GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araZsh in Pseudomonas fluorescens FW300-N1B4

Align Inner-membrane translocator (characterized, see rationale)
to candidate Pf1N1B4_6033 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= uniprot:A0KWY7
         (320 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_6033
          Length = 325

 Score =  124 bits (311), Expect = 3e-33
 Identities = 91/306 (29%), Positives = 151/306 (49%), Gaps = 6/306 (1%)

Query: 13  ASLLLTMFLVGTFQFDGFASGRVVTNLLRDNAFLLITALGMTLVIISGGIDLSVGAVIAL 72
           A  LL M  + +     F S    + L      L++ A+GMT V+I GGIDLSVG+V+AL
Sbjct: 24  AGALLAMVALFSVLSSHFLSYDTFSTLANQIPDLMVLAVGMTFVLIIGGIDLSVGSVLAL 83

Query: 73  SGVVTSLLITEYQWHPLLAFVVILPLGTLFGALMGTIIHVYKLQPFIVTLAGMFLARGLA 132
           +    S+ I  + W  L A ++ + +  L G + G+I   +++  FIV+L  + +ARGLA
Sbjct: 84  AASAVSVAILGWGWSVLPAALLGMAVAALAGTITGSITVAWRIPSFIVSLGVLEMARGLA 143

Query: 133 TTLSEESIAIDHPFYDAVAEMSIALPGNGALDLSSLIFILFFVIIAVVMHYTRFGTNVYA 192
             ++    A     Y   A   ++ P    +  S +I +L   I   V+  T FG  +  
Sbjct: 144 YQMTGSRTA-----YIGDAFAWLSNPIAFGISPSFIIALLIIFIAQAVLTRTVFGRYLIG 198

Query: 193 IGGNQHSAELMGISIAKTTISIYAISSFLATLAGIVFTFYTFSGYALGAIGVELDAIAAV 252
           IG N+ +  L GI+     I ++++   LA +A +       +       G+EL  IAAV
Sbjct: 199 IGTNEEAVRLAGINPKPYKILVFSLMGLLAGIAALFQISRLEAADPNAGSGLELQVIAAV 258

Query: 253 VIGGTLLTGGSGFVLGTVLGVILMGVIQTYITFDGSLSSWWTKIVIGLLLFFFILLQKLL 312
           VIGGT L GG G V+ T  GV+++ V+   +   G+      +I+ G ++   ++L    
Sbjct: 259 VIGGTSLMGGRGSVISTFFGVLIISVLAAGLAQIGATEP-TKRIITGAVIVVAVVLDTYR 317

Query: 313 NGRKTQ 318
           + R ++
Sbjct: 318 SQRASR 323


Lambda     K      H
   0.330    0.145    0.424 

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: 321
Number of extensions: 16
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: 320
Length of database: 325
Length adjustment: 28
Effective length of query: 292
Effective length of database: 297
Effective search space:    86724
Effective search space used:    86724
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 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