GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Desulfacinum infernum DSM 9756

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_073037017.1 BUB04_RS03595 ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_900129305.1:WP_073037017.1
          Length = 362

 Score =  207 bits (528), Expect = 3e-58
 Identities = 115/327 (35%), Positives = 194/327 (59%), Gaps = 25/327 (7%)

Query: 2   VRIIVKNVSKVFKKG--KVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPST 59
           + I +  ++K+++    K+ ALD V++ +     F +LGPSG GKTT +R + GL+ P  
Sbjct: 1   MEIRITGLTKIYESEGKKIHALDRVDLTVPANHIFTLLGPSGCGKTTLLRCLVGLESPDE 60

Query: 60  GELYFDDRLVASNGK-LIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIR 118
           GE+   + +V S  K + VPPE R +GMVFQT+A++P++T F+N+A+PL   ++ ++EIR
Sbjct: 61  GEISIGEEVVWSREKGVFVPPEKRGLGMVFQTYAIWPHMTVFDNVAYPLQVRRLPRDEIR 120

Query: 119 KRVEEVAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDS 178
            +V  V K++ +  + N    +LSGGQQQRVALARALV +P ++L DEP SNLDA++R+ 
Sbjct: 121 SKVAAVLKLVQLDALENRPATKLSGGQQQRVALARALVAEPKVILFDEPLSNLDAKLREE 180

Query: 179 ARALVKEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVA 238
            R  +++  + LG+T + V+HD  +  +++D + V+  G++V++G P+ +Y       VA
Sbjct: 181 TRKELRQFLTELGITAVYVTHDRVEALSLSDSIAVMKDGQIVEIGSPQKIYFQAEHPFVA 240

Query: 239 SLIGEINELEGKV-TNEGVVIG---------SLRFPVSVSSDRAIIGIRPEDVKLSKDVI 288
             IG  N + G V T E  ++          + R P     D   + +RPE +++  D +
Sbjct: 241 DFIGRANLIPGTVETREEDLVAVETPIGKVLAARGPKVARGDEVTVCVRPEFIRVVADPL 300

Query: 289 KD---------DSWILVG---KGKVKV 303
            +         +S + VG   +G+V+V
Sbjct: 301 AEGINTFSGVVESLVFVGEAHEGEVRV 327


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: 330
Number of extensions: 15
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 353
Length of database: 362
Length adjustment: 29
Effective length of query: 324
Effective length of database: 333
Effective search space:   107892
Effective search space used:   107892
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.

Links

Downloads

Related tools

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