Protein profile

KP13_01909

UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D- alanine ligase

Genome: KpKP13

Gene: AHE46350.1 murF Structure source: AlphaFold + ColabFold UniProt A0A0H3GRQ0

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Amino acids 452

Annotations 5

Features 28

PDB binders 18

Druggability 0.458

Overview

Basic information about this protein and its source genome.

Accession: KP13_01909
Assembly: Klebsiella pneumoniae subsp. pneumoniae Kp13, complete sequence
Gene: AHE46350.1 murF
Status: annotated
Amino acids: 452
Structure source: AlphaFold + ColabFold

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:0047480 Catalysis of the reaction: UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysine + ATP + D-alanyl-D-alanine = phosphate + UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine + ADP. GO:0016881 Catalysis of the ligation of an acid to an amino acid via a carbon-nitrogen bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate. GO:0071555 A process that results in the assembly, arrangement of constituent parts, or disassembly of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis. GO:0005524 Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.

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 (%): 84.071
DEG E-value: 0.0
Localization: Cytoplasmic
ColabFold pLDDT: 94.99

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 0.458

Structure A0A0H3GRQ0

Pocket Pocket 29

P2Rank 0.975

Structure A0A0H3GRQ0

Pocket Pocket 1

ColabFold model

FPocket 0.126 · Pocket 26

P2Rank 0.976 · Pocket 1

Core conservation Conserved core gene

Roary core

CoreCruncher core

Gut microbiome 137 / 4744 genomes with a hit

Normalized 0.029

Sequence

Primary amino-acid sequence viewer.

Functional Annotations

Enzyme classification and Gene Ontology terms linked to this protein.

5 GO

Gene Ontology (GO)

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:0047480 Catalysis of the reaction: UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysine + ATP + D-alanyl-D-alanine = phosphate + UDP-N-acetylmuramoyl-L-alanyl-D-glutamyl-L-lysyl-D-alanyl-D-alanine + ADP.
GO:0016881 Catalysis of the ligation of an acid to an amino acid via a carbon-nitrogen bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.
GO:0071555 A process that results in the assembly, arrangement of constituent parts, or disassembly of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis.
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.

28 records

Show feature table

Start	End	DB	Term	Name
29	446	NCBIfam	TIGR01143	UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase
29	446	InterPro	IPR005863	UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase
1	15	Phobius	SIGNAL_PEPTIDE	Signal peptide region
81	310	Gene3D	G3DSA:3.40.1190.10	-
81	310	InterPro	IPR036565	Mur-like, catalytic domain superfamily
1	97	SUPERFAMILY	SSF63418	MurE/MurF N-terminal domain
1	97	InterPro	IPR035911	MurE/MurF, N-terminal
1	80	Gene3D	G3DSA:3.40.1390.10	-
1	3	Phobius	SIGNAL_PEPTIDE_N_REGION	N-terminal region of a signal peptide.
101	310	SUPERFAMILY	SSF53623	MurD-like peptide ligases, catalytic domain
101	310	InterPro	IPR036565	Mur-like, catalytic domain superfamily
1	449	PANTHER	PTHR43024	UDP-N-ACETYLMURAMOYL-TRIPEPTIDE--D-ALANYL-D-ALANINE LIGASE
12	15	Phobius	SIGNAL_PEPTIDE_C_REGION	C-terminal region of a signal peptide.
4	11	Phobius	SIGNAL_PEPTIDE_H_REGION	Hydrophobic region of a signal peptide.
106	292	Pfam	PF08245	Mur ligase middle domain
106	292	InterPro	IPR013221	Mur ligase, central
313	446	SUPERFAMILY	SSF53244	MurD-like peptide ligases, peptide-binding domain
313	446	InterPro	IPR036615	Mur ligase, C-terminal domain superfamily
16	452	Phobius	NON_CYTOPLASMIC_DOMAIN	Region of a membrane-bound protein predicted to be outside the membrane, in the extracellular region.
313	391	Pfam	PF02875	Mur ligase family, glutamate ligase domain
313	391	InterPro	IPR004101	Mur ligase, C-terminal
4	447	Hamap	MF_02019	UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase [murF].
4	447	InterPro	IPR005863	UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase
312	452	Gene3D	G3DSA:3.90.190.20	-
312	452	InterPro	IPR036615	Mur ligase, C-terminal domain superfamily
81	310	FunFam	G3DSA:3.40.1190.10:FF:000007	UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase
24	95	Pfam	PF01225	Mur ligase family, catalytic domain
24	95	InterPro	IPR000713	Mur ligase, N-terminal catalytic 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...

