GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Pedobacter arcticus A12

Align Mannose-6-phosphate isomerase; EC 5.3.1.8; Phosphohexomutase; Phosphomannose isomerase; PMI (uncharacterized)
to candidate WP_017259472.1 B176_RS0114095 class I mannose-6-phosphate isomerase

Query= curated2:Q59935
         (316 letters)



>NCBI__GCF_000302595.1:WP_017259472.1
          Length = 324

 Score =  193 bits (491), Expect = 4e-54
 Identities = 114/305 (37%), Positives = 166/305 (54%), Gaps = 10/305 (3%)

Query: 1   MAEPLFLQSQMHKKIWGGNRLRKEFGYDI-PSETTGEYWAISAHPNGVSVVKNGVYKGVP 59
           M  PL  ++    KIWGG +++   G D  P    GE W IS   + VS++ NG   G  
Sbjct: 1   MLYPLKFKTIFKDKIWGGEKIKTYLGKDFAPLPNCGETWEISGVKSDVSIIANGPLTGTS 60

Query: 60  LDELYAEHR-ELFGNSK----SSVFPLLTKILDANDWLSVQVHPDNAYALEHEGELGKTE 114
           L +L A+ + EL G        + FPLL K +DAN+ LS+QVHP++  A +  G  GKTE
Sbjct: 61  LAQLLADQKGELIGKKNYERFGNEFPLLIKFIDANEDLSIQVHPNDELAEKRHGSKGKTE 120

Query: 115 CWYVISADEGAEIIYGHEAK-SKEELRQMIAAGDWDHLLTKIPVKAGDFFYVPSGTMHAI 173
            WYV+ ADEGA +I G   K  KE   +   AG+   +L K  VKAGD F++P+G +H I
Sbjct: 121 MWYVLQADEGATLISGFNQKLDKETYLKKFNAGELSDILNKEEVKAGDVFFLPAGRVHTI 180

Query: 174 GKGIMILETQQSSDTTYRVYDFDRKDDQGRKRALHIEQSIDVLTIGKPANATPAWLSLQG 233
           GKG++I E QQ+SD TYR+YDFDR DDQG KR LH+E+++D +           +     
Sbjct: 181 GKGLLIAEIQQTSDITYRIYDFDRVDDQGNKRELHVEEALDAIDYTFYDEYKTKYNDTIN 240

Query: 234 LETTVLVSSPFFTVYKWQISGSVKMQQTA--PYLLVSVLAGQGRITVGLEQYALRKGDHL 291
            E   LV   +FT      +       +A   +++   + G   +  G+E+  ++ GD +
Sbjct: 241 -EPVALVDCKYFTTNILTYTEDTLRDYSANDSFVIHVCVEGSYILKYGIEELPVQMGDCV 299

Query: 292 ILPNT 296
           ++P T
Sbjct: 300 LIPAT 304


Lambda     K      H
   0.317    0.135    0.408 

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: 259
Number of extensions: 18
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: 316
Length of database: 324
Length adjustment: 28
Effective length of query: 288
Effective length of database: 296
Effective search space:    85248
Effective search space used:    85248
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: 48 (23.1 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