GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Pseudomonas fluorescens FW300-N1B4

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate Pf1N1B4_409 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= uniprot:B2T9V8
         (351 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_409
          Length = 322

 Score =  151 bits (381), Expect = 3e-41
 Identities = 93/313 (29%), Positives = 160/313 (51%), Gaps = 20/313 (6%)

Query: 38  LRELALLPALALLIVIGAFISPSFLTKANL------ISVLGASAALALVVLAESLIVLTG 91
           L +  +L A   + V+   +  +FL+  N+      IS  G +A   L  LA      +G
Sbjct: 21  LDDWVMLLAAVGIFVLCTLLIDNFLSPLNMRGLGLAISTTGIAACTMLYCLA------SG 74

Query: 92  KFDLSLESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVVRL 151
            FDLS+ S +  A  V A+++    S   G+         A +V+G ++G ING ++ +L
Sbjct: 75  HFDLSVGSVIACAGVVAAVVMRDTDSVFLGVS--------AALVMGLIVGLINGIVIAKL 126

Query: 152 RLNAFIVTLAMLIVLRGMLVGATKGGTLFDMPTSFFALATTIVLGLPLSVWLAAAAFAIA 211
           R+NA I TLA + ++RG+      G  +      FF      + G+P+ + +    F   
Sbjct: 127 RVNALITTLATMQIVRGLAYIFANGKAVGVSQEQFFVFGNGQLFGVPVPILITIVCFLFF 186

Query: 212 AFMLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAIN 271
            ++L Y   GR   AIGGN EAA  AG+ V+R    +F +  ++ ++ G+I+   + +  
Sbjct: 187 GWLLNYTTYGRNTMAIGGNQEAALLAGVNVDRTKTLIFAVHGVIGALAGVILASRMTSGQ 246

Query: 272 ANQGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIY 331
              G G   TV +A V+GG+SL GG G +   + GVL+L +++N + L  + +F+   I 
Sbjct: 247 PMIGQGFELTVISACVLGGVSLSGGIGMIRHVIAGVLILAIIENAMNLKNIDTFYQYVIR 306

Query: 332 GAIILGSLMVARL 344
           G+I+L ++++ RL
Sbjct: 307 GSILLLAVVIDRL 319


Lambda     K      H
   0.326    0.140    0.397 

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: 242
Number of extensions: 7
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: 351
Length of database: 322
Length adjustment: 28
Effective length of query: 323
Effective length of database: 294
Effective search space:    94962
Effective search space used:    94962
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 (21.6 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