GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Burkholderia phytofirmans PsJN

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate BPHYT_RS29175 BPHYT_RS29175 ABC transporter ATP-binding protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__BFirm:BPHYT_RS29175
          Length = 390

 Score =  311 bits (796), Expect = 3e-89
 Identities = 165/356 (46%), Positives = 227/356 (63%), Gaps = 6/356 (1%)

Query: 10  NKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGGAILVDDADI 69
           N T   G    ++N++L +  GEF++L+GPSGCGKSTL++ IAGL  ++ G+I +   D+
Sbjct: 41  NLTIQLGANTVIENLDLDVQAGEFVVLLGPSGCGKSTLLHSIAGLIDVTDGSIEIAGEDM 100

Query: 70  SGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVSKLLQIEHLL 129
           +   PKDR IA+VFQSYALYPTMSV  N++F L+I   P AEI   VAR S++LQ+  LL
Sbjct: 101 TWADPKDRRIALVFQSYALYPTMSVERNLSFALRINGTPKAEIARRVARASEMLQLGPLL 160

Query: 130 SRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKLMHQRLKTTT 189
            RKP QLSGGQ+QRVA+GRA+ R   ++LFDEPLSNLDAKLR E+R E+K +HQRL  T 
Sbjct: 161 KRKPAQLSGGQRQRVAIGRAIVREADVFLFDEPLSNLDAKLRTELRRELKQLHQRLGATM 220

Query: 190 VYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPPMNFIPLRLQ 249
           +YVTHDQ+EAMTL  ++AVM+ G+IQQFGTP ++Y  P NLFVA+F+G+P MN I  RL+
Sbjct: 221 IYVTHDQVEAMTLATRMAVMRGGVIQQFGTPAEVYARPDNLFVATFLGTPAMNLIKGRLE 280

Query: 250 RKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQIILANGEANGLPTIRAEVQ 309
            +DG L    +  +         +         +LG+R E + LA G +       A+V 
Sbjct: 281 TRDGALHFCTEHWRLDVS-RYPFRTTPANGLPCVLGVRAEDVRLAEGASE-----HAKVS 334

Query: 310 VTEPTGPDTLVFVNLNDTKVCCRLAPDVAPAVGETLTLQFDPAKVLLFDAKTGERL 365
           + EP G   +++++ +  +V          A+G+     FD   V LFD   G RL
Sbjct: 335 LVEPMGNHRVIWLDYHGVQVASIDQTKTPLAIGDAAAFSFDSTHVSLFDEAGGARL 390


Lambda     K      H
   0.319    0.138    0.393 

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: 441
Number of extensions: 14
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: 386
Length of database: 390
Length adjustment: 30
Effective length of query: 356
Effective length of database: 360
Effective search space:   128160
Effective search space used:   128160
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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