.. DO NOT EDIT. .. THIS FILE WAS AUTOMATICALLY GENERATED BY SPHINX-GALLERY. .. TO MAKE CHANGES, EDIT THE SOURCE PYTHON FILE: .. "examples/gallery/sequence/pi3k_alignment.py" .. LINE NUMBERS ARE GIVEN BELOW. .. only:: html .. note:: :class: sphx-glr-download-link-note :ref:`Go to the end ` to download the full example code .. rst-class:: sphx-glr-example-title .. _sphx_glr_examples_gallery_sequence_pi3k_alignment.py: Comparison of human PI3K family =============================== .. currentmodule:: biotite.sequence.graphics The following script visualizes the sequence alignment of six proteins of the human Phosphoinositide 3-kinase (PI3K) family, including PI3K itself. At first we fetch the respective sequences. and align them using *Clustal Omega*. .. GENERATED FROM PYTHON SOURCE LINES 14-41 .. code-block:: Python # Code source: Patrick Kunzmann # License: BSD 3 clause import warnings import numpy as np import matplotlib.pyplot as plt import biotite import biotite.database.entrez as entrez import biotite.sequence as seq import biotite.sequence.align as align import biotite.sequence.graphics as graphics import biotite.sequence.io.fasta as fasta import biotite.application.clustalo as clustalo uids = ["5JHB_A", "5LUQ_A", "5FLC_B", "5YZ0_A", "5NP0_A", "4FUL_A"] names = ["PI3K", "DNA-PKcs", "mTOR", "ATR", "ATM", "hSMG-1"] sequences = [] file = fasta.FastaFile.read(entrez.fetch_single_file( uids, None, db_name="protein", ret_type="fasta" )) for header, seq_str in file.items(): sequences.append(seq.ProteinSequence(seq_str)) alignment = clustalo.ClustalOmegaApp.align(sequences) .. GENERATED FROM PYTHON SOURCE LINES 42-49 Since the sequences are relatively long, the display of the entire alignment using a :func:`plot_alignment` would be too big. Instead we use a heat map, which highlights the similarity in the alignment column using a color map. Like the :class:`LetterSimilarityPlotter` we will use the *average normalized similarity* as measure. .. GENERATED FROM PYTHON SOURCE LINES 49-88 .. code-block:: Python def get_average_normalized_similarity(trace_code, matrix, seq_i, pos_i): code1 = trace_code[seq_i, pos_i] if code1 == -1: return np.nan similarities = np.zeros(trace_code.shape[0]) for i in range(trace_code.shape[0]): code2 = trace_code[i, pos_i] if code2 == -1: similarities[i] = 0 else: sim = matrix[code1, code2] # Normalize (range 0.0 - 1.0) min_sim = np.min(matrix[code1]) max_sim = np.max(matrix[code1]) sim = (sim - min_sim) / (max_sim - min_sim) similarities[i] = sim # Delete self-similarity similarities = np.delete(similarities, seq_i) return np.average(similarities) matrix = align.SubstitutionMatrix.std_protein_matrix() # Get the alignment columns as symbols codes (-1 for gaps) trace_code = align.get_codes(alignment) similarities = np.zeros(trace_code.shape) for i in range(similarities.shape[0]): for j in range(similarities.shape[1]): similarities[i,j] = get_average_normalized_similarity( trace_code, matrix.score_matrix(), i, j ) figure = plt.figure(figsize=(8.0, 3.0)) ax = figure.add_subplot(111) heatmap = ax.pcolor( similarities, cmap="RdYlGn", vmin=0.0, vmax=1.0 ) cbar = figure.colorbar(heatmap) figure.tight_layout() .. image-sg:: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_001.png :alt: pi3k alignment :srcset: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_001.png :class: sphx-glr-single-img .. rst-class:: sphx-glr-script-out .. code-block:: none /home/runner/work/biotite/biotite/doc/examples/scripts/sequence/pi3k_alignment.py:85: MatplotlibDeprecationWarning: Getting the array from a PolyQuadMesh will return the full array in the future (uncompressed). To get this behavior now set the PolyQuadMesh with a 2D array .set_array(data2d). cbar = figure.colorbar(heatmap) .. GENERATED FROM PYTHON SOURCE LINES 89-95 As the plot creates a heatmap field for every alignment column, the