Merge pull request #10 from haddocking/9-unbound-variable-in-hsspget_…

…from_ftp

Refactor `get_from_ftp` to remove unbound variable

libwhiscy/hssp.py

@@ -1,13 +1,41 @@
-from ftplib import FTP
-import os
 import bz2
+import logging
+import os
+import sys
 import urllib.request
-from Bio import AlignIO
+from ftplib import FTP
+from typing import Union
 
+from Bio import AlignIO
 
-def get_from_ftp(pdb_code, path_to_store='.',
-                 ftp_server='ftp.cmbi.umcn.nl', ftp_path='/pub/molbio/data/hssp/'):
-    """Downloads using FTP protocol an HSSP alignment for the given pdb_code"""
+# Set logging
+logger = logging.getLogger("hssp_log")
+logger.setLevel(logging.INFO)
+ch = logging.StreamHandler(sys.stdout)
+ch.setLevel(logging.INFO)
+formatter = logging.Formatter("%(name)s [%(levelname)s] %(message)s")
+ch.setFormatter(formatter)
+logger.addHandler(ch)
+
+
+def get_from_ftp(
+    pdb_code: str,
+    path_to_store: str = ".",
+    ftp_server: str = "ftp.cmbi.umcn.nl",
+    ftp_path: str = "/pub/molbio/data/hssp/",
+) -> Union[str, None]:
+    """Downloads an HSSP alignment file for the given pdb_code using FTP protocol.
+
+    Args:
+        pdb_code (str): The PDB code for which to download the HSSP alignment file.
+        path_to_store (str, optional): The path where the downloaded file should be stored. Defaults to ".".
+        ftp_server (str, optional): The FTP server to connect to. Defaults to "ftp.cmbi.umcn.nl".
+        ftp_path (str, optional): The path on the FTP server where the HSSP alignments are stored. Defaults to "/pub/molbio/data/hssp/".
+
+    Returns:
+        Union[str, None]: The path to the downloaded file if successful, None otherwise.
+    """
+    path_to_file: str = ""
     # Start connection
     try:
         ftp = FTP(ftp_server)
@@ -16,33 +44,39 @@ def get_from_ftp(pdb_code, path_to_store='.',
         # Move to path where HSSP alignments are stored
         ftp.cwd(ftp_path)
         # File name format
-        file_name = '{}.hssp.bz2'.format(pdb_code.lower())
+        file_name = "{}.hssp.bz2".format(pdb_code.lower())
         # Retrieve file
         path_to_file = os.path.join(path_to_store, file_name)
-        ftp.retrbinary("RETR " + file_name, open(path_to_file, 'wb').write)
+        ftp.retrbinary("RETR " + file_name, open(path_to_file, "wb").write)
         # Close connection
         ftp.close()
 
         return path_to_file
-    except:
-        if os.path.exists(path_to_file):
+    except Exception as e:
+        logger.exception(e)
+        logger.error("There was an error downloading the file from the FTP server.")
+        if path_to_file != "" and os.path.exists(path_to_file):
             os.remove(path_to_file)
         return None
 
-def get_from_url(pdb_code, path_to_store='.',
-                 url='ftp://ftp.cmbi.umcn.nl/pub/molbio/data/hssp3/'):
+
+def get_from_url(
+    pdb_code, path_to_store=".", url="ftp://ftp.cmbi.umcn.nl/pub/molbio/data/hssp3/"
+):
     """Downloads from HSSP3 online db the HSSP file in stockholm format"""
-    file_name = '{}.hssp.bz2'.format(pdb_code.lower())
+    file_name = "{}.hssp.bz2".format(pdb_code.lower())
     # Make sure we use hssp3 instead of simple hssp to help identifying them
-    path_to_file = os.path.join(path_to_store, file_name.replace('hssp', 'hssp3'))
+    path_to_file = os.path.join(path_to_store, file_name.replace("hssp", "hssp3"))
     urllib.request.urlretrieve(url + file_name, path_to_file)
     return path_to_file
 
 
 def decompress_bz2(file_name_input, file_name_output):
-    """Decompresses file_name_input in BZ2 format into file_name_output""" 
-    with open(file_name_output, 'wb') as new_file, bz2.BZ2File(file_name_input, 'rb') as file:
-        for data in iter(lambda : file.read(100 * 1024), b''):
+    """Decompresses file_name_input in BZ2 format into file_name_output"""
+    with open(file_name_output, "wb") as new_file, bz2.BZ2File(
+        file_name_input, "rb"
+    ) as file:
+        for data in iter(lambda: file.read(100 * 1024), b""):
             new_file.write(data)
 
