GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Shewanella loihica PV-4

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate 5208657 Shew_1166 iron-containing alcohol dehydrogenase (RefSeq)

Query= BRENDA::P0DJA2
         (383 letters)



>FitnessBrowser__PV4:5208657
          Length = 382

 Score =  496 bits (1276), Expect = e-145
 Identities = 242/380 (63%), Positives = 301/380 (79%)

Query: 3   SSTFYIPFVNEMGEGSLEKAIKDLNGSGFKNALIVSDAFMNKSGVVKQVADLLKAQGINS 62
           ++ F+IP VN +G+ +++ AI D+   GF+ ALIV+D  + + G+V Q+ +   A GI S
Sbjct: 2   AAKFFIPSVNVLGQNAVDDAIGDIKTLGFQRALIVTDKPLVEIGLVGQIVEKFGAAGITS 61

Query: 63  AVYDGVMPNPTVTAVLEGLKILKDNNSDFVISLGGGSPHDCAKAIALVATNGGEVKDYEG 122
            ++DGV PNPTV  V  GL +LK N+ DFV+SLGGGSPHDCAK IALVATNGG +KDYEG
Sbjct: 62  TIFDGVQPNPTVGNVEAGLALLKANDCDFVVSLGGGSPHDCAKGIALVATNGGNIKDYEG 121

Query: 123 IDKSKKPALPLMSINTTAGTASEMTRFCIITDEVRHVKMAIVDRHVTPMVSVNDPLLMVG 182
           +D S KP LPL++INTTAGTASEMTRFCIITDE RH+KMAIVD+H TP++SVNDP LM+ 
Sbjct: 122 LDMSAKPQLPLVAINTTAGTASEMTRFCIITDEARHIKMAIVDKHTTPILSVNDPELMLL 181

Query: 183 MPKGLTAATGMDALTHAFEAYSSTAATPITDACALKAASMIAKNLKTACDNGKDMPAREA 242
            P GLTAATGMDALTHA EAY S AA PITDACA+KA  +I  NL  A +NG+ + AR+ 
Sbjct: 182 KPAGLTAATGMDALTHAIEAYVSIAANPITDACAIKAIELIKGNLVEAVENGQSLEARDQ 241

Query: 243 MAYAQFLAGMAFNNASLGYVHAMAHQLGGYYNLPHGVCNAVLLPHVLAYNASVVAGRLKD 302
           MAYAQFLAGMAFNNASLGYVHAMAHQLGG+Y+LPHGVCNA+LLPHV AYNA V A RLKD
Sbjct: 242 MAYAQFLAGMAFNNASLGYVHAMAHQLGGFYDLPHGVCNALLLPHVQAYNAQVAAPRLKD 301

Query: 303 VGVAMGLDIANLGDKEGAEATIQAVRDLAASIGIPANLTELGAKKEDVPLLADHALKDAC 362
           V  AMG+D++ + D++GA A I A++ L+ ++ IP NLT+LG K ED+P LAD+ALKDAC
Sbjct: 302 VAKAMGVDVSTMTDEQGATAAIDAIKALSVAVKIPENLTKLGVKAEDIPTLADNALKDAC 361

Query: 363 ALTNPRQGDQKEVEELFLSA 382
            LTNP+Q   +E+ ++F +A
Sbjct: 362 GLTNPKQATHEEICQIFTNA 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: 494
Number of extensions: 23
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