Alignments for a candidate for fruI in Pseudomonas putida KT2440

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruI in Pseudomonas putida KT2440

Align The fructose inducible fructose/xylitol porter, FruI (characterized)
to candidate PP_0795 PP_0795 fructose PTS permease - IIBC component

Query= TCDB::Q1LZ59
         (655 letters)



>FitnessBrowser__Putida:PP_0795
          Length = 580

 Score =  333 bits (855), Expect = 1e-95
 Identities = 206/514 (40%), Positives = 297/514 (57%), Gaps = 52/514 (10%)

Query: 148 ATEEEKKEATPAAPVADSHDF--LVAVTACTTGIAHTYMAEEALKKQAAEMGVGIKVETN 205
           A   E   A   AP A S     +VAVTAC TG+AHT+MA EAL++ A ++G  + VET 
Sbjct: 97  AANAELLAAVTGAPAAASSAGARIVAVTACPTGVAHTFMAAEALQQAAQQLGYQLTVETQ 156

Query: 206 GASGVGNKLTADDIKRAKGVIIAADKAVEMDRFNGKPLISRPVAEGIKKPEELINIILDG 265
           G+ G  N L+A+ I  A  V++AAD  V   RF GK +        +K+    ++  L  
Sbjct: 157 GSVGARNPLSAEAIAAADVVLLAADIEVPTARFAGKRIYRCGTGIALKQARATLDKAL-- 214

Query: 266 KAEAYVADNSDLSSEAS--SSEKAGLGSAFYKHLMSGVSQMLPFVIGGGIMIALSFLIDQ 323
            A+A V + +D ++  +   SEK G+    YKHL++GVS MLP V+ GG++IALSF+   
Sbjct: 215 -AQATVENGADAAAATTPTKSEKTGV----YKHLLTGVSFMLPMVVAGGLLIALSFVFGI 269

Query: 324 FMGVPKSSLSHLGNYHEIAAIFNQVGNAAFGFMIPVFAAYIAYSIAEKPGLVAGFVAGSM 383
                  +L         AA+    G AAF  M+P+ A YIA+SIA++PGL  G + G +
Sbjct: 270 EAYKEAGTLP--------AALMQIGGEAAFKLMVPLLAGYIAWSIADRPGLAPGMIGGLL 321

Query: 384 ATTGLAFNKVAFFEFGEKASQASLTGIPSGFLGALAGGFLAGGVILVLKKALAFVPRSLE 443
           A+T                       + +GF+G +  GFLAG     + +  A +P SLE
Sbjct: 322 AST-----------------------LGAGFIGGIVAGFLAGYSAKAIAR-WARLPSSLE 357

Query: 444 GIKSILLYPLLGVLVTGFLMLFV-NIPMAAINTALYNFLGNLSGGSAVLLGLIVGGMMAI 502
            +K IL+ PLL  L TG +M++V   P+AA+   L +FL ++   +A+LLGL++GGMM +
Sbjct: 358 ALKPILIIPLLASLFTGLVMIYVVGQPVAAMLEGLTHFLDSMGTTNAILLGLLLGGMMCV 417

Query: 503 DMGGPFNKAAYVFGTSTLTAAALAKGGSVVMASVMAGGMVPPLAVFVATLLFKNKFTQEE 562
           D+GGP NKAAY F    L +++ A      MA+ MA GMVPP+ + +AT L + KF Q E
Sbjct: 418 DLGGPINKAAYAFSVGLLASSSYAP-----MAATMAAGMVPPIGLGIATFLARRKFAQSE 472

Query: 563 HDAGLTNIVMGLSFITEGAIPFGAGDPARAIPSFIVGSAVTGALVGLSGIKLMAPHGGIF 622
            +AG   + +GL FI+EGAIPF A DP R IP+ I G A+TGAL    G KLMAPHGG+F
Sbjct: 473 REAGKAALALGLCFISEGAIPFAAKDPLRVIPASIAGGALTGALSMYFGCKLMAPHGGLF 532

Query: 623 VIAL---TSNPLLYLLYIAVGAVIAGILFGSLRK 653
           V+ +    ++ LLYLL I  G+++  +++  ++K
Sbjct: 533 VLLIPNAINHALLYLLAIVAGSLVTAVVYAVIKK 566


Lambda     K      H
   0.320    0.137    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: 810
Number of extensions: 31
Number of successful extensions: 6
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: 655
Length of database: 580
Length adjustment: 37
Effective length of query: 618
Effective length of database: 543
Effective search space:   335574
Effective search space used:   335574
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: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources