GapMind for catabolism of small carbon sources

 

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

Align L-arabinose-binding periplasmic protein; ABP (characterized)
to candidate Pf6N2E2_5968 L-arabinose-binding periplasmic protein precursor AraF (TC 3.A.1.2.2)

Query= SwissProt::P02924
         (329 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5968
          Length = 334

 Score =  375 bits (962), Expect = e-108
 Identities = 189/322 (58%), Positives = 242/322 (75%), Gaps = 2/322 (0%)

Query: 6   KALAAIGLAAVMSQSAMAENLKLGFLVKQPEEPWFQTEWKFADKAGKDLGFEVIKIAVPD 65
           +A  A+   ++ S    A+ +K+GFLVKQ EEPWFQTEW FA+KA KD GF++IKIAVPD
Sbjct: 12  RAALAVTAVSLSSHLLAADAVKIGFLVKQAEEPWFQTEWAFAEKAAKDKGFQLIKIAVPD 71

Query: 66  GEKTLNAIDSLAASGAKGFVICTPDPKLGSAIVAKARGYDMKVIAVDDQFVNAKGKPMDT 125
           GEKTL+AIDSLAA+GAKGFVIC PD  LG AIVAKA+  DMKVIAVDD+FV + GK M+ 
Sbjct: 72  GEKTLSAIDSLAANGAKGFVICPPDVSLGPAIVAKAKLNDMKVIAVDDRFVGSDGKFMED 131

Query: 126 VPLVMMAATKIGERQGQELYKEMQKRGWDVKESAVMAITANELDTARRRTTGSMDALKAA 185
           VP + MAA ++G++QG  +  E +KRGWD K++  +  T NELDT ++RT GS+DALK A
Sbjct: 132 VPYLGMAAFEVGQKQGGAMAAEAKKRGWDWKDTYAVINTYNELDTGKKRTDGSVDALKKA 191

Query: 186 GFPEKQIYQVPTKSNDIPGAFDAANSMLVQHPE-VKHWLIVGMNDSTVLGGVRATEGQGF 244
           G P   I     K+ D+PG+ D+ NS LV+ P   K+ +I GMND+TVLGGVRATE  GF
Sbjct: 192 GMPADHILYSALKTLDVPGSMDSTNSALVKLPSAAKNLIIGGMNDNTVLGGVRATEAAGF 251

Query: 245 KAADIIGIGINGVDAVSELSKAQATGFYGSLLPSPDVHGYKSSEMLYNWVAKDVEPPKFT 304
           KAA++IGIGING DA+ EL K   +GF+GS+LPSP + GYK++EM+Y W+    EPPK+T
Sbjct: 252 KAANVIGIGINGTDAIGELKKPD-SGFFGSMLPSPHIEGYKTAEMMYEWITTGKEPPKYT 310

Query: 305 EVTDVVLITRDNFKEELEKKGL 326
            + +V LITR+NFK+ELEK GL
Sbjct: 311 AMDEVTLITRENFKQELEKIGL 332


Lambda     K      H
   0.315    0.132    0.381 

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: 374
Number of extensions: 17
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: 329
Length of database: 334
Length adjustment: 28
Effective length of query: 301
Effective length of database: 306
Effective search space:    92106
Effective search space used:    92106
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: 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