Protein profile

KP13_03319

(Dimethylallyl)adenosine tRNA methylthiotransferase miaB

Genome: KpKP13

Gene: AHE45698.1 miaB Structure source: AlphaFold + ColabFold UniProt A0A0H3GTZ6
Amino acids 478
Annotations 10
Features 35
PDB binders 2
Druggability 0.045

Overview

Basic information about this protein and its source genome.

Accession
KP13_03319
Gene
AHE45698.1 miaB
Status
annotated
Amino acids
478
Structure source
AlphaFold + ColabFold

Target profile

Computed evidence for target prioritization.

Human off-target
hit
Human identity (%)
35.772
Human E-value
2.39e-86
Gut microbiome off-target
hit
Essential (DEG)
N
DEG identity (%)
0.0
Localization
Cytoplasmic
ColabFold pLDDT
91.57

Selected Druggability evidence

AlphaFold / UniProt model

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 0.045
Structure A0A0H3GTZ6
Pocket Pocket 28
P2Rank 0.929
Structure A0A0H3GTZ6
Pocket Pocket 1
ColabFold model
FPocket 0.709 · Pocket 7
P2Rank 0.938 · Pocket 1
Core conservation Conserved core gene
Roary core
CoreCruncher core
Gut microbiome 263 / 4744 genomes with a hit
Normalized 0.055

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:0051539 Binding to a 4 iron, 4 sulfur (4Fe-4S) cluster; this cluster consists of four iron atoms, with the inorganic sulfur atoms found between the irons and acting as bridging ligands.
  • GO:0035596 Catalysis of the addition of a methylthioether group (-SCH3) to a nucleic acid or protein acceptor.
  • GO:0016740 Catalysis of the transfer of a group, e.g. a methyl group, glycosyl group, acyl group, phosphorus-containing, or other groups, from one compound (generally regarded as the donor) to another compound (generally regarded as the acceptor). Transferase is the systematic name for any enzyme of EC class 2.
  • 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:0003824 Catalysis of a biochemical reaction at physiological temperatures. In biologically catalyzed reactions, the reactants are known as substrates, and the catalysts are naturally occurring macromolecular substances known as enzymes. Enzymes possess specific binding sites for substrates, and are usually composed wholly or largely of protein, but RNA that has catalytic activity (ribozyme) is often also regarded as enzymatic.
  • GO:0051536 Binding to an iron-sulfur cluster, a combination of iron and sulfur atoms.
  • GO:0005829 The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
  • GO:0046872 Binding to a metal ion.
  • GO:0035597 Catalysis of the reaction: N(6)-dimethylallyladenosine(37) in tRNA + [sulfur carrier]-SH + AH2 + 2 S-adenosyl-L-methionine = 2-methylsulfanyl-N(6)-dimethylallyladenosine(37) in tRNA + [sulfur carrier]-H + 5'-deoxyadenosine + L-methionine + A + S-adenosyl-L-homocysteine + 2 H+.

Sequence Features

Domain/signature hits from InterPro and related databases.

35 records
Show feature table
Start End DB Term Name
7 444 Hamap MF_01864 tRNA-2-methylthio-N(6)-dimethylallyladenosine synthase [miaB].
7 444 InterPro IPR006463 tRNA-2-methylthio-N(6)-dimethylallyladenosine synthase MiaB
382 444 Pfam PF01938 TRAM domain
382 444 InterPro IPR002792 TRAM domain
70 370 SFLD SFLDG01082 B12-binding domain containing
8 441 NCBIfam TIGR00089 MiaB/RimO family radical SAM methylthiotransferase
8 441 InterPro IPR005839 Methylthiotransferase
4 447 SFLD SFLDF00273 (dimethylallyl)adenosine tRNA methylthiotransferase (MiaB-like)
4 447 InterPro IPR006463 tRNA-2-methylthio-N(6)-dimethylallyladenosine synthase MiaB
149 382 FunFam G3DSA:3.80.30.20:FF:000001 tRNA-2-methylthio-N(6)-dimethylallyladenosine synthase 2
382 445 ProSiteProfiles PS50926 TRAM domain profile.
382 445 InterPro IPR002792 TRAM domain
155 175 ProSitePatterns PS01278 Methylthiotransferase radical SAM domain signature.
155 175 InterPro IPR020612 Methylthiotransferase, conserved site
3 447 PANTHER PTHR43020 CDK5 REGULATORY SUBUNIT-ASSOCIATED PROTEIN 1
131 376 SUPERFAMILY SSF102114 Radical SAM enzymes
7 133 Gene3D G3DSA:3.40.50.12160 -
7 133 InterPro IPR038135 Methylthiotransferase, N-terminal domain superfamily
7 124 ProSiteProfiles PS51449 Methylthiotransferase N-terminal domain profile.
7 124 InterPro IPR013848 Methylthiotransferase, N-terminal
155 329 Pfam PF04055 Radical SAM superfamily
155 329 InterPro IPR007197 Radical SAM
149 382 Gene3D G3DSA:3.80.30.20 tm_1862 like domain
149 382 InterPro IPR023404 Radical SAM, alpha/beta horseshoe
147 379 ProSiteProfiles PS51918 Radical SAM core domain profile.
147 379 InterPro IPR007197 Radical SAM
151 371 SMART SM00729 MiaB
151 371 InterPro IPR006638 Elp3/MiaA/NifB-like, radical SAM core domain
4 447 SFLD SFLDS00029 Radical SAM
4 447 InterPro IPR007197 Radical SAM
8 108 Pfam PF00919 Uncharacterized protein family UPF0004
8 108 InterPro IPR013848 Methylthiotransferase, N-terminal
8 444 NCBIfam TIGR01574 tRNA (N6-isopentenyl adenosine(37)-C2)-methylthiotransferase MiaB
160 361 CDD cd01335 Radical_SAM
7 134 FunFam G3DSA:3.40.50.12160:FF:000001 tRNA-2-methylthio-N(6)-dimethylallyladenosine synthase

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

0 + 2

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

Entry Method Resolution Chain Coverage Links Status
AlphaFold AF_A0A0H3GTZ6
AlphaFold full sequence Viewing
ColabFold KP13_03319
ColabFold full sequence Loaded
Pocket details FPocket · P2Rank — toggle visibility and zoom from here, or open full viewer

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 23.17 0.887
2 3.76 0.145
3 0.87 0.003

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.

15 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
CXS Q9X2H6 221.3 Da LogP 1.19 TPSA 66.4 ✓ Ro5 ✓ Clean C1CCC(CC1)NCCCS(=O)(=O)O
FS5 Q9X2H6 863.6 Da LogP 8.41 TPSA 0.0 2 viol. ✓ Clean S(SS[Fe]12[S]3[Fe]4[S]1[Fe]5[S]4[Fe]3[S]25)SS[F…

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.