GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Pseudomonas fluorescens FW300-N2E2

Align ABC transporter for Lactose, ATPase component (characterized)
to candidate Pf6N2E2_1649 Maltose/maltodextrin transport ATP-binding protein MalK (EC 3.6.3.19)

Query= reanno::Smeli:SM_b20002
         (358 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1649
          Length = 384

 Score =  352 bits (904), Expect = e-102
 Identities = 187/360 (51%), Positives = 248/360 (68%), Gaps = 6/360 (1%)

Query: 3   ELQLSDVRKSYGGLEVIKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSGDLTI 62
           +L+L +V K  GG  +++ V L+I +GEFVVFVGPSGCGKSTLLR+IAGL+ I  GDL I
Sbjct: 3   KLKLDNVNKQLGGARILRDVSLEISAGEFVVFVGPSGCGKSTLLRLIAGLDSICDGDLLI 62

Query: 63  DDVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAAHILE 122
           D  R+ND++P +RG+ MVFQSYALYPHM+V +N+ F L+ A   +A + +RV + A IL+
Sbjct: 63  DGRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTEKASLRERVLKTAQILQ 122

Query: 123 LGALLDRKPKQLSGGQRQRVAIGRAIVRHPKIFLFDEPLSNLDAELRVHMRIEIARLHKQ 182
           L  LL RKP++LSGGQRQRVA+GRA+ R P I LFDEPLSNLDA LRV MR EIARLH +
Sbjct: 123 LDKLLQRKPRELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHGR 182

Query: 183 LATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPKMNFL 242
           L +T++YVTHDQVEAMTLADKIVV+  G +EQVGSP +LY+ PA+ FVAGF+GSPKMNFL
Sbjct: 183 LGSTMIYVTHDQVEAMTLADKIVVLNGGRIEQVGSPRELYEHPASRFVAGFLGSPKMNFL 242

Query: 243 KGVIEIDEDQAYARLPDYGDAKIPV-TLQAAAGTAVTIGIRPEHFD---EAGPAALD-LA 297
              +    + +    P  G   +P  +   A G+ +T+GIRPEH       G A +  + 
Sbjct: 243 PARLHSPGETSQIDSPLLGMTPLPFDSAHLAVGSPLTLGIRPEHMSLKAAQGSAGVGVVG 302

Query: 298 IDMLEHLGGETFAYARHHGNGELIVVETKNGRGLKTGDRLTARFDPVSVLVFDGEGKRLR 357
           +  +E+LG ET+ +    G  E ++   +   G + GDR+  +    SV +FD +G  LR
Sbjct: 303 VVGVEYLGSETYVHL-ESGEDEPLICRCEVNAGWRVGDRVELQLAFGSVHLFDADGTALR 361


Lambda     K      H
   0.321    0.139    0.396 

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: 435
Number of extensions: 15
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: 358
Length of database: 384
Length adjustment: 30
Effective length of query: 328
Effective length of database: 354
Effective search space:   116112
Effective search space used:   116112
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