Ligand name: 3-[2-[(Z)-[3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-4-methyl-pyrrol-1-ium -2-ylidene]methyl]-5-[(Z)-[(3E)-3-ethylidene-4-methyl-5-oxidanylidene-pyrrolidin-2-ylidene]methyl]-4-methyl-1H-pyrrol-3- yl]propanoic acid
PDB ligand accession: LBV
DrugBank: n/a
PubChem: n/a
ChEMBL: n/a
InChI Key: DKMLMZVDTGOEGU-ISEYCTJISA-O
SMILES: CC=C1C(C(=O)NC1=Cc2c(c(c([nH]2)C=C3C(=C(C(=[NH+]3)C=C4C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O)C)C
Drug action: n/a

ClassyFire chemical classification:

List of PDB structures and/or AlphaFold models with target protein Q9RZA4

PDB/AF Accession PyMOL script Experimental / Predicted Interacting ECOD domains ECOD X-group name LigPlot
4Q0H Download Experimental e4q0hA1
e4q0hA2
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7Z9E Download Experimental e7z9eA1
e7z9eA2
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2O9C Download Experimental e2o9cA1
e2o9cA2
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6FHT Download Experimental e6fhtA2
e6fhtA3
e6fhtA4
e6fhtB1
e6fhtB3
e6fhtB4
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5AJG Download Experimental e5ajgA1
e5ajgA2
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5L8M Download Experimental e5l8mA1
e5l8mA2
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4Z1W Download Experimental e4z1wA1
e4z1wA2
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7Z9D Download Experimental e7z9dA1
e7z9dA2
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4O0P Download Experimental e4o0pA1
e4o0pA2
e4o0pA3
e4o0pB1
e4o0pB2
e4o0pB3
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5MG1 Download Experimental e5mg1A1
e5mg1A2
e5mg1A3
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3S7N Download Experimental e3s7nA1
e3s7nA2
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4Q0I Download Experimental e4q0iA1
e4q0iA2
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5NFX Download Experimental e5nfxA1
e5nfxA2
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5NWN Download Experimental e5nwnA1
e5nwnA2
e5nwnA3
e5nwnB1
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e5nwnC1
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e5nwnD1
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e5nwnD3
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5MG0 Download Experimental e5mg0A1
e5mg0A2
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6T3U Download Experimental e6t3uB1
e6t3uB2
e6t3uA1
e6t3uA2
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4O8G Download Experimental e4o8gA1
e4o8gA2
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3S7P Download Experimental e3s7pA1
e3s7pA2
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8AVV Download Experimental e8avvA1
e8avvA2
e8avvA3
e8avvB1
e8avvB2
e8avvB3
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3S7O Download Experimental e3s7oA1
e3s7oA2
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8AVW Download Experimental e8avwA1
e8avwA3
e8avwA4
e8avwB1
e8avwB2
e8avwB3
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4O01 Download Experimental e4o01A1
e4o01A2
e4o01A3
e4o01B1
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e4o01B3
e4o01C1
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e4o01D1
e4o01D2
e4o01D3
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LigPlot
6FTD Download Experimental e6ftdA1
e6ftdA2
e6ftdB1
e6ftdB2
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4IJG Download Experimental e4ijgA5
e4ijgA6
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LigPlot
3S7Q Download Experimental e3s7qA5
e3s7qA6
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5K5B Download Experimental e5k5bA1
e5k5bA2
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8BOR Download Experimental e8borA1
e8borA3
e8borB1
e8borB2
e8borD1
e8borC2
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e8borD1
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6T3L Download Experimental e6t3lB1
e6t3lB2
e6t3lA1
e6t3lA2
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5NM3 Download Experimental e5nm3A1
e5nm3A2
e5nm3A3
e5nm3B1
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e5nm3B3
e5nm3C1
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e5nm3D1
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LigPlot
4CQH Download Experimental e4cqhA1
e4cqhA2
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4Y5F Download Experimental e4y5fA1
e4y5fA2
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LigPlot
5LBR Download Experimental e5lbrA1
e5lbrA2
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4Q0J Download Experimental e4q0jA1
e4q0jA2
e4q0jA3
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2O9B Download Experimental e2o9bA1
e2o9bA2
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4Y3I Download Experimental e4y3iA1
e4y3iA2
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4ZRR Download Experimental e4zrrA1
e4zrrA2
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