GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcB in Burkholderia phytofirmans PsJN

Align Xylose ABC transporter, periplasmic xylose-binding protein XylF (characterized, see rationale)
to candidate BPHYT_RS16065 BPHYT_RS16065 LacI family transcriptional regulator

Query= uniprot:A0A0C4Y591
         (325 letters)



>FitnessBrowser__BFirm:BPHYT_RS16065
          Length = 317

 Score =  177 bits (450), Expect = 2e-49
 Identities = 116/313 (37%), Positives = 177/313 (56%), Gaps = 14/313 (4%)

Query: 8   ALATAALSLLCTGAAAQSAPDAAPASAAAQRPLKKVGVTLGSLGNPYFVALAHGAEAAAK 67
           A +TAAL+ L  G +  +AP       AAQ    K+G+T   L NPYFV +      AA 
Sbjct: 15  ARSTAALATLAFGLSFIAAP-------AAQAAPLKIGMTFQELNNPYFVTMQKALNDAAA 67

Query: 68  KINPDAKVTVLSADYDLNKQFSHIDSFIVSKVDLILINAADARAIEPAVRKARKAGIVVV 127
            I   A V V  A +D++KQ S ++  +  K+D++L+N  D+  I+ AV  A+KAG+VVV
Sbjct: 68  SIG--ATVVVTDAHHDVSKQVSDVEDMLQKKIDILLVNPTDSTGIQSAVTSAKKAGVVVV 125

Query: 128 AVDVAAAG-ADATVQTDNTRAGELACAFLAGRLGGRGNLIIQNGPPVSAVLDRVKGCKMV 186
           AVD  A G  D+ V + N  AGE+AC +LA  +GG G + I +G PV  +L+RV+GCK  
Sbjct: 126 AVDANANGPVDSFVGSKNYDAGEMACEYLAKSIGGSGEVAILDGIPVVPILERVRGCKAA 185

Query: 187 LGKHPGIHVLSDDQDGKGSREGGLNVMQLYLTRFPKIDAVFTINDPQAVGADLAARQLNR 246
           L K PG+  L D Q+GK  R   L+V +  +   P +  VF++ND  ++GA L+A + + 
Sbjct: 186 LAKAPGVK-LVDTQNGKQERATALSVTENMIQAHPNLKGVFSVNDGGSMGA-LSAIESSG 243

Query: 247 GGILIASVDGAPDIEAAL-KANTLVQASASQDPWAIARTAVEIGVGLMHGQAPANRTVLL 305
             I + SVDGAP+  AA+ K N+    +++Q P    R A+ I +    G A   +T+ +
Sbjct: 244 KDIKLTSVDGAPEAIAAIQKPNSKFVETSAQFPADQVRIALGIALAKKWG-ANVPKTIPV 302

Query: 306 PPTLVTRANVNEY 318
              ++ ++N   +
Sbjct: 303 DVKMIDKSNAKGF 315


Lambda     K      H
   0.318    0.132    0.377 

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: 184
Number of extensions: 13
Number of successful extensions: 5
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: 325
Length of database: 317
Length adjustment: 28
Effective length of query: 297
Effective length of database: 289
Effective search space:    85833
Effective search space used:    85833
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 (21.7 bits)
S2: 48 (23.1 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