GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Acidovorax sp. GW101-3H11

Align cyclohex-1-ene-1-carbonyl-CoA dehydrogenase (EC 1.3.8.10) (characterized)
to candidate Ac3H11_2996 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= BRENDA::Q39QF5
         (380 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2996
          Length = 376

 Score =  253 bits (645), Expect = 8e-72
 Identities = 151/376 (40%), Positives = 219/376 (58%), Gaps = 5/376 (1%)

Query: 4   LTEEQKLTLDMVRDVATREIAPRALELDEKSLFPEYARDLFAKLGLLNPLLPAAYGGTEM 63
           LT++Q++  D VRD A  E+ P A   D++  FP+ A    A LG     +P  +GG  +
Sbjct: 3   LTQDQEMIRDAVRDFAQTELWPHAARWDKEHHFPKDAHQGLAALGAYGICVPEEFGGANL 62

Query: 64  GVLTLALILEEL--GRVCASTALLLIAQTDGMLPIIHGGSPELKERYLRRFAGESTLLTA 121
             LTLAL+LEE+  G    STA+ +       + + +G + + ++       GE  +L A
Sbjct: 63  DYLTLALVLEEIAAGDGGTSTAISVTNCPVNAILMRYGNAQQKRDWLTPLARGE--MLGA 120

Query: 122 LAATEPAAGSDLLAMKTRAVRQGDKYVINGQKCFITNGSVADVIVVYAYTDPEKGSKGIS 181
              TEP  GSD  A++T AV+QGD+YVING K FIT+G    V +V A TD   G KG+S
Sbjct: 121 FCLTEPHVGSDASALRTTAVKQGDEYVINGVKQFITSGKNGQVAIVIAVTDKGAGKKGMS 180

Query: 182 AFVVEKGTPGLVYGRNESKMGMRGSINSELFFENMEVPAENIIGAEGTGFANLMQTLSTN 241
           AF+V    PG V  R E K+G   S  +++ F+N  +PAEN+IGAEG G+   +  L   
Sbjct: 181 AFLVPTNNPGYVVARLEDKLGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGG 240

Query: 242 RVFCAAQAVGIAQGALDIAVRHTQDRVQFGKPIAHLAPVQFMVADMATAVEASRLLTRKA 301
           R+  AAQ+VG+A+ A D A+ ++++R  FG  I +   V F +AD AT +EA+R L   A
Sbjct: 241 RIGIAAQSVGMARSAFDAALAYSKERESFGTAIFNHQAVGFRLADCATQIEAARQLIWHA 300

Query: 302 AELLDDGDKKAVLYGSMAKTMASDTAMRVTTDAVQVLGGSGYMKENGVERMMRDAKLTQI 361
           A L D G K  +   +MAK  AS+ A RV + A+Q LGG G + +  VER+ RD ++ QI
Sbjct: 301 AALRDAG-KPCLKEAAMAKLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRVCQI 359

Query: 362 YTGTNQITRMVTGRAL 377
           Y GT+ + +++  RAL
Sbjct: 360 YEGTSDVQKIIIQRAL 375


Lambda     K      H
   0.319    0.134    0.371 

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: 320
Number of extensions: 14
Number of successful extensions: 3
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: 380
Length of database: 376
Length adjustment: 30
Effective length of query: 350
Effective length of database: 346
Effective search space:   121100
Effective search space used:   121100
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: 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