GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Pseudomonas stutzeri RCH2

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate GFF658 Psest_0672 Alcohol dehydrogenase, class IV

Query= BRENDA::P0DJA2
         (383 letters)



>FitnessBrowser__psRCH2:GFF658
          Length = 382

 Score =  515 bits (1326), Expect = e-151
 Identities = 257/380 (67%), Positives = 306/380 (80%)

Query: 3   SSTFYIPFVNEMGEGSLEKAIKDLNGSGFKNALIVSDAFMNKSGVVKQVADLLKAQGINS 62
           SSTF+IP VN MG GSL++A+  +   GF+ ALIV+D  + ++GV ++VA LL A  I S
Sbjct: 2   SSTFFIPAVNMMGIGSLDEAMVAIANYGFRKALIVTDVGLARAGVAEKVATLLAAADIQS 61

Query: 63  AVYDGVMPNPTVTAVLEGLKILKDNNSDFVISLGGGSPHDCAKAIALVATNGGEVKDYEG 122
            V+DG  PNPTV  V +GL  L+++  DF+ISLGGGSPHDCAK IAL ATNGG + DYEG
Sbjct: 62  VVFDGAQPNPTVGNVEKGLSQLRESACDFIISLGGGSPHDCAKGIALCATNGGHIADYEG 121

Query: 123 IDKSKKPALPLMSINTTAGTASEMTRFCIITDEVRHVKMAIVDRHVTPMVSVNDPLLMVG 182
           +D+S KP LPL++INTTAGTASEMTRFCIITDE RHVKMAIVDR+VTP++SVNDP LMV 
Sbjct: 122 VDRSAKPQLPLVAINTTAGTASEMTRFCIITDESRHVKMAIVDRNVTPLLSVNDPALMVA 181

Query: 183 MPKGLTAATGMDALTHAFEAYSSTAATPITDACALKAASMIAKNLKTACDNGKDMPAREA 242
           MPKGLTAATGMDALTHA EAY STAATPITDACALKA  +I+ NL+TA  +G DMPAREA
Sbjct: 182 MPKGLTAATGMDALTHAVEAYVSTAATPITDACALKAIELISANLRTAVASGSDMPAREA 241

Query: 243 MAYAQFLAGMAFNNASLGYVHAMAHQLGGYYNLPHGVCNAVLLPHVLAYNASVVAGRLKD 302
           MAYAQFLAGMAFNNASLGYVHAMAHQLGG+Y+LPHGVCNAVLLPHV +YNASV   RL+D
Sbjct: 242 MAYAQFLAGMAFNNASLGYVHAMAHQLGGFYDLPHGVCNAVLLPHVESYNASVCPERLRD 301

Query: 303 VGVAMGLDIANLGDKEGAEATIQAVRDLAASIGIPANLTELGAKKEDVPLLADHALKDAC 362
           +  AMG++   L   +GAEA + A+R L+  IGIP  L ELGAK +D+P LA +A+ DAC
Sbjct: 302 IATAMGVETRGLDATQGAEAALAAIRTLSQDIGIPGGLAELGAKADDIPTLAANAMNDAC 361

Query: 363 ALTNPRQGDQKEVEELFLSA 382
            LTNPR+  Q+E+E +F SA
Sbjct: 362 GLTNPRRATQEEIEAIFHSA 381


Lambda     K      H
   0.316    0.132    0.373 

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: 508
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: 383
Length of database: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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 (21.6 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