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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_A0A0H3GRQ0	AlphaFold	—	—	full sequence	—	Viewing
ColabFold KP13_01909	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
29				0.458
1				0.355
20				0.213

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	30.28	0.934
2	1.82	0.035
3	1.68	0.028

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				30.11	0.933

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.

77 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
1LG	2AM1	Q8DNV6	500.4 Da LogP 4.08 TPSA 99.5	1 viol.	✓ Clean	`c1c(c(cc(c1S(=O)(=O)N2CCOCC2)Cl)Cl)C(=O)Nc3c(c4…`
2GN	3ZM6	Q8DNV6	659.6 Da LogP 3.94 TPSA 157.2	1 viol.	✓ Clean	`c1cc(ccc1CN2CCc3c(sc(c3C#N)NC(=O)c4cc(c(cc4Cl)C…`
2LG	2AM2	Q8DNV6	438.0 Da LogP 4.04 TPSA 90.3	✓ Ro5	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(c(c1)C(=O)Nc2c(c3c(s2)CCC…`
ACP	4CVL	Q9HVZ7	505.2 Da LogP -1.52 TPSA 269.9	3 viol.	✓ Clean	`c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)…`
ANP	4ZIY	A0A0D5YEC3	506.2 Da LogP -2.06 TPSA 281.9	3 viol.	✓ Clean	`c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)…`
API	1E8C	P22188	190.2 Da LogP -1.02 TPSA 126.6	✓ Ro5	✓ Clean	`C(C[C@H](C(=O)O)N)C[C@@H](C(=O)O)N`
IGM	3ZM5	Q8DNV6	607.5 Da LogP 4.46 TPSA 123.0	1 viol.	✓ Clean	`c1cc(ccc1CN2CCc3c(sc(c3C#N)NC(=O)c4cc(c(cc4Cl)C…`
JHP	7B9E	P22188	227.7 Da LogP 1.75 TPSA 46.9	✓ Ro5	✓ Clean	`Cn1cc(c(n1)C(=O)NC2CCCC2)Cl`
LVV	7B68	P22188	239.3 Da LogP 1.23 TPSA 37.4	✓ Ro5	✓ Clean	`Cc1ccc(cc1)CN2CCS(=O)(=O)CC2`
O3D	7B60	P22188	215.3 Da LogP 0.51 TPSA 50.5	✓ Ro5	✓ Clean	`c1cc(oc1)CN2CCS(=O)(=O)CC2`
SYQ	7B61	P22188	204.3 Da LogP 1.92 TPSA 42.0	✓ Ro5	✓ Clean	`Cc1cccc(n1)C(=O)N[C@@H](C)C2CC2`
SYZ	7B6N	P22188	278.3 Da LogP 1.42 TPSA 66.5	✓ Ro5	✓ Clean	`Cc1cccc(c1)C(=O)NCCN2C(=O)CSC2=O`
SZK	7B6L	P22188	241.3 Da LogP 3.26 TPSA 43.0	✓ Ro5	✓ Clean	`CCn1c2ccccc2nc1NCc3ccco3`
SZN	7B6M	P22188	260.3 Da LogP 0.87 TPSA 66.5	✓ Ro5	✓ Clean	`Cc1cccc(c1)C(=O)NCCN2C(=O)CCC2=O`
T3Z	7B61	P22188	204.3 Da LogP 1.92 TPSA 42.0	✓ Ro5	✓ Clean	`Cc1cccc(n1)C(=O)N[C@H](C)C2CC2`
UAG	1E8C	P22188	879.6 Da LogP -5.30 TPSA 427.7	3 viol.	✓ Clean	`C[C@@H](C(=O)N[C@H](CCC(=O)O)C(=O)O)NC(=O)[C@@H…`
UML	4C12	Q2FZP6	1007.8 Da LogP -5.68 TPSA 482.8	3 viol.	✓ Clean	`C[C@@H](C(=O)N[C@H](CCC(=O)N[C@@H](CCCCN)C(=O)O…`
WZD	7B6Q	P22188	213.2 Da LogP 2.77 TPSA 53.9	✓ Ro5	✓ Clean	`c1ccc2c(c1)[nH]c(n2)NCc3ccco3`

