GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA3 in Sinorhizobium meliloti 1021

Align L-rhamnonate dehydratase; RhamD; EC 4.2.1.90 (uncharacterized)
to candidate SM_b21107 SM_b21107 mandelate racemase or evolutionary related enzyme of the mandelate racemase muconate lactonizing enzyme family protein

Query= curated2:A9BQY2
         (395 letters)



>FitnessBrowser__Smeli:SM_b21107
          Length = 370

 Score =  123 bits (309), Expect = 8e-33
 Identities = 98/311 (31%), Positives = 140/311 (45%), Gaps = 28/311 (9%)

Query: 59  TLVVEIEDSAGRVG----FAVTTGGEPAAYIVEKHLARFLEGARVTDIERIWDQMYLSTL 114
           T +V I D+ G  G    + + TGG     ++  HL   L G     IE +W +M  +T 
Sbjct: 32  TPIVTITDADGATGTGYSYTIGTGGSSVMRLLSDHLVPILLGEDADCIEALWQKMEFATH 91

Query: 115 YYGRKGIVINTISGVDLALWDLLGKVRGEPVHQLLGGAVRDELQFYATG---------AR 165
                 I    ++ VD ALWDL  K +  P+ +L GGA ++    Y T          A 
Sbjct: 92  ATTIGAITALALAAVDTALWDLRAKKQKLPLWKLAGGA-KESCPLYTTEGGWLHIEKQAL 150

Query: 166 PD---LAQKMGFIGGKMPLHHGPAEGEEGLRRNLQELATMRERVGPDFWLMLDCWMSLDV 222
            D    A+  GF G K+ +  G   G E   R    L+ MR  +G  F +M DC     V
Sbjct: 151 VDDALQAKANGFSGSKVKI--GKPSGAEDYDR----LSAMRAALGDGFEIMTDCNQGFTV 204

Query: 223 NYATRLAQGAQAHGLKWIEEALPPDDYWGYAALRKNVPTGMLVTTGEHEATRWGFRQLLE 282
           + A R A   +   L WIEE LP DD  G+  L ++ PT + V  GE   +   FR+ ++
Sbjct: 205 DEAIRRAARLRELDLAWIEEPLPADDLDGHIRLTRSTPTPIAV--GESIYSIRHFREYMQ 262

Query: 283 MGCCDIIQPDVGWCGGITELLKISALADAHQALVIPHGSSVYSYHFVATRHNSPFAEFLM 342
            G C I+Q DV   GGIT  LK++  A+A    V PH         V    N  + E++ 
Sbjct: 263 KGACSIVQVDVARIGGITPWLKVAHAAEAFDIPVCPHFLMELHVSLVCAVPNGKYVEYI- 321

Query: 343 MAPKADEVVPM 353
             P+ D++  M
Sbjct: 322 --PQLDDLTQM 330


Lambda     K      H
   0.322    0.139    0.442 

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: 383
Number of extensions: 21
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: 395
Length of database: 370
Length adjustment: 30
Effective length of query: 365
Effective length of database: 340
Effective search space:   124100
Effective search space used:   124100
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 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