GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garD in Pedobacter sp. GW460-11-11-14-LB5

Align L-talarate dehydratase (EC 4.2.1.156); galactarate dehydratase (EC 4.2.1.42) (characterized)
to candidate CA265_RS12250 CA265_RS12250 enolase

Query= BRENDA::Q8ZL58
         (398 letters)



>FitnessBrowser__Pedo557:CA265_RS12250
          Length = 388

 Score =  139 bits (351), Expect = 1e-37
 Identities = 118/370 (31%), Positives = 177/370 (47%), Gaps = 35/370 (9%)

Query: 40  LATPVSDAKVLTGRQKPLTEVAIIIAEIRSRDGFEGVGFSYSKRAGGQGIYAHAKEIADN 99
           L  P+ +AK        LT   + +  I +  G +G G + +   G  GI A      +N
Sbjct: 11  LRCPIPEAKQHVSDYGLLTSFDMTLVVITTDSGLQGFGEAKAA-VGSCGICASIVNCIEN 69

Query: 100 -----LLGEDPNDIDKIYTKL---------LWAGAS---VGRSGMAVQAISPIDIALWDM 142
                LLG+   +I +++ ++         L  G     +GR G+ + A+S ID ALWD+
Sbjct: 70  ELKPMLLGKSVKNITRLWEEMYNGTRDHYALSRGRKFPILGRRGLTISAMSGIDTALWDL 129

Query: 143 KAKRAGLPLAKLLG-AHRDSVQCYNTSGGFLHTPLDQVLKNVVISRENGIGGIKLKVG-- 199
           K K   +P+A LLG A R  +  Y + G      + + L   V     G  G+K++VG  
Sbjct: 130 KGKMLNVPVADLLGGACRTKMPAYASGGWADEQNIGEQLMGYV---NKGFKGVKMRVGVM 186

Query: 200 QPNCAEDIRRLTAVREALGDEFPLMVDANQQWDRETAIRMGRKMEQFNLIWIEEPLDAYD 259
                + I R+ A R ALG +  LMVDA+  +    A +  R +E  N+ W EEP+   +
Sbjct: 187 DDTVQKSINRVKAARAALGPDIKLMVDAHGTFSVPEAKQFCRGVEDCNVYWFEEPISPDN 246

Query: 260 IEGHAQLAAALDTPIATGEM-LTSFREHEQLILGNASDFVQPDAPRVGGISPFLKIMDLA 318
            +G A++ AA D PIA GE   TSF  H+ L +  A D VQPDA  +GGIS  +++  LA
Sbjct: 247 RKGTAEVRAATDIPIAAGESEFTSFDIHDLLQI-RAIDVVQPDAAIIGGISEAMRVSHLA 305

Query: 319 AKHGRKLAPH-----FAMEVHLHLSAAYPLEPWLEHFEWLNP----LFNEQLELRDGRMW 369
           + H  +LAPH     F+    L ++ A      +E     NP    L NEQ+ + +G + 
Sbjct: 306 SVHQVELAPHCWGSAFSFMAGLTVAFASASATIIEFSLGGNPMMYDLVNEQIAVVNGEIS 365

Query: 370 ISDRHGLGFT 379
                GLG T
Sbjct: 366 APTAPGLGLT 375


Lambda     K      H
   0.319    0.136    0.410 

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: 356
Number of extensions: 22
Number of successful extensions: 2
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: 398
Length of database: 388
Length adjustment: 31
Effective length of query: 367
Effective length of database: 357
Effective search space:   131019
Effective search space used:   131019
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 17 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