GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupB in Phaeobacter inhibens BS107

Align RnsC, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized)
to candidate GFF2652 PGA1_c26920 ABC transporter, permease protein

Query= TCDB::Q8DU38
         (358 letters)



>FitnessBrowser__Phaeo:GFF2652
          Length = 349

 Score =  151 bits (382), Expect = 2e-41
 Identities = 98/327 (29%), Positives = 166/327 (50%), Gaps = 10/327 (3%)

Query: 6   QKLVVPLISVILGIILGAIIMMIFGYDPIWAYEGLFQKAFGSLKDIGEIFRAMSPLILIA 65
           ++L+ P ++++    L A++  I G +P+  +  +   AFGS   + E     +PLI   
Sbjct: 13  RRLMPPALALLATFALAALLAQIAGGEPLSIFGLILTGAFGSKFALLETLNRATPLIFTG 72

Query: 66  LGFAVASRAGFFNIGLSGQAYAGWIAAGWFALANPSLPRPLMILMTVLIGAASGGVVGAI 125
           L  AVA RA  +NIG   Q YAG +          +LP PL++ +       +G V+   
Sbjct: 73  LAIAVAFRAKLWNIGAEAQLYAGAVITVVLGTGALNLPAPLLLPLLGAAALIAGAVLLLG 132

Query: 126 PGFLRAYLGTSEVIVTIMMNYIVLYIGNAIIQDGFAKNIMRNSDSSIYVGHNASYQTEWL 185
           P  L+  LG  EV+ T++ N+I L   + +++      +      S  +  +A      L
Sbjct: 133 PALLKTRLGVDEVVTTLLFNFIFLLFVSYLLEGPLKDPMGMGWPKSPRLSADAR-----L 187

Query: 186 RALTNNSRMNIGFFLAIIAIVVVWYLLNKTTLGFEIRSVGLNPHASEYAGMSAKRTIVLS 245
             + +  R++ GF LA+I+ +V+W +  +TTLG+E+R+VG N  A+ +AG+   + I+ +
Sbjct: 188 PRVVDGLRLHWGFALALISALVIWVINTRTTLGYEMRAVGQNAEAARFAGIPVTKVILKT 247

Query: 246 MIISGALAGLGGVVEGLGTFGNVYVQTSSLAIGFDGMAVSLLASNSPIGIFLSAFLFGAL 305
            ++SG LAGL G  E  G  G + +  S    G+ G+ V++LA   PIG+  +A    A+
Sbjct: 248 ALLSGGLAGLAGYSEVSGLKGALTLDLSP-GFGYTGIVVAMLALLHPIGVVFAALFVAAI 306

Query: 306 SVGAPGMSISDATHVGTPPELIKVVTA 332
            VGA  MS +     G P  L  ++ A
Sbjct: 307 FVGADSMSRA----AGVPSYLADIMLA 329


Lambda     K      H
   0.325    0.141    0.416 

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: 275
Number of extensions: 15
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: 358
Length of database: 349
Length adjustment: 29
Effective length of query: 329
Effective length of database: 320
Effective search space:   105280
Effective search space used:   105280
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