GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaS in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

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 WP_068170334.1 HTA01S_RS10215 rhamnose ABC transporter substrate-binding protein

Query= TCDB::Q7BSH5
         (331 letters)



>NCBI__GCF_001592305.1:WP_068170334.1
          Length = 330

 Score =  388 bits (997), Expect = e-113
 Identities = 202/333 (60%), Positives = 256/333 (76%), Gaps = 5/333 (1%)

Query: 1   MKLAKTLALGVALAVAMMAGTASAKDIKIGLVVKSLGNGFFDAANKGAQEAAKELGGVEV 60
           MK ++      ALA+A+ A  A A D KI LVVKSLGNGFFDAA++GA EAAKEL  VE+
Sbjct: 1   MKKSRFALTAAALALAL-AQPAFAAD-KIALVVKSLGNGFFDAAHQGALEAAKELKDVEI 58

Query: 61  IYTGPTSTTAEGQIEVINSLIAQGVDAIAVSANDPDALVPALKKATQRGIKVISWDSGVA 120
           IYTGP   TAEGQIE++NSLIAQ V AI +SANDPDALVP+LKKA  RGIKVIS+DSGV 
Sbjct: 59  IYTGPAKATAEGQIEIVNSLIAQNVKAIVISANDPDALVPSLKKAMARGIKVISFDSGVK 118

Query: 121 PEGRILQLNPSSNELIGKMCLTLAKDHLEGGKGDFAILSATTTSTNQNIWIDQMKKQLK- 179
            EGR++QLNPS++ LIG+  + ++ + + G  G+ A+LSAT  +TNQNIWI +MKK L  
Sbjct: 119 KEGRLMQLNPSNSALIGEKLVKMS-EQVVGKTGEIAVLSATAQATNQNIWIGEMKKVLAK 177

Query: 180 -DFPGLNLVTTVYGDDLSDKSYREAEGLLKSNPNVKVIVAPTTVGVLAASKVVEDKGLVG 238
            ++ GL LV  VYGDD +DKSYREA+GL KS PN+K IVAPTTVG+ AA+K V+D+  VG
Sbjct: 178 PEYAGLKLVNVVYGDDQTDKSYREAQGLFKSYPNLKAIVAPTTVGIAAAAKAVQDEKKVG 237

Query: 239 KVYVTGLGLPSEMAGAIKSGATKEFAIWNPIDLGYSATQIAYRLVKGETDGKPGSEINAG 298
           +++VTGLGLPSEMAG ++SGA K FAIWNPIDLGYS+    +  +KG   G  G  I+ G
Sbjct: 238 QIFVTGLGLPSEMAGHVQSGAVKSFAIWNPIDLGYSSIHAVHAFMKGTVKGTKGEVISLG 297

Query: 299 RMGKIKVGDNGEAAMADPFVYNASNIDQFSKVF 331
           R+GK  + +NGEAAMA+PF Y+A+N+++FSK+F
Sbjct: 298 RVGKATLDENGEAAMAEPFTYDATNVEKFSKIF 330


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: 338
Number of extensions: 11
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: 331
Length of database: 330
Length adjustment: 28
Effective length of query: 303
Effective length of database: 302
Effective search space:    91506
Effective search space used:    91506
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 Apr 09 2024. 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