GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Geotalea uraniireducens Rf4

Align 2-methyl-branched-chain-enoyl-CoA reductase (EC 1.3.8.5) (characterized)
to candidate WP_011940133.1 GURA_RS16870 acyl-CoA dehydrogenase family protein

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



>NCBI__GCF_000016745.1:WP_011940133.1
          Length = 384

 Score =  284 bits (727), Expect = 3e-81
 Identities = 154/369 (41%), Positives = 215/369 (58%)

Query: 3   LTQDQEMIRDAVRDFAQTELWPHAARWDKEHHFPKDAHQGLAALGAYGICVPEEFGGANL 62
           L+  Q+  R+    F + E+ P A   D    FP +  + L A G  G  +P  +GGA L
Sbjct: 5   LSAAQKKARENACSFTEEEIIPFARENDANERFPLEIVRKLGARGLLGGTIPGAYGGAEL 64

Query: 63  DYLTLALVLEEIAAGDGGTSTAISVTNCPVNAILMRYGNAQQKRDWLTPLARGEMLGAFC 122
           D+++  L+ EEI  G     T +SV    V  ++  +G+  Q+R +L  L RGE+LG F 
Sbjct: 65  DWISDGLIFEEIGRGCSSVRTTVSVQVSLVEQVIFNWGSEAQRRSYLPGLCRGEILGCFA 124

Query: 123 LTEPHVGSDASALRTTAVKQGDEYVINGVKQFITSGKNGQVAIVIAVTDKGAGKKGMSAF 182
           LTEP VGSDA+ +  TA   GD +++NG K +IT+G    +AIV A T   AG KG+SAF
Sbjct: 125 LTEPGVGSDAAGIGATATPHGDGWLLNGTKNWITNGGVADIAIVFARTGPAAGNKGISAF 184

Query: 183 LVPTNNPGYVVARLEDKLGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGGRI 242
           +V T +PG+    +  KLG  +S TA + F +C +P + L+G  G G KIAL AL+ GR 
Sbjct: 185 IVDTKSPGFSSLEIRGKLGLRASSTAALTFRDCFLPGDALLGETGAGLKIALSALDNGRY 244

Query: 243 GIAAQSVGMARSAFDAALAYSKERESFGTAIFNHQAVGFRLADCATQIEAARQLIWHAAA 302
           G+AA  VG+ +   DA +AY++ R+ FG +I + Q V   +A  A  + AAR L++ A  
Sbjct: 245 GVAAGCVGIIQGCVDACVAYARRRQQFGRSIASFQLVQDMIARMAVDLAAARLLVFRAGE 304

Query: 303 LRDAGKPCLKEAAMAKLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRVCQIYEG 362
           L++ G     E +MAK FASE A R  + AIQ  G YG  N  PVER  RD +V  IYEG
Sbjct: 305 LKNRGAANSLETSMAKYFASEAAVRAATDAIQVHGAYGYSNAHPVERYLRDAKVATIYEG 364

Query: 363 TSDVQKIII 371
           TS +QK+II
Sbjct: 365 TSQIQKLII 373


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: 332
Number of extensions: 10
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: 384
Length adjustment: 30
Effective length of query: 346
Effective length of database: 354
Effective search space:   122484
Effective search space used:   122484
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 Apr 09 2024. 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