GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Pseudomonas putida KT2440

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate PP_0786 PP_0786 thioredoxin reductase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__Putida:PP_0786
          Length = 320

 Score =  589 bits (1519), Expect = e-173
 Identities = 295/319 (92%), Positives = 304/319 (95%)

Query: 1   MVEVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGL 60
           M EVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGD HGL
Sbjct: 1   MSEVRHSRVIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDPHGL 60

Query: 61  TGPALMERMREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYL 120
           TGPALM+RM+EHAERFETEIVFDHINAVD A KP+TL GDS  YTCDALIIATGASARYL
Sbjct: 61  TGPALMQRMQEHAERFETEIVFDHINAVDLANKPFTLQGDSGKYTCDALIIATGASARYL 120

Query: 121 GLPSEEAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRET 180
           GLPSEE FMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIAS VTL+HRRET
Sbjct: 121 GLPSEETFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASKVTLVHRRET 180

Query: 181 FRAEKILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNNDGSFDELKVDGVFI 240
           FRAEKIL+DKLNARVAEGKI LKLNA LDEVLGDNMGVTGARLKNNDGS DE+KVDGVFI
Sbjct: 181 FRAEKILVDKLNARVAEGKIELKLNATLDEVLGDNMGVTGARLKNNDGSSDEIKVDGVFI 240

Query: 241 AIGHTPNTSLFEGQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGA 300
           AIGHTPNTSLFEGQLTLKDGYLVV GGR+GNATAT+VEG+FAAGDVADHVYRQAITSAGA
Sbjct: 241 AIGHTPNTSLFEGQLTLKDGYLVVNGGREGNATATNVEGVFAAGDVADHVYRQAITSAGA 300

Query: 301 GCMAALDTERYLDGLQNAS 319
           GCMAALD ERYLDGL NAS
Sbjct: 301 GCMAALDVERYLDGLANAS 319


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: 479
Number of extensions: 13
Number of successful extensions: 1
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: 320
Length adjustment: 28
Effective length of query: 292
Effective length of database: 292
Effective search space:    85264
Effective search space used:    85264
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: 48 (23.1 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