GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Escherichia coli BW25113

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate 17511 b3450 ATP-binding component of sn-glycerol 3-phosphate transport system (VIMSS)

Query= BRENDA::Q8NMV1
         (376 letters)



>FitnessBrowser__Keio:17511
          Length = 356

 Score =  316 bits (809), Expect = 7e-91
 Identities = 176/375 (46%), Positives = 238/375 (63%), Gaps = 19/375 (5%)

Query: 1   MATVTFKDASLSYPGAKEPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDG 60
           MA +  +  + S+ G K   +K   L++ADGEF+V+VGPSGCGKST LRM+AGLE VT+G
Sbjct: 1   MAGLKLQAVTKSWDG-KTQVIKPLTLDVADGEFIVMVGPSGCGKSTLLRMVAGLERVTEG 59

Query: 61  AIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAA 120
            I+I D+ VT + P+DR IAMVFQNYALYPHM+V ENM + LKI G  + +I +RV EAA
Sbjct: 60  DIWINDQRVTEMEPKDRGIAMVFQNYALYPHMSVEENMAWGLKIRGMGKQQIAERVKEAA 119

Query: 121 ATLGLTEFLERKPKALSGGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAA 180
             L L   L+R+P+ LSGGQRQRVAMGRAIVR+P VFL DEPLSNLDAKLRVQ R ++  
Sbjct: 120 RILELDGLLKRRPRELSGGQRQRVAMGRAIVRDPAVFLFDEPLSNLDAKLRVQMRLELQQ 179

Query: 181 LQRKLGVTTVYVTHDQTEALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPA 240
           L R+L  T++YVTHDQ EA+T+  R+ V+  G  +Q+G P E+Y++PA++FVA FIGSPA
Sbjct: 180 LHRRLKTTSLYVTHDQVEAMTLAQRVMVMNGGVAEQIGTPVEVYEKPASLFVASFIGSPA 239

Query: 241 MNLGTFSVKDGDATSGHARIKLSPETLAAMTPEDNGRITIGFRPEALEIIPEGESTDLSI 300
           MNL T  V + + T       +              ++T+G RPE + +  + E     +
Sbjct: 240 MNLLTGRV-NNEGTHFELDGGIELPLNGGYRQYAGRKMTLGIRPEHIALSSQAEG---GV 295

Query: 301 PIKLDFVEELGSDSFLYGKLVGEGDLGSSSEDVPESGQIVVRAAPNAAPAPGSVFHARIV 360
           P+ +D +E LG+D+  +G+  GE              ++VVR A    P  GS     + 
Sbjct: 296 PMVMDTLEILGADNLAHGRW-GE-------------QKLVVRLAHQERPTAGSTLWLHLA 341

Query: 361 EGGQHNFSASTGKRL 375
           E   H F   TG+R+
Sbjct: 342 ENQLHLFDGETGQRV 356


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: 376
Number of extensions: 15
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: 356
Length adjustment: 30
Effective length of query: 346
Effective length of database: 326
Effective search space:   112796
Effective search space used:   112796
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