GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Burkholderia phytofirmans PsJN

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate BPHYT_RS26840 BPHYT_RS26840 NADH dehydrogenase

Query= curated2:Q93HX6
         (320 letters)



>FitnessBrowser__BFirm:BPHYT_RS26840
          Length = 530

 Score =  153 bits (386), Expect = 1e-41
 Identities = 105/317 (33%), Positives = 162/317 (51%), Gaps = 21/317 (6%)

Query: 10  IILGSGPAGYSAAVYAARANLKPLLITGMQA---GGQLTTTTEVDNWPGDVHGLTGPALM 66
           +I+G GPAG +AA+Y+AR  +     TG+ A   GGQ+  T  ++N+   V    GP   
Sbjct: 216 LIVGGGPAGAAAAIYSARKGIA----TGVVAERFGGQVLDTLAIENFVS-VTETEGPKFA 270

Query: 67  ERMREHAERFETEIV-FDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPSE 125
             + +H + +E +I+      A+           + A      +I+ATGA  R + +P E
Sbjct: 271 TALEQHVKTYEVDIMDVQRAEALIPGRINEVRLANGAVLKAKTIILATGARWREINVPGE 330

Query: 126 EAFMGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAEK 185
             +   GV+ C  CDG  ++ K VAV+GGGN+ VE A+ LA I   VTL     T RA++
Sbjct: 331 REYRNHGVAYCPHCDGPLFKGKRVAVIGGGNSGVEAAIDLAGIVREVTLFEFGATLRADE 390

Query: 186 ILIDKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKN-NDGSFDELKVDGVFIAIGH 244
           +L  KL +      + +   A   E+ GD   V G   K+   G   +++++GVF+ IG 
Sbjct: 391 VLQRKLRSL---ANVTVVTQAQTTEITGDGKKVNGLVYKDLRSGEVKQIELEGVFVQIGL 447

Query: 245 TPNTSLFEGQLTL-KDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCM 303
            PNT   +G + L K G +VV         ATSV G+FAAGDV    ++Q + + G G  
Sbjct: 448 VPNTEWLKGTVELSKHGEIVVDA-----RGATSVPGVFAAGDVTTVPFKQIVIAVGEGAK 502

Query: 304 AALDTERYLDGLQNASE 320
           A+L    +L  ++N+ E
Sbjct: 503 ASLSAFDHL--IRNSEE 517


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: 369
Number of extensions: 24
Number of successful extensions: 3
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: 530
Length adjustment: 31
Effective length of query: 289
Effective length of database: 499
Effective search space:   144211
Effective search space used:   144211
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