GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Herbaspirillum seropedicae SmR1

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate HSERO_RS16715 HSERO_RS16715 sugar ABC transporter ATP-binding protein

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



>FitnessBrowser__HerbieS:HSERO_RS16715
          Length = 361

 Score =  348 bits (893), Expect = e-100
 Identities = 194/363 (53%), Positives = 246/363 (67%), Gaps = 11/363 (3%)

Query: 1   MASVTLRNIRKAYDENEVMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGDL 60
           MASV +R ++K +   +++R +++DIADGEF V VGPSGCGKSTL+RM+AGLE+I+GG++
Sbjct: 1   MASVQIRAVKKQFGSTQIIRGVDIDIADGEFTVLVGPSGCGKSTLLRMLAGLEEITGGEI 60

Query: 61  TIDGMRVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAKI 120
            I G  VN+V P  R IAMVFQ+YALYPHMT+ DNMAF L LA   K  +D  V+ AA I
Sbjct: 61  LIGGTVVNNVQPKDRDIAMVFQNYALYPHMTVRDNMAFSLTLAKKDKAFVDERVKKAADI 120

Query: 121 LHIDHLLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARLH 180
           L ++ LLDR P+QLSGGQRQRVA+GRAI R P+VFLFDEPLSNLDA LRV+MR E   LH
Sbjct: 121 LGLNQLLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRTEIKELH 180

Query: 181 DELKTTMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFIGSPKMN 240
             LKTT IYVTHDQ+EAMT+AD+IVV+  G +EQ G P  LY  PAN FVAGFIGSP MN
Sbjct: 181 QRLKTTSIYVTHDQIEAMTMADQIVVMRDGLVEQRGRPLDLYDYPANLFVAGFIGSPAMN 240

Query: 241 FMEGVVQSVTHDGVTVRYETGETQRVAVEPAAVK--QGDKVTVGIRPEHLHVGMAEDGIS 298
           F+   ++     G  V +  G T+  A   AA++   G KVT G+RPEHL +G A  GI+
Sbjct: 241 FIPATLRR-NATGAEVEFADG-TRVPAPYGAALQGNDGQKVTYGVRPEHLSIGAAGQGIA 298

Query: 299 ARTMAVESLGDAAYLYAESSVAPDGLIARIPPLERHTKGETQKLGATPEH--CHLFDS-A 355
            + + VE  G    +++         I R    ERH  G    +   P+H   HLFD+ +
Sbjct: 299 TKVIVVEPTGADTEVFSRFGDTSLTSIFR----ERHDFGAGDVIHLVPDHSRTHLFDAES 354

Query: 356 GKA 358
           GK+
Sbjct: 355 GKS 357


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: 429
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: 369
Length of database: 361
Length adjustment: 30
Effective length of query: 339
Effective length of database: 331
Effective search space:   112209
Effective search space used:   112209
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: 49 (23.5 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:

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