Protein profile

KP13_00653

Gamma-glutamyltranspeptidase

Genome: KpKP13

Gene: ggt AHE42272.1 Structure source: AlphaFold + ColabFold UniProt A0A0H3GWX6

Export view

Amino acids 581

Annotations 6

Features 30

PDB binders 8

Druggability 0.442

Overview

Basic information about this protein and its source genome.

Accession: KP13_00653
Assembly: Klebsiella pneumoniae subsp. pneumoniae Kp13, complete sequence
Gene: ggt AHE42272.1
Status: annotated
Amino acids: 581
Structure source: AlphaFold + ColabFold

2.3.2.2 3.4.19.13

GO:0006751 The chemical reactions and pathways resulting in the breakdown of glutathione, the tripeptide glutamylcysteinylglycine, which acts as a coenzyme for some enzymes and as an antioxidant in the protection of sulfhydryl groups in enzymes and other proteins. GO:0036374 Catalysis of the reaction: glutathione + H2O = L-cysteinylglycine + L-glutamate. GO:0103068 OBSOLETE. Catalysis of the reaction: leukotriene C4 + a standard alpha amino acid = leukotriene D4 + an (gamma-L-glutamyl)-L-amino acid. GO:0006750 The chemical reactions and pathways resulting in the formation of glutathione, the tripeptide glutamylcysteinylglycine, which acts as a coenzyme for some enzymes and as an antioxidant in the protection of sulfhydryl groups in enzymes and other proteins.

Target profile

Computed evidence for target prioritization.

Human off-target: hit
Human identity (%): 40.876
Human E-value: 2.69e-24
Gut microbiome off-target: hit
Essential (DEG): Y
DEG identity (%): 88.966
DEG E-value: 0.0
Localization: Periplasmic
ColabFold pLDDT: 91.43

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 0.442

Structure A0A0H3GWX6

Pocket Pocket 6

P2Rank 0.711

Structure A0A0H3GWX6

Pocket Pocket 1

ColabFold model

FPocket 0.116 · Pocket 2

P2Rank 0.554 · Pocket 1

Core conservation Accessory gene

Roary core

CoreCruncher accessory

Gut microbiome 103 / 4744 genomes with a hit

Normalized 0.022

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

2 EC 4 GO

Enzyme Commission (EC)

Gene Ontology (GO)

GO:0006751 The chemical reactions and pathways resulting in the breakdown of glutathione, the tripeptide glutamylcysteinylglycine, which acts as a coenzyme for some enzymes and as an antioxidant in the protection of sulfhydryl groups in enzymes and other proteins.
GO:0036374 Catalysis of the reaction: glutathione + H2O = L-cysteinylglycine + L-glutamate.
GO:0103068 OBSOLETE. Catalysis of the reaction: leukotriene C4 + a standard alpha amino acid = leukotriene D4 + an (gamma-L-glutamyl)-L-amino acid.
GO:0006750 The chemical reactions and pathways resulting in the formation of glutathione, the tripeptide glutamylcysteinylglycine, which acts as a coenzyme for some enzymes and as an antioxidant in the protection of sulfhydryl groups in enzymes and other proteins.

Sequence Features

Domain/signature hits from InterPro and related databases.

