GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xad in Pedobacter sp. GW460-11-11-14-LB5

Align xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate CA265_RS13665 CA265_RS13665 galactonate dehydratase

Query= BRENDA::D4GP40
         (412 letters)



>FitnessBrowser__Pedo557:CA265_RS13665
          Length = 388

 Score =  205 bits (521), Expect = 2e-57
 Identities = 121/379 (31%), Positives = 202/379 (53%), Gaps = 18/379 (4%)

Query: 37  EITDVQTTMVDG-NYPWILVRVYTDAGVVGTGEAYWGGGDTAIIERMKPF---LVGENPL 92
           +ITDV+  +V+G  Y W L+++YTD G  G GEA    G   + E  K     ++G +P+
Sbjct: 2   KITDVKVWLVEGVKYNWTLLKIYTDTGHTGVGEATNWPGSPIVFEATKHVGQRIIGLDPM 61

Query: 93  DIDRLYEHLVQKMSGEGSVSGKVISAISGIEIALHDVAGKLLDVPAYQLVGGKYRDEVRV 152
             D ++  L + ++  G   G  + AISGI++AL D+  K+L VP Y+L+GG +R ++ +
Sbjct: 62  KTDFIWTKLYRDLNWMGPF-GASMCAISGIDMALLDLKAKVLGVPCYELLGGAFRKDILL 120

Query: 153 YCDLHTEDEANPQACAEEGVRVVEELGYDAIKFDLDVPSGH------EKDRANRHLRNPE 206
           Y +       +  A      + V+E G+  +KFD   P  H      E   +N  L  P+
Sbjct: 121 YANYWFTGGGHNTADYAAQAKKVKEAGFTGLKFD---PFAHTNYLYGEDLSSNLQLTAPQ 177

Query: 207 IDHKVEIVEAVTEAVGDRADVAFDCHWSFTGGSAKRLASELEDYDVWWLEDPVPPENHDV 266
            D    + +AV +AVG   D+  + H       A  +A  L + ++ W E+P  PEN + 
Sbjct: 178 QDLAFNVSKAVRDAVGPEFDIMIETHAMLNYRVAVTMAQRLSELNITWYEEPAGPENANT 237

Query: 267 QKLVTQS--TTTPIAVGENVYRKFGQRTLLEPQAVDIIAPDLPRVGGMRETRKIADLADM 324
            K +     +   I VGE  Y + G R +LE    DI+ PD+ R GG  E +++A + + 
Sbjct: 238 LKAMRDRIPSNVSICVGERHYTRHGIRDVLEKHICDIMMPDITRCGGPSEMKRMATMMEA 297

Query: 325 YYIPVAMHNVSSPIGTMASAQVAAAIPNSLALEYHSYQLGWWEDLVEED--DLIQNGHME 382
           Y + +A HN + P+ T+ASAQV A++PN    E+    + W ++++     D++QNGH++
Sbjct: 298 YNVLLAPHNPNGPLSTLASAQVCASVPNFFRQEFMFNDVPWRDEVISHPIADMVQNGHLK 357

Query: 383 IPEKPGLGLTLDLDAVEAH 401
           + ++PGLG+ L  + +E H
Sbjct: 358 LSDRPGLGVDLIEEEMEKH 376


Lambda     K      H
   0.315    0.135    0.401 

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: 466
Number of extensions: 24
Number of successful extensions: 5
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: 412
Length of database: 388
Length adjustment: 31
Effective length of query: 381
Effective length of database: 357
Effective search space:   136017
Effective search space used:   136017
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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