GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Echinicola vietnamensis KMM 6221, DSM 17526

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate Echvi_1212 Echvi_1212 Acyl-CoA dehydrogenases

Query= SwissProt::Q2LQN9
         (414 letters)



>FitnessBrowser__Cola:Echvi_1212
          Length = 379

 Score =  288 bits (736), Expect = 2e-82
 Identities = 163/377 (43%), Positives = 228/377 (60%), Gaps = 5/377 (1%)

Query: 37  LTEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTGM 96
           LTEE   + E  R  A   + P  IE D + +FP        +LG L  +V  +Y G GM
Sbjct: 5   LTEEHLAVQEAAREFAKSALLPGVIERDTHATFPHEQVKQMGELGFLGMMVAPQYNGGGM 64

Query: 97  DITTFAMVLEEIGKVCASTALMLLAQADGMLSIILD--GSPALKEKYLPRFGEKSTLMTA 154
           D  ++ + +EEI K+ AS A+ +    + ++   L+  GS   KEKYL        ++ A
Sbjct: 65  DTLSYVLAIEEISKIDASAAVAMSVN-NSLVCWGLEHYGSEQQKEKYLKPLAA-GEILGA 122

Query: 155 FAATEPGAGSDLLAMKTRAVKKGDKYVINGQKCFITNGSVADILTVWAYTDPSKGAKGMS 214
           F  +EP AGSD  + +T A K GD Y++NG K +ITNG  A +  V A T+P    KG+S
Sbjct: 123 FCLSEPEAGSDATSQRTMAEKHGDHYLLNGTKNWITNGGTASVYLVMAQTNPELKHKGIS 182

Query: 215 TFVVERGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSIN 274
           TF+VE+   G   G  E K+G+RG     L F D++VP EN +GE+G GF Y M +L   
Sbjct: 183 TFIVEKDMEGFQVGKKEDKLGIRGSDTHSLMFNDVKVPLENRIGEDGFGFTYAMHSLDGG 242

Query: 275 RVFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRKA 334
           R+  A+QA+GIA GA E A+ +++ER+ FGKPI+    IQF +ADMATE+EAAR+LV KA
Sbjct: 243 RIGIAAQALGIAAGAYELALAYSKERKAFGKPISQHQAIQFKLADMATEIEAARMLVWKA 302

Query: 335 TTLLDAKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQI 394
             L D  +        MAK +AS  AM  T +AVQ+ GG G+++EY VER+MR+AK+TQI
Sbjct: 303 AWLKDQGESYAH-ASAMAKLYASKVAMDTTIEAVQIHGGYGFVKEYHVERLMRDAKITQI 361

Query: 395 YTGTNQITRMVTGRSLL 411
           Y GT++I ++V  R+LL
Sbjct: 362 YEGTSEIQKIVISRNLL 378


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: 357
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: 414
Length of database: 379
Length adjustment: 31
Effective length of query: 383
Effective length of database: 348
Effective search space:   133284
Effective search space used:   133284
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