Alignments for a candidate for fruK in Trichormus variabilis ATCC 29413

GapMind for catabolism of small carbon sources

Alignments for a candidate for fruK in Trichormus variabilis ATCC 29413

Align Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized)
to candidate WP_011318959.1 AVA_RS10980 sugar ABC transporter ATP-binding protein

Query= SwissProt::Q8G847
         (513 letters)



>NCBI__GCF_000204075.1:WP_011318959.1
          Length = 517

 Score =  371 bits (952), Expect = e-107
 Identities = 194/485 (40%), Positives = 314/485 (64%), Gaps = 9/485 (1%)

Query: 6   PIVVMKGITIEFPGVKALDGVDLTLYPGEVHALMGENGAGKSTMIKALTGVYKINAGSIM 65
           P++ M+GI   F GV AL GV+LT+YPGEVHALMGENGAGKST++K L G Y  + G I 
Sbjct: 17  PVLEMQGIAKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIR 76

Query: 66  VDGKPQQFNGTLDAQNAGIATVYQEVNLCTNLSVGENVMLGHE-KRGPFGIDWKKTHEAA 124
           ++GK  +      A+ AGI  +YQE+N+  NL+V EN+ +G E  RG F +D K     A
Sbjct: 77  INGKGVKITDPGTARQAGINLIYQELNVAPNLTVTENIFMGSELTRGQF-LDRKAMELEA 135

Query: 125 KKYLAQMGLESIDPHTPLSSISIAMQQLVAIARAMVINAKVLILDEPTSSLDANEVRDLF 184
           ++ LA +G  S  P   + +++IA QQ V IARA+  N+++L++DEPT++L   E   LF
Sbjct: 136 QQVLASLG-ASFAPTDIVGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDRETERLF 194

Query: 185 AIMRKVRDSGVAILFVSHFLDQIYEITDRLTILRNGQFIKEVMTKDTPRDELIGMMIGKS 244
            ++RK+R+ G+AI+++SH +++IY + DR+++LR+GQ+I  +  ++     L+ MM+G+S
Sbjct: 195 EVIRKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLVQMMVGRS 254

Query: 245 AAELSQIGAKKARREITPGEKPIVDVKGLGKKGTINPVDVDIYKGEVVGFAGLLGSGRTE 304
             +  +      +R+  PG   +++V+ +     + P    +  GE++G AGL+G+GRTE
Sbjct: 255 MQDFYE-----HQRQSNPG-PVVLEVRNISDGRKVQPASFQLRAGEILGLAGLVGAGRTE 308

Query: 305 LGRLLYGADKPDSGTYTLNGKKVNISDPYTALKNKIAYSTENRRDEGIIGDLTVRQNILI 364
           + RL++GAD+  SG   LNGKK+ I  P  A+   I Y  E+R+D+G+  +++ R+NI +
Sbjct: 309 VSRLIFGADRKVSGEVFLNGKKLEIHSPSDAIAVGIGYVPEDRKDQGLFLEMSSRKNIGL 368

Query: 365 ALQATRGMFKPIPKKEADAIVDKYMKELNVRPADPDRPVKNLSGGNQQKVLIGRWLATHP 424
                      +     + I    ++  ++R A+ +    +LSGGNQQK+L+ RWLA +P
Sbjct: 369 NRLKQDANLGIVNWGSVNKIATDAVENFHIRLANLEIRAVDLSGGNQQKLLLARWLAINP 428

Query: 425 ELLILDEPTRGIDIGAKAEIQQVVLDLASQGMGVVFISSELEEVVRLSDDIEVLKDRHKI 484
            +L+LDEPTRG+DIGAK+EI +++ DL++QG+ ++ +SSEL E+V LSD + V+++   +
Sbjct: 429 RVLMLDEPTRGVDIGAKSEIYRIISDLSAQGVAILMVSSELPEIVGLSDRVLVMREGQLV 488

Query: 485 AEIEN 489
            E++N
Sbjct: 489 GELDN 493



 Score =  104 bits (259), Expect = 9e-27
 Identities = 69/237 (29%), Positives = 122/237 (51%), Gaps = 10/237 (4%)

Query: 266 PIVDVKGLGKK----GTINPVDVDIYKGEVVGFAGLLGSGRTELGRLLYGADKPDSGTYT 321
           P+++++G+ K+      +  V++ IY GEV    G  G+G++ L ++L GA   D G   
Sbjct: 17  PVLEMQGIAKRFHGVPALQGVNLTIYPGEVHALMGENGAGKSTLMKILAGAYIADEGEIR 76

Query: 322 LNGKKVNISDPYTALKNKIAYSTENRRDEGIIGDLTVRQNILIALQATRGMFKPIPKKEA 381
           +NGK V I+DP TA +  I    +   +  +  +LTV +NI +  + TRG F  + +K  
Sbjct: 77  INGKGVKITDPGTARQAGINLIYQ---ELNVAPNLTVTENIFMGSELTRGQF--LDRKAM 131

Query: 382 DAIVDKYMKELNVRPADPDRPVKNLSGGNQQKVLIGRWLATHPELLILDEPTRGIDIGAK 441
           +    + +  L    A  D  V  L+   QQ+V I R L  +  +L++DEPT  +     
Sbjct: 132 ELEAQQVLASLGASFAPTDI-VGTLAIAEQQQVEIARALKDNSRILVMDEPTAALSDRET 190

Query: 442 AEIQQVVLDLASQGMGVVFISSELEEVVRLSDDIEVLKDRHKIAEIENDDTVSQATI 498
             + +V+  L + G+ +++IS  +EE+  L+D I VL+D   I  +  ++   Q  +
Sbjct: 191 ERLFEVIRKLRNDGIAIIYISHRMEEIYALADRISVLRDGQYIGSLTREEISPQRLV 247


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: 667
Number of extensions: 29
Number of successful extensions: 9
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 513
Length of database: 517
Length adjustment: 35
Effective length of query: 478
Effective length of database: 482
Effective search space:   230396
Effective search space used:   230396
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