GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Burkholderia phytofirmans PsJN

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate BPHYT_RS11445 BPHYT_RS11445 putrescine/spermidine ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__BFirm:BPHYT_RS11445
          Length = 388

 Score =  408 bits (1048), Expect = e-118
 Identities = 205/371 (55%), Positives = 273/371 (73%)

Query: 6   PRPQAKTRKALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRML 65
           P   A T  A    +++ ++ K +    AV  V+L++ KGE+FALLG+SGCGKSTLLRM+
Sbjct: 17  PSLNAVTGDATDNFVQVVDVVKKFGETVAVKGVNLSVKKGELFALLGSSGCGKSTLLRMM 76

Query: 66  AGFEQPSAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAE 125
           AG E  S+G+I++DG DL+Q+PPY RP+NMMFQSYALFPHMTVE N+AFGLKQ+ +PKAE
Sbjct: 77  AGLESVSSGKILIDGEDLAQLPPYRRPVNMMFQSYALFPHMTVEGNVAFGLKQEGVPKAE 136

Query: 126 IASRVNEMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLR 185
           +  RV   L LV M  FAKRKP+QLSGGQ+QRVALARSL KRPKLLLLDEPM ALDK++R
Sbjct: 137 LKDRVQTALELVQMGRFAKRKPNQLSGGQQQRVALARSLVKRPKLLLLDEPMSALDKQIR 196

Query: 186 DRMQLEVVDILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRY 245
            R Q+E+V+IL++VGVTC+MVTHDQEEAMTMAGR+A+M+ G+ VQ+G P E+YE+P +R+
Sbjct: 197 QRTQIELVNILDKVGVTCMMVTHDQEEAMTMAGRLAVMSEGEIVQLGTPHEVYEYPNSRF 256

Query: 246 SAEFIGSVNVFEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLC 305
           SAEFIGS N+FEG   E + D + +++P L   L V    +    +PV +++RPE+I L 
Sbjct: 257 SAEFIGSTNLFEGHTVEDEPDYVFIETPDLPCRLYVSHGITGPLGMPVTISVRPERIALT 316

Query: 306 EEPPANGCNFAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRL 365
            +PP    N+  G V +IAY+G  S+YHV+L++G+ + A + +        PTWGDEV +
Sbjct: 317 RKPPEGAYNWGKGVVTNIAYMGGYSLYHVKLEAGKTVIANVTSLALTEIDPPTWGDEVYV 376

Query: 366 CWEVDSCVVLT 376
            W   + VVLT
Sbjct: 377 RWSASAGVVLT 387


Lambda     K      H
   0.321    0.137    0.400 

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: 424
Number of extensions: 8
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: 377
Length of database: 388
Length adjustment: 30
Effective length of query: 347
Effective length of database: 358
Effective search space:   124226
Effective search space used:   124226
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