GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Dechlorosoma suillum PS

Align furfuryl alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate Dsui_2228 Dsui_2228 Zn-dependent alcohol dehydrogenase

Query= metacyc::MONOMER-17184
         (342 letters)



>FitnessBrowser__PS:Dsui_2228
          Length = 340

 Score =  494 bits (1272), Expect = e-144
 Identities = 231/339 (68%), Positives = 278/339 (82%)

Query: 1   MPAMMKAAVVRAFGAPLTIDEVPVPQPGPGQVQVKIEASGVCHTDLHAADGDWPVKPTLP 60
           M  MMKAAVV  FG PL I+EVPVP+  PGQV VK+ ASGVCHTDLHAADGDWPVKP+LP
Sbjct: 1   MAQMMKAAVVHEFGKPLVIEEVPVPEVPPGQVLVKVVASGVCHTDLHAADGDWPVKPSLP 60

Query: 61  FIPGHEGVGYVSAVGSGVSRVKEGDRVGVPWLYSACGYCEHCLQGWETLCEKQQNTGYSV 120
           FIPGHEGVGYV+AVG+GV+ VKEGDRVGVPWL++ACG+CEHC+ GWETLC+ QQ TGY+V
Sbjct: 61  FIPGHEGVGYVAAVGAGVTHVKEGDRVGVPWLHTACGHCEHCITGWETLCDSQQMTGYTV 120

Query: 121 NGGYGEYVVADPNYVGLLPDKVGFVEIAPILCAGVTVYKGLKVTDTRPGQWVVISGIGGL 180
           NGGY EYV+ADP YVG LPD + F   AP+LCAGVTVYKGLKV + +PG WV ISGIGGL
Sbjct: 121 NGGYAEYVLADPGYVGKLPDTLEFAPAAPVLCAGVTVYKGLKVLECKPGDWVAISGIGGL 180

Query: 181 GHVAVQYARAMGLRVAAVDIDDAKLNLARRLGAEVAVNARDTDPAAWLQKEIGGAHGVLV 240
           GH+AVQYA+AMG  V AVD+ D KL LA+ LGA+V +NA   DP A +QK+I GAHG+LV
Sbjct: 181 GHMAVQYAKAMGFHVIAVDVADEKLALAKTLGADVTLNAARVDPVAEIQKQIKGAHGILV 240

Query: 241 TAVSPKAFSQAIGMVRRGGTIALNGLPPGDFGTPIFDVVLKGITIRGSIVGTRSDLQESL 300
           TAVS  AF QA+GM+ + GT++L GLPPGDFG PIFDVVL   T+RGSIVGTR DL+E+L
Sbjct: 241 TAVSRSAFGQALGMLHKRGTMSLVGLPPGDFGLPIFDVVLNAKTVRGSIVGTRKDLEEAL 300

Query: 301 DFAAHGDVKATVSTAKLDDVNDVFGRLREGKVEGRVVLD 339
            FA  G VK   ST +++++ND+FGR++ G ++GR+VL+
Sbjct: 301 AFAGEGKVKTHYSTDRIENINDIFGRMKAGHIDGRIVLN 339


Lambda     K      H
   0.319    0.139    0.427 

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: 446
Number of extensions: 14
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: 342
Length of database: 340
Length adjustment: 29
Effective length of query: 313
Effective length of database: 311
Effective search space:    97343
Effective search space used:    97343
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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