GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Clostridium tyrobutyricum FAM22553

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_039653163.1 PN53_RS10415 ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_000816635.1:WP_039653163.1
          Length = 361

 Score =  224 bits (570), Expect = 4e-63
 Identities = 130/336 (38%), Positives = 205/336 (61%), Gaps = 29/336 (8%)

Query: 4   IIVKNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGELY 63
           +++ NV K +K  K  A+D V++++  GE   ILGPSG+GKT+ +++IAG +  ++GE+ 
Sbjct: 8   LLMNNVEKYYKSFK--AVDKVSLSVNKGEFLTILGPSGSGKTSLLKLIAGFEKINSGEIL 65

Query: 64  FDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRVEE 123
            +   + +       P +R IGM+FQ +AL+P++T F+NIA+PL   K+SK++IR++V  
Sbjct: 66  LNKENIETK-----KPYERNIGMLFQNYALFPHMTIFDNIAYPLKIRKLSKDQIRQKVMA 120

Query: 124 VAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARALV 183
           + +++D+  V N +P++LSGGQQQRVALARA+V +P LLLLDEP   LD  +R   +  +
Sbjct: 121 MLEMVDLEGVENRYPKQLSGGQQQRVALARAIVFNPPLLLLDEPLGALDKNLRQKMQLEI 180

Query: 184 KEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLIGE 243
           K +Q ++G+T + V+HD  +   ++D+V ++ KGKL Q+  PE++Y  P S  VA  IGE
Sbjct: 181 KHIQQKVGITTISVTHDQEEALTMSDKVCIMNKGKLEQIDTPENIYQKPKSRFVAEFIGE 240

Query: 244 IN-------ELEGKVT-----NEGVVIGSLRFPVSVSSDRAI-IGIRPEDVKLSKDVIKD 290
           IN       E EGKV      N+ +V   +  P      +A+ I +RPE++ ++KD  K 
Sbjct: 241 INLIRGKILETEGKVAIIEIFNKQIVKAEMDEPDQFVQGKAVSIALRPENIYVTKDKPKY 300

Query: 291 DS--------WILVGKG-KVKVIGYQGGLFRITITP 317
           D+         I VG   KVKVI  +     I + P
Sbjct: 301 DNNISAIIKEVIFVGDALKVKVINKKQEEMMIKVKP 336


Lambda     K      H
   0.319    0.139    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: 347
Number of extensions: 17
Number of successful extensions: 3
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: 353
Length of database: 361
Length adjustment: 29
Effective length of query: 324
Effective length of database: 332
Effective search space:   107568
Effective search space used:   107568
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 (21.7 bits)
S2: 49 (23.5 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:

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