30 records

Show feature table

Start	End	DB	Term	Name
1	25	SignalP_EUK	SignalP-noTM	SignalP-noTM
392	416	ProSitePatterns	PS00462	Gamma-glutamyltranspeptidase signature.
392	416	InterPro	IPR000101	Gamma-glutamyltranspeptidase
1	25	Phobius	SIGNAL_PEPTIDE	Signal peptide region
392	581	Gene3D	G3DSA:3.60.20.40	-
392	581	InterPro	IPR043137	Gamma-glutamyltranspeptidase, small subunit
50	572	NCBIfam	TIGR00066	gamma-glutamyltransferase
50	572	InterPro	IPR000101	Gamma-glutamyltranspeptidase
43	573	PANTHER	PTHR43199	GLUTATHIONE HYDROLASE
392	410	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
416	434	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
72	97	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
481	498	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
262	278	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
292	311	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
145	163	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
457	472	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
163	182	PRINTS	PR01210	Gamma-glutamyltranspeptidase signature
10	21	Phobius	SIGNAL_PEPTIDE_H_REGION	Hydrophobic region of a signal peptide.
278	391	FunFam	G3DSA:1.10.246.130:FF:000004	Gamma-glutamyltranspeptidase (Ggt)
42	574	SUPERFAMILY	SSF56235	N-terminal nucleophile aminohydrolases (Ntn hydrolases)
42	574	InterPro	IPR029055	Nucleophile aminohydrolases, N-terminal
65	573	Pfam	PF01019	Gamma-glutamyltranspeptidase
392	581	FunFam	G3DSA:3.60.20.40:FF:000003	Gamma-glutamyltranspeptidase
1	25	SignalP_GRAM_POSITIVE	SignalP-TM	SignalP-TM
278	391	Gene3D	G3DSA:1.10.246.130	-
278	391	InterPro	IPR043138	Gamma-glutamyltranspeptidase, large subunit, C-terminal domain
26	581	Phobius	NON_CYTOPLASMIC_DOMAIN	Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region.
22	25	Phobius	SIGNAL_PEPTIDE_C_REGION	C-terminal region of a signal peptide.
1	9	Phobius	SIGNAL_PEPTIDE_N_REGION	N-terminal region of a signal peptide.

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...

Legend High Medium Low

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_A0A0H3GWX6	AlphaFold	—	—	full sequence	—	Viewing
ColabFold KP13_00653	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
6				0.442

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	Score	Probability
1	9.05	0.485
2	2.63	0.076
3	2.62	0.076
4	2.24	0.055
5	2.18	0.052

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	Score	Probability
1	5.91	0.29
2	2.3	0.059
3	1.78	0.033
4	1.57	0.024
5	1.37	0.016

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.

58 records

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.

Ligand	Source crystal	UniProt (homolog)	MW · LogP · TPSA	Lipinski	PAINS	SMILES
4UD	5BPK	O25743	144.1 Da LogP -0.83 TPSA 84.9	✓ Ro5	✓ Clean	`C1C=NO[C@@H]1[C@@H](C(=O)O)N`
6FY	5B5T	P18956	310.2 Da LogP -0.74 TPSA 156.0	✓ Ro5	✓ Clean	`CC[C@H](C(=O)NCC(=O)O)O[P@H](=O)CC[C@@H](C(=O)O…`
AVN	3FNM	O25743	178.6 Da LogP -0.26 TPSA 84.9	✓ Ro5	✓ Clean	`C1[C@H](ON=C1Cl)[C@@H](C(=O)O)N`
AZS	2Z8I	P18956	173.1 Da LogP -1.76 TPSA 126.0	✓ Ro5	Alert	`C([C@@H](C(=O)O)N)OC(=O)C=[N+]=[N-]`
DON	5Y9B	Q65KZ6	173.2 Da LogP -0.22 TPSA 116.6	✓ Ro5	Alert	`C(CC(=O)CN=N)[C@@H](C(=O)O)N`
GBL	7D9X	A0A6G6IRK3	86.1 Da LogP 0.32 TPSA 26.3	✓ Ro5	✓ Clean	`C1CC(=O)OC1`
GGL	2DBW	P18956	147.1 Da LogP -0.74 TPSA 100.6	✓ Ro5	✓ Clean	`C(CC(=O)O)[C@@H](C(=O)O)N`
GTB	2QMC	O25743	442.5 Da LogP -0.29 TPSA 202.0	✓ Ro5	✓ Clean	`c1cc(ccc1CSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H]…`

