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Reaction Details
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TargetProthrombin
LigandBDBM50288407
Substrate/Competitorn/a
Meas. Tech.ChEBML_208357
Ki 0.690000±n/a nM
Citation Galemmo, RAFevig, JMCarini, DJCacciola, JWells, BLHillyer, GLJr., JBRossi, KAStouten, PFAlexander, RSHilmer, RBostrom, LAbelman, MMLee, SLWeber, PCKettner, CAKnabb, RMWexler, RR (N-acyl-N-alkyl)glycyl borolysine analogs: A new class of potent thrombin inhibitors Bioorg Med Chem Lett6:2913-2918 (1996)    Article
More Info.:Get all data from this article,  Assay Method
 
Prothrombin
Name:Prothrombin
Synonyms:Activation peptide fragment 1 | Activation peptide fragment 2 | Coagulation factor II | F2 | Prothrombin precursor | THRB_HUMAN | Thrombin heavy chain | Thrombin light chain
Type:Protein
Mol. Mass.:70029.57
Organism:Homo sapiens (Human)
Description:P00734
Residue:622
Sequence:
MAHVRGLQLPGCLALAALCSLVHSQHVFLAPQQARSLLQRVRRANTFLEEVRKGNLEREC
VEETCSYEEAFEALESSTATDVFWAKYTACETARTPRDKLAACLEGNCAEGLGTNYRGHV
NITRSGIECQLWRSRYPHKPEINSTTHPGADLQENFCRNPDSSTTGPWCYTTDPTVRRQE
CSIPVCGQDQVTVAMTPRSEGSSVNLSPPLEQCVPDRGQQYQGRLAVTTHGLPCLAWASA
QAKALSKHQDFNSAVQLVENFCRNPDGDEEGVWCYVAGKPGDFGYCDLNYCEEAVEEETG
DGLDEDSDRAIEGRTATSEYQTFFNPRTFGSGEADCGLRPLFEKKSLEDKTERELLESYI
DGRIVEGSDAEIGMSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPWDKNFTEN
DLLVRIGKHSRTRYERNIEKISMLEKIYIHPRYNWRENLDRDIALMKLKKPVAFSDYIHP
VCLPDRETAASLLQAGYKGRVTGWGNLKETWTANVGKGQPSVLQVVNLPIVERPVCKDST
RIRITDNMFCAGYKPDEGKRGDACEGDSGGPFVMKSPFNNRWYQMGIVSWGEGCDRDGKY
GFYTHVFRLKKWIQKVIDQFGE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50288407
n/a
NameBDBM50288407
Synonyms:CHEMBL317137 | N-[(5-Amino-1-dihydroxyboranyl-pentylcarbamoyl)-methyl]-N-cyclopropyl-3-phenyl-propionamide
TypeSmall organic molecule
Emp. Form.C19H30BN3O4
Mol. Mass.375.27
SMILESNCCCC[C@H](NC(=O)CN(C1CC1)C(=O)CCc1ccccc1)B(O)O
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: