Protein profile
KP13_03319
(Dimethylallyl)adenosine tRNA methylthiotransferase miaB
Genome: KpKP13
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 modelSelected 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.
Sequence
Primary amino-acid sequence viewer.
Functional Annotations
Enzyme classification and Gene Ontology terms linked to this protein.
Enzyme Commission (EC)
1Gene 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.
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.
Loading 3D structure...
Structural evidence
0 + 2Experimental 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 |
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 |
|---|---|---|---|---|---|---|---|
| 7 | 0.709 |
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 | 25.18 | 0.904 | ||||||
| 2 | 3.02 | 0.099 |
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.
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.
No PDB structure with a co-crystallized ligand found for this exact protein.
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.
Experimental bioactivity from ChEMBL measured directly on this protein. Score = pchembl (−log Ki/IC₅₀; higher = more potent).
No ChEMBL bioactivity data found for this exact protein.
Bioactivity inferred from similar proteins in ChEMBL. Score = pchembl (−log Ki/IC₅₀; higher = more potent).
No ChEMBL hits found through similar proteins.
Proposed virtual-screening candidates from ZINC. Score = Tanimoto similarity to a known binder (0–1; higher = more similar).
| Ligand | Tanimoto | MW · LogP · TPSA | Lipinski | PAINS | SMILES |
|---|---|---|---|---|---|
| ZINC2004372 | 1.000 | 221.3 Da LogP 1.19 TPSA 66.4 | ✓ Ro5 | ✓ Clean |
O=S(=O)(O)CCCNC1CCCCC1
|
| ZINC38364153 | 0.926 | 235.3 Da LogP 1.58 TPSA 66.4 | ✓ Ro5 | ✓ Clean |
O=S(=O)(O)CCCCNC1CCCCC1
|
| ZINC1710230 | 0.786 | 207.3 Da LogP 0.80 TPSA 66.4 | ✓ Ro5 | ✓ Clean |
O=S(=O)(O)CCNC1CCCCC1
|
| ZINC5188799 | 0.630 | 280.5 Da LogP 4.39 TPSA 24.1 | ✓ Ro5 | ✓ Clean |
C(CCCNC1CCCCC1)CCNC1CCCCC1
|
| ZINC2509149 | 0.531 | 211.4 Da LogP 4.27 TPSA 12.0 | ✓ Ro5 | ✓ Clean |
CCCCCCCCNC1CCCCC1
|
| ZINC130127586 | 0.529 | 260.4 Da LogP 1.38 TPSA 58.2 | ✓ Ro5 | ✓ Clean |
O=S(=O)(NCCNC1CCCCCC1)C1CC1
|
| ZINC19367005 | 0.519 | 224.4 Da LogP 2.83 TPSA 24.1 | ✓ Ro5 | ✓ Clean |
C1CCC(NCCNC2CCCCC2)CC1
|
| ZINC1672446 | 0.500 | 228.3 Da LogP 1.49 TPSA 75.3 | ✓ Ro5 | ✓ Clean |
N[C@@H](CCCCNC1CCCCC1)C(=O)O
|
| ZINC2168583 | 0.500 | 237.3 Da LogP 0.16 TPSA 86.6 | ✓ Ro5 | ✓ Clean |
O=S(=O)(O)C[C@@H](O)CNC1CCCCC1
|
| ZINC2168584 | 0.500 | 237.3 Da LogP 0.16 TPSA 86.6 | ✓ Ro5 | ✓ Clean |
O=S(=O)(O)C[C@H](O)CNC1CCCCC1
|
| ZINC236994621 | 0.500 | 290.4 Da LogP 0.85 TPSA 75.3 | ✓ Ro5 | ✓ Clean |
CCS(=O)(=O)CC(=O)NCCNC1CCCCCC1
|
| ZINC44655186 | 0.500 | 213.4 Da LogP 3.12 TPSA 21.3 | ✓ Ro5 | ✓ Clean |
COCCCCNC1CCCCCCC1
|
| ZINC5840523 | 0.500 | 228.3 Da LogP 1.49 TPSA 75.3 | ✓ Ro5 | ✓ Clean |
N[C@H](CCCCNC1CCCCC1)C(=O)O
|
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.