GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Algoriphagus machipongonensis PR1

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_008203176.1 ALPR1_RS19205 acyl-CoA dehydrogenase

Query= reanno::ANA3:7024494
         (389 letters)



>NCBI__GCF_000166275.1:WP_008203176.1
          Length = 379

 Score =  301 bits (770), Expect = 3e-86
 Identities = 158/377 (41%), Positives = 229/377 (60%)

Query: 8   LNFGLGEEVDMLRDAVQDFAKHEIAPIAAKVDHDNAFPNEIWPVLGGMGLLGVTVPEEYG 67
           +NF   E   M+ D ++DF   EI P   + D    FP +++  LG +GL+GV VP ++G
Sbjct: 1   MNFNESENQRMIADMIRDFGAKEITPFRKEWDDTQFFPKDLFKKLGELGLMGVLVPTDFG 60

Query: 68  GANMGYLAHVVAMEEISRASASIGLSYGAHSNLCVNQINRNGNAEQKAKYLPKLVSGEHI 127
           GA  GY  +V A+ E+++   SIGLS  AH++LC   I   G+ EQK KYLPKL + E +
Sbjct: 61  GAGFGYDEYVTAIVEVTKLDPSIGLSLAAHNSLCTGHILLFGSEEQKQKYLPKLATCELL 120

Query: 128 GALAMSEPNAGSDVVSMKLHARKEGDRYILNGNKMWITNGPDANTYVIYAKTDLTKGAHG 187
           GA  ++EPN GSD  +MK  A K+GD +ILNG K +IT+G   +  V+ A+T     +HG
Sbjct: 121 GAWGLTEPNTGSDAGNMKTVAVKDGDYWILNGAKNFITHGVSGDLAVVIARTGEVGDSHG 180

Query: 188 ITAFIVERGFKGFSQAQKLDKLGMRGSNTCELVFEDVEVPEENILGGLNNGVKVLMSGLD 247
           +TAFIVERG  GF   +K DKLGMR S T E++FED ++ E  +LG + +G    M  LD
Sbjct: 181 MTAFIVERGTPGFKGGRKEDKLGMRASETAEMIFEDCKIHESQVLGNVGDGFIQSMKVLD 240

Query: 248 YERVVLSGGPLGIMNACMDIVVPYIHEREQFGKSIGEFQLVQGKLADMYTGMNAAKAYVY 307
             R+ ++   LGI    ++  + Y  EREQFGK I  FQ +  KLADM T + AAK  + 
Sbjct: 241 GGRISIAALSLGIAEGALEASIQYSKEREQFGKPISRFQGISFKLADMATQVEAAKLLIM 300

Query: 308 SVAKSCDRGETTRKDAAGAILYSAELATKMALDAIQLLGGNGYVNEYATGRLLRDAKLYE 367
             +   +RGE     +A A  Y++E+   ++ +A+Q+ GG G+  +Y   +  RD+KL  
Sbjct: 301 KASDMKNRGEKVTLASAQAKYYASEVCVSVSNEAVQIFGGYGFTKDYPVEKYYRDSKLCT 360

Query: 368 IGAGTSEIRRMLIGREL 384
           IG GTSEI++++I RE+
Sbjct: 361 IGEGTSEIQKLVIAREV 377


Lambda     K      H
   0.316    0.135    0.388 

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: 355
Number of extensions: 13
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: 389
Length of database: 379
Length adjustment: 30
Effective length of query: 359
Effective length of database: 349
Effective search space:   125291
Effective search space used:   125291
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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