Detail Information

P450 Protein:

P450 SymbolP450TbtJ1
Protein NameEngineering cytochrome P450
Uniprot ID
SpeciesThermobispora bispora DSM 43833
Txid 469371
P450 Protein Structure
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
Subcellular Location
Protein Sequence GO

Reaction Scheme:

Chemical Conversion C52H53N15O10S6 + C4H6N2O2 → C64H71N15O16S6 + N2
Reaction TypeOxidation
Chemical Bond
SolventsWater
Conditions16 h, pH 8, rt

2-{[(2-{1-[({2-[2-(1-{2-[1-({[2-(1-{2-[1-(acetylamino)vinyl]-1,3-thiazol-4-yl}-1,5-dioxo-2,6-diazahept-3-yl)-1,3-thiazol-4-yl]carbonyl}amino)vinyl]-1,3-thiazol-4-yl}-3-[(4-hydroxyphenyl)methyl]-7-methyl-1,4-dioxo-2,5-diazanon-6-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl}carbonyl)amino]vinyl}-1,3-thiazol-4-yl)carbonyl]amino}propanamide

+

Ethyl diazoacetate

P450TbtJ1

ethyl 2-[({2-[2-(1-{2-[1-({[2-(1-{2-[1-(acetylamino)-2-(ethoxycarbonyl)cyclopropyl]-1,3-thiazol-4-yl}-1,5-dioxo-2,6-diazahept-3-yl)-1,3-thiazol-4-yl]carbonyl}amino)-2-(ethoxycarbonyl)cyclopropyl]-1,3-thiazol-4-yl}-3-[(4-hydroxyphenyl)methyl]-7-methyl-1,4-dioxo-2,5-diazanon-6-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl}carbonyl)amino]-2-(4-{[(1-carbamoylethyl)amino]carbonyl}-1,3-thiazol-2-yl)cyclopropane-1-carboxylate

+

Nitrogen

Substrate Information:

Substrate Name 2-{[(2-{1-[({2-[2-(1-{2-[1-({[2-(1-{2-[1-(acetylamino)vinyl]-1,3-thiazol-4-yl}-1,5-dioxo-2,6-diazahept-3-yl)-1,3-thiazol-4-yl]carbonyl}amino)vinyl]-1,3-thiazol-4-yl}-3-[(4-hydroxyphenyl)methyl]-7-methyl-1,4-dioxo-2,5-diazanon-6-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl}carbonyl)amino]vinyl}-1,3-thiazol-4-yl)carbonyl]amino}propanamide
Substrate Chemical FormulaC52H53N15O10S6
Substrate SmilesO=C(NC(=C)C1=NC(=CS1)C(=O)NC(C(=O)N)C)C=2N=C(SC2)C=3N=C(SC3)C(NC(=O)C(NC(=O)C=4N=C(SC4)C(=C)NC(=O)C=5N=C(SC5)C(NC(=O)C=6N=C(SC6)C(=C)NC(=O)C)CC(=O)NC)CC7=CC=C(O)C=C7)C(C)CC
Substrate Structure
Substrate Name Ethyl diazoacetate
Substrate Chemical FormulaC4H6N2O2
Substrate PubChem CID12192
Substrate CAS Number623-73-4
Substrate Smiles[N-]=[N+]=CC(=O)OCC
Substrate Structure

Product Information:

Product Name ethyl 2-[({2-[2-(1-{2-[1-({[2-(1-{2-[1-(acetylamino)-2-(ethoxycarbonyl)cyclopropyl]-1,3-thiazol-4-yl}-1,5-dioxo-2,6-diazahept-3-yl)-1,3-thiazol-4-yl]carbonyl}amino)-2-(ethoxycarbonyl)cyclopropyl]-1,3-thiazol-4-yl}-3-[(4-hydroxyphenyl)methyl]-7-methyl-1,4-dioxo-2,5-diazanon-6-yl)-1,3-thiazol-4-yl]-1,3-thiazol-4-yl}carbonyl)amino]-2-(4-{[(1-carbamoylethyl)amino]carbonyl}-1,3-thiazol-2-yl)cyclopropane-1-carboxylate
Product Chemical FormulaC64H71N15O16S6
Product CAS Number2114284-06-7
Product SmilesO=C(OCC)C1CC1(NC(=O)C=2N=C(SC2)C=3N=C(SC3)C(NC(=O)C(NC(=O)C=4N=C(SC4)C5(NC(=O)C=6N=C(SC6)C(NC(=O)C=7N=C(SC7)C8(NC(=O)C)CC8C(=O)OCC)CC(=O)NC)CC5C(=O)OCC)CC9=CC=C(O)C=C9)C(C)CC)C%10=NC(=CS%10)C(=O)NC(C(=O)N)C
Product Structure
Product Name Nitrogen
Product Chemical FormulaN2
Product PubChem CID947
Product CAS Number7727-37-9
Product SmilesN#N
Product Structure

References:

Title: P450-Mediated Non-natural Cyclopropanation of Dehydroalanine-Containing Thiopeptides.
PMID: 28535034
Journal: ACS Chemical Biology
Year: 2017/5/23

Contact zhy1001@alu.uestc.edu.cn or yangzhang@cdutcm.edu.cn
© Department of Bioinformatics