GapMind for catabolism of small carbon sources

 

Alignments for a candidate for adhBqn in Rhizobium freirei PRF 81

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_037153268.1 RHSP_RS19630 cytochrome c

Query= SwissProt::Q47945
         (478 letters)



>NCBI__GCF_000359745.1:WP_037153268.1
          Length = 304

 Score =  164 bits (414), Expect = 5e-45
 Identities = 99/281 (35%), Positives = 149/281 (53%), Gaps = 19/281 (6%)

Query: 33  AAHAQDADEALIKRGEYVARLSDCIACHTALHGQPYA-----GGLEIKSPIGTIYSTNIT 87
           A+H  +  +  +K GE V     C +CH A   Q  A     GGL +KSP GT +  NI+
Sbjct: 34  ASHWTNLGDPDLKTGEMVFWAGGCTSCHAAPGAQGDAKLMLSGGLGLKSPFGTFHVPNIS 93

Query: 88  PDPEHGIGNYTLEDFTKALRKGIRKDGATVYPAMPYPEFARLSDDDIRAMYAFFMHGVKP 147
           PD + G+G++TL DF  A+++G+ ++G  +YP+ PY  ++R+SD DI  ++ F     K 
Sbjct: 94  PDEKAGLGSWTLADFGNAMKRGVGRNGEHLYPSFPYGSYSRMSDKDINDLWGFLKTLPKS 153

Query: 148 VALQNKAP--DISWPLSMRWPLGMWRAMFVPSMTPGVDKSISDPEVARGEYLVNGPGHCG 205
               N AP  ++ +P ++R  LG W+ +++    P V  + +D ++ RG+YLV GPGHCG
Sbjct: 154 ---SNVAPPHELPFPFNIRLALGAWKFLYLNDQ-PRVVLAKADDKIKRGQYLVEGPGHCG 209

Query: 206 ECHTPRGFGMQVKAYGTAGGNAYLAGGA-PIDNWIAPSLRSNSDTGLGRWSEDDIVTFLK 264
           ECHTPR       + G      +LAG   P      P +R  S   +G WS  DI  +L+
Sbjct: 210 ECHTPR------DSLGGFLSGQWLAGAPNPEGKGQIPDIRPGS-KAIGSWSAGDIANYLE 262

Query: 265 SGRIDHSAVFGGMADVVAYSTQHWSDDDLRATAKYLKSMPA 305
           +G   +    GG    V  +  H    D  A A YLK++PA
Sbjct: 263 TGFTPNYDSAGGSMAEVQQNIAHLPATDREAIAAYLKALPA 303


Lambda     K      H
   0.317    0.134    0.421 

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: 565
Number of extensions: 44
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 478
Length of database: 304
Length adjustment: 30
Effective length of query: 448
Effective length of database: 274
Effective search space:   122752
Effective search space used:   122752
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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