GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Actinomyces timonensis 7400942

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate WP_017177778.1 A1QA_RS0104755 ABC transporter ATP-binding protein

Query= reanno::WCS417:GFF4321
         (386 letters)



>NCBI__GCF_000295095.1:WP_017177778.1
          Length = 386

 Score =  240 bits (613), Expect = 4e-68
 Identities = 134/307 (43%), Positives = 184/307 (59%), Gaps = 21/307 (6%)

Query: 4   LELRNVNKTYGAGLPDT--LKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGGA 61
           LELR+V K +     D   +  + L I  GEF+ L+GPSGCGK+T +  IAG E  T G 
Sbjct: 19  LELRDVVKVFSNRGKDVYAVHGVSLDIAPGEFVTLLGPSGCGKTTTLRMIAGFEDTTSGQ 78

Query: 62  IMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVAK 121
           +++  Q++  + P  R ++MVFQSYAL+P +SVRENI +GLK+R     +I  +V     
Sbjct: 79  VVLDGQNMVSLPPNKRPMSMVFQSYALFPHLSVRENIAYGLKLRHTKPEEIREQVEIALT 138

Query: 122 LLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLM 181
            + +  L +R P +LSGGQQQRVA+ RA+  RPK+ LFDEPLSNLDAKLRV MR E++ +
Sbjct: 139 SMNLNSLADRAPNELSGGQQQRVALARAMVMRPKVLLFDEPLSNLDAKLRVRMRLEIRRL 198

Query: 182 HQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPPM 241
            QR+  T++YVTHDQ EAMT+ D++ VM  G I+Q  TP++IY  PA+ FVA FIG    
Sbjct: 199 QQRMGITSIYVTHDQAEAMTMSDRIVVMNAGTIEQVATPEKIYRRPASVFVADFIGR--A 256

Query: 242 NFVPLRLQRKDGRLVALLDSGQARC-------ELALNTTEAGLEDRDVILGLRPEQIMLA 294
           NF+    +          D G  RC       +L     E       V + +RPE + L+
Sbjct: 257 NFLAATAR----------DVGGGRCSARVLGADLQAACHEGVSAGSGVTVIVRPESVRLS 306

Query: 295 AGEGDSA 301
            G G+ A
Sbjct: 307 PGTGEGA 313


Lambda     K      H
   0.318    0.135    0.382 

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: 424
Number of extensions: 20
Number of successful extensions: 2
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: 386
Length of database: 386
Length adjustment: 30
Effective length of query: 356
Effective length of database: 356
Effective search space:   126736
Effective search space used:   126736
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: 50 (23.9 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