GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Pseudomonas fluorescens FW300-N1B4

Align m-Inositol ABC transporter, permease component (iatP) (characterized)
to candidate Pf1N1B4_409 L-arabinose transport system permease protein (TC 3.A.1.2.2)

Query= reanno::pseudo3_N2E3:AO353_21390
         (340 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_409
          Length = 322

 Score =  175 bits (444), Expect = 1e-48
 Identities = 108/338 (31%), Positives = 182/338 (53%), Gaps = 25/338 (7%)

Query: 5   LENKPAMAPAK--SRRRLPTELSIFLVLIGIGLVFEMFGWIVRDQSFLMNSQRLVLMILQ 62
           ++NK    P K    RR   +  + L  +GI   F +   ++ +    +N + L L I  
Sbjct: 3   VQNKALPTPRKPLDLRRFLDDWVMLLAAVGI---FVLCTLLIDNFLSPLNMRGLGLAI-- 57

Query: 63  VSIIGLLAIGVTQVIITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLPVWIP 122
            S  G+ A  +   + +   DLS GSV+A + ++AA + + +D             V++ 
Sbjct: 58  -STTGIAACTMLYCLASGHFDLSVGSVIACAGVVAAVVMRDTD------------SVFLG 104

Query: 123 VIAGLGVGLLAGAINGSIIAVTGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAI 182
           V A L +GL+ G ING +IA   +   I TL  M   RGLA  +  G+ V +  + +   
Sbjct: 105 VSAALVMGLIVGLINGIVIAKLRVNALITTLATMQIVRGLAYIFANGKAVGVSQEQFFVF 164

Query: 183 GHGAM-----PVIIFLVVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVY 237
           G+G +     P++I +V  + F   L YT YG+ T AIGGN +AA  +G+NV R   +++
Sbjct: 165 GNGQLFGVPVPILITIVCFLFFGWLLNYTTYGRNTMAIGGNQEAALLAGVNVDRTKTLIF 224

Query: 238 SIAGLLAGLAGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALI 297
           ++ G++  LAGV+ ++R  +GQ  +G  +EL  I+A V+GG SL+GG+G I   + G LI
Sbjct: 225 AVHGVIGALAGVILASRMTSGQPMIGQGFELTVISACVLGGVSLSGGIGMIRHVIAGVLI 284

Query: 298 LGVMASGFTFVGVDAYIQDIIKGLIIVIAVVIDQYRNK 335
           L ++ +      +D + Q +I+G I+++AVVID+ + +
Sbjct: 285 LAIIENAMNLKNIDTFYQYVIRGSILLLAVVIDRLKQR 322


Lambda     K      H
   0.326    0.140    0.394 

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: 265
Number of extensions: 13
Number of successful extensions: 2
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: 340
Length of database: 322
Length adjustment: 28
Effective length of query: 312
Effective length of database: 294
Effective search space:    91728
Effective search space used:    91728
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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.

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