GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas fluorescens GW456-L13

Align Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate PfGW456L13_1569 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= SwissProt::Q9YGA6
         (372 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1569
          Length = 372

 Score =  243 bits (619), Expect = 8e-69
 Identities = 141/304 (46%), Positives = 193/304 (63%), Gaps = 25/304 (8%)

Query: 4   VRLVDVWKVFGEV----TAVREMSLEVKDGEFMILLGPSGCGKTTTLRMIAGLEEPSRGQ 59
           V +  V KV+G+      A++ + L+++D EF  LLGPSGCGKTT LRMIAG E P+ G+
Sbjct: 12  VSIRSVRKVYGDPKTGPVALKSIDLDIRDNEFFTLLGPSGCGKTTLLRMIAGFEFPTEGE 71

Query: 60  IYIGDKLVADPEKGIFVPPKDRDIAMVFQSYALYPHMTVYDNIAFPLKL----RKVPRQE 115
           I +  + +AD       PP  R +  VFQ YAL+PHMT+ +N+AF L+     + + + +
Sbjct: 72  ILLYGENIADR------PPFQRPVNTVFQHYALFPHMTIAENLAFGLESHPMGKVLHKTQ 125

Query: 116 IDQRVREVAELLGLTELLNRKPRELSGGQRQRVALGRAIVRKPQVFLMDEPLSNLDAKLR 175
           + +RVRE+  L+ +    NRKP +LSGGQ+QRVAL RA+   P+V L+DEPLS LD KLR
Sbjct: 126 LAERVREMLALVQMERFANRKPAQLSGGQQQRVALARALAPHPKVLLLDEPLSALDLKLR 185

Query: 176 VRMRAELKKLQRQLGVTTIYVTHDQVEAMTMGDRIAVMNRGVLQQVGSPDEVYDKPANTF 235
             MR ELK +Q + G+T I+VTHDQ EA+TM DRIAV++ G +QQVG P+++Y++P N F
Sbjct: 186 QAMREELKTIQARTGITFIFVTHDQEEALTMSDRIAVLSEGEVQQVGRPEDIYERPRNRF 245

Query: 236 VAGFIGSPPMNFLDAIVT--EDGFVDFGEFRLKLLPDQ--FEVLGELGYVGREVIFGIRP 291
           VA FIG    NF++  VT  EDG   F       LP Q   +V      VG  V   +RP
Sbjct: 246 VADFIGE--TNFIEGTVTRVEDGLAWFAGPAGHPLPAQPCSDV-----RVGANVTLSVRP 298

Query: 292 EDLY 295
           E L+
Sbjct: 299 ERLH 302


Lambda     K      H
   0.323    0.142    0.406 

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: 362
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: 372
Length of database: 372
Length adjustment: 30
Effective length of query: 342
Effective length of database: 342
Effective search space:   116964
Effective search space used:   116964
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 49 (23.5 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