GapMind for catabolism of small carbon sources

 

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

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate PfGW456L13_1569 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1569
          Length = 372

 Score =  234 bits (597), Expect = 3e-66
 Identities = 132/303 (43%), Positives = 184/303 (60%), Gaps = 15/303 (4%)

Query: 4   IQLTDLTKRFGDT----VAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGD 59
           + +  + K +GD     VA+  + LDI D EF  L+GPSGCGK+T LRM+AG E PT G+
Sbjct: 12  VSIRSVRKVYGDPKTGPVALKSIDLDIRDNEFFTLLGPSGCGKTTLLRMIAGFEFPTEGE 71

Query: 60  IYIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEE---EGYTSAERDERVV 116
           I + G+++  R P  R +  VFQ YAL+PHMT+ +N+ FGLE     +     +  ERV 
Sbjct: 72  ILLYGENIADRPPFQRPVNTVFQHYALFPHMTIAENLAFGLESHPMGKVLHKTQLAERVR 131

Query: 117 EVAETLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTE 176
           E+   + +    +RKP +LSGGQQQRVAL RA+   P+V L+DEPLS LD KLR  MR E
Sbjct: 132 EMLALVQMERFANRKPAQLSGGQQQRVALARALAPHPKVLLLDEPLSALDLKLRQAMREE 191

Query: 177 LQNLQDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIG 236
           L+ +Q +  +T ++VTH+Q EA+TM+DRIAV+ +GE+QQV  P + Y  P N FVA+FIG
Sbjct: 192 LKTIQARTGITFIFVTHDQEEALTMSDRIAVLSEGEVQQVGRPEDIYERPRNRFVADFIG 251

Query: 237 EPMINLVRGTRSE-----STFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAP 291
           E   N + GT +      + F G    +PL       V    +  L VRPE + +  A  
Sbjct: 252 E--TNFIEGTVTRVEDGLAWFAGP-AGHPLPAQPCSDVRVGANVTLSVRPERLHLVPATT 308

Query: 292 DDA 294
           ++A
Sbjct: 309 ENA 311


Lambda     K      H
   0.317    0.135    0.386 

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: 342
Number of extensions: 16
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 383
Length of database: 372
Length adjustment: 30
Effective length of query: 353
Effective length of database: 342
Effective search space:   120726
Effective search space used:   120726
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 (21.6 bits)
S2: 50 (23.9 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