GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Bacteroides fluxus YIT 12057

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_009123484.1 HMPREF9446_RS00545 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>NCBI__GCF_000195635.1:WP_009123484.1
          Length = 567

 Score =  181 bits (458), Expect = 6e-50
 Identities = 124/367 (33%), Positives = 191/367 (52%), Gaps = 39/367 (10%)

Query: 37  KEAIDEMAELGLFGMLVPEQWGGSDTGYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPI 96
           K+ +D M + GL GM +P ++GG +     Y M  E +AA D     I S+ +   C+  
Sbjct: 92  KQNLDAMVKAGLNGMTMPRRFGGLNFPITPYTMCAEIVAAADAGFGNIWSLQD---CIET 148

Query: 97  L-RFGNEQQKEQFLTPLATGAMLGAFALTEPQAGSDASSLKTRARLE--GDHYVLNGSKQ 153
           L  FGNE Q  +F+  +  G  + +  LTEP AGSD  S+  +A  +   + + LNG K+
Sbjct: 149 LYEFGNEDQHSRFIPRICQGETM-SMDLTEPDAGSDLQSVMLKATFDEANNCWRLNGVKR 207

Query: 154 FITSGQ-NAGVVIVFAVTDPEAGKRGISAFIVPTDSPGYQVARVEDKLGQHASDTCQIVF 212
           FIT+G  N  +V+  +    + G RG+S FI   +  G  V R+E+KLG H S TC++V+
Sbjct: 208 FITNGDANLHLVLARSEEGTKDG-RGLSMFIYDKNEGGVDVRRIENKLGIHGSPTCELVY 266

Query: 213 DNVQVPVAN--RLGAEGEGYKIALANLEGGRIGIASQAVGMARAAFEVARDYANERQSFG 270
            N +  +    +LG      K  +A + G R+GIA+Q+VG+++AA+     YA +R+ FG
Sbjct: 267 KNAKAELCGDRKLGL----IKYVMALMNGARLGIAAQSVGLSQAAYNEGLAYAKDRKQFG 322

Query: 271 KPLIEHQAVAFRLADMATKISVARQMVLHAA-------ALRDAGR--------------- 308
           K +IE  AV   LA M  K+   R ++   +       AL D  R               
Sbjct: 323 KAIIEFPAVYDMLAIMKAKLDAGRSLLYQTSRYVDIYKALDDISRERKLTPEERQEQKKY 382

Query: 309 PALVEA--SMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEGTSDI 366
             L +A   +AK   SE A +   D++Q  GG G++ ++  +RIYRD R+  IYEGT+ +
Sbjct: 383 SKLADAFTPLAKGMNSEYANQNAYDSIQIHGGSGFMLEYACQRIYRDARITSIYEGTTQL 442

Query: 367 QRMVIAR 373
           Q +   R
Sbjct: 443 QTVAAIR 449


Lambda     K      H
   0.319    0.134    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: 473
Number of extensions: 31
Number of successful extensions: 7
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: 375
Length of database: 567
Length adjustment: 33
Effective length of query: 342
Effective length of database: 534
Effective search space:   182628
Effective search space used:   182628
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 51 (24.3 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