GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rhaS in Dinoroseobacter shibae DFL-12

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 3609045 Dshi_2434 rhamnose ABC transporter, periplasmic rhamnose-binding protein (RefSeq)

Query= TCDB::Q7BSH5
         (331 letters)



>FitnessBrowser__Dino:3609045
          Length = 333

 Score =  441 bits (1135), Expect = e-129
 Identities = 223/326 (68%), Positives = 270/326 (82%), Gaps = 2/326 (0%)

Query: 7   LALGVALAVAMMAGTASAKD-IKIGLVVKSLGNGFFDAANKGAQEAAKELGGVEVIYTGP 65
           L  G++LA ++   TA A+D ++I LVVK+LG GFF+AA +GA+EAA ELGGVE+IYTGP
Sbjct: 9   LTAGLSLAASLFGTTAMAQDEMRIALVVKALGIGFFEAAAQGAEEAAAELGGVEIIYTGP 68

Query: 66  TSTTAEGQIEVINSLIAQGVDAIAVSANDPDALVPALKKATQRGIKVISWDSGVAPEGRI 125
           T TTAEGQIEVINSLIAQGVDAIAVSAND DALVP LKKA QRGI VISWDSGVAPEGR 
Sbjct: 69  TDTTAEGQIEVINSLIAQGVDAIAVSANDTDALVPTLKKAMQRGITVISWDSGVAPEGRQ 128

Query: 126 LQLNPSSNELIGKMCLTLAKDHLEGGKGDFAILSATTTSTNQNIWIDQMKKQLKDFPGLN 185
           + LNPSSN LIG M + LA DHL  G GD A+LSATTTSTNQNIWI++M K L D+PG+N
Sbjct: 129 MHLNPSSNALIGNMIIKLAADHLPDG-GDVAVLSATTTSTNQNIWIEEMTKVLGDYPGIN 187

Query: 186 LVTTVYGDDLSDKSYREAEGLLKSNPNVKVIVAPTTVGVLAASKVVEDKGLVGKVYVTGL 245
           +V+TVYGDDL+DKSYREA+GL++S P++  I+APT+VG++AA++ V D G +G+V VTGL
Sbjct: 188 VVSTVYGDDLADKSYREAQGLMQSFPDLDAIIAPTSVGIVAAAQAVADAGKIGQVNVTGL 247

Query: 246 GLPSEMAGAIKSGATKEFAIWNPIDLGYSATQIAYRLVKGETDGKPGSEINAGRMGKIKV 305
           GLPSEMAGAI+SGA+K FAIWNPIDLGYSA  IA+ L  G    +PG+EI+ GR+G I +
Sbjct: 248 GLPSEMAGAIESGASKSFAIWNPIDLGYSAAMIAHALASGAATAEPGTEISIGRVGTITL 307

Query: 306 GDNGEAAMADPFVYNASNIDQFSKVF 331
            +N EAAMADPF+Y+ASNIDQF  +F
Sbjct: 308 DENNEAAMADPFIYDASNIDQFKSIF 333


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: 385
Number of extensions: 12
Number of successful extensions: 2
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: 333
Length adjustment: 28
Effective length of query: 303
Effective length of database: 305
Effective search space:    92415
Effective search space used:    92415
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