GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Phaeobacter inhibens BS107

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate GFF1190 PGA1_c12060 acyl-CoA dehydrogenase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2983
         (375 letters)



>FitnessBrowser__Phaeo:GFF1190
          Length = 383

 Score =  224 bits (571), Expect = 3e-63
 Identities = 130/373 (34%), Positives = 207/373 (55%), Gaps = 3/373 (0%)

Query: 5   DDQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGY 64
           D+ Q + DM   F      P    W ++    +    E   LG     VPE++GG    +
Sbjct: 12  DEHQMLADMTAQFITREWAPKFETWRKQGMMDRSTWNEAGALGLLCPSVPEEYGGVGGDF 71

Query: 65  LAYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFALT 124
              A  L E +  + A S    +H+ +    +L+YGT+EQK+R+L  + +G ++GA A+T
Sbjct: 72  GHEAAILIEGSRANLA-SWGHGIHSGIVAHYVLSYGTEEQKQRWLPKMITGELVGALAMT 130

Query: 125 EPQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFIV 184
           EP  GSD   +KT+A  +G+ Y L+G K FIT+GQ+A +++V A TDPS G +GIS   V
Sbjct: 131 EPSTGSDVQRIKTKAVKDGNAYRLSGQKTFITNGQHANLILVAAKTDPSQGSKGISLVAV 190

Query: 185 PTD-SPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRL-GEEGEGYRIALANLEGGRV 242
            TD + G+   R  DK+G HA+DT ++ F++V++   N L G EG+G+   +  L   R+
Sbjct: 191 ETDGADGFSRGRNLDKIGLHAADTSELFFDNVEIAPENILGGTEGQGFYQMMQQLPQERL 250

Query: 243 GIASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAA 302
            IA  +VG    A E    Y +ERE+FG P+ + Q   F+L +  T+  VAR  +     
Sbjct: 251 IIACGAVGAMEGAVERTITYCKEREAFGGPLTQFQNTRFKLVECQTKTKVARAFLDECMV 310

Query: 303 LRDSGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEG 362
               GK  + +A+MAK + ++    V    +Q  GGYG++ ++ V  ++ D RV +IY G
Sbjct: 311 EHLQGKLTVEKAAMAKYWITDTQGDVLDECVQLHGGYGFMQEYAVAEMWTDARVQRIYGG 370

Query: 363 TSDIQRMVISRNL 375
           T++I + +I+R+L
Sbjct: 371 TNEIMKELIARSL 383


Lambda     K      H
   0.320    0.135    0.394 

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: 352
Number of extensions: 17
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: 375
Length of database: 383
Length adjustment: 30
Effective length of query: 345
Effective length of database: 353
Effective search space:   121785
Effective search space used:   121785
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