GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Burkholderia phytofirmans PsJN

Align LacK, component of Lactose porter (characterized)
to candidate BPHYT_RS22760 BPHYT_RS22760 sugar ABC transporter ATP-binding protein

Query= TCDB::Q01937
         (363 letters)



>FitnessBrowser__BFirm:BPHYT_RS22760
          Length = 384

 Score =  351 bits (900), Expect = e-101
 Identities = 195/342 (57%), Positives = 243/342 (71%), Gaps = 17/342 (4%)

Query: 1   MAEVRLTDIRKSYGS-LEVIKGVNLEVSSGEFVVFVGPSGCGKSTLLRMIAGLEDISSGE 59
           MA + L  ++K+YG    VI+ V+LE+   EF VF+GPSGCGKSTLLRMIAGLED++ G+
Sbjct: 1   MASISLRGVQKAYGEGAPVIRDVDLEIGENEFCVFLGPSGCGKSTLLRMIAGLEDLTDGD 60

Query: 60  LTIGGTVMNDVDPSKRGIAMVFQTYALYPHMTVRENMGFALRFAGMAKDEIERRVNAAAK 119
           L+IGG +MNDV  ++RG+AMVFQ+YAL+PHM+V ENM F L+ A   KDE++R+V  AA+
Sbjct: 61  LSIGGKLMNDVPAAQRGVAMVFQSYALFPHMSVFENMAFGLKLAKTPKDEVDRKVREAAR 120

Query: 120 ILELDALMDRKPKALSGGQRQRVAIGRAIVRQPDVFLFDEPLSNLDAELRVHMRVEIARL 179
           IL+L+AL++RKPKALSGGQRQRVAIGRAIVR+P VFLFDEPLSNLDA LR   R+EIARL
Sbjct: 121 ILQLEALLERKPKALSGGQRQRVAIGRAIVREPGVFLFDEPLSNLDATLRGQTRIEIARL 180

Query: 180 HKEL-NATIVYVTHDQVEAMTLADKIVVM-------RGGIVEQVGAPLALYDDPDNMFVA 231
           HK+   A++VYVTHDQ+EAMTLADKIV++       R G + Q+GAPL LY  P + FVA
Sbjct: 181 HKQFAKASVVYVTHDQIEAMTLADKIVLLHAGKDTERYGSIAQIGAPLELYHRPKSRFVA 240

Query: 232 GFIGSPRMNFLPAVVIG-QAEGGQVTVALKARPDTQLTVACATPPQGGDAVTVGVRPEH- 289
           GFIGSPRMNFLP  V    A+G  VT+ L    +T          Q   AVT+GVRPEH 
Sbjct: 241 GFIGSPRMNFLPGRVASLDAQG--VTITLDHTQETVRVPVNGAGLQTSQAVTLGVRPEHL 298

Query: 290 -FLPAGS---GDTQLTAHVDVVEHLGNTSYVYAHTVPGEQII 327
            F+   S    D  LT  V +VE LG  SYV+     G  ++
Sbjct: 299 EFVDPSSVAPDDAVLTRTVSLVEQLGEHSYVHLDQPGGAALV 340


Lambda     K      H
   0.320    0.137    0.390 

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: 15
Number of successful extensions: 4
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: 363
Length of database: 384
Length adjustment: 30
Effective length of query: 333
Effective length of database: 354
Effective search space:   117882
Effective search space used:   117882
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 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