GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fadA in Halomonas xinjiangensis TRM 0175

Align 3-ketoacyl-CoA thiolase [isoleucine degradation] (EC 2.3.1.16) (characterized)
to candidate WP_043527088.1 JH15_RS03630 acetyl-CoA C-acyltransferase

Query= reanno::MR1:200842
         (396 letters)



>NCBI__GCF_000759345.1:WP_043527088.1
          Length = 394

 Score =  469 bits (1208), Expect = e-137
 Identities = 235/388 (60%), Positives = 305/388 (78%)

Query: 9   EIVIVAAKRTPMGSFQGSLSGITSLSLAATAIKALLADTQVAPDKVDEVLMGCVLPAGLG 68
           +IVI++A RTPMG  QGSLS +T+  LAATAI+A L   ++    +DE ++GCVLP G+ 
Sbjct: 5   DIVILSAARTPMGGMQGSLSSLTAPELAATAIRAALERAKLDSTSIDEGILGCVLPGGVK 64

Query: 69  QAPARQATLGAGLPLSVGATTVNKVCGSGMKTVMLAHDLIKAGSAKVVIAGGMESMSQAP 128
           Q PARQA   AG+P ++GATT+NK+CGSGMK  MLAHDLI+AGS ++V+AGGMESMS AP
Sbjct: 65  QGPARQAMRQAGIPDAIGATTINKLCGSGMKAAMLAHDLIRAGSGEIVLAGGMESMSNAP 124

Query: 129 YLLDKARAGIRMGHGKVLDHMFLDGLEDAYTGGAMGTFAQKTADEFGITREQMDAFALSS 188
           ++L KAR+G R+GHG++ DHMF DGLEDA TG  MG FAQ+ ADE G +RE+MD FA++S
Sbjct: 125 HILTKARSGYRLGHGELKDHMFYDGLEDAETGKLMGVFAQQVADERGYSRERMDDFAIAS 184

Query: 189 LEKANAAINSGAFKTEIVPVTVSDRRGDVTIDTDEQPGNARPEKIPTLRPAFAKDGTITA 248
           LE+A AA  +G  K E+ PVTV+ R+GD  +D DEQP  A+ +KI TLRPAFAKDGTITA
Sbjct: 185 LERAMAAHEAGHLKGEMAPVTVTTRQGDSVVDHDEQPFQAKLDKIRTLRPAFAKDGTITA 244

Query: 249 ANSSSISDGAAALMLTTRANAEQLGLTVLATIKGHTTHAQEPALFTTAPVGAMAKLLSNV 308
           AN+SSISDGA+AL+L +++ A+Q G   +A + GH TH+Q P+ FT APVGA+ KLL  +
Sbjct: 245 ANASSISDGASALILASQSAADQHGACPIARMLGHATHSQHPSEFTVAPVGAIDKLLKKL 304

Query: 309 GWSKDEVDLFEINEAFAMVTMLAVSELGLDMTKVNVNGGACALGHPIGCSGARLLVTLIH 368
            W  ++VDLFEINEAFA+VT+LA+  L +   KVNV GGACA GHP+G +G+R++ TLI+
Sbjct: 305 RWGVNDVDLFEINEAFAVVTLLAMDGLSISHDKVNVFGGACAQGHPVGSTGSRIIATLIN 364

Query: 369 ALKARGLKRGVASLCIGGGEATAMAIEV 396
           AL+ +G +RGVASLCIGGGEATA+AIE+
Sbjct: 365 ALRVKGGRRGVASLCIGGGEATAVAIEL 392


Lambda     K      H
   0.316    0.131    0.364 

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: 493
Number of extensions: 13
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: 396
Length of database: 394
Length adjustment: 31
Effective length of query: 365
Effective length of database: 363
Effective search space:   132495
Effective search space used:   132495
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 (21.6 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