GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iatP in Phaeobacter inhibens BS107

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 GFF2276 PGA1_c23080 ribose transport system permease protein RbsC

Query= TCDB::B8H230
         (332 letters)



>FitnessBrowser__Phaeo:GFF2276
          Length = 324

 Score =  171 bits (432), Expect = 3e-47
 Identities = 106/318 (33%), Positives = 176/318 (55%), Gaps = 11/318 (3%)

Query: 18  DLLAFARKHRTILFLLLLVAVFGAANERFLTARNALNILSEVSIYGIIAVGMTFVILIGG 77
           D+     K   ++   L +  F  AN +FLT  N  N++   +I G++A+G+TFV++ G 
Sbjct: 8   DIGKLLAKQGILIAFALFIIGFTIANPKFLTLDNFENVVRSSAILGVMALGVTFVVISGN 67

Query: 78  IDVAVGSLLAFASIAAAYVVTAVVGDGPATWLIALLVSTL-IGLAGGYVQGKAVTWLHVP 136
           +D++VGS+++F++I    +   +   GP   + A+   TL +G   G++ G    +L + 
Sbjct: 68  LDLSVGSMMSFSTIVVLDLHDKL---GPTLAIPAMFAMTLCLGALIGFLVG----YLKLN 120

Query: 137 AFIVTLGGMTVWRGATLLLNDGGPISGFNDAYRWW---GSGEILFLPVPVVIFALVAAAG 193
           + IVTLG ++   G TL  + G  +   +    W+   G G IL +  P++IF  +AA  
Sbjct: 121 SLIVTLGMLSAIHGLTLTYSGGKNMDIADKEGTWFAIFGQGNILGIQTPILIFIALAALL 180

Query: 194 HVALRYTRYGRQVYAVGGNAEAARLSGVNVDFITTSVYAIIGALAGLSGFLLSARLGSAE 253
            + L  T +GR+VYAVGGN  AA  SG+    +    Y +       +G + ++R   ++
Sbjct: 181 GIILAKTPFGRKVYAVGGNGTAATFSGIRRARVVFLCYIMSALCVATAGLIQASRSMGSQ 240

Query: 254 AVAGTGYELRVIASVVIGGASLTGGSGGVGGTVLGALLIGVLSNGLVMLHVTSYVQQVVI 313
              G G EL V+A+V++GGASL GGSG +  TV+G L++G + NGL+++ +   VQ VV 
Sbjct: 241 NTVGQGLELEVLAAVILGGASLLGGSGTIFKTVIGVLILGFIQNGLLLVGLDFSVQYVVT 300

Query: 314 GLIIVAAVAFDHYARTHK 331
            +II+ AV  D  A+  K
Sbjct: 301 WIIIILAVWLDIAAKRGK 318


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: 225
Number of extensions: 11
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: 324
Length adjustment: 28
Effective length of query: 304
Effective length of database: 296
Effective search space:    89984
Effective search space used:    89984
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