GapMind for catabolism of small carbon sources

 

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

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 3610403 Dshi_3784 Gluconate 2-dehydrogenase (acceptor) (RefSeq)

Query= SwissProt::Q47945
         (478 letters)



>FitnessBrowser__Dino:3610403
          Length = 305

 Score =  175 bits (443), Expect = 2e-48
 Identities = 113/292 (38%), Positives = 150/292 (51%), Gaps = 16/292 (5%)

Query: 21  AAAIGLM-AVSFGAAHAQDADEALIKRGEYVARLSDCIACHTALH--GQPYAGGLEIKSP 77
           AA++G++ A   G+A    A E  + RG Y+AR S CIACHT     G P AGG  +++P
Sbjct: 16  AASLGVVIAWPVGSAVTPIAIEGNVDRGAYLARASGCIACHTNFEAGGAPLAGGAPLETP 75

Query: 78  IGTIYSTNITPDPEHGIGNYTLEDFTKALRKGIRKDGATVYPAMPYPEFARLSDDDIRAM 137
            GT Y  N+T DPEHG+G +T E F KA+R+GI  DG   YP+ PY  +A  SD DI  +
Sbjct: 76  FGTFYPPNLTTDPEHGMGEWTAEQFAKAVRQGIGPDGTPYYPSFPYTFYADFSDQDIADL 135

Query: 138 YAFFMHGVKPVALQNKAPDISWPLSMRWPLGMWRAMFV--PSMTPGVDKSISDPEVARGE 195
           +A F   V PV       D+S+P   RW L +WRA F   P   P   +S       RG 
Sbjct: 136 WAAF-QTVPPVDEPAPENDVSFPFDQRWGLKLWRAAFFYDPDTEPIEGRS---DAWNRGR 191

Query: 196 YLVNGPGHCGECHTPRGFGMQVKAYGTAGGNAYLAGGAPIDNWIAPSLRSNSDTGLGRWS 255
            LV G  HCG CHTPR          +  GNA L GG+      AP++R   D     W+
Sbjct: 192 ELVRGAAHCGACHTPRNLAGGRDIGASFAGNAQLPGGSK-----APAIRP-KDLVKNDWT 245

Query: 256 EDDIVTFLKSGRIDHSAVFGG-MADVVAYSTQHWSDDDLRATAKYLKSMPAV 306
             ++   L++G       FGG MA+VV   T+  +  D  A A +L +   V
Sbjct: 246 VSNLAYALQTGITPSGDAFGGSMAEVVREGTRFLTPADREAMALFLLNKDTV 297


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: 528
Number of extensions: 35
Number of successful extensions: 6
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: 478
Length of database: 305
Length adjustment: 30
Effective length of query: 448
Effective length of database: 275
Effective search space:   123200
Effective search space used:   123200
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