GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Pseudomonas fluorescens FW300-N2E2

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate Pf6N2E2_5333 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= reanno::WCS417:GFF2713
         (383 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5333
          Length = 378

 Score =  255 bits (652), Expect = 1e-72
 Identities = 140/373 (37%), Positives = 207/373 (55%), Gaps = 1/373 (0%)

Query: 6   YTEEQVMIRDMARDFARGEIAPYAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGGTYV 65
           ++ E  + RD  R F   E  PY   WEK G +D  L  K GE G+L   +PE +GG   
Sbjct: 7   FSPEHELFRDSVRTFLEKEAVPYHSQWEKQGHVDRQLWNKAGEAGMLCSHLPEAYGGLDA 66

Query: 66  DYVAYALAVEEISAGDGATGALMSIHNSVGCGPILNYGTESQKQTWLADLASGQAIGCFC 125
           D++   + +EEI    G TG   S+H+ +    IL+YG+E+ K  +L  L SG+ +    
Sbjct: 67  DFLYSTVVIEEIGRL-GLTGIGFSLHSDIVAPYILHYGSEALKHKYLPKLVSGEMVTAIA 125

Query: 126 LTEPQAGSEAHNLRTRAELRDGHWVITGAKQFVSNGKRAKLAIVFAITDPELGKKGISAF 185
           +TEP AGS+   ++T A L    +VI G+K F++NG  A L IV A TDP+ G KG S F
Sbjct: 126 MTEPGAGSDLQGVKTTAVLDGDEYVINGSKTFITNGFLADLVIVVAKTDPKAGAKGTSLF 185

Query: 186 LVPTATPGFVVDRTEHKMGIRASDTCAVTLNQCTVPEANLLGERGKGLAIALSNLEGGRI 245
           LV   T GF   +   K+G++A DT  +      VP+ NLLG+ G G A  +  L   R+
Sbjct: 186 LVEAGTLGFEKGKRLEKVGMKAQDTSELFFQDVRVPKENLLGQAGMGFAYLMQELPQERL 245

Query: 246 GIAAQALGIARAAFEAALAYARDRVQFDKAIIEHQSVANLLADMQTQLNAARLLILHAAR 305
            +A   L  A AA +  L Y R+R  F K+I + Q+    LA+M T++   R+ +     
Sbjct: 246 TVAIGGLASAEAALQWTLDYTRERKAFGKSIADFQNTRFKLAEMATEIQIGRVFVDRCLE 305

Query: 306 LRSAGKPCLSEASQAKLFASEMAEKVCSSAMQIHGGYGYLEDYPVERYYRDARITQIYEG 365
           L   GK  +  A+ AK + +++  KV    +Q+HGGYG++ +YP+ R + DAR+ +IY G
Sbjct: 306 LHLQGKLDVPTAAMAKYWGTDLQCKVLDECVQLHGGYGFMWEYPIARAWADARVQRIYAG 365

Query: 366 TSEIQRMVIAREL 378
           T+EI + +IAR L
Sbjct: 366 TNEIMKEIIARSL 378


Lambda     K      H
   0.319    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: 318
Number of extensions: 15
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: 383
Length of database: 378
Length adjustment: 30
Effective length of query: 353
Effective length of database: 348
Effective search space:   122844
Effective search space used:   122844
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