Protein profile

PA2709

cysteine synthase A

Genome: NC_002516.2

Gene: PA2709 cysK Structure source: AlphaFold UniProt Q9I0D3

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Amino acids 324

Annotations 5

Features 18

PDB binders 5

Druggability 0.52

Overview

Basic information about this protein and its source genome.

Accession: PA2709
Assembly: Pseudomonas aeruginosa PAO1, complete genome
Gene: PA2709 cysK
Status: annotated
Amino acids: 324
Structure source: AlphaFold

2.5.1.47

GO:0005737 The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. GO:0004124 Catalysis of the reaction: O3-acetyl-L-serine + hydrogen sulfide = L-cysteine + acetate. GO:0080146 Catalysis of the reaction: L-cysteine + H2O = hydrogen sulfide + pyruvate + NH4+ + H+. GO:0006535 OBSOLETE. The chemical reactions and pathways resulting in the formation of cysteine from L- serine.

Target profile

Computed evidence for target prioritization.

Human off-target: hit
Human identity (%): 52.427
Human E-value: 8.11e-25
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 0.52

Structure –

Pocket –

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

1 EC 4 GO

Enzyme Commission (EC)

2.5.1.47

Gene Ontology (GO)

GO:0005737 The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
GO:0004124 Catalysis of the reaction: O3-acetyl-L-serine + hydrogen sulfide = L-cysteine + acetate.
GO:0080146 Catalysis of the reaction: L-cysteine + H2O = hydrogen sulfide + pyruvate + NH4+ + H+.
GO:0006535 OBSOLETE. The chemical reactions and pathways resulting in the formation of cysteine from L- serine.

Sequence Features

Domain/signature hits from InterPro and related databases.

18 records

Show feature table

Start	End	DB	Term	Name
9	313	NCBIfam	TIGR01136	cysteine synthase
9	313	InterPro	IPR005856	Cysteine synthase
33	51	ProSitePatterns	PS00901	Cysteine synthase/cystathionine beta-synthase P-phosphate attachment site.
33	51	InterPro	IPR001216	Cysteine synthase/cystathionine beta-synthase, pyridoxal-phosphate attachment site
9	313	NCBIfam	TIGR01139	cysteine synthase A
9	313	InterPro	IPR005859	Cysteine synthase CysK
45	143	FunFam	G3DSA:3.40.50.1100:FF:000002	Cysteine synthase
144	309	FunFam	G3DSA:3.40.50.1100:FF:000006	Cysteine synthase
6	312	SUPERFAMILY	SSF53686	Tryptophan synthase beta subunit-like PLP-dependent enzymes
6	312	InterPro	IPR036052	Tryptophan synthase beta chain-like, PALP domain superfamily
10	302	Pfam	PF00291	Pyridoxal-phosphate dependent enzyme
10	302	InterPro	IPR001926	Tryptophan synthase beta chain-like, PALP domain
13	309	CDD	cd01561	CBS_like
12	309	Gene3D	G3DSA:3.40.50.1100	-
12	309	InterPro	IPR036052	Tryptophan synthase beta chain-like, PALP domain superfamily
45	147	Gene3D	G3DSA:3.40.50.1100	-
45	147	InterPro	IPR036052	Tryptophan synthase beta chain-like, PALP domain superfamily
9	319	PANTHER	PTHR10314	CYSTATHIONINE BETA-SYNTHASE

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 PA2709	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
3				0.52
1				0.263

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.

70 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
0JO	5DBE	P45040	316.2 Da LogP 0.72 TPSA 149.5	✓ Ro5	✓ Clean	`Cc1c(c(c(cn1)COP(=O)(O)O)/C=N/C(=C)C(=O)O)O`
AA5	1Z7Y	P47998	378.3 Da LogP 1.33 TPSA 149.5	✓ Ro5	✓ Clean	`Cc1c(c(c(cn1)COP(=O)(O)O)C=N[C@@H](CCSC)C(=O)O)O`
AWH	3ZEI	P9WP55	412.4 Da LogP 3.08 TPSA 116.5	✓ Ro5	✓ Clean	`CN\1C(=O)/C(=C/c2ccccc2OCC(=O)O)/S/C1=N\c3cccc(…`
OAS	4ORE	P45040	147.1 Da LogP -1.04 TPSA 89.6	✓ Ro5	✓ Clean	`CC(=O)OC[C@@H](C(=O)O)N`
PDA	2Q3D	P9WP55	320.2 Da LogP 0.27 TPSA 149.2	✓ Ro5	✓ Clean	`Cc1c(c(c(cn1)COP(=O)(O)O)CNC(C)C(=O)O)O`

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).

