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_008198187.1 ALPR1_RS02465 acyl-CoA dehydrogenase

Query= reanno::Smeli:SM_b21121
         (387 letters)



>NCBI__GCF_000166275.1:WP_008198187.1
          Length = 379

 Score =  290 bits (741), Expect = 6e-83
 Identities = 157/377 (41%), Positives = 229/377 (60%)

Query: 6   LNFALGEEIDALRASVRRFASERIAPLADDADRSNAFPMSLWREMGELGLLGITADEAHG 65
           ++F L EE  A++ + R FA   + P   + D    FP    ++MGELG LG+     + 
Sbjct: 1   MDFQLTEEHLAVKEAAREFAQTELLPGVIERDTHGIFPKEQVKKMGELGFLGMMVKPENN 60

Query: 66  GAGLGYLAHCVAMEEISRASASVGLSYGAHSNLCVNQINRNGKPAQKSRYLPKLISGEHV 125
           G G+  L++ +AMEE+S+  AS  ++   +++L    + + G  AQK +YL  L SGE +
Sbjct: 61  GGGMDTLSYVIAMEELSKIDASASVAMSVNNSLVCWGLEKYGTEAQKEKYLRPLASGEVL 120

Query: 126 GALAMSEPGAGSDVVSMKLKADKRGDRYVLNGSKMWITNGPDADVLVVYAKTDPAAGPRG 185
           GA  +SEP AGSD  S + +A   GD Y+LNG+K WITNG  A + +V A+T P  G +G
Sbjct: 121 GAFCLSEPEAGSDATSQRTEAKLNGDHYILNGTKNWITNGNSASIYLVIAQTHPELGHKG 180

Query: 186 ITAFLVEKAFPGFSAGQKLDKLGMRGSNTSELIFTDCEVPEENVLGGVGEGVKVLMSGLD 245
           I+ F+VE+ + GF  G+K DKLG+RGS+T  L+FTD +VP EN +G  G G    M  L+
Sbjct: 181 ISVFIVEREWDGFVVGKKEDKLGIRGSDTHSLMFTDVKVPVENRIGEEGFGFTYAMETLN 240

Query: 246 YERVVLSAGPLGIMAACLDVVVPYLHERKQFGQPIGEFQLMQGKLADMYVTMNAARAYVY 305
             R+ ++A  LGI A   ++ + Y  ER+ FG+PI + Q +Q KLADM   + AAR  VY
Sbjct: 241 GGRIGIAAQALGIAAGAYELALAYSKEREAFGKPISKHQAIQFKLADMATQIEAARLLVY 300

Query: 306 AVAAACDRGETARKDAAGCILYAAEKATAMALEAIQALGGNGYTNDYPAGRLLRDAKLYE 365
             A   D+GE   + +A   LYA++ A  + +EAIQ  GG GY  +Y   RL+RDAK+ +
Sbjct: 301 KAAWTKDQGEDYSQASAIAKLYASQVAMDVTVEAIQVHGGYGYVKEYHVERLMRDAKITQ 360

Query: 366 IGAGTSEIRRMLIGREL 382
           I  GTSEI++++I R L
Sbjct: 361 IYEGTSEIQKIVISRSL 377


Lambda     K      H
   0.318    0.135    0.391 

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: 307
Number of extensions: 8
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: 387
Length of database: 379
Length adjustment: 30
Effective length of query: 357
Effective length of database: 349
Effective search space:   124593
Effective search space used:   124593
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 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