Autotests: #3204 - Charge Tool (#3242)

* - added tests for 'charge tool';
- added 1 test file;
- added expected snapshots

* - moved test files to folders

* - added ignored hotkeys to 'hotkeys.ts';
- deleted 'delay'

* - deleted 'delay' from import

* - changed name of folder 'Ket' to 'KET'

* - updated snapshot

* - updated expected snapshots;
- added folder path to some tests;
- delete 'fixme' from some tests

* - updated snapshots;
- code refactoring;
- added 'INPUT_DELAY' to functions 'cutAndPaste' and 'copyAndPaste'

* - deleted duplicate folder with tests

* -updated snapshots;
- fixed some tests

* - updated snapshots;
- fixed some tests

* - fix 1 test

* - fixed some tests;
- removed 'fixme' and 'skip'

* - updated snapshot

ketcher-autotests/tests/File-Management/Open-And-Save-Files/CDX-Files/cdx-files.spec.ts

@@ -1,8 +1,6 @@
 import { test } from '@playwright/test';
 import {
   clickInTheMiddleOfTheScreen,
-  TopPanelButton,
-  selectTopPanelButton,
   openFileAndAddToCanvas,
   takeEditorScreenshot,
   pasteFromClipboardAndAddToCanvas,
@@ -27,21 +25,19 @@ test.describe('CDX files', () => {
     await openFileAndAddToCanvas('cdx-expanded-contracted.cdx', page);
   });
 
-  test.fixme('opening cdx files with R-group', async ({ page }) => {
+  test('opening cdx files with R-group', async ({ page }) => {
     /* 
     Test case: EPMLSOPKET-6973
     Description: Open CDX files with R-group
     */
-    await openFileAndAddToCanvas('cdx_file.cdx', page);
+    await openFileAndAddToCanvas('r_group_cdx.cdx', page);
   });
 
-  test.fixme('opening cdx files from clipboard', async ({ page }) => {
+  test('opening cdx files from clipboard', async ({ page }) => {
     /* 
   Test case: EPMLSOPKET-6972
   Description: Open structure created in ChemDraw from clickboard
   */
-    await selectTopPanelButton(TopPanelButton.Open, page);
-    await page.getByText('Paste from clipboard').click();
     await pasteFromClipboardAndAddToCanvas(
       page,
       // eslint-disable-next-line max-len

ketcher-autotests/tests/File-Management/Open-And-Save-Files/Cml-files/cml-files.spec.ts

@@ -100,27 +100,26 @@ test.describe('CML files', () => {
     expect(cmlFile).toEqual(cmlFileExpected);
   });
 
-  test.fixme(
-    'Open and Save file - CML - CML for R-group and other features',
-    async ({ page }) => {
-      /**
-       * Test case: EPMLSOPKET-1948
-       * Description: Saved cml file with structure is compering with paste R-group from a mol file
-       */
-
-      await openFileAddToCanvasTakeScreenshot(page, 'cml-1948-R-group.mol');
-      // check that structure opened from file is displayed correctly
-
-      const expectedFile = await getCml(page);
-      await saveToFile('cml-1948-r-group-expected.cml', expectedFile);
-      const { file: cmlFile, fileExpected: cmlFileExpected } =
-        await receiveFileComparisonData({
-          page,
-          expectedFileName: 'tests/test-data/cml-1948-r-group-expected.cml',
-        });
-      // comparing cml file with golden cml file
-
-      expect(cmlFile).toEqual(cmlFileExpected);
-    },
-  );
+  test('Open and Save file - CML - CML for R-group and other features', async ({
+    page,
+  }) => {
+    /**
+     * Test case: EPMLSOPKET-1948
+     * Description: Saved cml file with structure is compering with paste R-group from a mol file
+     */
+
+    await openFileAddToCanvasTakeScreenshot(page, 'cml-1948-R-group.mol');
+    // check that structure opened from file is displayed correctly
+
+    const expectedFile = await getCml(page);
+    await saveToFile('cml-1948-r-group-expected.cml', expectedFile);
+    const { file: cmlFile, fileExpected: cmlFileExpected } =
+      await receiveFileComparisonData({
+        page,
+        expectedFileName: 'tests/test-data/cml-1948-r-group-expected.cml',
+      });
+    // comparing cml file with golden cml file
+
+    expect(cmlFile).toEqual(cmlFileExpected);
+  });
 });

