GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Burkholderia phytofirmans PsJN

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate BPHYT_RS02220 BPHYT_RS02220 butyryl-CoA dehydrogenase

Query= metacyc::MONOMER-11693
         (386 letters)



>FitnessBrowser__BFirm:BPHYT_RS02220
          Length = 376

 Score =  275 bits (702), Expect = 2e-78
 Identities = 153/372 (41%), Positives = 221/372 (59%), Gaps = 5/372 (1%)

Query: 12  LRRTVEEFAHDVVAPKIGDFYERHEFPYEIVREMGRMGLFGLPFPEEYGGMGGDYLALGI 71
           +R  +  F  + + P    +     FP ++ R++  +G +G+  PE YGG G D LAL +
Sbjct: 10  VRDALRTFVREAITPHAAVWDRERTFPKDVHRQLAELGAYGVLVPEAYGGAGMDALALAL 69

Query: 72  ALEELARVDSSVAITLEAGVSLGAMPIHLFGTDAQKAEWLPRLCSGEILGAFGLTEPDGG 131
            LEE+A  D   +  +          +  +G DAQK +WL  L  GE+LGAF LTEP  G
Sbjct: 70  ILEEIAAGDGGTSTAISVNNCPVCSILLTYGNDAQKRDWLTPLARGEMLGAFCLTEPQAG 129

Query: 132 SDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVTVTAVTGRKPDGKPLISSIIV 191
           SDA A RTTA  D     +V+NG K FIT+      G V +      K  GK  IS+ IV
Sbjct: 130 SDASALRTTATRDGDA--YVLNGVKQFITSGKN---GNVAIVMAVTDKAAGKRGISAFIV 184

Query: 192 PSGTPGFTVAAPYSKVGWNASDTRELSFADVRVPAANLLGEQGRGYAQFLRILDEGRIAI 251
           P+ T G+ VA    K+G ++SDT ++ F D RVPAANL+G +G GY   L  L+ GRI I
Sbjct: 185 PTDTKGYVVARVEDKLGQHSSDTAQIIFEDCRVPAANLIGAEGEGYRIALSGLEGGRIGI 244

Query: 252 SALATGLAQGCVDESVKYAGERHAFGRNIGAYQAIQFKIADMEMKAHMARVGWRDAASRL 311
           +A + G+A+   + ++ YA ER +FG  + ++QA+QF++ADM  +   AR     AAS  
Sbjct: 245 AAQSVGMARAAFEAALSYAKERESFGAPLFSHQAVQFRLADMATQLEAARQLIWHAASLK 304

Query: 312 VAGEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRDSKILEIGEGTS 371
            AG+P   EAA+AKL++S  A      A QIHGGYG+++++PV R++RD ++ +I EGTS
Sbjct: 305 DAGQPCLTEAAMAKLFASEAAERICSAALQIHGGYGYLSDFPVERIYRDVRVCQIYEGTS 364

Query: 372 EVQRMLIARELG 383
           ++Q++LIAR LG
Sbjct: 365 DIQKILIARGLG 376


Lambda     K      H
   0.318    0.136    0.402 

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: 406
Number of extensions: 16
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: 386
Length of database: 376
Length adjustment: 30
Effective length of query: 356
Effective length of database: 346
Effective search space:   123176
Effective search space used:   123176
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