GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Dechlorosoma suillum PS

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate Dsui_0977 Dsui_0977 acyl-CoA dehydrogenase

Query= SwissProt::Q2LQN9
         (414 letters)



>FitnessBrowser__PS:Dsui_0977
          Length = 378

 Score =  266 bits (681), Expect = 6e-76
 Identities = 151/377 (40%), Positives = 221/377 (58%), Gaps = 7/377 (1%)

Query: 37  LTEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTGM 96
           LT+EQ+++ + +R  A   +AP A E D+NH+FP  A     +LG +   VP E+GG GM
Sbjct: 3   LTQEQEMIRDSMRAFAQERLAPFAAEWDKNHTFPAEALKELGELGAMGMCVPEEWGGAGM 62

Query: 97  DITTFAMVLEEIGKVCASTALMLLAQADGMLSIILD-GSPALKEKYLPRF--GEKSTLMT 153
           D  +  + LEEI     +T+ ++  Q      I    G+   KE++L     GEK   + 
Sbjct: 63  DYMSLVLTLEEIAAGDGATSTIVSVQNSLACGITQKYGTDQQKEEWLKPLARGEK---LG 119

Query: 154 AFAATEPGAGSDLLAMKTRAVKKGDKYVINGQKCFITNGSVADILTVWAYTDPSKGAKGM 213
            F  TEP  GSD  A+ TRA + GD +V+NG K FIT G  A +  V+A TD + G KG+
Sbjct: 120 CFCLTEPHTGSDAAAITTRADRDGDHFVLNGVKQFITTGKHAHMAIVFAVTDKAAGKKGI 179

Query: 214 STFVVERGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSI 273
           S F+V   T G I G  E+KMG       ++ FED  VPA  L+G+EG+G+   +  L  
Sbjct: 180 SCFLVPTDTKGFIVGRTEEKMGQHASDTVQIIFEDCRVPASALLGKEGEGYKIALSNLEA 239

Query: 274 NRVFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRK 333
            R+  A+Q++G+A+ A E A+++ +ER  FG+PI     + F +ADM T ++AARL+V +
Sbjct: 240 GRIGIAAQSIGMARAAFEAAVRYAKERVTFGQPIIEHQAVNFRLADMNTLLDAARLMVWR 299

Query: 334 ATTLLDAKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQ 393
           A  L DA  K       MAK FAS+ A K+ +DA+Q+ GG GY  ++ VER+ R+ +++Q
Sbjct: 300 AAALKDA-GKPCLKEASMAKMFASEAAEKIASDAIQIHGGVGYTSDFPVERIYRDVRISQ 358

Query: 394 IYTGTNQITRMVTGRSL 410
           IY G N I R+V GRS+
Sbjct: 359 IYEGANDIQRLVIGRSI 375


Lambda     K      H
   0.318    0.133    0.375 

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: 376
Number of extensions: 15
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: 414
Length of database: 378
Length adjustment: 31
Effective length of query: 383
Effective length of database: 347
Effective search space:   132901
Effective search space used:   132901
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