GapMind for catabolism of small carbon sources

 

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

Align Trehalose import ATP-binding protein SugC; EC 7.5.2.- (characterized)
to candidate PfGW456L13_1799 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= SwissProt::P9WQI3
         (393 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1799
          Length = 351

 Score =  259 bits (661), Expect = 1e-73
 Identities = 149/317 (47%), Positives = 199/317 (62%), Gaps = 12/317 (3%)

Query: 1   MAEIVLDHVNKSYPDGHTAVRDLNLTIADGEFLILVGPSGCGKTTTLNMIAGLEDISSGE 60
           M+ ++L++V K Y     AV+D+NL + +G+ +  +GPSGCGKTT L MIAGLE +S GE
Sbjct: 1   MSGLILENVEKHYGSA-CAVKDVNLHLPEGKLVCFLGPSGCGKTTLLRMIAGLETLSGGE 59

Query: 61  LRIAGERVNEKAPKDRDIAMVFQSYALYPHMTVRQNIAFPLTLAKMRKADIAQKVSETAK 120
           +R+ GE +       R+  MVFQS AL+PHMTV +NIA+PL L  + KAD   +V E  +
Sbjct: 60  IRLDGEDIGHTPAHLRNFGMVFQSLALFPHMTVGENIAYPLKLRGVSKADQQARVVELLE 119

Query: 121 ILDLTNLLDRKPSQLSGGQRQRVAMGRAIVRHPKAFLMDEPLSNLDAKLRVQMRGEIAQL 180
           ++ L  +++R  ++LSGGQRQRVA+ RAI  HPK  L+DEPLS LDAKLR  M+ EI QL
Sbjct: 120 LIQLQAMINRPVAKLSGGQRQRVAIARAIANHPKILLLDEPLSALDAKLRESMQVEIRQL 179

Query: 181 QRRLGTTTVYVTHDQTEAMTLGDRVVVMYGGIAQQIGTPEELYERPANLFVAGFIGSPAM 240
           Q+RL  TT+ VTHDQ EAMT+ D VVV+     QQ+GTP E+Y  PAN FVA FIGS   
Sbjct: 180 QQRLNITTIMVTHDQREAMTMADIVVVLGEHKVQQVGTPIEIYRHPANEFVADFIGSG-- 237

Query: 241 NFFPARLTAIG-LTLPFGEVTLAPEVQGVIAAHPKPENVIVGVRPEHIQDAALIDAYQRI 299
           N FPA +   G ++LP G+    P    ++      E V + +RPE +Q    + A Q  
Sbjct: 238 NIFPATVLGNGKVSLPGGDALQVPICSSIVVG----EKVKMLIRPEDLQ----LSAPQAT 289

Query: 300 RALTFQVKVNLVESLGA 316
                  KV  V  +GA
Sbjct: 290 AGNRLLGKVTFVRDIGA 306


Lambda     K      H
   0.319    0.135    0.377 

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: 336
Number of extensions: 9
Number of successful extensions: 1
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: 393
Length of database: 351
Length adjustment: 30
Effective length of query: 363
Effective length of database: 321
Effective search space:   116523
Effective search space used:   116523
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