GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Phaeacidiphilus oryzae TH49

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate WP_037572389.1 BS73_RS14235 ABC transporter ATP-binding protein

Query= reanno::Smeli:SM_b21106
         (365 letters)



>NCBI__GCF_000744815.1:WP_037572389.1
          Length = 386

 Score =  237 bits (605), Expect = 3e-67
 Identities = 142/366 (38%), Positives = 204/366 (55%), Gaps = 27/366 (7%)

Query: 6   LKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAIEIGGR 65
           L  L K++G+   V G+DL +    F AL+G SGCGK+TTLRMI+GLE  + G I +G +
Sbjct: 21  LTGLTKKFGSFTAVDGVDLTIAQGSFFALLGASGCGKTTTLRMISGLEAPTAGRIHLGDQ 80

Query: 66  KVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAILDLAH 125
            V D  P  R ++ VFQ+YAL+PH+ + EN+ F L+  G     +K  V +   +++L H
Sbjct: 81  DVTDRKPYRRPVNTVFQNYALFPHLDIFENVAFGLRRRG--IRSVKKPVEDMLDLVELGH 138

Query: 126 LLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLHARMQA 185
           L  R+P+QLSGGQ+QR+A+ RA++ QP V L DEPL  LD KLR Q++ E+K++   +  
Sbjct: 139 LARRKPTQLSGGQQQRIALARALINQPQVLLLDEPLGALDLKLRRQMQIELKRIQLEVGL 198

Query: 186 TMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPM--NMEE 243
           T ++VTHDQ EAMT++D I +M  G IEQ+G+P +++  P T FVA F+G   +     E
Sbjct: 199 TFVHVTHDQEEAMTMADTIAVMNHGRIEQLGSPAELYENPNTTFVANFLGQSNLIAGTVE 258

Query: 244 AVLTDGKLAFASGATLPLPPRFRSLVREGQKVTFGLRPDDV--------YPSGHGLHAG- 294
           +V  D     A G +L LP   R     G  V  G+RP+ V         PSG     G 
Sbjct: 259 SVSGDVVQVAAHGRSLALPAA-RCRTTSG-PVILGVRPEKVRIAKTEAEVPSGANHLTGK 316

Query: 295 --DADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPLRPGEAVPMSFDLARA 352
             DA  +  +     +  P G E  VF Q  G++           RPG  V + +D ++ 
Sbjct: 317 VTDASFI-GVSTQYLVELPSGEELAVFEQNTGQE---------IQRPGAEVVVHWDPSQG 366

Query: 353 HLFDGE 358
              DGE
Sbjct: 367 FGLDGE 372


Lambda     K      H
   0.320    0.137    0.397 

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: 352
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: 365
Length of database: 386
Length adjustment: 30
Effective length of query: 335
Effective length of database: 356
Effective search space:   119260
Effective search space used:   119260
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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