GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucD in Tistlia consotensis USBA 355

Align L-fuconate dehydratase; FucD; EC 4.2.1.68 (characterized)
to candidate WP_085121732.1 B9O00_RS06885 mandelate racemase/muconate lactonizing enzyme family protein

Query= SwissProt::Q8P3K2
         (441 letters)



>NCBI__GCF_900177295.1:WP_085121732.1
          Length = 383

 Score =  112 bits (281), Expect = 2e-29
 Identities = 94/339 (27%), Positives = 143/339 (42%), Gaps = 61/339 (17%)

Query: 98  QLRWLGP----EKGVMHMAIGAVINAAWDLAARAANKPLWRFIAELTPEQLVDTIDFRYL 153
           Q R + P     +G  HMAI A+  A WD   R A +P+   +                 
Sbjct: 84  QARMVAPLAIDRRGQCHMAISALDIALWDAWGRIAGQPIHALLG---------------- 127

Query: 154 SDALTRDEALAILRDAQPQRAARTATLIEQGYPAYTTSPGWLGYSDEKLVRLAKEA---V 210
                       LRD                 PAY + P +L  + ++   LA E     
Sbjct: 128 ----------GALRDR---------------VPAYASGP-FLEAAPDRYGALAGEVERYA 161

Query: 211 ADGFRTIKLKVGANVQDDIRRCRLARAAIGPDIAMAVDANQRWDVGPAIDWMRQLAEFDI 270
           A GFR IKL+VG ++  D    R AR+ +G +  +  D N+   V  A+     +A+  +
Sbjct: 162 AAGFRAIKLRVGTDLATDASAIRQARSILGAEALLMADLNEGSTVRDAVALTEAVADARL 221

Query: 271 AWIEEPTSPDDVLGHAAIRQGITPVPVSTGEHTQNRVVFKQLLQAGAVDLIQIDAARVGG 330
           +WIEEP   DD+ G+  + Q +  +P++ GE       F+  L AGA+D++Q D A  GG
Sbjct: 222 SWIEEPIPHDDLPGYRRLAQ-LLSLPLAGGESFSGTQAFRDFLAAGALDIVQPDLAICGG 280

Query: 331 VNENLAILLLAAKFGVRVFPHAGGVGLCELVQHLAMADFVAI----TGKMEDRAIEF--- 383
           + E L +  LA  F   V PH  G G    +  LA   F A+     G +     E+   
Sbjct: 281 LTEGLRVAALADAFETAVAPHVWGTG----INFLASLQFAAVLTPRRGPVPFPLFEYDMG 336

Query: 384 VDHLHQHFLDPVRIQHGRYLAPEVPGFSAEMHPASIAEF 422
           ++ L     DP   + GR   P+ PG   E+    +A++
Sbjct: 337 INPLRSALYDPQPDRDGRLAVPDGPGLGIEISIDRLADY 375


Lambda     K      H
   0.321    0.136    0.409 

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: 475
Number of extensions: 30
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: 441
Length of database: 383
Length adjustment: 31
Effective length of query: 410
Effective length of database: 352
Effective search space:   144320
Effective search space used:   144320
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