Evolutionary tuning of a key helix drove androgen selectivity
Little, M.M., Ortlund, E.A.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 |
Ancestral androgen receptor | 248 | Escherichia coli | Mutation(s): 0  | ||
Entity Groups   | |||||
Sequence Clusters | 30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity | ||||
Sequence AnnotationsExpand | |||||
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Find similar proteins by: Sequence | 3D Structure
Entity ID: 2 | |||||
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Molecule | Chains | Sequence Length | Organism | Details | Image |
Nuclear receptor coactivator 2 | B [auth D] | 9 | Homo sapiens | Mutation(s): 0  | |
UniProt & NIH Common Fund Data Resources | |||||
Find proteins for Q15596 (Homo sapiens) Explore Q15596  Go to UniProtKB:  Q15596 | |||||
PHAROS:  Q15596 GTEx:  ENSG00000140396  | |||||
Entity Groups   | |||||
UniProt Group | Q15596 | ||||
Sequence AnnotationsExpand | |||||
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Ligands 2 Unique | |||||
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ID | Chains | Name / Formula / InChI Key | 2D Diagram | 3D Interactions | |
STR (Subject of Investigation/LOI) Query on STR | C [auth A] | PROGESTERONE C21 H30 O2 RJKFOVLPORLFTN-LEKSSAKUSA-N | |||
GOL Query on GOL | D [auth A] | GLYCEROL C3 H8 O3 PEDCQBHIVMGVHV-UHFFFAOYSA-N |
Length ( ? ) | Angle ( ? ) |
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a = 69.714 | ¦Á = 90 |
b = 69.714 | ¦Â = 90 |
c = 144.439 | ¦Ă = 90 |
Software Name | Purpose |
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PHENIX | refinement |
PDB-REDO | refinement |
HKL-2000 | data reduction |
HKL-2000 | data scaling |
PHASER | phasing |
Funding Organization | Location | Grant Number |
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National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Disease (NIH/NIDDK) | United States | R56DK115213 |