GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Tistlia consotensis USBA 355

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate WP_085125916.1 B9O00_RS27415 mandelate racemase/muconate lactonizing enzyme family protein

Query= BRENDA::A9CEQ8
         (378 letters)



>NCBI__GCF_900177295.1:WP_085125916.1
          Length = 382

 Score =  434 bits (1116), Expect = e-126
 Identities = 221/373 (59%), Positives = 265/373 (71%)

Query: 2   KITAVRTHLLEHRLDTPFESASMRFDRRAHVLVEIECDDGTVGWGECLGPARPNAAVVQA 61
           +I  VRTHLLEHRL   FES+  RF+ R   LVE+  +DGT GWGECLGP R NAAVV A
Sbjct: 6   RIADVRTHLLEHRLHDFFESSFSRFEARHACLVEVVAEDGTSGWGECLGPMRLNAAVVAA 65

Query: 62  YSGWLIGQDPRQTEKIWAVLYNALRDQGQRGLSLTALSGIDIALWDIKGKHYGASISMLL 121
               L+GQD    E++W  LY+  RDQGQRGL +TALSGI+IALWD+KGK + A +  LL
Sbjct: 66  MRPLLLGQDALDHERLWLHLYSQFRDQGQRGLVVTALSGIEIALWDLKGKRFEAPVHQLL 125

Query: 122 GGRWRESVRAYATGSFKRDNVDRVSDNASEMAERRAEGFHACKIKIGFGVEEDLRVIAAV 181
           GG +R+ V AYATG+F+R + DR +  A E A    EGF A KIKIG+GVEEDL  I AV
Sbjct: 126 GGAFRKEVPAYATGAFRRMSGDRPAYLAEETAGYVREGFSAVKIKIGYGVEEDLAAIRAV 185

Query: 182 REAIGPDMRLMIDANHGYTVTEAITLGDRAAGFGIDWFEEPVVPEQLDAYARVRAGQPIP 241
           REAIGP    MIDANHGY   EA+ LG  AA   I WFEEPVVPE L+ Y  VRAGQPIP
Sbjct: 186 REAIGPKAGFMIDANHGYDALEAVALGRAAAACDIGWFEEPVVPEDLEGYRAVRAGQPIP 245

Query: 242 VAGGETWHGRYGMWQALSAGAVDILQPDLCGCGGFSEIQKIATLATLHGVRIVPHVWGTG 301
           VAGGETW  R+G    +++  VDILQPD+CG GG SE  +IA +A+  G+R+VPHVWGTG
Sbjct: 246 VAGGETWFTRWGFRDVMTSRLVDILQPDVCGVGGLSEACRIAGMASAFGLRLVPHVWGTG 305

Query: 302 VQIAAALQFMAAMTPDPVRVNPIEPIMEFDRTHNPFRQAVLREPLEAVNGVVTIPDGPGL 361
           V +AAALQ++A + P P R    EP++EFDRT NPFRQAVL  P+E   G V +P+GPGL
Sbjct: 306 VALAAALQYLAVLPPVPPRHESREPLLEFDRTDNPFRQAVLTAPIEHREGRVAVPEGPGL 365

Query: 362 GIEINRDALTEFR 374
           GIE+ R AL  F+
Sbjct: 366 GIEVERAALERFK 378


Lambda     K      H
   0.321    0.138    0.431 

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: 520
Number of extensions: 16
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: 378
Length of database: 382
Length adjustment: 30
Effective length of query: 348
Effective length of database: 352
Effective search space:   122496
Effective search space used:   122496
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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