR018948 GTP-binding protein TrmE, N-terminal
12 455 NCBIfam TIGR00450 tRNA uridine-5-carboxymethylaminomethyl(34) synthesis GTPase MnmE
12 455 InterPro IPR004520 tRNA modification GTPase MnmE
216 378 ProSiteProfiles PS51709 TrmE-type guanine nucleotide-binding (G) domain profile.
216 378 InterPro IPR031168 TrmE-type guanine nucleotide-binding domain
122 455 Gene3D G3DSA:1.20.120.430 tRNA modification GTPase MnmE domain 2
122 455 InterPro IPR027368 tRNA modification GTPase MnmE domain 2
214 378 CDD cd04164 trmE
214 378 InterPro IPR031168 TrmE-type guanine nucleotide-binding domain
219 306 Pfam PF01926 50S ribosome-binding GTPase
219 306 InterPro IPR006073 GTP binding domain
217 367 NCBIfam TIGR00231 small GTP-binding protein domain
217 367 InterPro IPR005225 Small GTP-binding protein domain
6 455 Hamap MF_00379 tRNA modification GTPase MnmE [mnmE].
6 455 InterPro IPR004520 tRNA modification GTPase MnmE
7 120 Pfam PF10396 GTP-binding protein TrmE N-terminus
7 120 InterPro IPR018948 GTP-binding protein TrmE, N-terminal
73 373 SUPERFAMILY SSF52540 P-loop containing nucleoside triphosphate hydrolases
73 373 InterPro IPR027417 P-loop containing nucleoside triphosphate hydrolase
121 455 SUPERFAMILY SSF116878 TrmE connector domain
1 121 Gene3D G3DSA:3.30.1360.120 Probable tRNA modification gtpase trme; domain 1
1 121 InterPro IPR027266 GTP-binding protein TrmE/Aminomethyltransferase GcvT, domain 1
2 121 FunFam G3DSA:3.30.1360.120:FF:000001 tRNA modification GTPase MnmE
217 383 FunFam G3DSA:3.40.50.300:FF:000249 tRNA modification GTPase MnmE

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 PA5567
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
1 0.569
8 0.496

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.

55 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
ALF P25522 103.0 Da LogP 1.30 TPSA 0.0 ✓ Ro5 ✓ Clean F[Al-](F)(F)F
FON Q8KAS1 473.4 Da LogP -0.73 TPSA 219.8 1 viol. ✓ Clean c1cc(ccc1C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC[C@@H]2…
GCP P50743 521.2 Da LogP -2.22 TPSA 289.9 3 viol. ✓ Clean c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O…
GNP P50743 522.2 Da LogP -2.76 TPSA 301.9 3 viol. ✓ Clean c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O…
NH4 P25522 18.0 Da LogP 0.38 TPSA 36.5 ✓ Ro5 ✓ Clean [NH4+]

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.