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
CHEMBL272818	Q8DNV6	7.66	592.5 Da LogP 5.18 TPSA 119.7	2 viol.	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)c(Cl)cc2Cl)…`
CHEMBL91242	Q8DNV6	7.66	592.5 Da LogP 5.18 TPSA 119.7	2 viol.	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)c(Cl)cc2Cl)…`
CHEMBL272248	Q8DNV6	7.27	544.1 Da LogP 5.53 TPSA 110.5	2 viol.	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(Cl)c(C(=O)Nc2sc3c(c2C#N)C…`
CHEMBL91324	Q8DNV6	7.27	544.1 Da LogP 5.53 TPSA 110.5	2 viol.	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(Cl)c(C(=O)Nc2sc3c(c2C#N)C…`
CHEMBL271972	Q8DNV6	7.17	578.5 Da LogP 6.19 TPSA 110.5	2 viol.	✓ Clean	`CCN(CC)S(=O)(=O)c1cc(C(=O)Nc2sc3c(c2C#N)CC(c2cc…`
CHEMBL93913	Q8DNV6	7.17	578.5 Da LogP 6.19 TPSA 110.5	2 viol.	✓ Clean	`CCN(CC)S(=O)(=O)c1cc(C(=O)Nc2sc3c(c2C#N)CCC(c2c…`
CHEMBL329389	Q8DNV6	7.16	576.5 Da LogP 5.47 TPSA 99.5	2 viol.	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)c(Cl)cc2Cl)…`
CHEMBL411672	Q8DNV6	7.16	576.5 Da LogP 5.47 TPSA 99.5	2 viol.	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)c(Cl)cc2Cl)…`
CHEMBL92119	Q8DNV6	6.52	486.4 Da LogP 3.69 TPSA 99.5	✓ Ro5	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)c(Cl)cc2Cl)…`