ketcher-autotests/tests/File-Management/Smile-Files/smile-files.spec.ts

@@ -92,7 +92,7 @@ test.describe('SMILES files', () => {
     );
   });
 
-  test.skip('SmileString from mol file that contains abbreviation', async ({
+  test('SmileString from mol file that contains abbreviation', async ({
     page,
   }) => {
     /*
@@ -106,9 +106,7 @@ test.describe('SMILES files', () => {
     await page.getByText('Warnings').click();
   });
 
-  test.skip('SmileString  from mol file that contains Sgroup', async ({
-    page,
-  }) => {
+  test('SmileString  from mol file that contains Sgroup', async ({ page }) => {
     /*
     Test case: EPMLSOPKET-1914
     Description: In Daylight SMILES the structure will be saved without S-groups
@@ -124,7 +122,7 @@ test.describe('SMILES files', () => {
 
     await clearCanvasAndPasteSmiles(
       page,
-      'CCCCCCCCCCCCC.CCCCCCC.CCCCCCC.CCCCCCC.CCCCCCC |Sg:gen:16,17,15:,Sg:n:23,24,22:n:ht|',
+      'CCCCCCCCCCCCC.CCCCCCC.CCCCCCC.CCCCCCC.CCCCCCC |Sg:gen:16,17,15:,Sg:n:23,24,22:n:ht,SgD:38,37,36:fgfh:dsfsd::: :|',
     );
   });
 
@@ -149,27 +147,29 @@ test.describe('SMILES files', () => {
   });
 
   // flaky
-  test.fixme(
-    'SmileString from mol file that contains attached data',
-    async ({ page }) => {
-      /*
+  test('SmileString from mol file that contains attached data', async ({
+    page,
+  }) => {
+    /*
     Test case: EPMLSOPKET-1916
     Description: Warning tab: Structure contains query properties of atoms
     and bonds that are not supported in the SMILES. Query properties will not be reflected in the saved file
     */
-      await openFileAndAddToCanvas('Molfiles-V2000/attached-data.mol', page);
-      await getAndCompareSmiles(
-        page,
-        'tests/test-data/JSON/attached-data-expected.json',
-      );
+    await openFileAndAddToCanvas('Molfiles-V2000/attached-data.mol', page);
+    await getAndCompareSmiles(
+      page,
+      'tests/test-data/JSON/attached-data-expected.json',
+    );
 
-      await getPreviewForSmiles(page, 'MDL Molfile V2000', 'Daylight SMILES');
-      await page.getByText('Warnings').click();
-      await takeEditorScreenshot(page);
+    await getPreviewForSmiles(page, 'MDL Molfile V2000', 'Daylight SMILES');
+    await page.getByText('Warnings').click();
+    await takeEditorScreenshot(page);
 
-      await clearCanvasAndPasteSmiles(page, 'CCCC[C@@H](C)[C@@H](C)CC');
-    },
-  );
+    await clearCanvasAndPasteSmiles(
+      page,
+      'CCCC[C@@H](C)[C@@H](C)CC |SgD:4,5:Purity:Purity = 96%::: :|',
+    );
+  });
 
   test('SmileString from V2000 mol file contains abs stereochemistry', async ({
     page,
@@ -197,33 +197,32 @@ test.describe('SMILES files', () => {
   });
 