Ligand	UniProt (homolog)	pchembl	MW · LogP · TPSA	Lipinski	PAINS	SMILES
CHEMBL2418481	P9WP55	7.72	356.4 Da LogP 3.76 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(F)cc2)S/C1=N\c1cccc(C(=O)O)…`
CHEMBL2418529	P9WP55	7.59	444.5 Da LogP 5.20 TPSA 79.2	1 viol.	✓ Clean	`CN1C(=O)/C(=C/c2ccc(OCc3ccccc3)cc2)S/C1=N\c1ccc…`
CHEMBL2418524	P9WP55	7.47	368.4 Da LogP 3.63 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O)…`
CHEMBL2418487	P9WP55	7.43	381.5 Da LogP 3.68 TPSA 73.2	✓ Ro5	Alert	`CN1C(=O)/C(=C/c2ccc(N(C)C)cc2)S/C1=N\c1cccc(C(=…`
CHEMBL2418504	P9WP55	7.26	398.4 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O)…`
CHEMBL2418505	P9WP55	7.25	412.5 Da LogP 4.03 TPSA 88.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(OC)c(OC)c2)S/C1=N\c1cccc(C…`
CHEMBL2418502	P9WP55	7.22	384.4 Da LogP 3.33 TPSA 99.4	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O)c…`
CHEMBL2418568	P9WP55	7.20	354.4 Da LogP 3.32 TPSA 90.2	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N\c1cccc(C(=O)O)…`
CHEMBL2418489	P9WP55	7.16	428.5 Da LogP 3.64 TPSA 97.7	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O)c…`
CHEMBL2418545	P9WP55	7.02	382.4 Da LogP 4.10 TPSA 90.2	✓ Ro5	✓ Clean	`CCCN1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N\c1cccc(C(=O)…`
CHEMBL2418569	P9WP55	6.99	368.4 Da LogP 3.71 TPSA 90.2	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N\c1cccc(C(=O)O…`
CHEMBL2418548	P9WP55	6.96	380.4 Da LogP 3.88 TPSA 90.2	✓ Ro5	✓ Clean	`C=CCN1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N\c1cccc(C(=O…`
CHEMBL2418551	P9WP55	6.85	382.4 Da LogP 4.10 TPSA 90.2	✓ Ro5	✓ Clean	`CC(C)N1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N\c1cccc(C(=…`
CHEMBL2418514	P9WP55	6.79	368.4 Da LogP 3.63 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccccc1/C=C1\S/C(=N\c2cccc(C(=O)O)c2)N(C)C1=O`
CHEMBL4858734	P9WP55	6.20	844.9 Da LogP 1.49 TPSA 257.4	3 viol.	Alert	`C[C@@H]1O[C@@H](O[C@@H]2C[C@H](c3ccc4c(c3O)C(=O…`

