GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Belnapia rosea CPCC 100156

Align Sorbitol dehydrogenase; SDH; Polyol dehydrogenase; EC 1.1.1.- (characterized)
to candidate WP_090560791.1 BLR02_RS02430 L-idonate 5-dehydrogenase

Query= SwissProt::P0DMQ6
         (355 letters)



>NCBI__GCF_900101615.1:WP_090560791.1
          Length = 343

 Score =  197 bits (500), Expect = 4e-55
 Identities = 120/343 (34%), Positives = 184/343 (53%), Gaps = 9/343 (2%)

Query: 9   AVVVHRAGDLRLENRPIPEPGPNEVLLRMHSVGICGSDVHYWQHGRIGDFVVKDPMVLGH 68
           +VV+H   DLR+E      PG  +V +R+ + GICGSD+HY+ HG  G   +++PMVLGH
Sbjct: 3   SVVIHAPKDLRIEEAAAVAPGAGQVAIRIKAGGICGSDLHYYLHGGFGAVRLREPMVLGH 62

Query: 69  EASGTVIKVGAGVTHLKPGDRVAIEPGVPRETDEFCKTGRYNLSPTIFFCAT----PPDD 124
           E +G V  +G GV  L PG  VA+ P +P      C  GR N    + F  +    P   
Sbjct: 63  EIAGIVEALGEGVQGLSPGQAVAVNPSLPCGACRQCLAGRPNHCLDMRFYGSAMRMPHVQ 122

Query: 125 GNLCRYYKHSASYCYKLPDSVTFEEGALIEPLSVGIHACKRAGVTLGSRVFVSGSGPIGL 184
           G         A     LP  +     A  EPL+V +HA ++AG  LG+RV V+G+GPIG 
Sbjct: 123 GGFSELLVCEAERAVPLPAGMAPALAAFAEPLAVCLHAARQAGPMLGARVLVTGAGPIGN 182

Query: 185 VNVIIAKMMGAAAVVVTDLSASRLQTAKELGADFTIQIKNETPQEVAAKVESLLGCMPEI 244
           + + +A+  GA  VVVTDL ++ L TA+ +GAD T+ +  +    +   ++   G   ++
Sbjct: 183 LAIAVARHAGAREVVVTDLHSTPLLTARRMGADRTLSMSEDPDGLLPYAIDK--GYF-DL 239

Query: 245 TVECTGVQACIQASIYATRSGGTLVLVGLGPEMVTVPIVNAAVREVDIRGIFRYCNTWPV 304
             E +G  A + ++I   R G  +V +GLG + V +P+     +EV +RG FR+   +  
Sbjct: 240 VFEASGSGAALASAIQVARPGAVIVQLGLGGD-VGLPLSALVAKEVALRGTFRFHEEFAQ 298

Query: 305 AISLLASKRINIKPLVTHRFPLEKALEAFE-TTKRGEGVKIML 346
           A+ +LA   I+ +PL+T   P+  A+ AFE    R   +K+ L
Sbjct: 299 AVEVLARGAIDPRPLLTATMPMADAVAAFELAADRSRAMKVQL 341


Lambda     K      H
   0.320    0.137    0.415 

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: 328
Number of extensions: 24
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: 355
Length of database: 343
Length adjustment: 29
Effective length of query: 326
Effective length of database: 314
Effective search space:   102364
Effective search space used:   102364
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: 49 (23.5 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