GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Phyllobacterium brassicacearum STM 196

Align Sorbitol dehydrogenase; SDH; (R,R)-butanediol dehydrogenase; L-iditol 2-dehydrogenase; Polyol dehydrogenase; Ribitol dehydrogenase; RDH; Xylitol dehydrogenase; XDH; EC 1.1.1.-; EC 1.1.1.4; EC 1.1.1.14; EC 1.1.1.56; EC 1.1.1.9 (characterized)
to candidate WP_106713530.1 CU102_RS23605 L-idonate 5-dehydrogenase

Query= SwissProt::Q00796
         (357 letters)



>NCBI__GCF_003010955.1:WP_106713530.1
          Length = 343

 Score =  216 bits (549), Expect = 9e-61
 Identities = 125/330 (37%), Positives = 195/330 (59%), Gaps = 9/330 (2%)

Query: 11  SLVVHGPGDLRLENYPIPEPGPNEVLLRMHSVGICGSDVHYWEYGRIGNFIVKKPMVLGH 70
           ++V H   D+R+E+    + GP EV LR+ + GICGSD+HY+ +G  G   +K+PM+LGH
Sbjct: 3   AIVAHAAKDVRIEDVREEQAGPGEVKLRLATGGICGSDLHYYNHGGFGTVRLKQPMILGH 62

Query: 71  EASGTVEKVGSSVKHLKPGDRVAIEPGAPRENDEFCKMGRYNLSPSIFFCAT----PPDD 126
           E S TVE +G  V+    GD VA+ P  P  + ++C+ G +N   ++ F  +    P   
Sbjct: 63  EVSATVEALGEGVEGFAVGDLVAVSPSRPCRSCKYCQEGLHNQCLNMRFYGSAMPFPHIQ 122

Query: 127 GNLCRFYKHNAAFCYKLPDNVTFEEGALIEPLSVGIHACRRGGVTLGHKVLVCGAGPIGM 186
           G        +A  C    D +T  E A+ EPL+V +HA RR G  LG +VLV G GPIG+
Sbjct: 123 GAFRESLVADAFQCVPAGD-LTPGEAAMAEPLAVTLHATRRAGEMLGKRVLVTGCGPIGV 181

Query: 187 VTLLVAKAMGAAQVVVTDLSATRLSKAKEIGADLVLQISKESPQEIARKVEGQLGCKPEV 246
           +++L A+  GAA++V TDLS   L+ AK   AD  +  +K+ P+ +A     +     +V
Sbjct: 182 LSILSARRAGAAEIVATDLSDFTLAMAKTACADRTIN-TKDEPEALAAYSANK--GTFDV 238

Query: 247 TIECTGAEASIQAGIYATRSGGNLVLVGLGSEMTTVPLLHAAIREVDIKGVFRYCNTWPV 306
             EC+GA A++ +GI A R  G +V +GLG +M ++P++    +E+D++G FR+   +  
Sbjct: 239 LYECSGAAAALSSGIAALRPRGVIVQLGLGGDM-SLPMMAITAKELDLRGSFRFHEEFAT 297

Query: 307 AISMLASKSVNVKPLVTHRFPLEKALEAFE 336
            +S++ +  ++VKPL+TH   LE AL AFE
Sbjct: 298 GVSLMRNGLIDVKPLITHTVRLEDALLAFE 327


Lambda     K      H
   0.319    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: 18
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: 357
Length of database: 343
Length adjustment: 29
Effective length of query: 328
Effective length of database: 314
Effective search space:   102992
Effective search space used:   102992
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 (21.7 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