GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Dyella japonica UNC79MFTsu3.2

Align Alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate N515DRAFT_2489 N515DRAFT_2489 alcohol dehydrogenase, propanol-preferring

Query= reanno::Cup4G11:RR42_RS34260
         (342 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2489
          Length = 343

 Score =  546 bits (1406), Expect = e-160
 Identities = 261/342 (76%), Positives = 294/342 (85%)

Query: 1   MTAMMKAAVVREFGAPLTIDEVPVPQPGRGQIQVKIEASGVCHTDLHAAEGDWPVKPTLP 60
           M+  MKAAVVR FG PL+IDEVPVP PG G++ VKIEA GVCHTDLHA +GDWPVKP  P
Sbjct: 1   MSKTMKAAVVRAFGQPLSIDEVPVPTPGLGEVLVKIEACGVCHTDLHAVDGDWPVKPKPP 60

Query: 61  FIPGHEGVGYVSAVGAGVSRVKEGDRVGVPWLYSACGYCEHCLQGWETLCEKQQNTGYSV 120
           FIPGHEGVGYV A+G GV+ +KEGDRVG+PWLYSACG+CEHCL GWETLCE QQNTGYSV
Sbjct: 61  FIPGHEGVGYVVAIGPGVTHLKEGDRVGIPWLYSACGHCEHCLGGWETLCESQQNTGYSV 120

Query: 121 NGGYGEYVVADPNYVGLLPDSVGFVEIAPILCAGVTVYKGLKVTDTRPGQWVVISGIGGL 180
           NGG+ EY +A  +YVG LPD +GFVEIAP+LCAGVTVYKGLKVTDTRPG WVVISGIGGL
Sbjct: 121 NGGFAEYALAAADYVGHLPDGIGFVEIAPVLCAGVTVYKGLKVTDTRPGNWVVISGIGGL 180

Query: 181 GHVAVQYARAMGLRVAAVDIDDKKLELARKLGAEVTVNARTTDPVAFLQKEIGGAHGALV 240
           GH+AVQYA AMGL VAAVDIDD KL+LAR+LGA++ +NAR  DPVA ++KEIGGAHGALV
Sbjct: 181 GHMAVQYAAAMGLNVAAVDIDDAKLDLARRLGAQLIINARHADPVAVVKKEIGGAHGALV 240

Query: 241 TAVSPKAFGQAIGMVRRGGTIALNGLPPGDFPTPIFDVVLKGITIRGSIVGTRSDLQESL 300
           TAVSPKAFGQA+ MVRRGGT++LNGLPPG F   IFD+VL G+T+RGSIVGTR DLQESL
Sbjct: 241 TAVSPKAFGQAMNMVRRGGTVSLNGLPPGSFDLSIFDMVLNGVTVRGSIVGTRLDLQESL 300

Query: 301 DFAAHGAVKATVSTAPLEKINEIFTRMRAGDIEGRVVMDFAA 342
           DFA  G VKATV+T  LE INE+F RM  G IEGRVV+D A+
Sbjct: 301 DFAKAGKVKATVTTDRLENINEVFRRMHQGQIEGRVVLDMAS 342


Lambda     K      H
   0.319    0.138    0.420 

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: 457
Number of extensions: 15
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: 343
Length adjustment: 29
Effective length of query: 313
Effective length of database: 314
Effective search space:    98282
Effective search space used:    98282
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.

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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