GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Pseudovibrio axinellae Ad2

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 WP_068009667.1 PsAD2_RS19325 ribose ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>NCBI__GCF_001623255.1:WP_068009667.1
          Length = 314

 Score =  245 bits (625), Expect = 1e-69
 Identities = 138/307 (44%), Positives = 198/307 (64%), Gaps = 9/307 (2%)

Query: 22  FARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGGIDVA 81
           F  ++++++ L++L+A    AN  FL   N LNIL + SI  +IA+GMTFVIL  GID++
Sbjct: 6   FISENKSLIGLIILMAAVSFANANFLGVDNMLNILRQTSINAVIAMGMTFVILTSGIDLS 65

Query: 82  VGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTLIGLAGGYVQGKAVTWLHVPAFIVT 141
           VGS+LAFA    A ++     D P   ++AL  + ++G   G   G  +++ +V  FI T
Sbjct: 66  VGSILAFAGAICASLIGM---DTPL--VVALFATIMVGAGLGATSGVIISYFNVQPFIAT 120

Query: 142 LGGMTVWRGATLLLNDGGPIS-GFND---AYRWWGSGEILFLPVPVVIFALVAAAGHVAL 197
           L GMT+ RGATL+   G P+S G +D   ++  +G+G I  +P PV++  ++ A     L
Sbjct: 121 LVGMTMIRGATLVYTQGRPVSTGSHDVAESFYQFGAGYIFGIPHPVILMIVIFAICWFIL 180

Query: 198 RYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAEAVAG 257
             TR+GR VYA+GGN   ARLSG+NV  +   VYA+ GALA L+G +L+ARL SA+  AG
Sbjct: 181 SQTRFGRYVYAIGGNENVARLSGINVKKVKILVYALSGALAALAGIILTARLESAQPTAG 240

Query: 258 TGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVIGLII 317
            GYEL  IA+VV+GG SL GG G V GT++GAL+IGVL+N L ++ V+SY Q +  G +I
Sbjct: 241 LGYELDAIAAVVLGGTSLAGGKGRVFGTIIGALIIGVLNNALNIMDVSSYYQMIAKGAVI 300

Query: 318 VAAVAFD 324
           + AV  D
Sbjct: 301 LLAVVVD 307


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: 252
Number of extensions: 15
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: 314
Length adjustment: 28
Effective length of query: 304
Effective length of database: 286
Effective search space:    86944
Effective search space used:    86944
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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