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
ZINC100260795	1.000	412.4 Da LogP 3.08 TPSA 116.5	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccccc2OCC(=O)O)S/C1=N/c1cccc(C(…`
ZINC4575663	1.000	398.4 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC4599096	1.000	384.4 Da LogP 3.33 TPSA 99.4	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)c…`
ZINC5065718	1.000	381.5 Da LogP 3.68 TPSA 73.2	✓ Ro5	Alert	`CN1C(=O)/C(=C/c2ccc(N(C)C)cc2)S/C1=N/c1cccc(C(=…`
ZINC100321212	0.867	398.4 Da LogP 3.72 TPSA 99.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(OC)c(O)c2)S/C1=N/c1cccc(C(…`
ZINC100936755	0.867	398.4 Da LogP 3.72 TPSA 99.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(O)c(OC)c2)S/C1=N/c1cccc(C(…`
ZINC33684545	0.867	398.4 Da LogP 3.72 TPSA 99.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C\c2ccc(O)c(OC)c2)S/C1=N\c1cccc(C(…`
ZINC100260846	0.862	384.4 Da LogP 3.33 TPSA 99.4	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC4660262	0.860	382.4 Da LogP 3.94 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC100309209	0.852	461.3 Da LogP 4.78 TPSA 79.2	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(OC)c(Br)c2)S/C1=N/c1cccc(C…`
ZINC6878883	0.850	442.4 Da LogP 3.09 TPSA 125.7	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)c…`
ZINC100318601	0.845	402.9 Da LogP 4.28 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC100928204	0.845	447.3 Da LogP 4.39 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC8438503	0.845	494.3 Da LogP 4.23 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC100318659	0.844	436.5 Da LogP 4.03 TPSA 88.4	✓ Ro5	✓ Clean	`C#CCOc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(CC)C…`
ZINC100260861	0.840	338.4 Da LogP 3.62 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccccc2)S/C1=N/c1cccc(C(=O)O)c1`
ZINC8642766	0.840	338.4 Da LogP 3.62 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccccc2)S/C1=N\c1cccc(C(=O)O)c1`
ZINC4698831	0.836	368.4 Da LogP 3.63 TPSA 79.2	✓ Ro5	✓ Clean	`COc1cccc(/C=C2/S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O…`
ZINC83316693	0.828	412.4 Da LogP 3.08 TPSA 116.5	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccccc2OCC(=O)O)S/C1=N/c1ccc(C(=…`
ZINC100309361	0.827	354.4 Da LogP 3.32 TPSA 90.2	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(O)cc2)S/C1=N/c1cccc(C(=O)O)…`
ZINC2296453232	0.827	354.4 Da LogP 3.32 TPSA 90.2	✓ Ro5	✓ Clean	`CN1C(=O)C(=Cc2ccc(O)cc2)SC1=Nc1cccc(C(=O)O)c1`
ZINC5024864	0.827	352.4 Da LogP 3.93 TPSA 70.0	✓ Ro5	✓ Clean	`Cc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)c…`
ZINC6878881	0.825	428.5 Da LogP 3.64 TPSA 97.7	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)c…`
ZINC100927880	0.820	491.3 Da LogP 3.84 TPSA 116.5	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2cc(Br)ccc2OCC(=O)O)S/C1=N/c1ccc…`
ZINC4591268	0.820	398.4 Da LogP 3.72 TPSA 99.4	✓ Ro5	✓ Clean	`CCOc1cc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC100260791	0.817	412.4 Da LogP 3.08 TPSA 116.5	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(OCC(=O)O)cc2)S/C1=N/c1cccc(…`
ZINC100260761	0.811	372.8 Da LogP 4.27 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(Cl)cc2)S/C1=N/c1cccc(C(=O)O…`
ZINC8642746	0.811	372.8 Da LogP 4.27 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(Cl)cc2)S/C1=N\c1cccc(C(=O)O…`
ZINC100927270	0.810	384.4 Da LogP 3.33 TPSA 99.4	✓ Ro5	✓ Clean	`COc1cc(/C=C2\S/C(=N/c3ccc(C(=O)O)cc3)N(C)C2=O)c…`
ZINC6878882	0.810	422.5 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`C#CCOc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2…`
ZINC100260755	0.807	368.4 Da LogP 3.63 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccccc1/C=C1\S/C(=N/c2cccc(C(=O)O)c2)N(C)C1=O`
ZINC1007728	0.804	396.4 Da LogP 3.41 TPSA 96.3	✓ Ro5	✓ Clean	`COC(=O)c1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)…`
ZINC4680392	0.804	340.4 Da LogP 3.63 TPSA 62.1	✓ Ro5	✓ Clean	`COc1cc(/C=C2/S/C(=N/c3ccccc3)N(C)C2=O)ccc1O`
ZINC97456580	0.804	398.4 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3ccc(C(=O)O)cc3)N(C)C2=O)…`
ZINC4466315	0.792	336.4 Da LogP 4.18 TPSA 52.9	✓ Ro5	✓ Clean	`C=CCN1C(=O)/C(=C\c2ccc(O)cc2)S/C1=N/c1ccccc1`
ZINC100937907	0.790	488.5 Da LogP 4.90 TPSA 116.5	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccccc2OCc2ccc(C(=O)O)cc2)S/C1=N…`
ZINC4664355	0.789	368.5 Da LogP 4.33 TPSA 51.1	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C\c2ccc(OC)c(OC)c2)S/C1=N/c1ccccc1`
ZINC4698651	0.789	398.4 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`COc1ccc(OC)c(/C=C2/S/C(=N\c3cccc(C(=O)O)c3)N(C)…`
ZINC8399628	0.783	426.5 Da LogP 4.42 TPSA 88.4	✓ Ro5	✓ Clean	`CCOc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O…`
ZINC5033940	0.782	380.5 Da LogP 4.74 TPSA 70.0	✓ Ro5	✓ Clean	`CC(C)c1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2…`
ZINC100215266	0.778	381.5 Da LogP 3.68 TPSA 73.2	✓ Ro5	Alert	`CN1C(=O)/C(=C/c2ccc(N(C)C)cc2)S/C1=N/c1ccc(C(=O…`
ZINC5558020	0.778	368.4 Da LogP 3.63 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3ccc(C(=O)O)cc3)N(C)C2=O)…`
ZINC100260866	0.776	398.4 Da LogP 3.64 TPSA 88.4	✓ Ro5	✓ Clean	`COc1ccc(/C=C2\S/C(=N/c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC4691610	0.776	382.4 Da LogP 3.94 TPSA 79.2	✓ Ro5	✓ Clean	`COc1ccc(/C=C2/S/C(=N\c3cccc(C(=O)O)c3)N(C)C2=O)…`
ZINC100311577	0.769	491.4 Da LogP 4.79 TPSA 88.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2cc(Br)c(OC)c(OC)c2)S/C1=N/c1cc…`
ZINC100319088	0.769	432.9 Da LogP 4.38 TPSA 99.4	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2cc(Cl)c(O)c(OC)c2)S/C1=N/c1ccc…`
ZINC100931254	0.769	356.4 Da LogP 3.76 TPSA 70.0	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(F)cc2)S/C1=N/c1ccc(C(=O)O)c…`
ZINC100309245	0.768	370.4 Da LogP 4.15 TPSA 70.0	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C/c2ccc(F)cc2)S/C1=N/c1cccc(C(=O)O…`
ZINC4949945	0.768	370.4 Da LogP 4.15 TPSA 70.0	✓ Ro5	✓ Clean	`CCN1C(=O)/C(=C\c2ccc(F)cc2)S/C1=N\c1cccc(C(=O)O…`
ZINC100938831	0.767	480.3 Da LogP 3.93 TPSA 90.2	✓ Ro5	✓ Clean	`CN1C(=O)/C(=C/c2ccc(O)c(I)c2)S/C1=N/c1cccc(C(=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.