Protein profile
KP13_02008
Trifunctional NAD biosynthesis/regulator protein NadR
Genome: KpKP13
Overview
Basic information about this protein and its source genome.
- Accession
- KP13_02008
- Gene
- AHE46445.1 nadR
- Status
- annotated
- Amino acids
- 410
- Structure source
- AlphaFold + ColabFold
Target profile
Computed evidence for target prioritization.
- Human off-target
- No hit
- Human identity (%)
- 0.0
- Gut microbiome off-target
- hit
- Essential (DEG)
- Y
- DEG identity (%)
- 54.441
- DEG E-value
- 9.78e-141
- Localization
- Cytoplasmic
- ColabFold pLDDT
- 91.39
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.
Gene Ontology (GO)
9- GO:0009058 A cellular process consisting of the biochemical pathways by which a living organism synthesizes chemical substances. This typically represents the energy-requiring part of metabolism in which simpler substances are transformed into more complex ones.
- GO:0009435 The chemical reactions and pathways resulting in the formation of nicotinamide adenine dinucleotide (NAD+), a coenzyme that interconverts with its reduced form, NADH, in many redox and catabolic reactions. NAD+ is derived from various sources including vitamin B3.
- GO:0000309 Catalysis of the reaction: beta-nicotinamide D-ribonucleotide + ATP + H+ = diphosphate + NAD+.
- 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:0050262 Catalysis of the reaction: beta-nicotinamide D-riboside + ATP = beta-nicotinamide D-ribonucleotide + ADP + H+.
- GO:0003677 Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid).
- GO:0005737 The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
- GO:0005886 The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
- GO:0005524 Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
Sequence Features
Domain/signature hits from InterPro and related databases.
Show feature table
| Start | End | DB | Term | Name |
|---|---|---|---|---|
| 2 | 410 | PIRSF | PIRSF004776 | NadR_NMNAT/RNK |
| 2 | 410 | InterPro | IPR016429 | NAD biosynthesis/regulator protein NadR |
| 63 | 230 | Gene3D | G3DSA:3.40.50.620 | HUPs |
| 63 | 230 | InterPro | IPR014729 | Rossmann-like alpha/beta/alpha sandwich fold |
| 232 | 386 | SUPERFAMILY | SSF52540 | P-loop containing nucleoside triphosphate hydrolases |
| 232 | 386 | InterPro | IPR027417 | P-loop containing nucleoside triphosphate hydrolase |
| 5 | 60 | FunFam | G3DSA:1.10.260.40:FF:000020 | Trifunctional nicotinamide-nucleotide adenylyltransferase/ribosylnicotinamide kinase/transcriptional regulator NadR |
| 7 | 62 | ProSiteProfiles | PS50943 | Cro/C1-type HTH domain profile. |
| 7 | 62 | InterPro | IPR001387 | Cro/C1-type helix-turn-helix domain |
| 66 | 409 | PANTHER | PTHR37512 | TRIFUNCTIONAL NAD BIOSYNTHESIS/REGULATOR PROTEIN NADR |
| 64 | 395 | NCBIfam | TIGR01526 | nicotinamide-nucleotide adenylyltransferase |
| 64 | 395 | InterPro | IPR006417 | Nicotinamide-nucleotide adenylyltransferase |
| 7 | 59 | CDD | cd00093 | HTH_XRE |
| 7 | 59 | InterPro | IPR001387 | Cro/C1-type helix-turn-helix domain |
| 6 | 62 | SMART | SM00530 | mbf_short4 |
| 6 | 62 | InterPro | IPR001387 | Cro/C1-type helix-turn-helix domain |
| 63 | 230 | FunFam | G3DSA:3.40.50.620:FF:000091 | Trifunctional nicotinamide-nucleotide adenylyltransferase/ribosylnicotinamide kinase/transcriptional regulator NadR |
| 66 | 136 | NCBIfam | TIGR00125 | cytidyltransferase-like domain |
| 66 | 136 | InterPro | IPR004821 | Cytidyltransferase-like domain |
| 66 | 227 | CDD | cd02167 | NMNAT_NadR |
| 66 | 227 | InterPro | IPR041749 | NadR, nicotinamide/nicotinate mononucleotide adenylyltransferase domain |
| 7 | 58 | Pfam | PF01381 | Helix-turn-helix |
| 7 | 58 | InterPro | IPR001387 | Cro/C1-type helix-turn-helix domain |
| 231 | 397 | FunFam | G3DSA:3.40.50.300:FF:000672 | Trifunctional nicotinamide-nucleotide adenylyltransferase/ribosylnicotinamide kinase/transcriptional regulator NadR |
| 231 | 397 | Gene3D | G3DSA:3.40.50.300 | - |
| 231 | 397 | InterPro | IPR027417 | P-loop containing nucleoside triphosphate hydrolase |
| 6 | 60 | SUPERFAMILY | SSF47413 | lambda repressor-like DNA-binding domains |
| 6 | 60 | InterPro | IPR010982 | Lambda repressor-like, DNA-binding domain superfamily |
| 66 | 229 | SUPERFAMILY | SSF52374 | Nucleotidylyl transferase |
| 233 | 260 | CDD | cd02019 | NK |
| 5 | 60 | Gene3D | G3DSA:1.10.260.40 | - |
| 5 | 60 | InterPro | IPR010982 | Lambda repressor-like, DNA-binding domain superfamily |
| 234 | 394 | Pfam | PF13521 | AAA domain |
| 234 | 394 | InterPro | IPR038727 | NadR/Ttd14, AAA domain |
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_A0A0H3GM95
|
AlphaFold | — | — | full sequence | — | Viewing |
|
ColabFold
KP13_02008
|
ColabFold | — | — | full sequence | — | Loaded |
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 | 0.958 | ||||||
| 17 | 0.816 | ||||||
| 7 | 0.261 |
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 | 24.94 | 0.902 | ||||||
| 2 | 10.42 | 0.56 | ||||||
| 3 | 2.77 | 0.084 | ||||||
| 4 | 1.77 | 0.033 |
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 | 0.812 | ||||||
| 2 | 0.738 | ||||||
| 10 | 0.212 |
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 | 14.61 | 0.728 | ||||||
| 2 | 12.09 | 0.638 | ||||||
| 3 | 5.17 | 0.239 | ||||||
| 4 | 2.21 | 0.053 | ||||||
| 5 | 1.2 | 0.011 |