GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Sinorhizobium meliloti 1021

Align Erythritol/L-threitol dehydrogenase; EC 1.1.1.- (characterized)
to candidate SM_b20853 SM_b20853 sugar-alcohol dehydrogenase

Query= SwissProt::A0QXD8
         (362 letters)



>FitnessBrowser__Smeli:SM_b20853
          Length = 339

 Score =  138 bits (348), Expect = 2e-37
 Identities = 105/341 (30%), Positives = 155/341 (45%), Gaps = 33/341 (9%)

Query: 9   MQAVVCHGPHDYRLEEVAVPQRKPGEALIRVEAVGICASDLKCYHGAAKFWGDENRPAWA 68
           M+A+V H P D RLE    P   PGE L+RV +VG+C SDL              + AW 
Sbjct: 1   MRAIVLHAPGDIRLETRPKPVAGPGEVLLRVASVGVCGSDLPRMLV---------KGAW- 50

Query: 69  ETMVIPGHEFVGRVVELDDEAAQRWGIAVGDRVVSEQIVPCWECLFCKRGQYHMCQPHDL 128
           +  +I GHEF G +  L +      G  +G+      ++PC +C+ CK G +  C+ +D 
Sbjct: 51  KMPLITGHEFSGHIHALGENVE---GWEIGELTAIAPLMPCNQCIECKTGNFSRCRDYDY 107

Query: 129 YGFKRRTPGAMASYMVYPAEALVHKVSPDIPAQHAAFAEPLSCSLHAVERAQ-ITFEDTV 187
           +G +R   GA A ++  P E L+ K    +  +  A  +P S +LHA+ +A  IT   T 
Sbjct: 108 FGSRR--DGAYAEFVAVPVENLI-KTPQHVDPRAIAMTDPASIALHAIWKAGGITAGQTG 164

Query: 188 VVAGCGPIGLGMIAGAKAKSPMRVIALDMAPDKLKLAEKCGADLTINIAEQDAEKIIKDL 247
            V GCGPIGL  I   +     RVIA+D+  +KL LA + GADL I  A+    K     
Sbjct: 165 AVVGCGPIGLFAIQWMRIMGTSRVIAVDVTEEKLALARQAGADLCILSADFADNK----- 219

Query: 248 TGGYGADVYIEGTGHTSAVPQGLNLLRKLGRYVEYGVFGSDVTVDWSI--------ISDD 299
                AD+ IE  G  S +   + L    G     G+   DV +  +         +S  
Sbjct: 220 ---ERADLVIEAVGIDSTINAAVMLAAPGGHVTFIGIPVPDVKLSNATFQRFLRQEVSLH 276

Query: 300 KELDVLGAHLGPYCWPAAIKMIESGALPMDEICTHQFPLTE 340
              +  GA      W   ++   +G L  + + +H   L E
Sbjct: 277 GSWNSFGAPFPGPQWTTTVQKFATGELKWEFMISHDLDLAE 317


Lambda     K      H
   0.320    0.137    0.428 

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: 343
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: 362
Length of database: 339
Length adjustment: 29
Effective length of query: 333
Effective length of database: 310
Effective search space:   103230
Effective search space used:   103230
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