GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Skermanella stibiiresistens SB22

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_051511581.1 N825_RS05320 ABC transporter permease

Query= TCDB::B8H230
         (332 letters)



>NCBI__GCF_000576635.1:WP_051511581.1
          Length = 338

 Score =  213 bits (541), Expect = 7e-60
 Identities = 127/328 (38%), Positives = 185/328 (56%), Gaps = 9/328 (2%)

Query: 3   APSSPAPLATDKPRFDLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIY 62
           APSS     T     +   F  ++  +L L++++ V    +  FL+ RN  N+L   ++ 
Sbjct: 16  APSSKMGAQTGASSINWTRFLVQYSNVLALIVILVVASLLSPYFLSTRNIFNVLRGATMV 75

Query: 63  GIIAVGMTFVILIGGIDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTLIGLAG 122
           GI+A+GMT+VIL  GID++VGSL+  ++   A      +G       IA  +  + GL  
Sbjct: 76  GIVAIGMTYVILNRGIDLSVGSLVGLSAALTASFADYGIG-------IAASIGLVSGLVL 128

Query: 123 GYVQGKAVTWLHVPAFIVTLGGMTVWRGATLLLNDGGPI--SGFNDAYRWWGSGEILFLP 180
           G   G  +T L +  FI TLG M   RG   +  +G  I      DA+ W GS  I  +P
Sbjct: 129 GLANGLMITKLRLQPFIATLGMMIFARGLVFVYTNGSNIVVDKPTDAFTWLGSAYIGPVP 188

Query: 181 VPVVIFALVAAAGHVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGL 240
           VPVV+F L+ A   + LRYT +GR+++AVG N EAARLSG+NVD     VY I G LA  
Sbjct: 189 VPVVVFVLIWALCALVLRYTVFGREIFAVGANEEAARLSGINVDRNKIRVYCISGVLAAF 248

Query: 241 SGFLLSARLGSAEAVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLV 300
           +G ++++RL   E   GT +EL  IA+ +IGG +  GG G V GTVLG L++  LSN L 
Sbjct: 249 AGVIMASRLTVGEPNGGTLFELDAIAATLIGGTTFDGGVGSVHGTVLGVLILAFLSNVLN 308

Query: 301 MLHVTSYVQQVVIGLIIVAAVAFDHYAR 328
           +L+++ Y Q ++ G+IIV AV    + +
Sbjct: 309 LLNISPYSQMLLKGVIIVLAVVVSEWRK 336


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: 271
Number of extensions: 18
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: 332
Length of database: 338
Length adjustment: 28
Effective length of query: 304
Effective length of database: 310
Effective search space:    94240
Effective search space used:    94240
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 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