   // flaky
-  test.fixme(
-    'SmileString from mol file that contains combination of different features',
-    async ({ page }) => {
-      /*
+  test('SmileString from mol file that contains combination of different features', async ({
+    page,
+  }) => {
+    /*
     Test case: EPMLSOPKET-1920
     Description: SmileString is correctly generated from structure and vise versa structure is
     correctly generated from SmileString.
     Structure appears without attached data and brackets, query features,
     Rgroup labels are rendered as R# symbols.
     */
-      await openFileAndAddToCanvas('different-features.mol', page);
-      await getAndCompareSmiles(
-        page,
-        'tests/test-data/smiles-different-features-expected.json',
-      );
-
-      await getPreviewForSmiles(page, 'MDL Molfile V2000', 'Daylight SMILES');
-      await takeEditorScreenshot(page);
-
-      await clearCanvasAndPasteSmiles(
-        page,
-        // eslint-disable-next-line max-len
-        'S=CC(F)CCCCC[C@@](CCO)/C=C/[C@@](N)CCC[C]C([13C]CC([C+2]CC(CC%91)CC(C)CCC)CCC)CC%92.[*:2]%92.[*:1]%91 |$;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;_R2;_R1$,rb:32:*,u:3|',
-      );
-      await delay(DELAY_IN_SECONDS.THREE);
-    },
-  );
+    await openFileAndAddToCanvas('different-features.mol', page);
+    await getAndCompareSmiles(
+      page,
+      'tests/test-data/smiles-different-features-expected.json',
+    );
+
+    await getPreviewForSmiles(page, 'MDL Molfile V2000', 'Daylight SMILES');
+    await takeEditorScreenshot(page);
+
+    await clearCanvasAndPasteSmiles(
+      page,
+      // eslint-disable-next-line max-len
+      'S=CC(F)CCCCC[C@@](CCO)/C=C/[C@@](N)CCC[C]C([13C]CC([C+2]CC(CC%91)CC(C)CCC)CCC)CC%92.[*:2]%92.[*:1]%91 |$;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;_R2;_R1$,rb:32:*,u:3|',
+    );
+    await delay(DELAY_IN_SECONDS.THREE);
+  });
 
   test('SmileString from file that contains Cis/Trans configuration', async ({
     page,
@@ -248,7 +247,7 @@ test.describe('SMILES files', () => {
     );
   });
 
-  test.skip('SmileString from file that contains alias and pseudoatom', async ({
+  test('SmileString from file that contains alias and pseudoatom', async ({
     page,
   }) => {
     /*
@@ -265,7 +264,7 @@ test.describe('SMILES files', () => {
     await getPreviewForSmiles(page, 'MDL Molfile V2000', 'Daylight SMILES');
     await takeEditorScreenshot(page);
 
-    await clearCanvasAndPasteSmiles(page, '');
+    await clearCanvasAndPasteSmiles(page, 'CCCC*CC |$;;alias123;;GH*;;$|');
   });
 
   test('SmileString from reaction consists of two or more reaction arrows and structures', async ({

ketcher-autotests/tests/Indigo-Tools/Aromatize-Dearomatize/aromatize-dearomatize.spec.ts

@@ -66,29 +66,28 @@ test.describe('Aromatize/Dearomatize Tool', () => {
     await selectTopPanelButton(TopPanelButton.Dearomatize, page);
   });
 
-  test.fixme(
-    'Aromatic structures - interchanged Single and Double bonds',
-    async ({ page }) => {
-      /*
+  test('Aromatic structures - interchanged Single and Double bonds', async ({
+    page,
+  }) => {
+    /*
     Test case: EPMLSOPKET-1870
     Description: The aromatic structures appear with circle inside the cycles.
     Aromatize function affects all canvas.
     The structures appears in a Kekule form: with interchanged Single and Double bonds.
     Dearomatize function affects all canvas.
     */
-      await openFileAndAddToCanvas(
-        'Molfiles-V2000/aromatic-structures.mol',
-        page,
-      );
-      await waitForSpinnerFinishedWork(page, async () => {
-        await selectTopPanelButton(TopPanelButton.Aromatize, page);
-      });
-      await takeEditorScreenshot(page);
-      await waitForSpinnerFinishedWork(page, async () => {
-        await selectTopPanelButton(TopPanelButton.Dearomatize, page);
-      });
-    },
-  );
+    await openFileAndAddToCanvas(
+      'Molfiles-V2000/aromatic-structures.mol',
+      page,
+    );
+    await waitForSpinnerFinishedWork(page, async () => {
+      await selectTopPanelButton(TopPanelButton.Aromatize, page);
+    });
+    await takeEditorScreenshot(page);
+    await waitForSpinnerFinishedWork(page, async () => {
+      await selectTopPanelButton(TopPanelButton.Dearomatize, page);
+    });
+  });
 
