GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Pseudarthrobacter sulfonivorans Ar51

Align Sorbitol dehydrogenase; SDH; Polyol dehydrogenase; EC 1.1.1.- (characterized)
to candidate WP_058930523.1 AU252_RS09660 L-idonate 5-dehydrogenase

Query= SwissProt::P0DMQ6
         (355 letters)



>NCBI__GCF_001484605.1:WP_058930523.1
          Length = 382

 Score =  202 bits (513), Expect = 2e-56
 Identities = 128/356 (35%), Positives = 182/356 (51%), Gaps = 25/356 (7%)

Query: 9   AVVVHRAGDLRLENRPIPEPGPNEVLLRMHSVGICGSDVHYWQHGRIGDFVVKDPMVLGH 68
           AVV H AGDLR+E+ P+  P  ++ ++ +   GICGSD+HYW HG  G+ V+K PMVLGH
Sbjct: 23  AVVAHAAGDLRVEDIPLTPPPADQAVVEIAYGGICGSDLHYWLHGAAGESVLKAPMVLGH 82

Query: 69  EASGTVIKVGAGVTHLKPGDRVAIEPGVPRETDEF------CKTGRYNLSPTIFFCAT-- 120
           E  G V++  A  T    G  VA+ P  P                R NLSP   +  +  
Sbjct: 83  EIVGVVVRAAADGTGPAEGCAVAVHPATPGPGPGAGPGIVKYPEDRPNLSPGCTYLGSAA 142

Query: 121 --PPDDGNLCRYYKHSASYCYKLPDSVTFEEGALIEPLSVGIHACKRAGVTLGSRVFVSG 178
             P  +G   RY          LPD +  +  ALIEP SV  HA  RAG   G    V G
Sbjct: 143 RFPHTNGAFSRYSNLPTRMLRVLPDGLDLKTAALIEPASVAWHAVARAGDVAGKTALVIG 202

Query: 179 SGPIGLVNVIIAKMMGAAAVVVTDLSASRLQTAKELGADFTIQIKNETPQEVAAKVESLL 238
           SGPIG + V + K  GAA +   D+ A  L+ A  +GAD  +Q         A   E+++
Sbjct: 203 SGPIGALVVAVLKRAGAARITAVDMHAKPLEIAAAVGADEVLQ---------AGDAEAIV 253

Query: 239 GCMPEITVECTGVQACIQASIYATRSGGTLVLVGL---GPEMVTVPIVNAAVREVDIRGI 295
               ++ +E +G    + ++I     GG +V+VGL   GP+ V + +  A  RE+++ G 
Sbjct: 254 AVQADVVIESSGSHHGLASAIKGAVRGGKVVMVGLLPSGPQPVLISL--AITRELELLGS 311

Query: 296 FRYCNTWPVAISLLASKRINIKPLVTHRFPLEKALEAFETTKR-GEGVKIMLKCDP 350
           FR+ +     I+ LA   + + P++TH FPLE+ LEAFET K   E  K++L   P
Sbjct: 312 FRFNDEIDDVITALADGSLFVDPVITHVFPLERGLEAFETAKNSAESGKVLLSFAP 367


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: 436
Number of extensions: 28
Number of successful extensions: 4
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: 382
Length adjustment: 30
Effective length of query: 325
Effective length of database: 352
Effective search space:   114400
Effective search space used:   114400
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 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