The Crystal Structure of human DHFR from Biortus
Wang, F., Cheng, W., Xu, C., Qi, J., Bao, X., Miao, Q.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 |
Dihydrofolate reductase | 204 | Homo sapiens | Mutation(s): 0  Gene Names: DHFR EC: 1.5.1.3 | ||
UniProt & NIH Common Fund Data Resources | |||||
Find proteins for P00374 (Homo sapiens) Explore P00374  Go to UniProtKB:  P00374 | |||||
PHAROS:  P00374 GTEx:  ENSG00000228716  | |||||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
UniProt Group | P00374 | ||||
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 | B [auth A] | NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE C21 H28 N7 O17 P3 XJLXINKUBYWONI-NNYOXOHSSA-N | |||
FOL Query on FOL | C [auth A] | FOLIC ACID C19 H19 N7 O6 OVBPIULPVIDEAO-LBPRGKRZSA-N |
Length ( ? ) | Angle ( ? ) |
---|---|
a = 61.569 | ¦Á = 90 |
b = 61.569 | ¦Â = 90 |
c = 94.068 | ¦Ă = 90 |
Software Name | Purpose |
---|---|
REFMAC | refinement |
XDS | data reduction |
Aimless | data scaling |
PHASER | phasing |