GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Paraburkholderia bryophila 376MFSha3.1

Align Ribose import permease protein RbsC (characterized)
to candidate H281DRAFT_00427 H281DRAFT_00427 monosaccharide ABC transporter membrane protein, CUT2 family

Query= SwissProt::P0AGI1
         (321 letters)



>FitnessBrowser__Burk376:H281DRAFT_00427
          Length = 341

 Score =  239 bits (609), Expect = 9e-68
 Identities = 130/315 (41%), Positives = 196/315 (62%), Gaps = 9/315 (2%)

Query: 10  RYFTKAWLMEQKSLIALLVLIAIVSTLSPNFFTINNLFNILQQTSVNAIMAVGMTLVILT 69
           R F+   L +  +  +L++L+   S  SP F  ++N+  ILQ T+VN ++A+  T VI+T
Sbjct: 22  RIFSPTALQKLLAFASLILLLVFFSFASPAFMQMDNILGILQATAVNGVLAIASTFVIIT 81

Query: 70  SGIDLSVGSLLALTGAVAASIVGI-EVNALVAVAAALALGAAIGAVTGVIVAKGRVQAFI 128
            GIDLSVG+L+  T  +    +    +   + V AA+  GA  G ++G + AK ++  FI
Sbjct: 82  GGIDLSVGTLMTFTAVICGVFLTYWHLPMWLGVIAAIGTGAICGTISGTLTAKMKIPPFI 141

Query: 129 ATLVMMLLLRGVTMVYTNGSPVNTGFTENA------DLFGWFGIGRPLGVPTPVWIMGIV 182
           ATL MMLLL+G+++V +   P+    TEN        L G+     P  +P  V I+  +
Sbjct: 142 ATLGMMLLLKGLSLVVSADKPIYFTDTENFYMISQDSLIGYLVPSLP--IPNAVLILFFL 199

Query: 183 FLAAWYMLHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARL 242
            + +   L+ T LGRY +ALG NE A RLSG+NV++ KI +Y L G +  +AG++  +RL
Sbjct: 200 AIVSSVTLNRTALGRYTFALGSNEEAVRLSGVNVDRWKIAIYGLGGAICGIAGLLIASRL 259

Query: 243 SSAQPTAGTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQ 302
           +SAQP  G GYEL+AIAAVV+GGTSL+GG G I+GT+IGA I+  L NGL ++ V+  +Q
Sbjct: 260 NSAQPALGQGYELEAIAAVVIGGTSLSGGSGTILGTIIGAFIMSVLTNGLRIMSVAQEWQ 319

Query: 303 MIVKAVVILLAVLVD 317
           ++V  ++I+LAV  D
Sbjct: 320 IVVTGLIIILAVYAD 334


Lambda     K      H
   0.324    0.139    0.393 

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: 260
Number of extensions: 12
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: 321
Length of database: 341
Length adjustment: 28
Effective length of query: 293
Effective length of database: 313
Effective search space:    91709
Effective search space used:    91709
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 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