GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bamH in Dinoroseobacter shibae DFL-12

Align Benzoyl-CoA reductase electron transfer protein, putative (characterized, see rationale)
to candidate 3607908 Dshi_1316 NADH-quinone oxidoreductase, F subunit (RefSeq)

Query= uniprot:Q39TW5
         (635 letters)



>FitnessBrowser__Dino:3607908
          Length = 433

 Score =  292 bits (747), Expect = 2e-83
 Identities = 161/391 (41%), Positives = 238/391 (60%), Gaps = 11/391 (2%)

Query: 167 LFQMTPEDVMGEIKKSNLRGRGGGGFPAWRKW----EESRNAPDPIKYVIVNADEGDPGA 222
           L QM  +D++  +K S LRGRGG GFP   KW    +ES   P    Y++VNADE +PG 
Sbjct: 35  LIQMGRDDIVKIMKDSGLRGRGGAGFPTGLKWSFMPKESDGRPH---YLVVNADESEPGT 91

Query: 223 FMDRALIEGNPHSILEGLIIGAYAVGAHEGFIYVRQEYPLAVENINLAIRQASERGFVGK 282
             DR ++  +PH+++EG +I ++A+GAH  +IY+R EY    E +  AI +A E G +GK
Sbjct: 92  CKDREIMRHDPHTLIEGCLIASFAMGAHASYIYIRGEYIREREALQAAIDEAYEAGLLGK 151

Query: 283 DILGSGFDFTVKVHMGAGAFVCGESSALMTALEGRAGEPRPKYIHTAVKGVWDHPSVLNN 342
           +  GSG+DF + +  GAGA++CGE +AL+ +LEG+ G PR K    A  G++  P+ +NN
Sbjct: 152 NAAGSGWDFDLYLTHGAGAYICGEETALIESLEGKKGMPRMKPPFPAGAGLYGCPTTVNN 211

Query: 343 VETWANVTQIITKGADWFTSYGTAGSTGTKIFSLVGKITNTGLVEVPMGVTLRDIITKVG 402
           VE+ A V  I+ +GADWF  +G   + GTK+F++ G +    +VE  M ++  ++I K  
Sbjct: 212 VESIAVVPTILRRGADWFAQFGRPNNAGTKLFAISGHVNQPCVVEEAMSISFEELIDKHC 271

Query: 403 GGIPGG-KKFKAVQTGGPSGGCI-PEAMLDLPVDFDELT-KAGSMMGSGGMIVMDEDTCM 459
           GGI GG    KAV  GG S  C+  E M D  +DFD L  + GS +G+  +IVMD+ T +
Sbjct: 272 GGIRGGWDNLKAVIPGGSSVPCVRGENMRDAIMDFDYLRGELGSGLGTAAVIVMDQSTDI 331

Query: 460 VDIARYFIDFLKDESCGKCTPCREGIRQMLAVLTRITVGKGKEGDIELLEELAEST-GAA 518
           +        F K ESCG+CTPCREG   M+ V+ R+  G+ +  +I++L ++ +   G  
Sbjct: 332 IKAIWRLSAFYKHESCGQCTPCREGTGWMMRVMDRLVRGEAEVEEIDMLFDVTKQVEGHT 391

Query: 519 LCALGKSAPNPVLSTIRYFRDEYEAHIREKK 549
           +CALG +A  P+   IR FRDE E  I+ +K
Sbjct: 392 ICALGDAAAWPIQGLIRNFRDEIEDRIKAQK 422


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: 742
Number of extensions: 39
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: 635
Length of database: 433
Length adjustment: 35
Effective length of query: 600
Effective length of database: 398
Effective search space:   238800
Effective search space used:   238800
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: 52 (24.6 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