GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Pseudomonas fluorescens FW300-N2E3

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 AO353_21390 AO353_21390 ABC transporter

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_21390
          Length = 340

 Score =  211 bits (537), Expect = 2e-59
 Identities = 128/338 (37%), Positives = 190/338 (56%), Gaps = 26/338 (7%)

Query: 13  DKPRFDLLAFARKHRTILFLLLLVAVFGAANERF----------LTARNALNILSEVSIY 62
           +KP        R+  T L + L++   G   E F          + ++  + ++ +VSI 
Sbjct: 7   NKPAMAPAKSRRRLPTELSIFLVLIGIGLVFEMFGWIVRDQSFLMNSQRLVLMILQVSII 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
               +GL  G + G  +    +P FI TLG M   RG      +G P+S  +D+Y   G 
Sbjct: 125 AGLGVGLLAGAINGSIIAVTGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGH 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 VMASGFTFVGVDAYIQDIIKGLIIVIAVVIDQYRNKRK 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: 276
Number of extensions: 13
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:

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