Alignments for a candidate for fruII-ABC in Klebsiella michiganensis M5al

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruII-ABC in Klebsiella michiganensis M5al

Align The fructose porter, FruA (fructose-1-P forming IIABC) (Delobbe et al. 1975) FruA is 39% identical to 4.A.2.1.1). fructose can be metabolized to Fru-1-P via this system as well as Fru-6-P by another PTS system (characterized)
to candidate BWI76_RS19725 BWI76_RS19725 PTS fructose transporter subunit EIIBC

Query= TCDB::P71012
         (635 letters)



>FitnessBrowser__Koxy:BWI76_RS19725
          Length = 558

 Score =  421 bits (1081), Expect = e-122
 Identities = 219/470 (46%), Positives = 310/470 (65%), Gaps = 18/470 (3%)

Query: 165 APAGKGKILAVTACPTGIAHTFMAADALKEKAKELGVEIKVETNGSSGIKHKLTAQEIED 224
           A  G  +I+AVTACPTG+AHTFMAA+A++ +AK+ G  +KVET GS G  + +T +E+E 
Sbjct: 99  AANGPKRIVAVTACPTGVAHTFMAAEAIETEAKKRGWWVKVETRGSVGAGNAITPEEVEQ 158

Query: 225 APAIIVAADKQVEMERFKGKRVLQVPVTAGIRRPQELIEKAMNQDAPIYQGSGGGSAASN 284
           A  ++VAAD +V++ +F GK + +      +++  + ++KA+ +  P YQ +G   AA+ 
Sbjct: 159 ADLVVVAADIEVDLAKFAGKPMYRTTTGLALKKTAQELDKAVVEAKP-YQPAGKSQAAAE 217

Query: 285 DDEEAKGKSGSGIGNTFYKHLMSGVSNMLPFVVGGGILVAISFFWGIHSADPNDPSYNTF 344
             +E+ G          Y+HL++GVS MLP VV GG+ +A+SF +GI + +  D    T 
Sbjct: 218 GKKESAGA---------YRHLLTGVSYMLPMVVAGGLCIALSFAFGIKAFEVKD----TL 264

Query: 345 AAALNFIGGDNALKLIVAVLAGFIAMSIADRPGFAPGMVGGFMATQANAGFLGGLIAGFL 404
           AAAL  IGG +A  L+V VLAGFIA SIADRPG  PG++GG +A    +GF+GG+IAGFL
Sbjct: 265 AAALMQIGGGSAFALMVPVLAGFIAFSIADRPGLTPGLIGGMLAVSTGSGFIGGIIAGFL 324

Query: 405 AGYVVILLKKVFTFIPQSLDGLKPVLIYPLFGIFITGVLMQFVVNTPVAAFMNFLTNWLE 464
           AGYV   +      +PQS++ LKP+LI PL    I G+ M +++  PVA  +  LT+WL+
Sbjct: 325 AGYVAKAISTKLK-LPQSMEALKPILIIPLVSSLIVGLAMIYLIGKPVAGILEGLTHWLQ 383

Query: 465 SLGTGNLVLMGIILGGMMAIDMGGPLNKAAFTFGIAMIDAGNYAPHAAIMAGGMVPPLGI 524
           ++GT N VL+G ILGGMM  DMGGP+NKAA+ FG+ ++    YAP AAIMA GMVPPL +
Sbjct: 384 TMGTANAVLLGAILGGMMCTDMGGPVNKAAYAFGVGLLSTQTYAPMAAIMAAGMVPPLAL 443

Query: 525 ALATTIFRNKFTQRDREAGITCYFMGAAFVTEGAIPFAAADPLRVIPAAVVGAAVAGGLT 584
            LAT I R KF +  +E G     +G  F+TEGAIPFAA DP+RV+P  +VG AV G ++
Sbjct: 444 GLATLIARKKFDKAQQEGGKAALVLGLCFITEGAIPFAARDPMRVLPCCIVGGAVTGAMS 503

Query: 585 EFFRVTLPAPHGGVFVAFITN--HPML-YLLSIVIGAVVMAIILGIVKKP 631
            +    L APHGG+FV  I     P+L YL++IV+G +V  +   ++K+P
Sbjct: 504 MWVGAKLMAPHGGLFVLLIPGAITPVLGYLMAIVVGTLVAGLSYAVLKRP 553


Lambda     K      H
   0.320    0.137    0.390 

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: 844
Number of extensions: 39
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: 635
Length of database: 558
Length adjustment: 37
Effective length of query: 598
Effective length of database: 521
Effective search space:   311558
Effective search space used:   311558
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)
Organisms (tab-delimited)
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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