Binding of two substrate analogue molecules to dihydroflavonol-4-reductase alters the functional geometry of the catalytic site
Petit, P., Langlois d'Estaintot, B., Granier, T., Gallois, B.To be published.
Experimental Data Snapshot
Starting Model: experimental
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Entity ID: 1 | |||||
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Molecule | Chains | Sequence Length | Organism | Details | Image |
Dihydroflavonol 4-reductase | 337 | Vitis vinifera | Mutation(s): 0  Gene Names: dfr1 EC: 1.1.1.219 (PDB Primary Data), 1.1.1.234 (UniProt) | ||
UniProt | |||||
Find proteins for P51110 (Vitis vinifera) Explore P51110  Go to UniProtKB:  P51110 | |||||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | P51110 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 2 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
NAP Query on NAP | E [auth A], H [auth B], K [auth C], N [auth D] | NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE C21 H28 N7 O17 P3 XJLXINKUBYWONI-NNYOXOHSSA-N | |||
MYC Query on MYC | F [auth A] G [auth A] I [auth B] J [auth B] L [auth C] | 3,5,7-TRIHYDROXY-2-(3,4,5-TRIHYDROXYPHENYL)-4H-CHROMEN-4-ONE C15 H10 O8 IKMDFBPHZNJCSN-UHFFFAOYSA-N |
Length ( ? ) | Angle ( ? ) |
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a = 47.231 | ¦Á = 90 |
b = 177.958 | ¦Â = 104.77 |
c = 92.597 | ¦Ă = 90 |
Software Name | Purpose |
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SCALA | data scaling |
AMoRE | phasing |
REFMAC | refinement |
PDB_EXTRACT | data extraction |
ProDC | data collection |
MOSFLM | data reduction |