GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaS in Sinorhizobium meliloti 1021

Align RhaS, component of Rhamnose porter (Richardson et al., 2004) (Transport activity is dependent on rhamnokinase (RhaK; AAQ92412) activity (Richardson and Oresnik, 2007) This could be an example of group translocation!) (characterized)
to candidate SM_b21016 SM_b21016 sugar ABC transporter substrate-binding protein

Query= TCDB::Q7BSH5
         (331 letters)



>FitnessBrowser__Smeli:SM_b21016
          Length = 343

 Score =  172 bits (435), Expect = 1e-47
 Identities = 100/312 (32%), Positives = 172/312 (55%), Gaps = 8/312 (2%)

Query: 3   LAKTLALGVALAVAMMAGTASAK-----DIKIGLVVKSLGNGFFDAANKGAQEAAKELGG 57
           + KT+    ALA A++AGT  A      + +I  + K +G GFF +   GA +A +E+G 
Sbjct: 1   MIKTIMKSSALAAALLAGTVLASGAAHAENQIAFIPKLVGVGFFTSGGAGAVKAGEEVGA 60

Query: 58  VEVIYTGPTSTTAEGQIEVINSLIAQGVDAIAVSANDPDALVPALKKATQRGIKVISWDS 117
            +V Y GPT  +  GQ++ IN+ + QG +A+ VS+  PD L PALK+A +RG+ V++WDS
Sbjct: 61  -KVTYDGPTEPSVSGQVQFINNFVNQGYNALIVSSVSPDGLCPALKRAMERGVLVMTWDS 119

Query: 118 GVAPEGRILQLNPSSNELIGKMCLTLAKDHLEGGKGDFAILSATTTSTNQNIWIDQMKKQ 177
            V P+ R   +N  + E +G + + +A + ++  K   A   ++ T T+QN W +  K +
Sbjct: 120 DVNPDCRSYYINQGTPEQLGGLLVDMAAEGVKKEKAKVAFFYSSPTVTDQNAWAEAAKAK 179

Query: 178 L-KDFPGLNLVTTVYGDDLSDKSYREAEGLLKSNPNVKVIVAPTTVGVLAASKVVEDKGL 236
           + K+ PG  +VTT YG + + KS + AE +L++ P++  I+AP    + AA++  E+   
Sbjct: 180 IAKEHPGWEIVTTQYGYNDAQKSLQTAESILQTYPDLDAIIAPDANALPAAAQAAENLKR 239

Query: 237 VGKVYVTGLGLPSEMAGAIKSGATKEFAIWNPIDLGYSATQIAYRLVKGETDGKPGSEIN 296
              V + G   P+ M   I+ G  + F +W+    G  +  +A  ++K     K G ++ 
Sbjct: 240 AEGVTIVGFSTPNVMRPYIERGTIQRFGLWDVTQQGKISVFVADHVLK-NGPMKVGEKLE 298

Query: 297 AGRMGKIKVGDN 308
              +G ++V  N
Sbjct: 299 IPGVGTVEVSAN 310


Lambda     K      H
   0.313    0.131    0.365 

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: 263
Number of extensions: 8
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: 331
Length of database: 343
Length adjustment: 28
Effective length of query: 303
Effective length of database: 315
Effective search space:    95445
Effective search space used:    95445
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 (21.9 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