GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Desulfacinum infernum DSM 9756

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate WP_073039911.1 BUB04_RS12255 ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_900129305.1:WP_073039911.1
          Length = 383

 Score =  125 bits (315), Expect = 1e-33
 Identities = 101/320 (31%), Positives = 151/320 (47%), Gaps = 8/320 (2%)

Query: 14  LAFAPLAHAD-ITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEKVVLELADD 72
           L F  +  AD + IGL+APLTG  AA G  V N  + AV+++NK GGILG++V L   DD
Sbjct: 16  LPFGAVQAADTLKIGLLAPLTGFAAADGASVLNSVKLAVEKVNKDGGILGKQVELVAYDD 75

Query: 73  AGEPKQGVSAANKVV-GDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATAPDLTKRG 131
             + K+ V  A K++  D +  VVG   S  +  V+ +  E  +  +   A  PD+TK G
Sbjct: 76  RADGKEAVGLAQKLIQRDQVVGVVGGSYSTPSRAVAPLFQEEEIPFIAAYAVHPDITKAG 135

Query: 132 LTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATL--NAGGIT 189
                R       +   AA   + N K K++A++     +G+ LA  FK  L  NA  + 
Sbjct: 136 -DYCFRNGFLGMVEGRAAAYVAVSNLKAKKIALLTSDNDFGRTLAAGFKEYLSKNAPEVE 194

Query: 190 EVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATIIGGDGL 249
            V   A    +KDF      IK +  D+++  GY+ + G +  Q  ++   ATI G +G 
Sbjct: 195 LVYEQAYPFKEKDFKPYLAAIKEKNPDLIFASGYYFQTGPIVSQAREMGITATIFGEEGA 254

Query: 250 SNTEFWAI-GTDAAGGTIFTNASDATKSPDSKAAADALAAK-NIPAEAFTLNAYAAVEVL 307
            + +F  I G  A G  I TN +     P+ +        +  I  +    +AY A  +L
Sbjct: 255 DSPKFLEIAGKAAEGFLIVTNLNRDDPRPEVQEFLKQYRERYQIEPDMVGASAYDAFMLL 314

Query: 308 KAGIEKAGSAEDAEAVATAL 327
              I +AG   D  AV  AL
Sbjct: 315 CDAIRRAGKT-DGAAVRDAL 333


Lambda     K      H
   0.312    0.131    0.362 

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: 323
Number of extensions: 20
Number of successful extensions: 4
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: 367
Length of database: 383
Length adjustment: 30
Effective length of query: 337
Effective length of database: 353
Effective search space:   118961
Effective search space used:   118961
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 50 (23.9 bits)

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

Links

Downloads

Related tools

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