Alignments for a candidate for fruK in Rhizobium leguminosarum bv. trifolii WSM1325

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruK in Rhizobium leguminosarum bv. trifolii WSM1325

Align Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized)
to candidate WP_012757420.1 RLEG_RS09440 sugar ABC transporter ATP-binding protein

Query= SwissProt::Q8G847
         (513 letters)



>NCBI__GCF_000023185.1:WP_012757420.1
          Length = 507

 Score =  446 bits (1146), Expect = e-129
 Identities = 238/501 (47%), Positives = 336/501 (67%), Gaps = 6/501 (1%)

Query: 3   DKNPIVVMKGITIEFPGVKALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINAG 62
           D   ++   GI+  FPG  ALD VD TL  GEVHAL+GENGAGKST+IK +TG Y  + G
Sbjct: 4   DFENVLAASGISKFFPGAVALDKVDFTLRRGEVHALLGENGAGKSTLIKCITGAYHRDEG 63

Query: 63  SIMVDGKPQQFNGTLDAQNAGIATVYQEVNLCTNLSVGENVMLGHEKRGPFGIDWKKTHE 122
           S+M++G+      TL AQ  GI TVYQEVNL +NLSV EN+ LG + R     D +  + 
Sbjct: 64  SLMLEGQEINPANTLAAQKLGIGTVYQEVNLLSNLSVAENLFLGRQPRRFGMTDVRSMNR 123

Query: 123 AAKKYLAQMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSLDANEVRD 182
            A+  LA  G++ ID    L   S+A+QQ+VAIARA+ ++ KVLILDEPT+SLD  EV  
Sbjct: 124 KARDLLAGYGVD-IDVTAELGRFSVAVQQVVAIARAVDLSGKVLILDEPTASLDNQEVAL 182

Query: 183 LFAIMRKVRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDELIGMMIG 242
           LF I+  ++  G+ I+F++HFL+Q+Y I+DR+T+LRNG+ +      D PR  LI MM+G
Sbjct: 183 LFRIIEDLKKRGLGIVFITHFLEQVYAISDRITVLRNGKLVGTRDAADLPRQGLIAMMLG 242

Query: 243 KSAAELSQIGAKKARREITPGEKPIVDVKGLGKKGTINPVDVDIYKGEVVGFAGLLGSGR 302
           +   EL+ +      R +  G+       G GK+G + P D+++  GEVVG AGLLGSGR
Sbjct: 243 R---ELAHVEETVRERSLAAGDVRY-HFAGYGKRGKVKPFDLEVRAGEVVGVAGLLGSGR 298

Query: 303 TELGRLLYGADKPDSGTYTLNGKKVNISDPYTALKNKIAYSTENRRDEGIIGDLTVRQNI 362
           TE   LL+G +  DSG+ T++G+ V IS P  A+     +  E+R+ +GIIGDL++R+NI
Sbjct: 299 TETAELLFGIEHADSGSATIDGQPVTISSPRAAIAKGFGFCPEDRKTDGIIGDLSIRENI 358

Query: 363 LIALQATRGMFKPIPKKEADAIVDKYMKELNVRPADPDRPVKNLSGGNQQKVLIGRWLAT 422
            +ALQA RG  +P+ + E + + D+Y+K L++R  D ++P++ LSGGNQQK ++ RWLAT
Sbjct: 359 ALALQARRGWTRPLSRAEQNTLADRYIKALDIRTTDREKPIRLLSGGNQQKAILARWLAT 418

Query: 423 HPELLILDEPTRGIDIGAKAEIQQVVLDLASQGMGVVFISSELEEVVRLSDDIEVLKDRH 482
           +P+ LILDEPTRGID+GA AEI +++ +L + GM ++ ISSELEE+V  S  + VL+DR 
Sbjct: 419 NPKFLILDEPTRGIDVGAHAEIIRLIEELCAGGMSLIVISSELEELVAYSSRVIVLRDRQ 478

Query: 483 KIAEIENDDTVSQATIVETIA 503
            IAE+   + ++ A IVE IA
Sbjct: 479 HIAEL-TGERITAAGIVEAIA 498


Lambda     K      H
   0.316    0.135    0.376 

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: 693
Number of extensions: 32
Number of successful extensions: 7
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: 513
Length of database: 507
Length adjustment: 34
Effective length of query: 479
Effective length of database: 473
Effective search space:   226567
Effective search space used:   226567
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: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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:

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 2024 update 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