GapMind for catabolism of small carbon sources

 

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

Align D-galactono-lactonase (EC 3.1.1.-) (characterized)
to candidate CA265_RS25055 CA265_RS25055 6-phosphogluconolactonase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3314
         (389 letters)



>FitnessBrowser__Pedo557:CA265_RS25055
          Length = 369

 Score =  228 bits (582), Expect = 2e-64
 Identities = 135/367 (36%), Positives = 212/367 (57%), Gaps = 19/367 (5%)

Query: 21  ASAEDYQLLVGSYTA-GQSQGIYRLAFDSRTGQIDASPLQVIKSANPSWLTLSKDQRHLF 79
           A   +Y L+VG+YTA G+S+GIY   F++ T       +    +ANPS+L +S DQ+ ++
Sbjct: 19  AQKANYNLIVGTYTAPGKSEGIYTYNFNASTAATTIKSITK-NTANPSYLAVSPDQKFVY 77

Query: 80  VVNENGPGQTDPVGRVSSFAIDPKTHALSLISQVQSLGNEPTHSSLSIDGSHLFVSNYSV 139
           VVNE G   T     VS+F  +  + AL+ +++V S G +P    +++D  ++ V+NYS 
Sbjct: 78  VVNETGATST-----VSAFKYNAASGALTFLNKVDSHGADPCF--ITVDAKNVIVANYS- 129

Query: 140 AEDPGGTLAVLPVAADGKLKAVVQMSSHPASRVNPE-RQASAHVHSTIPSPDGRYVFAND 198
               GG+LA+    ADG L   +Q   H    ++P+ RQ SAHVH    +PD +++  ND
Sbjct: 130 ----GGSLAIFSRKADGALTEALQTIEHTGKSIDPKGRQESAHVHMVKFTPDYKHLIVND 185

Query: 199 LGADKVFAYRFDPKANPELPLTPATPAFVQLPPGSGPRHLLFSADGKHAWLTMEMSAQVA 258
           LG D+++ Y + P A   + LT    + ++   G+GPRH+ FS +GK A+L  E +  + 
Sbjct: 186 LGEDRIYIYNYKPAAKENI-LT--VKSVIKTNAGTGPRHITFSPNGKFAYLAHEFNGSIT 242

Query: 259 VFDYHDGQLEQTQMVDLAAGQPVSDKAAAALHASADGKFLYVSNRGTANQLLVFAIDPAT 318
            F Y +G L + Q +   +        AA +H SADGKFLY +NRG AN +  F++ P T
Sbjct: 243 AFAYSNGSLTKIQEIGTTSKDFTGKVDAADIHVSADGKFLYETNRGDANSISAFSVLP-T 301

Query: 319 GHLSELQRRAVEGDHPREFSLDPSGKFLLIANQKSNQIVVVERDARTGLLGKTVQKLPMD 378
           G L  ++  +  G  PR F++DP+GKFLLI +Q +N IV+ +R+  TG L  + +++ + 
Sbjct: 302 GKLKFIETVSTLGKGPRNFTIDPTGKFLLIGHQYTNNIVIFKRNKTTGKLSDSGKRIDVG 361

Query: 379 APSDLRF 385
           AP  L F
Sbjct: 362 APVCLVF 368


Lambda     K      H
   0.316    0.132    0.382 

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: 408
Number of extensions: 28
Number of successful extensions: 7
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: 389
Length of database: 369
Length adjustment: 30
Effective length of query: 359
Effective length of database: 339
Effective search space:   121701
Effective search space used:   121701
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 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