GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Halomonas desiderata SP1

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_086509764.1 BZY95_RS09860 acyl-CoA dehydrogenase

Query= reanno::Phaeo:GFF1011
         (386 letters)



>NCBI__GCF_002151265.1:WP_086509764.1
          Length = 383

 Score =  268 bits (684), Expect = 2e-76
 Identities = 137/372 (36%), Positives = 222/372 (59%), Gaps = 2/372 (0%)

Query: 17  LRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFGGAGMSYLAHTV 76
           L D + R+ +ER+ P    + +++  PAEL +EM E+GL G+++PEE+GG G++     +
Sbjct: 11  LIDTISRFVRERLIPNEARLAEEDAVPAELLEEMKEMGLFGLSIPEEYGGLGLTMEEEAL 70

Query: 77  AVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLVSGEHVGALAMSEAGAG 136
              EI + S +    +G ++ +    I ++G  EQKAKY+PRL +GE + +  ++E  AG
Sbjct: 71  VAMEIGKTSPAFRSIFGTNNGIGAQGILIDGTPEQKAKYVPRLATGELLSSFCLTEPDAG 130

Query: 137 SDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDP-DAGSKGMTAFLIEKEF 195
           SD  S+   A +  DHY LNG K +ITNGP+AD   V A+TDP + G+ G+TAF++E + 
Sbjct: 131 SDAASLRTTAVRDGDHYVLNGTKRFITNGPEADVFTVMARTDPGNKGAGGITAFIVEGDT 190

Query: 196 KGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVL-GEEGKGVRVLMSGLDYERVVLAGI 254
            G        K+G +G++T +++FED  VP EN++ G EGKG +  M  LD  R+ ++ +
Sbjct: 191 PGLKRGPADSKMGQKGAHTCDIIFEDCRVPAENIIGGVEGKGFKTAMKVLDRGRLHISAV 250

Query: 255 GTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYVYEVAKACDKG 314
             G+    ++E + Y  ERKQFG P+   QL+Q  +AD  T     R  V + A+  D G
Sbjct: 251 CVGVAERLVEESLNYAIERKQFGVPLAEHQLVQAMLADSKTEAYAGRTMVLDAARRKDAG 310

Query: 315 TVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLMEIGAGTSEIR 374
                 A+ C L+ +E+    A +AVQ  GGAGY+++  V R +RD +L  I  GT++I+
Sbjct: 311 ENASTLASCCKLFCAEMVGRVADRAVQVHGGAGYMAEYAVERFYRDVRLFRIYEGTTQIQ 370

Query: 375 RMLIGRELMSQM 386
           +++I R ++ ++
Sbjct: 371 QVVIARNMVREV 382


Lambda     K      H
   0.318    0.132    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: 384
Number of extensions: 23
Number of successful extensions: 3
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: 386
Length of database: 383
Length adjustment: 30
Effective length of query: 356
Effective length of database: 353
Effective search space:   125668
Effective search space used:   125668
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