GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bmpA in Sinorhizobium meliloti 1021

Align RnsA, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized)
to candidate SMc02884 SMc02884 lipoprotein

Query= TCDB::Q8DU36
         (349 letters)



>FitnessBrowser__Smeli:SMc02884
          Length = 330

 Score =  144 bits (362), Expect = 4e-39
 Identities = 111/341 (32%), Positives = 167/341 (48%), Gaps = 35/341 (10%)

Query: 15  VLGLAACGNRAAREKGKAKTDLKVAIVTDTGGVDDKSFNQSAWEGLQAWGKDNGLSKGNG 74
           +LGL A    +A        D+K AI+ D GG  DKSFN++A+ G + +  + G+     
Sbjct: 5   ILGLLAFSMMSATALA---ADIKPAIIYDLGGKFDKSFNEAAFNGAEKFKTETGIE---- 57

Query: 75  FDYFQSASESDYATNLDTASSSGYKLIFGIGYALHDAIEKTAADNKNIHYVIIDDVIQKK 134
           +  F+ A+++     L   +S G   I   G+    ++EK A +  +  + IID V++K 
Sbjct: 58  YREFEIANDAQREQALRRFASDGNSPIVMAGFNWAASLEKLAGEYPDTKFAIIDMVVEKP 117

Query: 135 NNVASVTFADNEAAYLAGIAAAKTTKSKKVGFVGGVKSEVITRFEKGFEAGVKSVDSSIQ 194
           N V S+ F + E +YL G+ A   +K+K V FVGG+   +I +F  G+  G KS  + ++
Sbjct: 118 N-VKSIVFKEQEGSYLVGVLAGLASKTKTVSFVGGMDIPLIHKFACGYVGGAKSTGADVK 176

Query: 195 IQVDYAG----SFGDAAKGKTIAAAQYASGADVIYQAAGGTGAGVFSEAKAVNEKKKENK 250
           +   Y G    ++ D  KG  IA +Q   G+DV+Y AAGGTG GV   A    +      
Sbjct: 177 VLEAYTGTTPDAWNDPVKGGEIAKSQIDQGSDVVYHAAGGTGVGVLQAAADAGKLG---- 232

Query: 251 KVWVIGVDRDQAAEGKYTSKDGKKSNFVLASSLKEVGKAVQLISTNTSKKKFPGGKVTTY 310
               IGVD +Q        + GK    VL S LK V  AV          KF  G ++  
Sbjct: 233 ----IGVDSNQ-----NMLQPGK----VLTSMLKRVDVAVYDSFMAAKDDKFEFG-ISNL 278

Query: 311 GLKDKGVDLV-----PTHLSKEGKKAVDDAKKKIVSGDVKV 346
           GLK+ GV           ++ E K+AV+  K  I+SG V+V
Sbjct: 279 GLKEDGVGYALDEHNQVLITPEMKEAVEKVKADIISGKVQV 319


Lambda     K      H
   0.310    0.128    0.352 

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: 280
Number of extensions: 13
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: 349
Length of database: 330
Length adjustment: 28
Effective length of query: 321
Effective length of database: 302
Effective search space:    96942
Effective search space used:    96942
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.7 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