 
@@ -53,7 +87,7 @@ def _parse_hssp_proteins(line_buffer):
         if line.startswith("  NR.") or line.startswith("##"):
             continue
         # Only get the id and name of the protein in the alignment
-        fields = (line[:20]).split(':')
+        fields = (line[:20]).split(":")
         seq_id = int(fields[0]) - 1
         name = fields[1].strip()[:10]
         proteins[seq_id] = name
@@ -67,30 +101,30 @@ def _parse_hssp_alignments(line_buffer, chain_id, num_alignments):
     last_alignment = 0
     current_num_alignments = 0
     for line in line_buffer:
-        if line.startswith(" SeqNo") or line[12] == '!':
+        if line.startswith(" SeqNo") or line[12] == "!":
             continue
         if line.startswith("## ALIGNMENTS"):
-            fields = (line[13:]).split('-')
+            fields = (line[13:]).split("-")
             # We are now parsing alignments from first to last specified
             # in the ALINGMENTS header
             first_alignment = int(fields[0]) - 1
             last_alignment = int(fields[1]) - 1
             current_num_alignments = last_alignment - first_alignment + 1
         else:
-            if line[12] == chain_id and line[14] != 'X':
-                for i, s in enumerate(line[51:51+current_num_alignments]):
+            if line[12] == chain_id and line[14] != "X":
+                for i, s in enumerate(line[51 : 51 + current_num_alignments]):
                     # We will convert spaces or dots to -
-                    if s == '.' or s == ' ':
-                        s = '-'
+                    if s == "." or s == " ":
+                        s = "-"
                     # We leave residues in minor case as if to not forget insertions
                     alignments[first_alignment + i].append(s)
-    alignments = [(''.join(s)) for s in alignments]
+    alignments = [("".join(s)) for s in alignments]
     return alignments
 
 
 def hssp_file_to_phylip(hssp_file_name, phylip_file_name, chain_id, master_sequence):
     """Parses an HSSP file and returns a list of the sequences"""
-    # We're only interested in the lenght of the sequence of our given chain_id, 
+    # We're only interested in the lenght of the sequence of our given chain_id,
     # SEQLENGHT header gives us the sum of all.
     seqlength = len(master_sequence)
     num_alignments = 0
@@ -103,13 +137,13 @@ def hssp_file_to_phylip(hssp_file_name, phylip_file_name, chain_id, master_seque
     with open(hssp_file_name, "rU") as handle:
         for line in handle:
             line = line.rstrip(os.linesep)
-            if line.startswith('NCHAIN'):
+            if line.startswith("NCHAIN"):
                 num_chains = int(line.split()[1])
-            if line.startswith('NALIGN'):
+            if line.startswith("NALIGN"):
                 num_alignments = int(line.split()[1])
-            
-            parsing = (seqlength != 0 and num_chains != 0 and num_alignments != 0)
-            
+
+            parsing = seqlength != 0 and num_chains != 0 and num_alignments != 0
+
             if parsing:
                 if line.startswith("## ALIGNMENTS"):
                     parsing_alignment = True
@@ -130,33 +164,45 @@ def hssp_file_to_phylip(hssp_file_name, phylip_file_name, chain_id, master_seque
                     prot_line_buffer.append(line)
 
         proteins = _parse_hssp_proteins(prot_line_buffer)
-        alignments = _parse_hssp_alignments(line_buffer, chain_id.upper(), num_alignments)
+        alignments = _parse_hssp_alignments(
+            line_buffer, chain_id.upper(), num_alignments
+        )
 
-        all_zero = (sum([len(a) for a in alignments]) == 0)
+        all_zero = sum([len(a) for a in alignments]) == 0
 
         if all_zero:
-            raise Exception("Not a single alignment found for chain {}".format(chain_id))
-
-        non_valid = [k for k in proteins.keys() if alignments[k].count('-') >= seqlength]
-        with open(phylip_file_name, 'w') as output_handle:
+            raise Exception(
+                "Not a single alignment found for chain {}".format(chain_id)
+            )
+
+        non_valid = [
+            k for k in proteins.keys() if alignments[k].count("-") >= seqlength
+        ]
+        with open(phylip_file_name, "w") as output_handle:
             # Write header, MASTER also counts
-            output_handle.write("{}  {}{}".format(len(proteins) - len(non_valid) + 1, seqlength, os.linesep))
+            output_handle.write(
+                "{}  {}{}".format(
+                    len(proteins) - len(non_valid) + 1, seqlength, os.linesep
+                )
+            )
             # Write master sequence
             output_handle.write("MASTER    {}{}".format(master_sequence, os.linesep))
             # Write the rest of non null alignments
             for k in sorted(proteins.keys()):
                 if k not in non_valid:
-                    output_handle.write("{:10s}{}{}".format(proteins[k], alignments[k], os.linesep))
+                    output_handle.write(
+                        "{:10s}{}{}".format(proteins[k], alignments[k], os.linesep)
+                    )
 
 
 def hssp3_file_to_phylip(hssp3_file_name, phylip_file_name, chain_id, master_sequence):
     """Reads a HSSP file in stockholm format and writes a new msa file in phylip-sequential format
     only containing the given chain"""
-    alignments = list(AlignIO.parse(hssp3_file_name, format='stockholm'))
+    alignments = list(AlignIO.parse(hssp3_file_name, format="stockholm"))
     for align in alignments:
-        if align[0].name[4] == '/':
+        if align[0].name[4] == "/":
             chain = align[0].name[5].upper()
             if chain == chain_id:
-                align[0].id = align[0].name = align[0].description = 'MASTER'
-                #align[0].seq = align[0].seq.ungap('-')
-                AlignIO.write(align, phylip_file_name, format='phylip-sequential')
+                align[0].id = align[0].name = align[0].description = "MASTER"
+                # align[0].seq = align[0].seq.ungap('-')
+                AlignIO.write(align, phylip_file_name, format="phylip-sequential")