GapMind for catabolism of small carbon sources

 

Alignments for a candidate for adhBqn in Marivita geojedonensis DPG-138

Align Alcohol dehydrogenase (quinone), cytochrome c subunit; ADH; Alcohol dehydrogenase (quinone), subunit II; Cytochrome c-553; Cytochrome c553; Ethanol:Q2 reductase; G3-ADH subunit II; Quinohemoprotein-cytochrome c complex; Ubiquinol oxidase; EC 1.1.5.5 (characterized)
to candidate WP_085635893.1 MGEO_RS06505 cytochrome c

Query= SwissProt::P0A388
         (468 letters)



>NCBI__GCF_002115805.1:WP_085635893.1
          Length = 294

 Score =  138 bits (348), Expect = 2e-37
 Identities = 99/287 (34%), Positives = 140/287 (48%), Gaps = 31/287 (10%)

Query: 17  LAGTALAQTPDADSALVQKGAYVARLGDCVACHTALHGQS-----YAGGLEIKSPIGTIY 71
           L  TALA   DAD A    G  V     C +CH A   +       AGG    S  GT  
Sbjct: 29  LDDTALAGI-DADPA---NGETVFTAAGCASCHAAPDAEGEAKLVLAGGQRFASDFGTFI 84

Query: 72  STNITPDPTYGIGRYTFAEFDEAVRHGIRKDGSTLYPAMPYPSFSRMTKEDMQALYAYFM 131
           + N++P P  GIG +T AEF  AV  G+  +G   YPA PY ++  MT++D+  L+AY+ 
Sbjct: 85  APNVSPHPEAGIGGWTLAEFASAVTRGVSPEGQHYYPAFPYAAYLHMTEQDVADLWAYW- 143

Query: 132 HGVKPVAQPDKQPDISWPLSMRWPLGIWRMMFSPSPKDFTPAPGTDPEIARGDYLVTGPG 191
             +   A P +  ++ +P ++R  +G+W+ ++     D+  A     +IARG YLV    
Sbjct: 144 QTLPQDATPSEPHEVGFPFNIRRAVGVWKQLYMTD--DWVMASAETDQIARGRYLVEALA 201

Query: 192 HCGACHTPRGFAMQEKALDAAGGPD---FLSGGA-PIDNWVAPSLRNDPVVGLGRWSEDD 247
           HCG CHTPR         DA GG D   +L+G   P      PSL  D +     W   +
Sbjct: 202 HCGECHTPR---------DALGGLDRDAWLAGAPNPSGRGTIPSLTPDDLT----WGSTE 248

Query: 248 IYTFLKSG-RIDHSAVFGGMGDVVAWSTQYFTDDDLHAIAKYLKSLP 293
           I  +L++G   D  +  G M  V+A  T+     D  A+A YLK+LP
Sbjct: 249 IAYYLETGFTPDFDSAGGHMVAVIANFTK-LPASDREAVAAYLKALP 294


Lambda     K      H
   0.317    0.134    0.425 

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: 472
Number of extensions: 37
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: 468
Length of database: 294
Length adjustment: 30
Effective length of query: 438
Effective length of database: 264
Effective search space:   115632
Effective search space used:   115632
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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