GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Dechlorosoma suillum PS

Align 2-methyl-branched-chain-enoyl-CoA reductase (EC 1.3.8.5) (characterized)
to candidate Dsui_0977 Dsui_0977 acyl-CoA dehydrogenase

Query= reanno::acidovorax_3H11:Ac3H11_2996
         (376 letters)



>FitnessBrowser__PS:Dsui_0977
          Length = 378

 Score =  496 bits (1276), Expect = e-145
 Identities = 240/376 (63%), Positives = 297/376 (78%)

Query: 1   MLLTQDQEMIRDAVRDFAQTELWPHAARWDKEHHFPKDAHQGLAALGAYGICVPEEFGGA 60
           M+LTQ+QEMIRD++R FAQ  L P AA WDK H FP +A + L  LGA G+CVPEE+GGA
Sbjct: 1   MILTQEQEMIRDSMRAFAQERLAPFAAEWDKNHTFPAEALKELGELGAMGMCVPEEWGGA 60

Query: 61  NLDYLTLALVLEEIAAGDGGTSTAISVTNCPVNAILMRYGNAQQKRDWLTPLARGEMLGA 120
            +DY++L L LEEIAAGDG TST +SV N     I  +YG  QQK +WL PLARGE LG 
Sbjct: 61  GMDYMSLVLTLEEIAAGDGATSTIVSVQNSLACGITQKYGTDQQKEEWLKPLARGEKLGC 120

Query: 121 FCLTEPHVGSDASALRTTAVKQGDEYVINGVKQFITSGKNGQVAIVIAVTDKGAGKKGMS 180
           FCLTEPH GSDA+A+ T A + GD +V+NGVKQFIT+GK+  +AIV AVTDK AGKKG+S
Sbjct: 121 FCLTEPHTGSDAAAITTRADRDGDHFVLNGVKQFITTGKHAHMAIVFAVTDKAAGKKGIS 180

Query: 181 AFLVPTNNPGYVVARLEDKLGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGG 240
            FLVPT+  G++V R E+K+GQH+SDT QI F++CR+PA  L+G EGEGYKIAL  LE G
Sbjct: 181 CFLVPTDTKGFIVGRTEEKMGQHASDTVQIIFEDCRVPASALLGKEGEGYKIALSNLEAG 240

Query: 241 RIGIAAQSVGMARSAFDAALAYSKERESFGTAIFNHQAVGFRLADCATQIEAARQLIWHA 300
           RIGIAAQS+GMAR+AF+AA+ Y+KER +FG  I  HQAV FRLAD  T ++AAR ++W A
Sbjct: 241 RIGIAAQSIGMARAAFEAAVRYAKERVTFGQPIIEHQAVNFRLADMNTLLDAARLMVWRA 300

Query: 301 AALRDAGKPCLKEAAMAKLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRVCQIY 360
           AAL+DAGKPCLKEA+MAK+FASE AE++ S AIQ  GG G  +DFPVERIYRDVR+ QIY
Sbjct: 301 AALKDAGKPCLKEASMAKMFASEAAEKIASDAIQIHGGVGYTSDFPVERIYRDVRISQIY 360

Query: 361 EGTSDVQKIIIQRALA 376
           EG +D+Q+++I R++A
Sbjct: 361 EGANDIQRLVIGRSIA 376


Lambda     K      H
   0.319    0.134    0.396 

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: 448
Number of extensions: 5
Number of successful extensions: 1
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: 376
Length of database: 378
Length adjustment: 30
Effective length of query: 346
Effective length of database: 348
Effective search space:   120408
Effective search space used:   120408
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 (21.8 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