3JWQ: Chimeric PDE5/PDE6 catalytic domain

Crystal structure of chimeric PDE5/PDE6 catalytic domain complexed with sildenafil. Determined by X-ray diffraction at 2.87 Å resolution. Released 13 Oct 2009.

Method
X-ray diffraction
Resolution
2.87 Å
Organism
Homo sapiens
Chains
4
Atoms
10,723
Mol. weight
155.39 kDa
Ligands
ZN, MG, VIA
Released
13 Oct 2009

Explore 3JWQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3JWQ contains 90 α-helices and 0 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 22 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix537-5459
α-helix568-58114
α-helix584-5885
α-helix592-60413
α-helix615-62915
α-helix635-6373
α-helix640-65213
α-helix662-6676
α-helix672-6754
α-helix680-69314
α-helix706-72116
α-helix725-74016
α-helix749-76416
α-helix766-7694
α-helix772-79524
α-helix803-8053
α-helix807-8126
α-helix813-8208
α-helix821-8255
α-helix826-83510
α-helix837-8393
α-helix840-85718
Chain B: 22 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix537-5459
α-helix551-5544
α-helix568-58114
α-helix584-5885
α-helix592-60413
α-helix615-63016
α-helix635-6373
α-helix640-65213
α-helix662-6676
α-helix671-6755
α-helix680-69314
α-helix706-72116
α-helix725-74016
α-helix749-76416
α-helix766-7694
α-helix772-79625
α-helix803-8053
α-helix813-8208
α-helix821-8255
α-helix826-83510
α-helix837-8393
α-helix840-85617
Chain C: 23 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix538-5458
α-helix551-5544
α-helix568-58114
α-helix584-5885
α-helix592-60413
α-helix615-62915
α-helix635-6373
α-helix640-65213
α-helix662-6676
α-helix672-6754
α-helix680-69314
α-helix706-72116
α-helix725-74016
α-helix749-76416
α-helix766-7694
α-helix772-79524
α-helix803-8053
α-helix810-8123
α-helix813-8208
α-helix821-8255
α-helix826-83510
α-helix837-8393
α-helix840-85617
Chain D: 23 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix538-5458
α-helix568-58114
α-helix584-5885
α-helix592-60413
α-helix615-62915
α-helix635-6373
α-helix640-65213
α-helix662-6676
α-helix671-6744
α-helix680-69314
α-helix706-72116
α-helix725-74016
α-helix749-76416
α-helix766-7694
α-helix772-79524
α-helix799-8013
α-helix803-8053
α-helix807-8126
α-helix813-8208
α-helix821-8255
α-helix826-83510
α-helix837-8393
α-helix840-85718

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic…A, B, C, Dprotein330Homo sapiensO76074 (AlphaFold model), P51160 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>3JWQ_1 cGMP-specific 3',5'-cyclic phosphodiesterase catalytic domain, Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha chimera (chains A, B, C, D)
GSHMEETRELQSLAAAVVPSAQTLKITDFSFSDFELSDLETALCTIRMFTDLNLVQNFQM
KHEVLCRWILSVKKNYRKNVAYHNWRHAFNTAQCMFAALKAGKIQNKLTDLEILALLIAA
LSHDLDHRGVNNSYIQRSEHPLAQLYCHSIMEHHHFDQCLMILNSPGNQILSGLSIEEYK
TTLKIIKQAILATDLALYIKRRGEFFELIRKNQFNLEDPHQKELFLAMLMTACDLSAITK
PWPIQQRIAELVATEFWEQGDLERTVLQQQPIPMMDRNKRDELPKLQVGFIDFVCTQLYE
ALTHVSEDCFPLLDGCRKNRQKWQALAEQQ

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn4
MGMagnesium ionMg4
VIA5-{2-ethoxy-5-[(4-methylpiperazin-1-yl)sulfonyl]phenyl}-1-methyl-3-propyl-1H,6H…C22 H30 N6 O4 S4

Primary citation

Structural basis of phosphodiesterase 6 inhibition by the C-terminal region of the gamma-subunit. Barren, B., Gakhar, L., Muradov, H. et al. EMBO J (2009) 28:3613-3622. DOI 10.1038/emboj.2009.284 · PubMed

Other PDB entries of the same protein (UniProt O76074 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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