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
ZINC19851827	1.000	215.3 Da LogP 0.51 TPSA 50.5	✓ Ro5	✓ Clean	`O=S1(=O)CCN(Cc2ccco2)CC1`
ZINC25773506	1.000	204.3 Da LogP 1.92 TPSA 42.0	✓ Ro5	✓ Clean	`Cc1cccc(C(=O)N[C@H](C)C2CC2)n1`
ZINC25773508	1.000	204.3 Da LogP 1.92 TPSA 42.0	✓ Ro5	✓ Clean	`Cc1cccc(C(=O)N[C@@H](C)C2CC2)n1`
ZINC467615	1.000	227.7 Da LogP 1.75 TPSA 46.9	✓ Ro5	✓ Clean	`Cn1cc(Cl)c(C(=O)NC2CCCC2)n1`
ZINC47693073	1.000	278.3 Da LogP 1.42 TPSA 66.5	✓ Ro5	✓ Clean	`Cc1cccc(C(=O)NCCN2C(=O)CSC2=O)c1`
ZINC513005	1.000	213.2 Da LogP 2.77 TPSA 53.9	✓ Ro5	✓ Clean	`c1coc(CNc2nc3ccccc3[nH]2)c1`
ZINC513479	1.000	241.3 Da LogP 3.26 TPSA 43.0	✓ Ro5	✓ Clean	`CCn1c(NCc2ccco2)nc2ccccc21`
ZINC59601259	1.000	239.3 Da LogP 1.23 TPSA 37.4	✓ Ro5	✓ Clean	`Cc1ccc(CN2CCS(=O)(=O)CC2)cc1`
ZINC72818936	1.000	260.3 Da LogP 0.87 TPSA 66.5	✓ Ro5	✓ Clean	`Cc1cccc(C(=O)NCCN2C(=O)CCC2=O)c1`
ZINC854136	1.000	438.0 Da LogP 4.04 TPSA 90.3	✓ Ro5	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(Cl)c(C(=O)Nc2sc3c(c2C#N)C…`
ZINC2487640	0.971	241.7 Da LogP 2.14 TPSA 46.9	✓ Ro5	✓ Clean	`Cn1cc(Cl)c(C(=O)NC2CCCCC2)n1`
ZINC468315	0.971	255.7 Da LogP 2.53 TPSA 46.9	✓ Ro5	✓ Clean	`Cn1cc(Cl)c(C(=O)NC2CCCCCC2)n1`
ZINC827259	0.964	452.0 Da LogP 4.43 TPSA 90.3	✓ Ro5	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(Cl)c(C(=O)Nc2sc3c(c2C#N)C…`
ZINC3055005	0.882	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	0.882	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	0.882	204.2 Da LogP -0.63 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@H](CCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC105469665	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@@](=O)(O)CP(=O…`
ZINC13527614	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@](=O)(O)CP(=O)…`
ZINC219330894	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@](=O)(O)CP(=O)…`
ZINC3873852	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](CO[P@](=O)(O)CP(=O)…`
ZINC3873853	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](CO[P@](=O)(O)CP(=O…`
ZINC3873854	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](CO[P@](=O)(O)CP(=O)…`
ZINC3873855	0.873	425.2 Da LogP -1.64 TPSA 223.4	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](CO[P@](=O)(O)CP(=O…`
ZINC12360002	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@@](=O)(O)OP(=O…`
ZINC12360703	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@@](=O)(O)OP(=O…`
ZINC12503599	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@@](=O)(O)OP(=O…`
ZINC31977053	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](CO[P@](=O)(O)OP(=O)…`
ZINC4806433	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO[P@@](=O)(O)OP(=O…`
ZINC53683898	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](CO[P@@](=O)(O)OP(=…`
ZINC8586019	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](CO[P@](=O)(O)OP(=O)…`
ZINC8586020	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](CO[P@@](=O)(O)OP(=…`
ZINC8586021	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](CO[P@@](=O)(O)OP(=O…`
ZINC8586022	0.839	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](CO[P@@](=O)(O)OP(=…`
ZINC1555366	0.833	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	0.833	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	0.833	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	0.833	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	0.833	218.3 Da LogP -0.24 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@@H](CCCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC1720130	0.833	218.3 Da LogP -0.24 TPSA 126.6	✓ Ro5	✓ Clean	`N[C@H](CCCCC[C@@H](N)C(=O)O)C(=O)O`
ZINC513251	0.814	255.3 Da LogP 3.65 TPSA 43.0	✓ Ro5	✓ Clean	`CCCn1c(NCc2ccco2)nc2ccccc21`
ZINC16546165	0.810	427.2 Da LogP -1.75 TPSA 232.6	2 viol.	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@H](CO[P@](=O)(O)OP(=O)(…`
ZINC1433755	0.781	452.0 Da LogP 3.04 TPSA 99.5	✓ Ro5	✓ Clean	`N#Cc1c(NC(=O)c2cc(S(=O)(=O)N3CCOCC3)ccc2Cl)sc2c…`
ZINC944845	0.780	403.5 Da LogP 3.39 TPSA 90.3	✓ Ro5	✓ Clean	`CCN(CC)S(=O)(=O)c1ccc(C(=O)Nc2sc3c(c2C#N)CCC3)c…`
ZINC13518964	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](COP(=O)(O)O)[C@H](…`
ZINC2046931	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@@H](COP(=O)(O)O)[C@H](…`
ZINC2126310	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](…`
ZINC3201893	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](COP(=O)(O)O)[C@@H](…`
ZINC3830180	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@H]1O[C@@H](COP(=O)(O)O)[C@@H](…`
ZINC3860156	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](…`
ZINC8613167	0.768	347.2 Da LogP -1.86 TPSA 186.1	✓ Ro5	✓ Clean	`Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@H](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.