GapMind for catabolism of small carbon sources

 

Aligments for a candidate for hisJ in Burkholderia phytofirmans PsJN

Align histidine ABC transporter, periplasmic histidine-binding protein HisJ (characterized)
to candidate BPHYT_RS35100 BPHYT_RS35100 ABC transporter substrate-binding protein

Query= CharProtDB::CH_018185
         (260 letters)



>lcl|FitnessBrowser__BFirm:BPHYT_RS35100 BPHYT_RS35100 ABC
           transporter substrate-binding protein
          Length = 263

 Score =  228 bits (582), Expect = 7e-65
 Identities = 112/255 (43%), Positives = 166/255 (65%), Gaps = 3/255 (1%)

Query: 5   ALSLSLVLAFSSATAAFAAIPQKIRIGTDPTYAPFESKNAQGELVGFDIDLAKELCKRIN 64
           ALS +L  A + +T+AFA  P  +R+G DP+Y P ++K   G   GFD+DL  E+CKRI+
Sbjct: 11  ALSTALSAALAFSTSAFAVEPTTLRLGIDPSYPPMDAKAPDGSFKGFDVDLGNEICKRIH 70

Query: 65  TQCTFVENPLDALIPSLKAKKIDAIMSSLSITEKRQQEIAFTDKLYAADSRLVVAKNSDI 124
            +C +VE     +IP+L+A+KIDAI+SS++ITEKR+Q+I F+ KL+   SRL+  + S +
Sbjct: 71  ARCQWVELEFSGMIPALQARKIDAILSSMAITEKREQQILFSSKLFQFKSRLIARQGSAL 130

Query: 125 QPTVASLKGKRVGVLQGTTQETFGNEHWAPKGIEIVSYQGQDNIYSDLTAGRIDAAFQDE 184
                +L GK++GV  GT  E +  ++WAP G  +V+Y+ QD +++DL  GR+D A    
Sbjct: 131 AGGTNALAGKQIGVQSGTQFEGYALKNWAPLGAHVVAYKSQDEVFADLQNGRLDGALLGS 190

Query: 185 VAASEGFLKQPVGKDYKFGGPAVKDEKLFGVGTGMGLRKEDNELREALNKAFAEMRADGT 244
           V A  GFL+ P GK + F G  +    +   G G+GLRK++  ++ ++N A A M  DGT
Sbjct: 191 VEADIGFLRTPAGKGFAFVGEPL---SMGDRGVGIGLRKDETAVQASINAAIASMLKDGT 247

Query: 245 YEKLAKKYFDFDVYG 259
           Y ++AKKYFDFD YG
Sbjct: 248 YAQIAKKYFDFDPYG 262


Lambda     K      H
   0.316    0.133    0.372 

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: 189
Number of extensions: 9
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: 260
Length of database: 263
Length adjustment: 25
Effective length of query: 235
Effective length of database: 238
Effective search space:    55930
Effective search space used:    55930
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: 47 (22.7 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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