GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malE_Aa in Halomonas desiderata SP1

Align Maltodextrin-binding protein (characterized, see rationale)
to candidate WP_086508157.1 BZY95_RS01095 maltose/maltodextrin ABC transporter substrate-binding protein MalE

Query= uniprot:Q9RHZ6
         (427 letters)



>NCBI__GCF_002151265.1:WP_086508157.1
          Length = 395

 Score =  164 bits (416), Expect = 3e-45
 Identities = 104/363 (28%), Positives = 176/363 (48%), Gaps = 14/363 (3%)

Query: 54  GQTITVWSWQTGPELQDVKQIAAQWAKAHGDKVIVVDQSSNPKGFQFYATAARTGKGPDV 113
           G  +T+W          ++++A Q+A   G +V +V+  +    FQ    AA +G+GPD+
Sbjct: 29  GDRLTIWMGDN-KGYDGIREVARQFADDTGIEVRIVNPDNLTDRFQ---QAAGSGQGPDI 84

Query: 114 VFGMPHDNNGVFAEEGLMAPVPSGVLNTGLYAPNTIDAIKVNGTMYSVPVSVQVAAIYYN 173
           V    HD  G +A+ GL+APV         Y   T DA   +G  Y  P+SV+   + YN
Sbjct: 85  VI-WAHDRIGEWAQSGLLAPVSPSSDFRERYFDFTWDATLWSGEHYGYPISVEALGLIYN 143

Query: 174 KKLVPQPPQTWAEFVK------DANAHGFMYDQANLYFDYAIIGGYGGYVFKDNNGTLDP 227
           K LV  PP+++AE  +      +      ++D    Y+ + ++   GGY F+      D 
Sbjct: 144 KALVETPPESFAELAQLDAELAEQGRKAILFDYGEPYYGWTLLAANGGYPFRRTEEGFDV 203

Query: 228 NNIGLDTPGAVQAYTLMRDMVSKYHWMTPSTNGSIAKAEFLAGKIGMYVSGPWDTADIEK 287
           ++IG++  GA+Q   L+ +++     +   T+ SI    F  G++   +SGPW  +++E+
Sbjct: 204 DDIGVNNEGALQGAELLVELIES-GVLPRGTDYSIMDTRFNRGEVAAMISGPWAWSNLEQ 262

Query: 288 AKIDFGVTPWPTLPNGKHATPFLGVITAFVNKESKTQAADWSLVQALTSAQAQQMYFRDS 347
           + ID+GV   P +   + A P  GV+ A +N  S         ++    ++     F   
Sbjct: 263 SGIDYGVALLPKVGE-ERAKPMFGVMAAMINTASPNDFLAVEFLENYLLSEEGMRTFNSD 321

Query: 348 QQIPALLSVQRSSAVQSSPTFKAFVEQLRYAVPMPNIPQMQAVWQAMS-ILQNIIAGKVS 406
             + A+  +     ++S P   A +E     +PMPNIP+M A W AM   LQNI +G+ S
Sbjct: 322 STLGAVAHIAYQQELESDPNIAATLENAELGMPMPNIPEMGAFWAAMEPALQNIGSGRQS 381

Query: 407 PEQ 409
           P +
Sbjct: 382 PRE 384


Lambda     K      H
   0.315    0.130    0.392 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 438
Number of extensions: 31
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 427
Length of database: 395
Length adjustment: 31
Effective length of query: 396
Effective length of database: 364
Effective search space:   144144
Effective search space used:   144144
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory