GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Pedobacter sp. GW460-11-11-14-LB5

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate CA265_RS09630 CA265_RS09630 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>FitnessBrowser__Pedo557:CA265_RS09630
          Length = 396

 Score =  211 bits (536), Expect = 4e-59
 Identities = 121/373 (32%), Positives = 199/373 (53%), Gaps = 5/373 (1%)

Query: 6   LSEDQRMIRDMARDFARREIAPHAQAWEKAGWIDDTLVAQMGELGLLGMVVPEEWGGSYI 65
           L+++ ++IR  ARD+ ++E++P  + + +       L+  + ++G  G  +P E+GG+ +
Sbjct: 22  LTDEHKLIRATARDWVKKEVSPIIEDYAQKAEFPKHLIKGLADIGAFGPTIPVEYGGAGL 81

Query: 66  DYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGRAIGCFA 125
           DY AY + ++EI  GD    +  S+  S+   P+  YGS+ Q+ ++L +LASG  +GCF 
Sbjct: 82  DYTAYGILMQEIERGDSGIRSTASVQGSLVMYPIYAYGSEEQRKKYLPKLASGEMMGCFG 141

Query: 126 LTEPQAGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGKKGLSAF 185
           LTEP  GS    + T  +    H++LNG+K + SNA  + +A+V+A    E GK  +   
Sbjct: 142 LTEPDHGSNPGGMVTNIKDAGSHYILNGAKMWISNAPFADIAVVWA--KDESGK--IRGL 197

Query: 186 LVPTDTPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIALSNLEGGRI 245
           +V     GF+   + HK  +RAS T  +   + ++P+ N+  E   GL   L  L   R 
Sbjct: 198 IVERGMEGFSTPETHHKWSLRASATGELVFDNVKVPKENIFPEI-SGLKGPLGCLNQARY 256

Query: 246 GIGAQALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAARLLILHAAR 305
           GI   ALG A   ++ AL Y++ERVQFGKPI   Q     LA+M T++   +LL+     
Sbjct: 257 GIAWGALGAAMDCYDTALRYSKERVQFGKPIGGFQLQQKKLAEMVTEITKGQLLVWRLGV 316

Query: 306 LKSAGLPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDARITQIYEG 365
           LKS       + S AK  + E+A  +   A Q+ GG G   +Y + R+  +      YEG
Sbjct: 317 LKSENRASAEQISMAKRNSVEIALDIARNARQMLGGMGITGEYSIMRHMMNLESVVTYEG 376

Query: 366 SSEIQRLLIAREL 378
           + +I  L+   ++
Sbjct: 377 THDIHLLITGMDV 389


Lambda     K      H
   0.318    0.133    0.390 

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: 337
Number of extensions: 15
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: 383
Length of database: 396
Length adjustment: 30
Effective length of query: 353
Effective length of database: 366
Effective search space:   129198
Effective search space used:   129198
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 (21.7 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