GapMind for catabolism of small carbon sources

 

Alignments for a candidate for treV in Phaeobacter inhibens BS107

Align TreV, component of Trehalose porter (characterized)
to candidate GFF2754 PGA1_c27970 ATP-binding transport protein SmoK

Query= TCDB::Q97ZC0
         (324 letters)



>FitnessBrowser__Phaeo:GFF2754
          Length = 331

 Score =  254 bits (648), Expect = 3e-72
 Identities = 133/312 (42%), Positives = 198/312 (63%), Gaps = 5/312 (1%)

Query: 3   VELIDIVKKYGKNIVINGITEKIETGEFFVILGPSGEGKSTLLKILAGIEKLDKGKIIAD 62
           ++L ++ K +G   V+  I   +E GEF V +GPSG GKSTLL++++G+E    G+I   
Sbjct: 4   LQLTNVCKSFGPVEVLKDINLTVEDGEFVVFVGPSGCGKSTLLRVISGLEDATAGEISIG 63

Query: 63  GADITDKPPEKRNVAMVFQNYALYPNMSVRDNIAFPLKMRGMKKEEIIERVEKAAKLLGI 122
           G  +T  PP KR +AMVFQ+YALYP++SVR+N+A  LK     KEEI  RV +A+++L +
Sbjct: 64  GQTVTTTPPAKRGIAMVFQSYALYPHLSVRENMALALKQERQPKEEIAARVAEASRMLSL 123

Query: 123 SEILDKKVTQISGGQQQRVALARAIVRNPSYFLLDEPLSNLDARVRTTARGELKRIQKEL 182
            + LD++ +++SGGQ+QRVA+ RA+VR P  FL DEPLSNLDA +R   R E+ R+ ++L
Sbjct: 124 EDYLDRRPSELSGGQRQRVAIGRAVVREPKLFLFDEPLSNLDAALRMNTRLEIARLHRQL 183

Query: 183 KGTFIYVTHDQKEALSLADRIAILHKGKFEQVSDPKTLYEYPKTKWVAQFVGEFPMNFLP 242
             + IYVTHDQ EA++LAD+I +L  G+ EQV  P  LY  P  ++VA+F+G   MNF+P
Sbjct: 184 SASMIYVTHDQIEAMTLADKIVVLRDGRIEQVGTPMELYNNPANRFVAEFIGAPAMNFVP 243

Query: 243 GE-LMKEKAQEIGFRPEWVEVGK-GNLSCMVESVEASGESRYLICNFKNN---NITILSQ 297
            + L     Q IG RPE+  +   G L+  V  VE  G    ++ +   +      +  Q
Sbjct: 244 AQRLGGNPGQFIGIRPEYARISPVGPLAGEVIHVEKLGGDTNILVDMGEDLTFTARLFGQ 303

Query: 298 EFYDVGQEVRFE 309
              +VG+ ++F+
Sbjct: 304 HDTNVGETLQFD 315


Lambda     K      H
   0.318    0.137    0.385 

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: 12
Number of successful extensions: 1
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: 324
Length of database: 331
Length adjustment: 28
Effective length of query: 296
Effective length of database: 303
Effective search space:    89688
Effective search space used:    89688
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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