GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Pantoea rwandensis LMG 26275

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_084932508.1 HA51_RS04785 NAD(P)-dependent alcohol dehydrogenase

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_002095475.1:WP_084932508.1
          Length = 344

 Score =  263 bits (672), Expect = 5e-75
 Identities = 128/340 (37%), Positives = 202/340 (59%), Gaps = 2/340 (0%)

Query: 10  KAAVMHNTREIKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYVVEKPFILG 69
           +AA + + R++++    +P+++ DEV+I++  +G+CGSD+H+Y +G    +    PFILG
Sbjct: 4   RAAFVLDNRKMEVRDTVMPELHPDEVMIRMKKIGVCGSDVHFYEHGE-PEFPDVYPFILG 62

Query: 70  HECAGEIAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATPPVDGAF 129
           HE AGE+  VG++V   K GDRV +EPGV C  CE C  G+YNLCP V F + P   G  
Sbjct: 63  HEGAGEVVEVGAAVSHLKAGDRVCLEPGVPCRVCEWCTSGKYNLCPTVYFPSAPRALGMM 122

Query: 130 VQYIKMRQDFVFLIPDSLSYEEAALIEPFSVGIHAAARTKLQPGSTIAIMGMGPVGLMAV 189
             +I  + D  F +PD++S++E AL+EP +VGIHA   + ++ G +  I+G G +GL+ +
Sbjct: 123 RNFITHKADLCFKLPDNVSFQEGALVEPLAVGIHAVRESGIKMGQSATILGSGCIGLVTL 182

Query: 190 AAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEEIKTITNDRGVDVAWETA 249
            + KA G   I V D+  +RLE AK++GA H+IN    D +  +K +    G D  +ETA
Sbjct: 183 LSLKAAGVDDITVVDIHDIRLEKAKELGARHLINASNTDMISAVKDVYGGIGPDFIFETA 242

Query: 250 GNPAALQSALASVRRGGKLAIVGLPSQNEIPLNVPFIADNEIDIYGIFRYANTYPKGIEF 309
           GN     +++  ++RGG + I+G     + P+N   + + E  I   FRY N YP  +  
Sbjct: 243 GNRVTASNSVPMIKRGGTIMIIG-NVVGDTPVNFQMLGNKEATIKATFRYRNIYPSALSA 301

Query: 310 LASGIVDTKHLVTDQYSLEQTQDAMERALQFKNECLKVMV 349
           L+SG ++   +V+D Y  E TQ A E ++  K   +K M+
Sbjct: 302 LSSGRINVNSIVSDFYKFEDTQSAFEDSINNKATVVKAMI 341


Lambda     K      H
   0.320    0.137    0.401 

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: 310
Number of extensions: 16
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: 353
Length of database: 344
Length adjustment: 29
Effective length of query: 324
Effective length of database: 315
Effective search space:   102060
Effective search space used:   102060
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