GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Herbaspirillum seropedicae SmR1

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate HSERO_RS16715 HSERO_RS16715 sugar ABC transporter ATP-binding protein

Query= BRENDA::Q8NMV1
         (376 letters)



>FitnessBrowser__HerbieS:HSERO_RS16715
          Length = 361

 Score =  314 bits (804), Expect = 3e-90
 Identities = 179/359 (49%), Positives = 232/359 (64%), Gaps = 23/359 (6%)

Query: 21  VKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDGAIFIGDKDVTHVAPRDRDIA 80
           ++  +++IADGEF VLVGPSGCGKST LRMLAGLE +T G I IG   V +V P+DRDIA
Sbjct: 19  IRGVDIDIADGEFTVLVGPSGCGKSTLLRMLAGLEEITGGEILIGGTVVNNVQPKDRDIA 78

Query: 81  MVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAAATLGLTEFLERKPKALSGGQ 140
           MVFQNYALYPHMTV +NM F+L +A K +  +++RV +AA  LGL + L+R P+ LSGGQ
Sbjct: 79  MVFQNYALYPHMTVRDNMAFSLTLAKKDKAFVDERVKKAADILGLNQLLDRYPRQLSGGQ 138

Query: 141 RQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAALQRKLGVTTVYVTHDQTEAL 200
           RQRVAMGRAIVR+PQVFL DEPLSNLDAKLRVQ RT+I  L ++L  T++YVTHDQ EA+
Sbjct: 139 RQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRTEIKELHQRLKTTSIYVTHDQIEAM 198

Query: 201 TMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPAMNLGTFSVKDGDATSGHARI 260
           TM D+I V++DG ++Q G P +LYD PAN+FVAGFIGSPAMN    +++  +AT      
Sbjct: 199 TMADQIVVMRDGLVEQRGRPLDLYDYPANLFVAGFIGSPAMNFIPATLR-RNATGAEVEF 257

Query: 261 ----KLSPETLAAMTPEDNGRITIGFRPEALEIIPEGESTDLSIPIKLDFVEELGSDSFL 316
               ++     AA+   D  ++T G RPE L I   G+     I  K+  VE  G+D+ +
Sbjct: 258 ADGTRVPAPYGAALQGNDGQKVTYGVRPEHLSIGAAGQ----GIATKVIVVEPTGADTEV 313

Query: 317 YGKLVGEGDLGSSSEDVPESGQIVVRAAPNAAPAPGSVFHARIVEGGQHNFSASTGKRL 375
           + +  G+  L S   +  + G              G V H        H F A +GK L
Sbjct: 314 FSRF-GDTSLTSIFRERHDFG-------------AGDVIHLVPDHSRTHLFDAESGKSL 358


Lambda     K      H
   0.316    0.135    0.380 

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: 382
Number of extensions: 10
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: 376
Length of database: 361
Length adjustment: 30
Effective length of query: 346
Effective length of database: 331
Effective search space:   114526
Effective search space used:   114526
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 (21.6 bits)
S2: 49 (23.5 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