Detail Information

P450 Protein:

P450 SymbolCYP1251 C3
Protein NameCytochrome P450Blt
Uniprot IDA0ACD6BAH8
EC Number1.14.-.-
SpeciesMicromonospora sp. MW-13
Txid 2094022
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 C21H29N5O5 → C21H27N5O5
Reaction TypeCyclization
Chemical Bond
SolventsWater
Conditionsovernight, 30°C

(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-4-methylpentanoyl]amino]-3-(1H-imidazol-5-yl)propanoic acid

CYP1251 C3

(8S,11S,14S)-8-amino-3-hydroxy-11-(2-methylpropyl)-9,12-dioxo-1,10,13,17-tetrazatricyclo[14.2.1.12,6]icosa-2(20),3,5,17-tetraene-14-carboxylic acid

Substrate Information:

Substrate Name (2S)-2-[[(2S)-2-[[(2S)-2-amino-3-(4-hydroxyphenyl)propanoyl]amino]-4-methylpentanoyl]amino]-3-(1H-imidazol-5-yl)propanoic acid
Substrate Chemical FormulaC21H29N5O5
Substrate PubChem CID145458691
Substrate SmilesCC(C)C[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CC2=CC=C(C=C2)O)N
Substrate Structure

Product Information:

Product Name (8S,11S,14S)-8-amino-3-hydroxy-11-(2-methylpropyl)-9,12-dioxo-1,10,13,17-tetrazatricyclo[14.2.1.12,6]icosa-2(20),3,5,17-tetraene-14-carboxylic acid
Product Chemical FormulaC21H27N5O5
Product CAS Number2951912-73-3
Product SmilesOC1=C2N3C=C(N=C3)C[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(=C2)C=C1
Product Structure

References:

Title: Cytochrome P450(Blt) Enables Versatile Peptide Cyclisation to Generate Histidine- and Tyrosine-Containing Crosslinked Tripeptide Building Blocks.
PMID: 35851739
Journal: Angewandte Chemie, International Edition
Year: 2022/7/18

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