GapMind for catabolism of small carbon sources

 

Aligments for a candidate for PS417_17590 in Phaeobacter inhibens BS107

Align ABC transporter substrate-binding protein; SubName: Full=Histidine transport system substrate-binding protein (characterized, see rationale)
to candidate GFF3832 PGA1_262p02360 putative histidine-binding periplasmic protein

Query= uniprot:A0A1N7UK26
         (258 letters)



>lcl|FitnessBrowser__Phaeo:GFF3832 PGA1_262p02360 putative
           histidine-binding periplasmic protein
          Length = 259

 Score =  170 bits (431), Expect = 2e-47
 Identities = 101/255 (39%), Positives = 149/255 (58%), Gaps = 10/255 (3%)

Query: 7   LFAALLLPLCATAHAQEWKEIRFGVFPE-YPPFESVAADGSLQGFDIELGNAICAKLEVK 65
           L AA +   CA A A+    ++ GV  E YPPF S+ + G   G++I++ NA+CA  E+ 
Sbjct: 12  LAAATVAATCAVAQAEP---VKIGVAAEPYPPFASLDSSGQWVGWEIDVINAVCAAAELD 68

Query: 66  CTWVHNEFDGMIPALRARKFDAIMSSMAVTPAREKIIDFSDRLFLSPTSVITRKSADFGD 125
           C      +DG+IP+L  ++ DAIM+SM++T  R K IDFSD  + +P  ++  KS D   
Sbjct: 69  CVITPVAWDGIIPSLTGQQVDAIMASMSITEERLKTIDFSDPYYNTPAVIVADKSMDIEA 128

Query: 126 TPESLMGKQVGVLQGSLQEAYARAHLAKLGAQIKAYQSQDQNYADLQNGRLDATLTDKLE 185
           TPESL GK VG+   ++ +AYA+ H     ++++ YQ+QD+   DL  GR+DAT  D + 
Sbjct: 129 TPESLAGKVVGIQASTIHQAYAQEHFK--DSELRVYQTQDEANQDLFAGRIDATQADSI- 185

Query: 186 AQLNFLSKPEGS--DFKTGPAFKDPTLPLDIAMGLRKNDQALRALINKGIAAVQADGTYA 243
           A  +F+    G   + K   A  +  L   +  G+RK D  + A +NKGIAA+ ADGT+A
Sbjct: 186 AMADFVGSDAGGCCEIKGAVANDEAILGKGVGAGVRKGDSDVLAALNKGIAAILADGTHA 245

Query: 244 QIQKKYFGDQDIYHE 258
           +I  KYF    IY E
Sbjct: 246 EITSKYF-TTSIYSE 259


Lambda     K      H
   0.319    0.135    0.393 

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: 155
Number of extensions: 9
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: 258
Length of database: 259
Length adjustment: 24
Effective length of query: 234
Effective length of database: 235
Effective search space:    54990
Effective search space used:    54990
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 47 (22.7 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 preprint 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