GapMind for catabolism of small carbon sources

 

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

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate Echvi_1212 Echvi_1212 Acyl-CoA dehydrogenases

Query= reanno::Phaeo:GFF1011
         (386 letters)



>FitnessBrowser__Cola:Echvi_1212
          Length = 379

 Score =  286 bits (732), Expect = 7e-82
 Identities = 155/378 (41%), Positives = 228/378 (60%)

Query: 6   MTFDLGEDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFG 65
           M F L E+  A+++    +A+  + P   E D    FP E  ++MGELG LG+ V  ++ 
Sbjct: 1   MNFTLTEEHLAVQEAAREFAKSALLPGVIERDTHATFPHEQVKQMGELGFLGMMVAPQYN 60

Query: 66  GAGMSYLAHTVAVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLVSGEHV 125
           G GM  L++ +A+EEI++  AS +++   +++L    ++  G+ +QK KYL  L +GE +
Sbjct: 61  GGGMDTLSYVLAIEEISKIDASAAVAMSVNNSLVCWGLEHYGSEQQKEKYLKPLAAGEIL 120

Query: 126 GALAMSEAGAGSDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPDAGSKG 185
           GA  +SE  AGSD  S    AEK  DHY LNG K WITNG  A   +V A+T+P+   KG
Sbjct: 121 GAFCLSEPEAGSDATSQRTMAEKHGDHYLLNGTKNWITNGGTASVYLVMAQTNPELKHKG 180

Query: 186 MTAFLIEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVLMSGLD 245
           ++ F++EK+ +GF   +  DKLG+RGS+T  L+F DV+VP EN +GE+G G    M  LD
Sbjct: 181 ISTFIVEKDMEGFQVGKKEDKLGIRGSDTHSLMFNDVKVPLENRIGEDGFGFTYAMHSLD 240

Query: 246 YERVVLAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYVY 305
             R+ +A    GI A   +  + Y KERK FG+PI   Q +Q K+ADM T +  AR  V+
Sbjct: 241 GGRIGIAAQALGIAAGAYELALAYSKERKAFGKPISQHQAIQFKLADMATEIEAARMLVW 300

Query: 306 EVAKACDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLME 365
           + A   D+G      +A   LYAS+VAM    +AVQ  GG G++ +  V R+ RDAK+ +
Sbjct: 301 KAAWLKDQGESYAHASAMAKLYASKVAMDTTIEAVQIHGGYGFVKEYHVERLMRDAKITQ 360

Query: 366 IGAGTSEIRRMLIGRELM 383
           I  GTSEI++++I R L+
Sbjct: 361 IYEGTSEIQKIVISRNLL 378


Lambda     K      H
   0.318    0.132    0.382 

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: 364
Number of extensions: 22
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: 386
Length of database: 379
Length adjustment: 30
Effective length of query: 356
Effective length of database: 349
Effective search space:   124244
Effective search space used:   124244
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