GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Pseudomonas fluorescens FW300-N2E2

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate Pf6N2E2_1960 Various polyols ABC transporter, ATP-binding component

Query= BRENDA::Q8NMV1
         (376 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1960
          Length = 365

 Score =  302 bits (773), Expect = 1e-86
 Identities = 160/323 (49%), Positives = 216/323 (66%), Gaps = 16/323 (4%)

Query: 1   MATVTFKDASLSYPGAKEPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDG 60
           MAT+  ++    + G     +K  +LE+ D EF+V VGPSGCGKST LR++AGLE+VT G
Sbjct: 1   MATLKIENLKKGFEGLS--IIKGIDLEVKDKEFVVFVGPSGCGKSTLLRLIAGLEDVTSG 58

Query: 61  AIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAA 120
            I +  +D+T V P  RD+AMVFQ YALYPHMTV +N+ FAL +AG+ + ++ ++V EAA
Sbjct: 59  TIELDGRDITEVTPAKRDLAMVFQTYALYPHMTVRKNLSFALDLAGEKKPDVERKVAEAA 118

Query: 121 ATLGLTEFLERKPKALSGGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAA 180
             L L   L+RKPK LSGGQRQRVA+GRAIVRNP++FL DEPLSNLDA LRVQTR +++ 
Sbjct: 119 RILELGSLLDRKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQTRLELSR 178

Query: 181 LQRKLGVTTVYVTHDQTEALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPA 240
           L ++L  T +YVTHDQ EA+T+  ++ VL  G ++Q+G+P ELY  PAN+FVAGF+G+P 
Sbjct: 179 LHKELQATMIYVTHDQVEAMTLATKVVVLNAGRIEQIGSPLELYHHPANLFVAGFLGTPK 238

Query: 241 MNLGTFSVKDGDATSGHARIKLSPETLAAMTPEDNG------RITIGFRPEALEIIPEGE 294
           M     +V    A+    R   S  TL  + P D+        +TIG RPE L +  EG+
Sbjct: 239 MGFLQATVHAVHASGVEVRF-ASGTTL--LIPRDSSALSVGQSVTIGIRPEHLTLSAEGQ 295

Query: 295 STDLSIPIKLDFVEELGSDSFLY 317
                +P+  D  E LGSD+F +
Sbjct: 296 -----VPVTTDVTERLGSDTFCH 313


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: 391
Number of extensions: 16
Number of successful extensions: 3
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: 365
Length adjustment: 30
Effective length of query: 346
Effective length of database: 335
Effective search space:   115910
Effective search space used:   115910
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.

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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