GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Dechlorosoma suillum PS

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate Dsui_0977 Dsui_0977 acyl-CoA dehydrogenase

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



>FitnessBrowser__PS:Dsui_0977
          Length = 378

 Score =  273 bits (697), Expect = 8e-78
 Identities = 159/379 (41%), Positives = 230/379 (60%), Gaps = 7/379 (1%)

Query: 5   LTPELEELRRTVEEFAHDVVAPKIGDFYERHEFPYEIVREMGRMGLFGLPFPEEYGGMGG 64
           LT E E +R ++  FA + +AP   ++ + H FP E ++E+G +G  G+  PEE+GG G 
Sbjct: 3   LTQEQEMIRDSMRAFAQERLAPFAAEWDKNHTFPAEALKELGELGAMGMCVPEEWGGAGM 62

Query: 65  DYLALGIALEELARVDSSVAITLEAGVSLGAMPIHLFGTDAQKAEWLPRLCSGEILGAFG 124
           DY++L + LEE+A  D + +  +    SL       +GTD QK EWL  L  GE LG F 
Sbjct: 63  DYMSLVLTLEEIAAGDGATSTIVSVQNSLACGITQKYGTDQQKEEWLKPLARGEKLGCFC 122

Query: 125 LTEPDGGSDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVTVTAVTGRKPDGKP 184
           LTEP  GSDA A   T R D   + +V+NG K FIT        +  V AVT  K  GK 
Sbjct: 123 LTEPHTGSDAAAI--TTRADRDGDHFVLNGVKQFITTGKH--AHMAIVFAVTD-KAAGKK 177

Query: 185 LISSIIVPSGTPGFTVAAPYSKVGWNASDTRELSFADVRVPAANLLGEQGRGYAQFLRIL 244
            IS  +VP+ T GF V     K+G +ASDT ++ F D RVPA+ LLG++G GY   L  L
Sbjct: 178 GISCFLVPTDTKGFIVGRTEEKMGQHASDTVQIIFEDCRVPASALLGKEGEGYKIALSNL 237

Query: 245 DEGRIAISALATGLAQGCVDESVKYAGERHAFGRNIGAYQAIQFKIADMEMKAHMARVG- 303
           + GRI I+A + G+A+   + +V+YA ER  FG+ I  +QA+ F++ADM      AR+  
Sbjct: 238 EAGRIGIAAQSIGMARAAFEAAVRYAKERVTFGQPIIEHQAVNFRLADMNTLLDAARLMV 297

Query: 304 WRDAASRLVAGEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRDSKI 363
           WR AA +  AG+P  KEA++AK+++S  A   A +A QIHGG G+ +++PV R++RD +I
Sbjct: 298 WRAAALK-DAGKPCLKEASMAKMFASEAAEKIASDAIQIHGGVGYTSDFPVERIYRDVRI 356

Query: 364 LEIGEGTSEVQRMLIAREL 382
            +I EG +++QR++I R +
Sbjct: 357 SQIYEGANDIQRLVIGRSI 375


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: 381
Number of extensions: 13
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: 378
Length adjustment: 30
Effective length of query: 356
Effective length of database: 348
Effective search space:   123888
Effective search space used:   123888
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