GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacD in Paraburkholderia phymatum STM815

Align D-xylonate dehydratase subunit (EC 4.2.1.25; EC 4.2.1.82) (characterized)
to candidate WP_012399852.1 BPHY_RS02165 galactonate dehydratase

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



>NCBI__GCF_000020045.1:WP_012399852.1
          Length = 382

 Score =  211 bits (538), Expect = 2e-59
 Identities = 140/387 (36%), Positives = 207/387 (53%), Gaps = 21/387 (5%)

Query: 3   KISEIEAYILGKEVTSAQWASLMVLVRVTTNDGRVGWGETVSALRAEAVANFVKKINTVL 62
           KI++IE +I+       +W      V++ T++G VGWGE V   RA  VA  V +++  L
Sbjct: 2   KITKIETFIV-----PPRWC----FVKIETDEGIVGWGEPVVEGRAHTVAAAVDELSDYL 52

Query: 63  KGNDVFNVEKNRLEWYKHDFNMTISLESTTAYSAVDIASWDIIGKELGAPLYKLLGGKTR 122
            G D  N+E +    Y+  F     + S +A + VD A WDI GK  G P++ LLGG+ R
Sbjct: 53  LGKDPRNIEDHWQVMYRAGFYRGGPI-SMSAIAGVDQALWDIKGKFHGVPVHTLLGGQVR 111

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

Query: 183 AVREAVGDNVDILIEHHGRFNANSAIMIAKRLEKYNPLFMEEPIHPEDVEGLRKYRNNTS 242
           AVREAVG NV I ++ HGR +   A ++AK L+ Y  +F+EEP+  E+ E LR   N TS
Sbjct: 169 AVREAVGPNVGIGVDFHGRVHKPMAKVLAKELDPYKLMFIEEPVLSENAEALRDIVNQTS 228

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

Query: 303 GPILNAVTLQFDAFIPNFLIQESFYDWFPSWKRELI-YNGTP----IDNGYAIIPERPGL 357
           GPI  A  LQ DA   N  IQE       +   +L+ Y   P     ++G+  IP+ PGL
Sbjct: 289 GPIALATCLQIDAVSYNAFIQEQSLGIHYNQGNDLLDYIKNPEVFKYEDGFVSIPQGPGL 348

Query: 358 GVEVNEKMLDSLKVKGEEYFNPEEPVW 384
           G+EVNE+ +  +   G  + N   PVW
Sbjct: 349 GIEVNEEKVREMAKVGHRWRN---PVW 372


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: 402
Number of extensions: 25
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.

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