Nomosis Docs
The Nomosis Viewer

Visual Settings & Camera

Control the global scene, camera, lighting, effects, image quality, and presentation style.

Use Display to style individual molecular components. Use Settings, the top-bar controls, and camera gestures to control the complete scene. Keeping these scopes separate makes visual changes more predictable.

Global settings versus component settings

You want to changeUse
Protein or ligand representation, color, visibility, or opacityDisplay
Background, lighting, effects, projection, or anti-aliasingSettings
Quick background colorBG in the top bar
Complete coordinated visual treatmentStyle in the top bar
Camera framingFit and viewport navigation

Camera navigation

GoalControl
RotateLeft-drag
ZoomScroll
PanMiddle-drag
Focus a picked atomDouble-click
Focus the complete sceneFit → All (reset)
Focus the ligandFit → Ligand
SelectClick
Add or remove from selectionCtrl/Cmd+click
Open contextual actionsRight-click

Use Fit → All (reset) as the recovery action whenever the structure is lost, clipped, or framed too closely.

Choose a projection

ProjectionBest forTradeoff
PerspectiveNatural depth and presentation viewsApparent size changes with distance
OrthographicStructural comparison and technical figuresDepth feels flatter

Use the same projection and a saved camera when comparing two scenes. Otherwise, camera changes can look like structural differences.

Background

Choose a solid, horizontal-gradient, or radial-gradient background in Settings. The top-bar BG swatches provide fast solid-color options.

  • Dark backgrounds work well for interactive review and bright molecular colors.
  • White backgrounds integrate easily into many documents and figures.
  • Transparent backgrounds are selected at image export time, not by making the viewport transparent.

Lighting and exposure

Lighting controls include ambient intensity, direct-light intensity, inclination, azimuth, and exposure. Adjust them as a coordinated set:

Set the final background first.
Raise ambient light until shadowed regions remain readable.
Use direct light to reveal form without washing out colors.
Adjust inclination and azimuth so the subject, not an empty surface, receives the strongest modeling.
Set exposure last and inspect both the brightest ligand atoms and the darkest protein regions.

Effects

EffectAddsUse carefully when
OutlineStronger silhouettes and separationDense atomic scenes can become visually busy
Ambient OcclusionContact shadows and depth cuesDark pockets may lose detail
ShadowsDirectional depthScientific detail must remain visible
Depth of FieldFocus separationThe full structure needs to remain interpretable
BloomGlow around bright featuresBright atom colors can lose precision
FogAtmospheric depthDistant components still matter
SharpeningStronger local edge contrastThin lines or labels may become harsh

Effects should support structure reading, not compensate for a weak component hierarchy.

Anti-aliasing and field of view

  • Choose SMAA or FXAA when smoother edges improve the scene; use Off only for diagnostic or performance reasons.
  • Adjust field of view only when using perspective projection and the default framing does not suit the scene.
  • Recheck labels, interaction lines, and thin bonds after changing image-quality settings.

Style presets

The top-bar Style menu applies a coordinated starting point.

PresetUse it for
DefaultBalanced general review
PublicationClean figure-oriented scene
Publication (solvent)Publication styling while retaining solvent context
IllustrativeDiagram-like structural communication
PrettyPolished presentation view
Binding SiteLigand and nearby-residue focus
Binding Site (dry)Binding-site focus without water clutter

Apply a preset early, then refine components and camera. Applying another preset later may replace several coordinated visual choices.

Before applying a new Style preset to a carefully prepared scene, save the viewer session or create a story scene. A preset is a multi-setting change, not a single color adjustment.

Prepare a consistent figure

Choose the final projection and background.
Frame the scientific subject with deliberate margins.
Reduce the scene to components that support the conclusion.
Check contrast for protein, ligand, interactions, measurements, and labels.
Save the viewer session as a reproducible source state.
Open Studio and inspect the final output resolution before exporting.

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