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
ZINC2031112	0.824	200.2 Da LogP 1.43 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCC(=O)OCCCCO1`
ZINC113251999	0.778	228.3 Da LogP 2.21 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCC(=O)OCCCCCCO1`
ZINC34542648	0.778	228.3 Da LogP 2.21 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCOC(=O)CCCCCO1`
ZINC4023310	0.778	212.3 Da LogP 3.83 TPSA 26.3	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCCCO1`
ZINC4023520	0.778	240.4 Da LogP 4.61 TPSA 26.3	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCCCCCO1`
ZINC4026026	0.778	256.3 Da LogP 2.99 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCCCO1`
ZINC4026253	0.778	284.4 Da LogP 3.77 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCCCCCO1`
ZINC4026492	0.778	270.4 Da LogP 3.38 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCCCCO1`
ZINC4676827	0.778	270.4 Da LogP 3.38 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCC(=O)OCCCCCCO1`
ZINC33802904	0.765	344.4 Da LogP 1.29 TPSA 105.2	✓ Ro5	✓ Clean	`O=C1CCCCC(=O)OCCOC(=O)CCCCC(=O)OCCO1`
ZINC35906424	0.765	344.4 Da LogP 1.29 TPSA 105.2	✓ Ro5	✓ Clean	`O=C1CCC(=O)OCCCCOC(=O)CCC(=O)OCCCCO1`
ZINC4026344	0.750	254.4 Da LogP 3.79 TPSA 43.4	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCC(=O)OCCC1`
ZINC196715962	0.722	456.6 Da LogP 4.41 TPSA 105.2	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCOC(=O)CCCCCCCCC(=O)OCCO1`
ZINC4015272	0.722	228.3 Da LogP 2.21 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCO1`
ZINC4024376	0.722	270.4 Da LogP 3.38 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCCC(=O)OCCO1`
ZINC4026271	0.722	214.3 Da LogP 1.82 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCC(=O)OCCO1`
ZINC4794429	0.722	256.3 Da LogP 2.99 TPSA 52.6	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCC(=O)OCCO1`
ZINC3870210	0.698	473.4 Da LogP -0.53 TPSA 245.1	✓ Ro5	✓ Clean	`N[C@@H](CCC(=O)N[C@@H](CSc1ccc([N+](=O)[O-])cc1…`
ZINC2106542	0.667	245.3 Da LogP 1.99 TPSA 100.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCCCCCCC(=O)O)C(=O)O`
ZINC2106543	0.667	245.3 Da LogP 1.99 TPSA 100.6	✓ Ro5	✓ Clean	`N[C@H](CCCCCCCCCC(=O)O)C(=O)O`
ZINC2108713	0.667	217.3 Da LogP 1.21 TPSA 100.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCCCCC(=O)O)C(=O)O`
ZINC2108714	0.667	217.3 Da LogP 1.21 TPSA 100.6	✓ Ro5	✓ Clean	`N[C@H](CCCCCCCC(=O)O)C(=O)O`
ZINC3881672	0.667	256.4 Da LogP 3.85 TPSA 35.5	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCOCCCCO1`
ZINC4026039	0.667	256.4 Da LogP 3.85 TPSA 35.5	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCOCCCCCO1`
ZINC5189357	0.667	256.4 Da LogP 3.85 TPSA 35.5	✓ Ro5	✓ Clean	`O=C1CCCCCCCCOCCCCCCO1`