   test('Cycles with Aromatic Bonds', async ({ page }) => {
     /*
@@ -104,26 +103,25 @@ test.describe('Aromatize/Dearomatize Tool', () => {
     await selectTopPanelButton(TopPanelButton.Dearomatize, page);
   });
 
-  test.fixme(
-    '(Undo/Redo) Manipulations with cyclic structures with a circle inside the cycle',
-    async ({ page }) => {
-      /*
+  test('(Undo/Redo) Manipulations with cyclic structures with a circle inside the cycle', async ({
+    page,
+  }) => {
+    /*
     Test case: EPMLSOPKET-1872
     Description: Only six-cycle structures appear in a Kekule form: with interchanged Single and Double bonds.
     All other structures are rendered with a circle inside the cycles. The actions are Undone/Redone.
     */
-      await openFileAndAddToCanvas('cycles-with-aromatic-bonds.mol', page);
-      await waitForSpinnerFinishedWork(page, async () => {
-        await selectTopPanelButton(TopPanelButton.Aromatize, page);
-      });
-      await waitForSpinnerFinishedWork(page, async () => {
-        await selectTopPanelButton(TopPanelButton.Dearomatize, page);
-      });
-      await selectTopPanelButton(TopPanelButton.Undo, page);
-      await takeEditorScreenshot(page);
-      await selectTopPanelButton(TopPanelButton.Redo, page);
-    },
-  );
+    await openFileAndAddToCanvas('cycles-with-aromatic-bonds.mol', page);
+    await waitForSpinnerFinishedWork(page, async () => {
+      await selectTopPanelButton(TopPanelButton.Aromatize, page);
+    });
+    await waitForSpinnerFinishedWork(page, async () => {
+      await selectTopPanelButton(TopPanelButton.Dearomatize, page);
+    });
+    await selectTopPanelButton(TopPanelButton.Undo, page);
+    await takeEditorScreenshot(page);
+    await selectTopPanelButton(TopPanelButton.Redo, page);
+  });
 
   test('(Copy/Paste) Manipulations with cyclic structures with a circle inside the cycle', async ({
     page,

ketcher-autotests/tests/Indigo-Tools/Calculated-Values-Tool/calculated-values.spec.ts

@@ -184,7 +184,7 @@ test.describe('Calculated Values Tools', () => {
     Description: Calculation of exact mass for the reaction
     should be correct: '[78.047] > [155.957]'.
     */
-    await openFileAndAddToCanvas('benzene-bromination.rxn', page);
+    await openFileAndAddToCanvas('Rxn-V2000/benzene-bromination.rxn', page);
     await selectTopPanelButton(TopPanelButton.Calculated, page);
   });
 

ketcher-autotests/tests/Indigo-Tools/Layout/layout.spec.ts

@@ -27,7 +27,7 @@ test.describe('Indigo Tools - Layout', () => {
 
   test('Center molecule after layout', async ({ page }) => {
     // Related Github issue: https://github.com/epam/ketcher/issues/2078
-    const anyStructure = 'benzene-rings.mol';
+    const anyStructure = 'Molfiles-V2000/benzene-rings.mol';
     await openFileWithShift(anyStructure, page);
     await selectTopPanelButton(TopPanelButton.Layout, page);
     await takeEditorScreenshot(page);