GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Pseudomonas fluorescens FW300-N1B4

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 3/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate Pf1N1B4_4787 Butyryl-CoA dehydrogenase (EC 1.3.99.2)

Query= BRENDA::Q18AQ1
         (378 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4787
          Length = 375

 Score =  348 bits (894), Expect = e-100
 Identities = 171/359 (47%), Positives = 245/359 (68%)

Query: 18  FAENEVKPLATELDEEERFPYETVEKMAKAGMMGIPYPKEYGGEGGDTVGYIMAVEELSR 77
           FA+  +KP A E D E RFP E + +MA  G  G+  P+++GG     + Y MA+EE++ 
Sbjct: 17  FAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTGYLAYAMALEEIAA 76

Query: 78  VCGTTGVILSAHTSLGSWPIYQYGNEEQKQKFLRPLASGEKLGAFGLTEPNAGTDASGQQ 137
             G    I+S H S+G  PI ++GN++QK++FL+PLASG  LGAF LTEP AG+DAS  +
Sbjct: 77  GDGACSTIMSVHNSVGCVPILKFGNDDQKERFLKPLASGAMLGAFALTEPQAGSDASSLK 136

Query: 138 TTAVLDGDEYILNGSKIFITNAIAGDIYVVMAMTDKSKGNKGISAFIVEKGTPGFSFGVK 197
           T A LDGD Y+LNG K FIT+     + +V A+TD S G +GI+A IV   +PG+     
Sbjct: 137 TRARLDGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGITALIVPTDSPGYKVARV 196

Query: 198 EKKMGIRGSATSELIFEDCRIPKENLLGKEGQGFKIAMSTLDGGRIGIAAQALGLAQGAL 257
           E K+G   S T +++FED ++P  N LG+EG+G+KIA++ L+GGR+GIA+Q++G+A+ A 
Sbjct: 197 EDKLGQHASDTCQILFEDVKVPVANRLGEEGEGYKIALANLEGGRVGIASQSVGMARAAF 256

Query: 258 DETVKYVKERVQFGRPLSKFQNTQFQLADMEVKVQAARHLVYQAAINKDLGKPYGVEAAM 317
           +    Y +ER  FG+P+ + Q   F+LADM  ++  AR +V+ AA  +D GKP  VEA+M
Sbjct: 257 EAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAALRDSGKPALVEASM 316

Query: 318 AKLFAAETAMEVTTKAVQLHGGYGYTRDYPVERMMRDAKITEIYEGTSEVQRMVISGKL 376
           AKLFA+E A +V + A+Q  GGYGY  D+P+ER+ RD ++ +IYEGTS++QRMVIS  L
Sbjct: 317 AKLFASEMAEKVCSSALQTLGGYGYLNDFPLERIYRDVRVCQIYEGTSDIQRMVISRNL 375


Lambda     K      H
   0.315    0.133    0.373 

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: 12
Number of successful extensions: 1
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: 378
Length of database: 375
Length adjustment: 30
Effective length of query: 348
Effective length of database: 345
Effective search space:   120060
Effective search space used:   120060
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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