GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Lactobacillus shenzhenensis LY-73

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_022528631.1 L248_RS03205 ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_000469325.1:WP_022528631.1
          Length = 362

 Score =  204 bits (520), Expect = 2e-57
 Identities = 121/357 (33%), Positives = 204/357 (57%), Gaps = 29/357 (8%)

Query: 7   KNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGELYFDD 66
           KNV+K F  G   AL N+N  ++ G+ + +LGPSG+GKTT +R IAG   P++G + F  
Sbjct: 9   KNVNKFF--GDFQALKNINFALDQGKFYSLLGPSGSGKTTILRTIAGFTSPTSGTVLFQG 66

Query: 67  RLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRVEEVAK 126
           +   +     +P   RK+  +FQ +AL+P+L  F+N+AF L+   + K+EI  RV +  K
Sbjct: 67  QPQNN-----IPANKRKVNTIFQNYALFPHLNVFDNVAFGLSIRHVPKDEIETRVMDNLK 121

Query: 127 ILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARALVKEV 186
           ++ +  + N    ELSGGQQQRVA+ARA++ +P LLLLDEP S LD ++R   +  ++E+
Sbjct: 122 LVHLQDLANREINELSGGQQQRVAIARAIINEPVLLLLDEPLSALDKKLRQDMQYELREL 181

Query: 187 QSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLIGEINE 246
           Q RLG+T + V+HD  +  A++D + V+  G+++Q G P D+YD P++  VA  IGE N 
Sbjct: 182 QQRLGITFVFVTHDQEEALALSDEIFVMDAGEILQNGTPVDIYDEPINHFVADFIGESNI 241

Query: 247 LEGKVTNE-GVVIGSLRFPVSVS----SDRAIIGIRPEDVKLS-----KDVIKDDSWILV 296
           ++G +  +  V     RF  + +    ++   + +RPED+ ++     K V++ DS +  
Sbjct: 242 VKGTMIKDYEVEFVGKRFECADAGMKPNEPVEVVLRPEDLDVTTPEKGKLVVQVDSQL-- 299

Query: 297 GKGKVKVIGYQGGLFRITITPLDSEEEIFTYSDHPIHSGEEVLVYVRKDKIKVFEKN 353
                    ++G  F +     D  E +  +S +P+   +++ ++   + I V   N
Sbjct: 300 ---------FRGDHFEVVAYDADHNEWLI-HSTNPVEEDKDIGLFFEPEDIHVMRFN 346


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: 348
Number of extensions: 15
Number of successful extensions: 2
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: 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 Sep 24 2021. 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