GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Shewanella loihica PV-4

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate 5209711 Shew_2164 acyl-CoA dehydrogenase domain-containing protein (RefSeq)

Query= metacyc::G1G01-166-MONOMER
         (393 letters)



>FitnessBrowser__PV4:5209711
          Length = 596

 Score = 97.4 bits (241), Expect = 9e-25
 Identities = 102/376 (27%), Positives = 171/376 (45%), Gaps = 51/376 (13%)

Query: 56  FREMGEVGLLGATIPEQYGGSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEF 115
           +++  + G    T   +YGG GL   C G+ A E++   +   +M    +      I+  
Sbjct: 82  YQQYVDNGWATLTSDPEYGGQGLPE-CIGVFATEMKTATNMAFAMYPGLTHGAYAAIHAH 140

Query: 116 GTEAQKQKYLPKLASGEWIGCFGLTEPNHGSDPGSMITRARKV-DGGYRLTGSKMWITNS 174
           G++A K KYL KL SGEW G   LTE + G+D   + T+A+ V +  Y ++G K++I++ 
Sbjct: 141 GSDALKAKYLEKLVSGEWTGTMNLTEAHAGTDLALLRTKAKPVGEDTYAISGEKIFISSG 200

Query: 175 --PIAD--VFVVWAK-DDAGD-IRGFVL---------EKGW----QGLSAPAIHGKVGLR 215
              +AD  V +V A+  DA D ++G  L         + G      G+ A A+  K+G+ 
Sbjct: 201 DHDLADNIVHLVLARLPDAPDGVKGISLFAVPKYLVNDDGTLGCRNGVEASALEHKMGIH 260

Query: 216 ASITGEIVMDNVFVPEENIFPDVRGLKGPFTCLNSARYGISWGALGAAEACWHTARQYTL 275
            + T  +V D      E +    +GL+  FT +N AR G+    LG +E  +  A  Y  
Sbjct: 261 GNSTCVMVFDGAI--GELVGEPHQGLRAMFTMMNEARLGVGVQGLGVSEIAYQNALSYAR 318

Query: 276 DRQQFGRPLA-----------------ANQLIQKKLADMQTEITLALQGCLRLG---RMK 315
           +R Q GR L+                   +++  + A  Q    L  Q  L L    R +
Sbjct: 319 ERLQ-GRALSGVKESESPADPILVHGDVRRMLMAQKAFNQGARALMGQQALWLDESHRHQ 377

Query: 316 DEGTAAVE------ITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNLEVVN 369
           D+  A +        T ++K     +       A+ + GG+G   E+G+ + + +  +  
Sbjct: 378 DKAKATIAAKLAALFTPVVKGFVTDQGFKACVDAQQVYGGHGYIHEWGMEQFVRDSRIAM 437

Query: 370 TYEGTHDVHAL-ILGR 384
            YEGT+ V AL ++GR
Sbjct: 438 IYEGTNGVQALDLVGR 453


Lambda     K      H
   0.320    0.137    0.413 

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: 521
Number of extensions: 24
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 393
Length of database: 596
Length adjustment: 34
Effective length of query: 359
Effective length of database: 562
Effective search space:   201758
Effective search space used:   201758
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: 52 (24.6 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