GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Cupriavidus basilensis 4G11

Align Sorbitol dehydrogenase; SDH; Polyol dehydrogenase; EC 1.1.1.- (characterized)
to candidate RR42_RS35005 RR42_RS35005 L-idonate 5-dehydrogenase

Query= SwissProt::P0DMQ6
         (355 letters)



>FitnessBrowser__Cup4G11:RR42_RS35005
          Length = 342

 Score =  194 bits (494), Expect = 2e-54
 Identities = 111/332 (33%), Positives = 179/332 (53%), Gaps = 13/332 (3%)

Query: 7   NLAVVVHRAGDLRLENRPIPEPGPNEVLLRMHSVGICGSDVHYWQHGRIGDFVVKDPMVL 66
           +L   +H + DLR        PGP EV +R+ + GICGSD+HY+ HG++G FV+++P+  
Sbjct: 2   SLVCHIHASEDLRFTQVEPAAPGPFEVEVRLGAAGICGSDLHYYFHGKVGAFVIREPLTP 61

Query: 67  GHEASGTVIKVGAGVTHLKPGDRVAIEPGVPRETDEFCKTGRYNLSPTIFFCAT----PP 122
           GHEA+G V +VG+ VT + PG++VAI P       ++C+ GR NL  ++ F  +    P 
Sbjct: 62  GHEAAGIVSRVGSAVTRVAPGNKVAINPSHACGQCDYCRAGRDNLCRSMRFLGSASIYPH 121

Query: 123 DDGNLCRYYKHSASYCYKLPDSVTFEEGALIEPLSVGIHACKRAGVTLGSRVFVSGSGPI 182
             G    ++         +   ++  E A  EPLSV +H   RAG  LG  V V+G G I
Sbjct: 122 VQGMFREHFLMHERQLTPVDSDISLGELAFAEPLSVALHGVNRAGELLGKTVLVTGGGTI 181

Query: 183 GLVNVIIAKMMGAAAVVVTDLSASRLQTAKELGADFTIQIKNETPQEVAAKVESLLGCMP 242
           G + V+ A++ GAA ++  D++   L+ A  +GAD  I+   E P+         L  + 
Sbjct: 182 GSLAVMAARLAGAAHIIACDIADRPLEVALRVGADQVIRTDREPPR--------ALQDLA 233

Query: 243 EITVECTGVQACIQASIYATRSGGTLVLVGLGP-EMVTVPIVNAAVREVDIRGIFRYCNT 301
           ++ +E  G  A +   + A R G  +V +G  P E +  P  N   RE++  G FR+   
Sbjct: 234 DVCLEAAGSGAALDTCLLAARRGARIVQIGTLPAEGLHFPANNIMARELEYVGAFRFGRE 293

Query: 302 WPVAISLLASKRINIKPLVTHRFPLEKALEAF 333
           +  A+  L   R++++PL++ + PL +A+EAF
Sbjct: 294 FDWAVRYLTQGRLDVRPLLSAQLPLAQAVEAF 325


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: 313
Number of extensions: 17
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: 342
Length adjustment: 29
Effective length of query: 326
Effective length of database: 313
Effective search space:   102038
Effective search space used:   102038
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 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