GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xad in Herbaspirillum seropedicae SmR1

Align D-xylonate dehydratase subunit (EC 4.2.1.25; EC 4.2.1.82) (characterized)
to candidate HSERO_RS05150 HSERO_RS05150 galactonate dehydratase

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



>FitnessBrowser__HerbieS:HSERO_RS05150
          Length = 382

 Score =  207 bits (528), Expect = 3e-58
 Identities = 134/382 (35%), Positives = 206/382 (53%), Gaps = 18/382 (4%)

Query: 3   KISEIEAYILGKEVTSAQWASLMVLVRVTTNDGRVGWGETVSALRAEAVANFVKKINTVL 62
           KI++I  +I+       +W  L    ++ T++G VGWGE +   RA +VA  V++++  L
Sbjct: 2   KITKITTFIV-----PPRWCFL----KIETDEGVVGWGEPIVEGRAHSVAAAVEELSDYL 52

Query: 63  KGNDVFNVEKNRLEWYKHDFNMTISLESTTAYSAVDIASWDIIGKELGAPLYKLLGGKTR 122
            G D  N+E +    Y+  F    ++  + A + +D A WDI GK+LG P+++LLGG  R
Sbjct: 53  IGKDPRNIEDHWTVLYRGGFYRGGAIHMS-ALAGIDQALWDIKGKDLGVPVHQLLGGAVR 111

Query: 123 DKVLVYANGWYQNCVKPEDFAEKAKEIVKMGYKALKFDPFGPYFNDISKKGLDIAEERVK 182
           + + VY+  W     +P D A  AK  V  G+ A+K +         S   +++    V+
Sbjct: 112 NSIRVYS--WIGGD-RPADTAAAAKSAVARGFTAVKMNGTEELQFIDSHDKIELTLANVQ 168

Query: 183 AVREAVGDNVDILIEHHGRFNANSAIMIAKRLEKYNPLFMEEPIHPEDVEGLRKYRNNTS 242
           AVREAVG NV I ++ HGR +   A  + K LE Y  +F+EEP+  E+ E L++  + TS
Sbjct: 169 AVREAVGPNVGIGVDFHGRVHKPMAKALIKELEPYKLMFIEEPVLSENAEALKEIAHLTS 228

Query: 243 LRIALGERIINKQQALYFMKEGLVDFLQADLYRIGGVTETKKVVGIAETFDVQMAFHNAQ 302
             IALGER+ ++      + EG VD +Q D+   GG+TET+K+  +AE +DV +A H   
Sbjct: 229 TPIALGERLYSRWDFKRILSEGYVDIIQPDVSHAGGITETRKIAMMAEAYDVALALHCPL 288

Query: 303 GPILNAVTLQFDAFIPNFLIQESFYDWFPSWKRELI-----YNGTPIDNGYAIIPERPGL 357
           GPI  A  LQ DA   N  IQE       +   +L+      N    ++GY  IP+ PGL
Sbjct: 289 GPIALASCLQVDAGSYNAFIQEQSLGIHYNESNDLLDYIRDKNVFAYEDGYVKIPQGPGL 348

Query: 358 GVEVNEKMLDSLKVKGEEYFNP 379
           G+E+NE+ +      G  + NP
Sbjct: 349 GIEINEEYVRQRAEVGHRWRNP 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: 389
Number of extensions: 15
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: 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 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