GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Derxia gummosa DSM 723

Align Sugar ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_028311054.1 H566_RS0108150 polyamine ABC transporter ATP-binding protein

Query= uniprot:A0A165KQ08
         (355 letters)



>NCBI__GCF_000482785.1:WP_028311054.1
          Length = 365

 Score =  231 bits (588), Expect = 3e-65
 Identities = 138/339 (40%), Positives = 202/339 (59%), Gaps = 18/339 (5%)

Query: 23  VLRKVDIHVAPGEFLILVGPSGCGKSTLLNIIAGLDEPTEGEIRIGGKNVVGMPPRDRDI 82
           ++R +D+ +  GEFL L+GPSG GK+T L ++AG + PT GEIR+GGK +  +PP  R+I
Sbjct: 23  IVRDLDLDIERGEFLTLLGPSGSGKTTCLMMLAGFETPTAGEIRLGGKVINKLPPWRRNI 82

Query: 83  AMVFQSYALYPTLSVADNIGFALEMRKMPKPERQKRIDEVAAMLQISHLLDRRPSQLSGG 142
            +VFQ+YAL+P ++V +NI F L +RK+P  E  +++ +  AM+++    +R P QLSGG
Sbjct: 83  GVVFQNYALFPHMTVRENIRFPLAVRKLPAHEIDQKVKQALAMVKLDAFGERYPQQLSGG 142

Query: 143 QRQRVAMGRALARQPQLFLFDEPLSNLDAKLRVEMRAEIKRLHQASGITSVYVTHDQVEA 202
           Q+QR+A+ RAL   P+L L DEPL  LD +LR  M+ EIK LH + GIT V+VTHDQ EA
Sbjct: 143 QQQRIALARALVFSPELVLMDEPLGALDKQLREHMQMEIKHLHDSLGITFVFVTHDQSEA 202

Query: 203 MTLGSRIAVMKGGVVQQLGTPDEIYNRPANTYVATFIGSPTMNLLRGAVT---GGQFGIQ 259
           +T+  RIAV   G +QQL   D +Y RPAN +VA FIG    N L   V    G +  ++
Sbjct: 203 LTMSDRIAVFDKGRIQQLDRADALYERPANAFVAGFIGE--SNALAATVEQHHGAECSLR 260

Query: 260 ---GAALNLAPPPSSA-NEVLLGVRPEHLVMQ---ETAPWRGRVSVVEPT--GPDTYVMV 310
              G+ L  +     A N   + +RPE +++    E AP R   +V E    G    + +
Sbjct: 261 LADGSLLRASVGDLGAENTATVSIRPERVLIDQAAEAAPNRFTATVKELVYLGDHLRLRL 320

Query: 311 DTAA-GSVTLRTDA---QTRVQPGEHVGLALAPAHAHWF 345
           D A  G+  ++  A     +V P + + + + P HA  F
Sbjct: 321 DLAGNGNFMVKLPAGALDRQVLPEQTIAVGIRPEHARAF 359


Lambda     K      H
   0.318    0.135    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: 333
Number of extensions: 14
Number of successful extensions: 1
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: 355
Length of database: 365
Length adjustment: 29
Effective length of query: 326
Effective length of database: 336
Effective search space:   109536
Effective search space used:   109536
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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