GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Phaeobacter inhibens BS107

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate GFF1190 PGA1_c12060 acyl-CoA dehydrogenase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2985
         (383 letters)



>FitnessBrowser__Phaeo:GFF1190
          Length = 383

 Score =  220 bits (561), Expect = 5e-62
 Identities = 128/379 (33%), Positives = 201/379 (53%), Gaps = 3/379 (0%)

Query: 2   HDIELSEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDGLVAKMGELGLLGMVVPEEWG 61
           H   +++E  M+ DM   F   E AP  + W K G +D     + G LGLL   VPEE+G
Sbjct: 6   HSSWMTDEHQMLADMTAQFITREWAPKFETWRKQGMMDRSTWNEAGALGLLCPSVPEEYG 65

Query: 62  GTYVDYVAYALAVEEISAGDGATGAFMSIHNSVGCGPVLNYGSEEQKQTWLADLASGQVI 121
           G   D+   A  + E S  + A+     IH+ +    VL+YG+EEQKQ WL  + +G+++
Sbjct: 66  GVGGDFGHEAAILIEGSRANLASWGH-GIHSGIVAHYVLSYGTEEQKQRWLPKMITGELV 124

Query: 122 GCFCLTEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGKRAKLAIVFAVTDPDLGKRG 181
           G   +TEP  GS+   ++T+A      + ++G K F++NG+ A L +V A TDP  G +G
Sbjct: 125 GALAMTEPSTGSDVQRIKTKAVKDGNAYRLSGQKTFITNGQHANLILVAAKTDPSQGSKG 184

Query: 182 ISAFLVPTDTA-GFIVDRTEHKMGIRASDTCAVTLNNCTIPEANLL-GERGKGLAIALSN 239
           IS   V TD A GF   R   K+G+ A+DT  +  +N  I   N+L G  G+G    +  
Sbjct: 185 ISLVAVETDGADGFSRGRNLDKIGLHAADTSELFFDNVEIAPENILGGTEGQGFYQMMQQ 244

Query: 240 LEGGRIGIAAQALGIARAAFEAALAYSRDRVQFGKAINEHQSIANLLADMHMQLNAARLM 299
           L   R+ IA  A+G    A E  + Y ++R  FG  + + Q+    L +   +   AR  
Sbjct: 245 LPQERLIIACGAVGAMEGAVERTITYCKEREAFGGPLTQFQNTRFKLVECQTKTKVARAF 304

Query: 300 ILHAARLRTAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVEKYYRDARI 359
           +         GK  + +A+ AK + ++    V    +Q+HGGYG++++Y V + + DAR+
Sbjct: 305 LDECMVEHLQGKLTVEKAAMAKYWITDTQGDVLDECVQLHGGYGFMQEYAVAEMWTDARV 364

Query: 360 TQIYEGSSEIQRMVIAREL 378
            +IY G++EI + +IAR L
Sbjct: 365 QRIYGGTNEIMKELIARSL 383


Lambda     K      H
   0.319    0.134    0.393 

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: 355
Number of extensions: 15
Number of successful extensions: 4
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: 383
Length adjustment: 30
Effective length of query: 353
Effective length of database: 353
Effective search space:   124609
Effective search space used:   124609
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