| Reaction Details |
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 | Report a problem with these data |
| Target | Promotilin |
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| Ligand | BDBM85614 |
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| Substrate/Competitor | n/a |
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| Ki | 3.6±n/a nM |
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| Comments | PDSP_6650 |
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| Citation |  Tsukamoto, K; Kuboyama, N; Yamano, M; Nakazawa, T; Suzuki, T In vitro pharmacological profile of SK-896, a new human motilin analogue. Pharmacology60:128-35 (2000) [PubMed] Article |
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| More Info.: | Get all data from this article |
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| Promotilin |
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| Name: | Promotilin |
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| Synonyms: | MLN | MOTI_HUMAN | Motilin | Promotilin |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 12919.83 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Motilin 0 HUMAN::P12872 |
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| Residue: | 115 |
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| Sequence: | MVSRKAVAALLVVHVAAMLASQTEAFVPIFTYGELQRMQEKERNKGQKKSLSVWQRSGEE
GPVDPAEPIREEENEMIKLTAPLEIGMRMNSRQLEKYPATLEGLLSEMLPQHAAK
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| BDBM85614 |
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| n/a |
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| Name | BDBM85614 |
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| Synonyms: | [Leu13]motilin | [leu13]pMOT(1-22) |
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| Type | Small organic molecule |
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| Emp. Form. | C121H190N34O35 |
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| Mol. Mass. | 2681.0101 |
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| SMILES | [#6]-[#6]-[#6@H](-[#6])-[#6@H](-[#7]-[#6](=O)-[#6@@H]-1-[#6]-[#6]-[#6]-[#7]-1-[#6](=O)-[#6@@H](-[#7]-[#6](=O)-[#6@@H](-[#7])-[#6]-c1ccccc1)-[#6](-[#6])-[#6])-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-[#6@@H](-[#6@@H](-[#6])-[#8])-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccc(-[#8])cc1)-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#8])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#8])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#6]-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#8])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#7])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]-[#6]-[#7])-[#6](=O)-[#7]-[#6]-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6](-[#7])=O)-[#6](-[#8])=O |r| |
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| Structure | 
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