GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Phaeacidiphilus oryzae TH49

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate WP_084703891.1 BS73_RS07930 ABC transporter ATP-binding protein

Query= reanno::BFirm:BPHYT_RS16095
         (369 letters)



>NCBI__GCF_000744815.1:WP_084703891.1
          Length = 389

 Score =  204 bits (520), Expect = 3e-57
 Identities = 136/366 (37%), Positives = 189/366 (51%), Gaps = 23/366 (6%)

Query: 4   VTLRNIRKAYDENEVMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGDLTID 63
           ++  ++  AY +  V+    LD+A GE V  +GPSG GK+T +R +AG      G + I 
Sbjct: 32  ISFEDVTVAYRDQVVLNGFTLDVAAGEVVALLGPSGSGKTTALRTVAGFTAPVRGRVGIG 91

Query: 64  GMRVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAKILHI 123
           G  V  + P +RGI MV Q YAL+PH+ +  N+AFGLK   T + ++   V  A ++  +
Sbjct: 92  GRDVTGLPPHRRGIGMVVQQYALFPHLRVEQNVAFGLKAHRTPRAQVPGRVAEALEMTGM 151

Query: 124 DHLLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARLHDEL 183
                R P++LSGGQ+QRVA+ RA+  +P+V L DEPLS LDA LR  M  E ARLH EL
Sbjct: 152 AGYARRYPRELSGGQQQRVALARALAIRPEVLLLDEPLSALDAGLRAGMLAELARLHREL 211

Query: 184 -KTTMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFIGSPKMNFM 242
            + +++YVTHDQ+EA+TLAD+I VL    L   G+P  LY  PA+ F A F+G  + N +
Sbjct: 212 PEVSILYVTHDQIEALTLADRIAVLRDARLVDCGTPERLYRRPADAFTASFVG--RANLL 269

Query: 243 EGVVQSVTHDGVTVRYETGETQRVAVEPAA---VKQGDKVTVGIRPEHLHVGMAEDG--- 296
             V      D V +   T  T  V +   A      G    + +RP  L     E G   
Sbjct: 270 P-VTAGQEPDRVVLGAATHRTGAVELRITAQDGFPAGSPALLCVRPHQLRPA-TEGGPNL 327

Query: 297 ISARTMAVESLGDAAYLYAESSVAP------DGLIARIPPLERHTKGETQKLGATPEHCH 350
           +  R   V+ LG    +  +    P       GL  R+PP      GE   LG  PE   
Sbjct: 328 LRGRVSDVQWLGSTHRVQVDLDAGPRVAAELSGL--RVPP----AAGEELALGFDPEDGV 381

Query: 351 LFDSAG 356
           L  + G
Sbjct: 382 LLPAEG 387


Lambda     K      H
   0.320    0.135    0.384 

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: 396
Number of extensions: 12
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: 369
Length of database: 389
Length adjustment: 30
Effective length of query: 339
Effective length of database: 359
Effective search space:   121701
Effective search space used:   121701
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