GapMind for catabolism of small carbon sources

 

Aligments for a candidate for iatP in Pseudomonas fluorescens FW300-N1B4

Align Inositol ABC transport system, permease protein IatP, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate Pf1N1B4_4287 Inositol transport system permease protein

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4287
          Length = 340

 Score =  213 bits (543), Expect = 4e-60
 Identities = 129/338 (38%), Positives = 192/338 (56%), Gaps = 26/338 (7%)

Query: 13  DKPRFDLLAFARKHRTILFLLLLVAVFGAANERF----------LTARNALNILSEVSIY 62
           +KP    +   R+  T L + L++   G   E F          + ++  + ++ +VSI 
Sbjct: 7   NKPAAVPVKSRRRFPTELSIFLVLIGIGLVFEMFGWIVRDQSFLMNSQRLVLMILQVSII 66

Query: 63  GIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYV---------VTAVVGDGPATWLIALL 113
           G++A+G+T VI+  GID++ GS+LA +++ AA +         V   + D P  W I ++
Sbjct: 67  GLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPV-W-IPVI 124

Query: 114 VSTLIGLAGGYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWWGS 173
           V   +GL  G + G  +    +P FI TLG M   RG      +G P+S  +D+Y   G 
Sbjct: 125 VGLGVGLLAGAINGSIIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGH 184

Query: 174 GEILFLPVPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAI 233
           G +     PV+IF +VA   H+ALRYT+YG+  YA+GGN +AAR SG+NV      VY+I
Sbjct: 185 GAM-----PVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVYSI 239

Query: 234 IGALAGLSGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIG 293
            G LAGL+G + SAR  + +A  G  YEL  IA+ VIGG SL GG G + GTV+GAL++G
Sbjct: 240 AGLLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILG 299

Query: 294 VLSNGLVMLHVTSYVQQVVIGLIIVAAVAFDHYARTHK 331
           V+++G   + V +Y+Q ++ GLIIV AV  D Y    K
Sbjct: 300 VMASGFTFVGVDAYIQDIIKGLIIVVAVVIDQYRNKRK 337


Lambda     K      H
   0.325    0.140    0.413 

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: 273
Number of extensions: 12
Number of successful extensions: 4
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: 332
Length of database: 340
Length adjustment: 28
Effective length of query: 304
Effective length of database: 312
Effective search space:    94848
Effective search space used:    94848
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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