GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Shewanella sp. ANA-3

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate 7026184 Shewana3_3326 FAD-dependent pyridine nucleotide-disulphide oxidoreductase (RefSeq)

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__ANA3:7026184
          Length = 525

 Score =  159 bits (401), Expect = 2e-43
 Identities = 105/309 (33%), Positives = 162/309 (52%), Gaps = 17/309 (5%)

Query: 9   VIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPALMER 68
           V+++G GPAG +AA+YAAR  L+  ++   + GGQ+  T  ++N+   V    GP L+  
Sbjct: 213 VLVVGGGPAGAAAAIYAARKGLRTGVVAD-KFGGQVAETVGIENFIS-VKATEGPKLVAN 270

Query: 69  MREHAERFETEIVFDHINAVDFAAKPY--TLTGDSATYTCDALIIATGASARYLGLPSEE 126
           +  H   +E +I+ D+  AV  A+           AT     +++ATGA  R + +P E+
Sbjct: 271 LEAHVRDYEVDIM-DNQKAVKLASDGLFELELASGATLRSRTILLATGARWREMNVPGEK 329

Query: 127 AFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAEKI 186
            + GKGV+ C  CDG  ++ K VAV+GGGN+ +E A+ LANI   VT++      RA+ +
Sbjct: 330 EYRGKGVAYCPHCDGPLFKGKRVAVIGGGNSGIEAAIDLANIVEHVTVLEFDSKLRADDV 389

Query: 187 LIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNN-DGSFDELKVDGVFIAIGHT 245
           L  K     + G I +   A   EV GD   V G    +   G    + + G+F+ IG  
Sbjct: 390 LQRK---AASMGNIHIITQAMTTEVTGDGTRVNGLNYTDRATGESHHIALAGIFVQIGLV 446

Query: 246 PNTSLFEG--QLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCM 303
           PN    +G   LT +   +V + G+      TS+ G+FAAGDV +  Y+Q I + G+G  
Sbjct: 447 PNAEWLKGTVDLTPRGEIIVDERGQ------TSIPGVFAAGDVTNSPYKQIIIAMGSGAN 500

Query: 304 AALDTERYL 312
           A+L    YL
Sbjct: 501 ASLGAFDYL 509


Lambda     K      H
   0.318    0.135    0.386 

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: 380
Number of extensions: 17
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: 320
Length of database: 525
Length adjustment: 31
Effective length of query: 289
Effective length of database: 494
Effective search space:   142766
Effective search space used:   142766
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 (21.7 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