GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaS in Herbaspirillum seropedicae SmR1

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 HSERO_RS22225 HSERO_RS22225 ABC transporter substrate-binding protein

Query= TCDB::Q7BSH5
         (331 letters)



>FitnessBrowser__HerbieS:HSERO_RS22225
          Length = 325

 Score =  400 bits (1029), Expect = e-116
 Identities = 207/327 (63%), Positives = 257/327 (78%), Gaps = 4/327 (1%)

Query: 7   LALGVALAVAMMAGTASAKDIKIGLVVKSLGNGFFDAANKGAQEAAKELGGVEVIYTGPT 66
           LA G A+ +   A   +A+ ++I +VVKSLGNGFFDAA++GA+EAA+ELG VEVIYTGPT
Sbjct: 1   LAAG-AIGLIAAAPAHAAEKVRIAMVVKSLGNGFFDAAHEGAKEAARELGDVEVIYTGPT 59

Query: 67  STTAEGQIEVINSLIAQGVDAIAVSANDPDALVPALKKATQRGIKVISWDSGVAPEGRIL 126
           + TAEGQIE++NSLI+Q VDAI +SAND +ALVP  K+A QRG+KV+S+DSG+A  GR++
Sbjct: 60  TPTAEGQIEIVNSLISQKVDAIVISANDANALVPITKRAMQRGVKVLSFDSGIAKGGRLM 119

Query: 127 QLNPSSNELIGKMCLTLAKDHLEGGKGDFAILSATTTSTNQNIWIDQMKKQLK--DFPGL 184
           QLNPS+ ELIG   + +A + + GG GD AILSAT  +TNQNIWI +MKK L   +F  +
Sbjct: 120 QLNPSNAELIGLKQIQMAAEAI-GGAGDVAILSATAQATNQNIWIGEMKKALARPEFSRM 178

Query: 185 NLVTTVYGDDLSDKSYREAEGLLKSNPNVKVIVAPTTVGVLAASKVVEDKGLVGKVYVTG 244
            LV TVYGDD SDKSYREA GLL+S+P +K I+APTTVG+ AA K V D+ LVGKVYVTG
Sbjct: 179 KLVATVYGDDQSDKSYREAIGLLRSHPGLKAIIAPTTVGINAAGKAVVDEKLVGKVYVTG 238

Query: 245 LGLPSEMAGAIKSGATKEFAIWNPIDLGYSATQIAYRLVKGETDGKPGSEINAGRMGKIK 304
           LGLPSEMAG +KSGA K FAIWNPIDLGY+AT  AY+ VKG+  GK G  I  GRMG IK
Sbjct: 239 LGLPSEMAGHVKSGAVKSFAIWNPIDLGYAATYAAYQFVKGKAQGKEGESIAVGRMGSIK 298

Query: 305 VGDNGEAAMADPFVYNASNIDQFSKVF 331
           +   GEAA+A PF Y+ASN+D+F+K+F
Sbjct: 299 LDAAGEAALAPPFTYDASNVDKFAKIF 325


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: 356
Number of extensions: 8
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: 325
Length adjustment: 28
Effective length of query: 303
Effective length of database: 297
Effective search space:    89991
Effective search space used:    89991
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