GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bamH in Dechlorosoma suillum PS

Align Benzoyl-CoA reductase electron transfer protein, putative (characterized, see rationale)
to candidate Dsui_3045 Dsui_3045 NADH-quinone oxidoreductase, F subunit

Query= uniprot:Q39TW5
         (635 letters)



>FitnessBrowser__PS:Dsui_3045
          Length = 442

 Score =  346 bits (887), Expect = 1e-99
 Identities = 175/404 (43%), Positives = 255/404 (63%), Gaps = 4/404 (0%)

Query: 150 SMDDYLAIGGYSALSKVLFQMTP-EDVMGEIKKSNLRGRGGGGFPAWRKWEESRNAPDPI 208
           S+ DY+A GGY AL K+L +  P E V+ E+K S LRGRGG GFP   KW     +    
Sbjct: 22  SLKDYVARGGYEALKKILAEKIPQEQVIAEVKTSVLRGRGGAGFPTGLKWSFMPRSFPGD 81

Query: 209 KYVIVNADEGDPGAFMDRALIEGNPHSILEGLIIGAYAVGAHEGFIYVRQEYPLAVENIN 268
           KYV+ N+DEG+PG F DR ++  NPHS++EG+ I AYA+GA  G+ Y+  E     +   
Sbjct: 82  KYVVCNSDEGEPGTFKDRDILRYNPHSVIEGMAIAAYAMGATRGYNYIHGEIWEVYKRFE 141

Query: 269 LAIRQASERGFVGKDILGSGFDFTVKVHMGAGAFVCGESSALMTALEGRAGEPRPKYIHT 328
            A+ +A   GF+G++ILGSGF+F +  H G GA++CGE +AL+ ++EG+ G+PR K    
Sbjct: 142 DALDEARAAGFIGQNILGSGFNFELFAHHGYGAYICGEETALLESIEGKKGQPRFKPPFP 201

Query: 329 AVKGVWDHPSVLNNVETWANVTQIITKGADWFTSYGTAGSTGTKIFSLVGKITNTGLVEV 388
           A  G++  P+ +NN ET+ ++  II  G + F + G   + GTK+FS+ G +   G  E+
Sbjct: 202 ASFGLYGKPTTINNTETFGSIPFIIRDGGEKFLNLGKPNNGGTKLFSISGHVNRPGNYEI 261

Query: 389 PMGVTLRDIITKVGGGIPGGKKFKAVQTGGPSGGCIP-EAMLDLPVDFDELTKAGSMMGS 447
           P+G     ++ ++ GG+ GG+K KAV  GG S   +P + M++  +D+D ++KAGSM+GS
Sbjct: 262 PLGTPFSTLL-EMAGGVRGGRKLKAVIPGGSSAPVLPGDVMMECTMDYDSISKAGSMLGS 320

Query: 448 GGMIVMDEDTCMVDIARYFIDFLKDESCGKCTPCREGIRQMLAVLTRITVGKGKEGDIEL 507
           G +IVMDE TCMV        F  +ESCG+CTPCREG   +  V++RI  G G+  D++L
Sbjct: 321 GAVIVMDETTCMVKALERLSFFYHEESCGQCTPCREGTPWLYKVVSRIEHGLGRPDDLDL 380

Query: 508 LEELAES-TGAALCALGKSAPNPVLSTIRYFRDEYEAHIREKKC 550
           L+ + E   G  +CALG +A  PV S I++FRDE+  HI  K C
Sbjct: 381 LDSVCEGIMGRTICALGDAAAFPVKSFIKHFRDEFVHHIEHKTC 424


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: 811
Number of extensions: 33
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: 442
Length adjustment: 35
Effective length of query: 600
Effective length of database: 407
Effective search space:   244200
Effective search space used:   244200
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