plot looks quite confusing. It is not clearly visible, which parts of the sequences have a low or high similarity to each other. Hence, we create bins, that contain the mean similarity over a range of columns. .. GENERATED FROM PYTHON SOURCE LINES 95-124 .. code-block:: Python def calculate_bins(similarities, bin_count): edges = np.linspace(0, similarities.shape[1], bin_count, dtype=int) edges = np.append(edges, similarities.shape[1]) binned_similarities = np.zeros(similarities.shape) for i in range(similarities.shape[0]): for j in range(len(edges) - 1): binned_similarities[i, edges[j]:edges[j+1]] = \ np.nanmean(similarities[i, edges[j]:edges[j+1]]) return binned_similarities with warnings.catch_warnings(): # Catch warnings about empty slice for gap-only parts warnings.simplefilter("ignore") similarities = calculate_bins(similarities, 100) figure = plt.figure(figsize=(8.0, 3.0)) ax = figure.add_subplot(111) heatmap = ax.pcolor( similarities, cmap="RdYlGn", vmin=0.0, vmax=1.0 ) cbar = figure.colorbar(heatmap) # Furthermore, add some labels to the figure cbar.set_label("Average normalized similarity") ax.set_xlabel("Alignment position") ax.set_yticks([0.5, 1.5, 2.5, 3.5, 4.5, 5.5]) ax.set_yticklabels(names) figure.tight_layout() .. image-sg:: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_002.png :alt: pi3k alignment :srcset: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_002.png :class: sphx-glr-single-img .. rst-class:: sphx-glr-script-out .. code-block:: none /home/runner/work/biotite/biotite/doc/examples/scripts/sequence/pi3k_alignment.py:116: MatplotlibDeprecationWarning: Getting the array from a PolyQuadMesh will return the full array in the future (uncompressed). To get this behavior now set the PolyQuadMesh with a 2D array .set_array(data2d). cbar = figure.colorbar(heatmap) .. GENERATED FROM PYTHON SOURCE LINES 126-132 Finally we show the alignment columns without the terminal gaps of the PI3K sequence, comprising the more conserved parts. Since the alignment is still relatively long, we will reduce the size of the font and the backgrounbd boxes, to fit more alignment columns into one line. .. GENERATED FROM PYTHON SOURCE LINES 132-165 .. code-block:: Python # Find start position and exclusive stop position of 'PI3K' sequence # (index 0) trace = alignment.trace # From beginning of the sequence... for i in range(len(trace)): # Check if all sequences have no gap at the given position if trace[i,0] != -1: start_index = i break # ...and the end of the sequence for i in range(len(trace)-1, -1, -1): # Check if all sequences have no gap at the given position if trace[i,0] != -1: stop_index = i+1 break # Truncate alignment to region where the 'PI3K' sequence exists alignment.trace = alignment.trace[start_index:stop_index] matrix = align.SubstitutionMatrix.std_protein_matrix() fig = plt.figure(figsize=(8.0, 15)) ax = fig.add_subplot(111) # The alignment is quite long # -> Reduce font size to reduce figure size graphics.plot_alignment_similarity_based( ax, alignment, matrix=matrix, symbols_per_line=80, labels=names, show_numbers=True, label_size=10, number_size=10, symbol_size=6, color=biotite.colors["orange"] ) fig.tight_layout() plt.show() .. image-sg:: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_003.png :alt: pi3k alignment :srcset: /examples/gallery/sequence/images/sphx_glr_pi3k_alignment_003.png :class: sphx-glr-single-img .. _sphx_glr_download_examples_gallery_sequence_pi3k_alignment.py: .. only:: html .. container:: sphx-glr-footer sphx-glr-footer-example .. container:: sphx-glr-download sphx-glr-download-jupyter :download:`Download Jupyter notebook: pi3k_alignment.ipynb ` .. container:: sphx-glr-download sphx-glr-download-python :download:`Download Python source code: pi3k_alignment.py ` .. only:: html .. rst-class:: sphx-glr-signature `Gallery generated by Sphinx-Gallery `_