GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Pseudomonas fluorescens FW300-N2E3

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate AO353_25130 AO353_25130 ABC transporter

Query= reanno::Smeli:SMc03065
         (362 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_25130
          Length = 381

 Score =  340 bits (872), Expect = 4e-98
 Identities = 189/367 (51%), Positives = 246/367 (67%), Gaps = 15/367 (4%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  L L ++ K  G V ++  + L+I  GEFVVFVGPSGCGKSTLLR+IAGL+ I  GD+
Sbjct: 1   MIKLKLDNVNKQLGGVRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICAGDL 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            ID  RVND+ P +RG+ MVFQSYALYPHM+VYDN++FG+++A+  K  +  RV   A +
Sbjct: 61  LIDERRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKSSLRERVLRTAQI 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           LQL   L R PK LSGGQRQRVA+GRA+ R P + LFDEPLSNLDA+LRV  R EIA+L 
Sbjct: 121 LQLDKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
            R+  +TMIYVTHDQVEAMTLAD+IVVL+ G +EQVG+P ELYERPA+ FVA F+GSP M
Sbjct: 181 ARLG-STMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRM 239

Query: 241 NVIPATITATGQQTAVS--LAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLF 298
           N + A + A G+ + V   + G  S+  D    A++     S GVRPE + +  AD    
Sbjct: 240 NFLAARLHAPGETSLVDTPVLGMTSLPFDSSNLAADT--PLSLGVRPEHVSLKAAD---- 293

Query: 299 EGTVSI----VEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFD 354
            GTV +    VE LG  T ++++   +++P+I +    A    GD+V    D   LHLFD
Sbjct: 294 -GTVGVIVTGVEYLGSETYVHLD-TGQDDPLICRCEVNAGWQVGDRVELQLDIGNLHLFD 351

Query: 355 TNGQSYR 361
            +G + R
Sbjct: 352 ADGTALR 358


Lambda     K      H
   0.320    0.137    0.387 

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: 368
Number of extensions: 14
Number of successful extensions: 3
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: 362
Length of database: 381
Length adjustment: 30
Effective length of query: 332
Effective length of database: 351
Effective search space:   116532
Effective search space used:   116532
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: 49 (23.5 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