GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Desulfacinum infernum DSM 9756

Align Glucosaminate ammonia-lyase; EC 4.3.1.9; D-glucosaminate dehydratase alpha-subunit; GlcNA-DH alpha subunit; GlcNADH-alpha (uncharacterized)
to candidate WP_073036231.1 BUB04_RS01360 FAD-dependent oxidoreductase

Query= curated2:Q93HX6
         (320 letters)



>NCBI__GCF_900129305.1:WP_073036231.1
          Length = 538

 Score =  172 bits (435), Expect = 2e-47
 Identities = 109/301 (36%), Positives = 168/301 (55%), Gaps = 16/301 (5%)

Query: 9   VIILGSGPAGYSAAVYAARANLKPLLITGMQAGGQLTTTTEVDNWPGDVHGLTGPALMER 68
           ++I+G GPAG +A +YA R+ L+  ++     GGQ+ TT  V+N+PG +  + G  L++ 
Sbjct: 232 LVIVGGGPAGLTAGIYAVRSGLRAAVVERGNLGGQVATTPMVENYPG-LSRVPGKTLVDI 290

Query: 69  MREHAERFETEIVFDHINAVDFAAKPYTLTGDSATYTCDALIIATGASARYLGLPSEEAF 128
           M  HA  +      + +  V    +   +T     +T  A+++ATGAS R LG+P E+  
Sbjct: 291 MVSHALEYVEIFPNEEVVEVRPNGRLEVVT-TRRRFTARAVLLATGASYRRLGVPGEDRL 349

Query: 129 MGKGVSACATCDGFFYRNKPVAVVGGGNTAVEEALYLANIASTVTLIHRRETFRAEKILI 188
            G+GVS C+TCDG  YR K   VVGGGN+AV EAL+L +I   V L+HRR++ RA++ L+
Sbjct: 350 AGRGVSYCSTCDGPLYRGKKAVVVGGGNSAVTEALHLHHIGVEVALVHRRDSLRAQEHLV 409

Query: 189 DKLNARVAEGKIILKLNANLDEVLGDNMGVTGARLKNN-DGSFDELKVDGVFIAIGHTPN 247
             L       +I +  N  + E++G    V    LKNN  G     + D VF+AIG+   
Sbjct: 410 KALEG----AEIPVLWNTEVQEIVGGRF-VEAVLLKNNKTGETFTRETDAVFVAIGYVAE 464

Query: 248 TSLFE--GQLTLKDGYLVVQGGRDGNATATSVEGIFAAGDVADHVYRQAITSAGAGCMAA 305
           T+L +  G     DG++     R   +  T++ G++ AGDV +  YRQ +T+  AG  AA
Sbjct: 465 TTLAKKLGLPLTPDGFV-----RHDGSHRTAIPGVYTAGDV-EGGYRQIVTATAAGAAAA 518

Query: 306 L 306
           +
Sbjct: 519 M 519


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: 403
Number of extensions: 20
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: 538
Length adjustment: 31
Effective length of query: 289
Effective length of database: 507
Effective search space:   146523
Effective search space used:   146523
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 Apr 09 2024. 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