GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacD in Rhizobium leguminosarum WSM1325

Align D-xylonate dehydratase subunit (EC 4.2.1.25; EC 4.2.1.82) (characterized)
to candidate WP_011653629.1 RLEG_RS18610 galactonate dehydratase

Query= metacyc::MONOMER-18070
         (393 letters)



>NCBI__GCF_000023185.1:WP_011653629.1
          Length = 382

 Score =  207 bits (528), Expect = 3e-58
 Identities = 134/382 (35%), Positives = 207/382 (54%), Gaps = 18/382 (4%)

Query: 3   KISEIEAYILGKEVTSAQWASLMVLVRVTTNDGRVGWGETVSALRAEAVANFVKKINTVL 62
           KI+++  YI+       +W    + ++V T++G VGWGE V   RA  V   V ++   L
Sbjct: 2   KITKLTTYIV-----PPRW----LFLKVETDEGIVGWGEPVVEGRALTVQAAVHELEDYL 52

Query: 63  KGNDVFNVEKNRLEWYKHDFNMTISLESTTAYSAVDIASWDIIGKELGAPLYKLLGGKTR 122
            G D F +E +    Y+  F    ++  + A S +D A WDI GK LG P++ LLGG+ R
Sbjct: 53  IGKDPFLIEDHWTVMYRGGFYRGGAVHMS-AISGIDQALWDIKGKALGQPIHSLLGGQLR 111

Query: 123 DKVLVYANGWYQNCVKPEDFAEKAKEIVKMGYKALKFDPFGPYFNDISKKGLDIAEERVK 182
           D++ VY+  W     +P D A  AKE+V  G+KA+K +         + + ++ A E + 
Sbjct: 112 DRIKVYS--WIGGD-RPSDVANNAKEVVARGFKAIKLNGCEEMQIVDTNEKVEKAVETIA 168

Query: 183 AVREAVGDNVDILIEHHGRFNANSAIMIAKRLEKYNPLFMEEPIHPEDVEGLRKYRNNTS 242
           A+REA+G ++ I ++ HGR +   A ++AK L+ Y  +F+EEP+  E+ E LR   N+TS
Sbjct: 169 AIREAIGPHIGIGVDFHGRVHKPMAKVLAKELDPYKLMFIEEPVLSENKEALRDIVNHTS 228

Query: 243 LRIALGERIINKQQALYFMKEGLVDFLQADLYRIGGVTETKKVVGIAETFDVQMAFHNAQ 302
             IALGER+ ++      + +G VD +Q DL   GG+TE +K+  +AE +DV +A H   
Sbjct: 229 TPIALGERLFSRWDFKQVLSDGYVDIIQPDLSHAGGITECRKIAAMAEAYDVALAPHCPL 288

Query: 303 GPILNAVTLQFDAFIPNFLIQESFYDWFPSWKREL---IYNGTPID--NGYAIIPERPGL 357
           GPI  A  LQ DA   N  IQE       +   ++   I N       +G+  IP+ PGL
Sbjct: 289 GPIALAACLQVDAVSYNAFIQEQSLGIHYNKGNDILDYISNKEVFQYADGFVSIPQGPGL 348

Query: 358 GVEVNEKMLDSLKVKGEEYFNP 379
           G+EV+E  +     +G  + NP
Sbjct: 349 GIEVDEAYVIERAKEGHRWRNP 370


Lambda     K      H
   0.319    0.137    0.409 

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: 400
Number of extensions: 16
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: 393
Length of database: 382
Length adjustment: 30
Effective length of query: 363
Effective length of database: 352
Effective search space:   127776
Effective search space used:   127776
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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