GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Sphingomonas indica Dd16

Align 2-methyl-branched-chain-enoyl-CoA reductase (EC 1.3.8.5) (characterized)
to candidate WP_085218433.1 B9N75_RS08665 acyl-CoA dehydrogenase

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



>NCBI__GCF_900177405.1:WP_085218433.1
          Length = 380

 Score =  257 bits (656), Expect = 4e-73
 Identities = 138/367 (37%), Positives = 214/367 (58%), Gaps = 2/367 (0%)

Query: 9   MIRDAVRDFAQTELWPHAARWDKEHHFPKDAHQGLAALGAYGICVPEEFGGANLDYLTLA 68
           + RD VR F    L PH  RW++E    +D        G     VPEE+GG  LD+   A
Sbjct: 16  LFRDQVRRFFDKALIPHLDRWEEEGIVDRDLWTQCGETGLLCPTVPEEYGGLGLDFRYNA 75

Query: 69  LVLEEIAAGDGGTSTAISVTNCPVNAILMRYGNAQQKRDWLTPLARGEMLGAFCLTEPHV 128
           ++ EE+A    G++  I++ +  V   ++ YG+  QK+ WL  +  GE   A  +TEP  
Sbjct: 76  VIDEELAYA--GSTAGITLHSDIVADYIVVYGSEAQKQHWLPRMISGETPTAIAMTEPGA 133

Query: 129 GSDASALRTTAVKQGDEYVINGVKQFITSGKNGQVAIVIAVTDKGAGKKGMSAFLVPTNN 188
           GSD   +RTTA++ GD YVING K +IT+G++  + IV+A TD   G KG S  LV  + 
Sbjct: 134 GSDLQGVRTTAIRDGDSYVINGSKTYITNGQHADLVIVVAKTDPSQGAKGTSLILVEADR 193

Query: 189 PGYVVARLEDKLGQHSSDTAQINFDNCRIPAENLIGAEGEGYKIALGALEGGRIGIAAQS 248
            G+   R  DK+G HS DT+++ F++ R+PA+NL+G EG G+   +  L   R+ IA  +
Sbjct: 194 EGFARGRNLDKIGLHSQDTSEMFFNDVRVPADNLLGQEGAGFAYLMNQLPQERLSIACSA 253

Query: 249 VGMARSAFDAALAYSKERESFGTAIFNHQAVGFRLADCATQIEAARQLIWHAAALRDAGK 308
            G A+ AFD ALA++++R++FG ++ + Q   F LAD AT+++     +  A     AG+
Sbjct: 254 QGAAQRAFDEALAFTRDRKAFGKSVLDFQNTRFTLADLATKLQVGWAHLDWAITRHVAGE 313

Query: 309 PCLKEAAMAKLFASEMAERVCSAAIQTLGGYGVVNDFPVERIYRDVRVCQIYEGTSDVQK 368
               EA+ AKL+ +E+    C  A+Q  GG G +N++ + R++RD RV +I+ GT+++ K
Sbjct: 314 LTATEASAAKLWHTELQGEACDTALQLHGGAGYMNEYLIARLWRDARVTRIFGGTNEIMK 373

Query: 369 IIIQRAL 375
            +I R L
Sbjct: 374 EVIGRGL 380


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: 358
Number of extensions: 18
Number of successful extensions: 2
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: 380
Length adjustment: 30
Effective length of query: 346
Effective length of database: 350
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 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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