GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Halomonas desiderata SP1

Align glutaryl-CoA dehydrogenase (EC 1.3.8.6) (characterized)
to candidate WP_086511950.1 BZY95_RS21595 acyl-CoA dehydrogenase

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



>NCBI__GCF_002151265.1:WP_086511950.1
          Length = 393

 Score =  739 bits (1908), Expect = 0.0
 Identities = 360/387 (93%), Positives = 376/387 (97%)

Query: 6   SFNWIDPLLLDQQLTEEERMVRDSAYQFAQDKLAPRVLEAFRHEQTDPAIFREMGEVGLL 65
           +F+W DPLLLDQQLTEEERMV+ SA QFA DKLAPRVLEAFRHEQTDPAIFREMGE GLL
Sbjct: 6   AFHWQDPLLLDQQLTEEERMVQQSAAQFAADKLAPRVLEAFRHEQTDPAIFREMGETGLL 65

Query: 66  GATIPEQYGGSGLNYVCYGLIAREVERIDSGYRSMMSVQSSLVMVPINEFGTEAQKQKYL 125
           GATIPEQYGGSGLNYVCYGLIARE+ER+DSGYRSMMSVQSSLVMVPIN FG EA +QKYL
Sbjct: 66  GATIPEQYGGSGLNYVCYGLIAREIERVDSGYRSMMSVQSSLVMVPINAFGNEATRQKYL 125

Query: 126 PKLASGEWIGCFGLTEPNHGSDPGSMITRARKVDGGYRLTGSKMWITNSPIADVFVVWAK 185
           PKLASGEWIGCFGLTEPNHGSDPG+M+TRAR+VDGGYRLTGSKMWITNSPIADVFVVWAK
Sbjct: 126 PKLASGEWIGCFGLTEPNHGSDPGAMVTRARRVDGGYRLTGSKMWITNSPIADVFVVWAK 185

Query: 186 DDAGDIRGFVLEKGWQGLSAPAIHGKVGLRASITGEIVMDNVFVPEENIFPDVRGLKGPF 245
           DD GDIRGFVLEKGW+GLSAPAIHGKVGLRASITGEIVMD+VFVPEEN+FP+VRGLKGPF
Sbjct: 186 DDEGDIRGFVLEKGWEGLSAPAIHGKVGLRASITGEIVMDSVFVPEENMFPEVRGLKGPF 245

Query: 246 TCLNSARYGISWGALGAAEACWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTEITLAL 305
           TCLNSARYGISWGALGAAE CWHTARQYTLDRQQFGRPLAANQLIQKKLADMQT+I LAL
Sbjct: 246 TCLNSARYGISWGALGAAEDCWHTARQYTLDRQQFGRPLAANQLIQKKLADMQTDICLAL 305

Query: 306 QGCLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARMARDMLGGNGISDEFGVARHLVNL 365
           QGCLRLGRMKDEGTAAVEITSIMKRNSCGKALDIAR+ARDMLGGNGISDEFGVARHLVNL
Sbjct: 306 QGCLRLGRMKDEGTAAVEITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNL 365

Query: 366 EVVNTYEGTHDVHALILGRAQTGIQAF 392
           EVVNTYEGTHDVHALILGRAQTG+QAF
Sbjct: 366 EVVNTYEGTHDVHALILGRAQTGLQAF 392


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: 638
Number of extensions: 10
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: 393
Length of database: 393
Length adjustment: 31
Effective length of query: 362
Effective length of database: 362
Effective search space:   131044
Effective search space used:   131044
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: 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