ZINC139862480	0.650	304.3 Da LogP 0.70 TPSA 80.3	✓ Ro5	✓ Clean	`O=C1CCCCC(=O)OCCOCCOCCOCCO1`
ZINC5188445	0.650	216.2 Da LogP 0.66 TPSA 61.8	✓ Ro5	✓ Clean	`O=C1CCCCC(=O)OCCOCCO1`
ZINC2242694	0.643	276.2 Da LogP -1.39 TPSA 167.0	✓ Ro5	✓ Clean	`N[C@@H](CCC(=O)N[C@@H](CCC(=O)O)C(=O)O)C(=O)O`
ZINC2547582	0.643	276.2 Da LogP -1.39 TPSA 167.0	✓ Ro5	✓ Clean	`N[C@@H](CCC(=O)N[C@H](CCC(=O)O)C(=O)O)C(=O)O`
ZINC4096970	0.643	405.4 Da LogP -2.04 TPSA 233.4	1 viol.	✓ Clean	`N[C@@H](CCC(=O)N[C@@H](CCC(=O)N[C@@H](CCC(=O)O)…`
ZINC4545890	0.643	276.2 Da LogP -1.39 TPSA 167.0	✓ Ro5	✓ Clean	`N[C@H](CCC(=O)N[C@@H](CCC(=O)O)C(=O)O)C(=O)O`
ZINC4545891	0.643	276.2 Da LogP -1.39 TPSA 167.0	✓ Ro5	✓ Clean	`N[C@H](CCC(=O)N[C@H](CCC(=O)O)C(=O)O)C(=O)O`
ZINC3055005	0.619	204.2 Da LogP -0.63 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCC[C@H](N)C(=O)O)C(=O)O`
ZINC3055007	0.619	204.2 Da LogP -0.63 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC3055010	0.619	204.2 Da LogP -0.63 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@H](CCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC4024200	0.619	300.4 Da LogP 3.00 TPSA 61.8	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCCC(=O)OCCOCCO1`
ZINC4863091	0.619	316.4 Da LogP 2.24 TPSA 71.1	✓ Ro5	✓ Clean	`O=C1CCCCCCCCC(=O)OCCOCCOCCO1`
ZINC18024709	0.600	269.4 Da LogP 4.05 TPSA 58.9	✓ Ro5	✓ Clean	`O=C1CCCCCCCCCC/C(=N\O)CCCO1`
ZINC72334032	0.600	241.3 Da LogP 3.27 TPSA 58.9	✓ Ro5	✓ Clean	`O=C1CCCCCCCC/C(=N\O)CCCO1`
ZINC13537379	0.593	256.3 Da LogP 1.24 TPSA 106.5	✓ Ro5	✓ Clean	`N[C@@H](CSCc1ccc([N+](=O)[O-])cc1)C(=O)O`
ZINC1530265	0.593	219.2 Da LogP -0.80 TPSA 126.9	✓ Ro5	✓ Clean	`N[C@H](CCOC(=O)CCC(=O)O)C(=O)O`
ZINC1532858	0.593	219.2 Da LogP -0.80 TPSA 126.9	✓ Ro5	✓ Clean	`N[C@@H](CCOC(=O)CCC(=O)O)C(=O)O`
ZINC1576202	0.593	204.2 Da LogP -1.62 TPSA 129.7	✓ Ro5	✓ Clean	`N[C@@H](CCC(=O)NCC(=O)O)C(=O)O`
ZINC1680890	0.593	256.3 Da LogP 1.24 TPSA 106.5	✓ Ro5	✓ Clean	`N[C@H](CSCc1ccc([N+](=O)[O-])cc1)C(=O)O`
ZINC3995565	0.593	204.2 Da LogP -1.62 TPSA 129.7	✓ Ro5	✓ Clean	`N[C@H](CCC(=O)NCC(=O)O)C(=O)O`
ZINC1555366	0.591	232.3 Da LogP 0.15 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCCC[C@H](N)C(=O)O)C(=O)O`
ZINC1555367	0.591	232.3 Da LogP 0.15 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC1555369	0.591	232.3 Da LogP 0.15 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@H](CCCCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC1720127	0.591	218.3 Da LogP -0.24 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCC[C@H](N)C(=O)O)C(=O)O`
ZINC1720128	0.591	218.3 Da LogP -0.24 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCC[C@@H](N)C(=O)O)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.