GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Pseudovibrio axinellae Ad2

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate WP_068005085.1 PsAD2_RS09075 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_2941
         (350 letters)



>NCBI__GCF_001623255.1:WP_068005085.1
          Length = 363

 Score =  295 bits (756), Expect = 1e-84
 Identities = 157/335 (46%), Positives = 225/335 (67%), Gaps = 10/335 (2%)

Query: 2   AYLQLRGIEKFFGEHRAIKGIDLTIQQGEFIVFVGPSGCGKSTLLRLIAGLEAIDGGSLM 61
           A+L+L  + K +G+  A+  ++L++  G F V +GPSGCGKST LRLIAGLE    G + 
Sbjct: 8   AHLELSNLTKSWGDTTAVNQVNLSVTGGSFTVLLGPSGCGKSTTLRLIAGLEEATSGQIS 67

Query: 62  LDGRDITDQPSSKRDLAMVFQSYALYPHMSVYENMSFALKLAKVDKQVIDEKVQNAARIL 121
           + GRD+T +  ++RD++MVFQ+YAL+PH+SV EN+ F LK+ KV +   D ++++AA +L
Sbjct: 68  IGGRDVTHRSPAQRDISMVFQNYALFPHISVAENILFGLKVRKVGRAERDGRLKHAADLL 127

Query: 122 NLTQYLQRTPKELSGGQRQRVAIGRAIVRAPKVFLFDEPLSNLDAALRGQTRVEIAKLHR 181
            ++  L+R P +LSGGQ+QRVA+GRAIV    V L DEPLSNLDA LR + RVE+  L +
Sbjct: 128 GISHLLERKPSQLSGGQQQRVALGRAIVSQKPVCLMDEPLSNLDAKLRQEMRVELRALQQ 187

Query: 182 DLGATTIYVTHDQVEAMTLADRVVVLRDGIIEQVGTPLELYDKPANQFVAQFIGTPQMNV 241
            LG T +YVTHDQ EA+T+AD+VV++ +G +EQ  +P E+Y++PA+ F A+FIGTP MN+
Sbjct: 188 QLGLTMVYVTHDQTEAITMADQVVLMNNGQVEQAASPKEIYERPASVFTARFIGTPPMNI 247

Query: 242 VPVDKL----PQPVQQQAPAAPAGAAVGAIGLRPENITVRTTGATPVGGQVDLIEALGAE 297
           V +D +    P  VQ   P    G+    +GLRPE+I  R TG   + GQV  +E +GA+
Sbjct: 248 VSLDAIRSVTPLTVQHLLPKTSVGS---RLGLRPEDI--RLTGENGIPGQVLSLEYMGAD 302

Query: 298 TLIYVTTPGGAQFVSRQNDRTDLRVGDAVSLDIDA 332
           TL   +  GG + + R    T+L+ G  V L  DA
Sbjct: 303 TLANCSV-GGEKMLVRVKGTTELKPGQTVGLTWDA 336


Lambda     K      H
   0.320    0.137    0.388 

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: 341
Number of extensions: 18
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: 350
Length of database: 363
Length adjustment: 29
Effective length of query: 321
Effective length of database: 334
Effective search space:   107214
Effective search space used:   107214
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. 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