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TargetPlasminogen
LigandBDBM50289435
Substrate/Competitorn/a
Meas. Tech.ChEBML_222787
IC50>2500±n/a nM
Citation Tamura, SYShamblin, BMBrunck, TKRipka, WC RATIONAL DESIGN, SYNTHESIS, AND SERINE PROTEASE INHIBITORY ACTIVITY OF NOVEL P1-ARGININOYL HETEROCYCLES Bioorg Med Chem Lett7:1359-1364 (1997)    Article
More Info.:Get all data from this article,  Assay Method
 
Plasminogen
Name:Plasminogen
Synonyms:PLMN_RAT | Plasmin | Plasminogen | Plg
Type:Protein
Mol. Mass.:90541.87
Organism:Rattus norvegicus
Description:Q01177
Residue:812
Sequence:
MDHKEIILLFLLFLKPGQGDSLDGYVSTQGASLHSLTKKQLAAGSIADCLAKCEGETDFI
CRSFQYHSKEQQCVIMAENSKTSSIIRMRDVILFEKRVYLSECKTGIGKGYRGTMSKTKT
GVTCQKWSDTSPHVPKYSPSTHPSEGLEENYCRNPDNDEQGPWCYTTDPDQRYEYCNIPE
CEEECMYCSGEKYEGKISKTMSGLDCQSWDSQSPHAHGYIPAKFPSKNLKMNYCRNPDGE
PRPWCFTTDPNKRWEYCDIPRCTTPPPPPGPTYQCLKGRGENYRGTVSVTASGKTCQRWS
EQTPHRHNRTPENFPCKNLEENYCRNPDGETAPWCYTTDSQLRWEYCEIPSCGSSVSPDQ
SDSSVLPEQTPVVQECYQGNGKSYRGTSSTTNTGKKCQSWVSMTPHSHSKTPANFPDAGL
EMNYCRNPDNDQRGPWCFTTDPSVRWEYCNLKRCSETGGGVAESAIVPQVPSAPGTSETD
CMYGNGKEYRGKTAVTAAGTPCQEWAAQEPHSHRIFTPQTNPRAGLEKNYCRNPDGDVNG
PWCYTMNPRKLYDYCNIPLCASLSSFECGKPQVEPKKCPGRVVGGCVANPHSWPWQISLR
TRFSGQHFCGGTLISPEWVLTAAHCLEKSSRPEFYKVILGAHEERILGSDVQQIAVTKLV
LEPNDADIALLKLSRPATITDNVIPACLPSPNYVVADRTLCYITGWGETKGTPGAGRLKE
AQLPVIENKVCNRAEYLNNRVKSTELCAGHLAGGIDSCQGDSGGPLVCFEKDKYILQGVT
SWGLGCARPNKPGVYVRVSRYVNWIEREMRND
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50289435
n/a
NameBDBM50289435
Synonyms:(S)-1-[(R)-2-(3,3-Dimethyl-butyrylamino)-3-phenyl-propionyl]-pyrrolidine-2-carboxylic acid [(S)-1-(1H-benzoimidazole-2-carbonyl)-4-guanidino-butyl]-amide; TFA | CHEMBL27008
TypeSmall organic molecule
Emp. Form.C33H44N8O4
Mol. Mass.616.7537
SMILESCC(C)(C)CC(=O)N[C@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)c1nc2ccccc2[nH]1
Structure
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