GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Thermodesulforhabdus norvegica DSM 9990

Align Lactaldehyde reductase (characterized, see rationale)
to candidate WP_093396479.1 BM091_RS13315 alcohol dehydrogenase

Query= uniprot:Q8A199
         (384 letters)



>NCBI__GCF_900114975.1:WP_093396479.1
          Length = 380

 Score =  208 bits (530), Expect = 2e-58
 Identities = 126/374 (33%), Positives = 202/374 (54%), Gaps = 7/374 (1%)

Query: 12  FGAGCRSVIAVEAARRGFKKAFFVTDKDLIKFGVAAEIIKVFDDNHIPYELYSDVKANPT 71
           FG G     A+ A R G +K F V+D  L K G   E+I + + + + +  + DV +NP 
Sbjct: 13  FGRGSMKYTALCARRLGAEKVFLVSDPGLEKVGWVDELINILEAHQLEWVYFGDVVSNPR 72

Query: 72  IANVQNGVAAYKASGADFIVALGGGSSIDTAKGIGIVVNNPDFADVKSLEGVADTKHKAV 131
              ++ G   Y +  AD ++ALGGGS +D AKGI IV +N     +   EG         
Sbjct: 73  DYQIERGARLYLSERADVVIALGGGSPMDAAKGIAIVASNG--GSIHDYEGANRIHRPLP 130

Query: 132 PTFALPTTAGTAAEVTINYVIIDEDARKKMVCVDPNDIPAVAIVDPELMYSMPKGLTAAT 191
           P   LPTTAG+ ++++   +I D   R KM  +    +P ++I+DP  + + P+ L  ++
Sbjct: 131 PMVFLPTTAGSGSDISQFAIITDTRRRVKMSIISRTLVPNISIIDPLFLQTKPRELVLSS 190

Query: 192 GMDALTHAIESYITPGAWAMSDMFELKAIEMIAQNL-KAAVDNGKDTVAREAMSQAQYIA 250
            +DAL+HAIES+++  A   ++M  LKAIE++A+ L  AAV    DT+  EA+S A   A
Sbjct: 191 AIDALSHAIESFVSVIASPFTEMQSLKAIELVAKYLPTAAVSLELDTL--EALSTASTAA 248

Query: 251 GMGFSNVGLGIVHSMAHPLGAFYDTPHGVANALLLPYVMEYNAESPAAPKYIHIAKAMGV 310
            M FSN GLG VH+++H +G  YD  HG  + +LLP VM +N E+    K   I + +  
Sbjct: 249 AMAFSNAGLGAVHALSHAIGGMYDVLHGHVHPVLLPPVMRFNMEA-CLDKMAQIGRIISG 307

Query: 311 NTDGMTETEGVKAAIEAVKALSLSIGIPQKLHEINVKEEDIPALAVAAFNDVCTGGNPRP 370
                 ++  ++  IE ++ + LS+ +  +L +I   + +I  L   A  DVC   NPRP
Sbjct: 308 RRRRSKKSTAIE-GIETLREMFLSLNMKVRLRDILPDDHNIELLCRMAIQDVCVVTNPRP 366

Query: 371 TSVAEIEVLYRKAF 384
            +  ++  +  +A+
Sbjct: 367 VTWKDLVKICEEAW 380


Lambda     K      H
   0.317    0.133    0.379 

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: 310
Number of extensions: 16
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: 384
Length of database: 380
Length adjustment: 30
Effective length of query: 354
Effective length of database: 350
Effective search space:   123900
Effective search space used:   123900
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 24 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