GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Bradyrhizobium sp. BTAi1

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_041750694.1 BBTA_RS16625 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_000015165.1:WP_041750694.1
          Length = 353

 Score =  344 bits (882), Expect = 2e-99
 Identities = 187/365 (51%), Positives = 238/365 (65%), Gaps = 16/365 (4%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           M+ V +  + K++ G     +    + I+D EF V VGPSGCGK+T LRM+AGLE+IT G
Sbjct: 1   MSSVQIRDVRKSFGGFE--VLHGVTIPIEDGEFVVLVGPSGCGKSTLLRMLAGLENITSG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + IG+R VN+V PK+RDIAMVFQNYALYPHMTV  NM F LKLR     +I + V  AA
Sbjct: 59  TISIGERVVNNVQPKERDIAMVFQNYALYPHMTVADNMGFSLKLRGARPEDIKKGVARAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           +IL +  LLDR P+ LSGGQRQRVA+GRAIVR+PQVFL DEPLSNLDAKLRV MR EI++
Sbjct: 119 EILALTPLLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVAMRTEIKE 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LHQRL+TT +YVTHDQ EAMTM D+IVVM DG+++Q  +P  +Y +P N FVAGFIGSPA
Sbjct: 179 LHQRLKTTTVYVTHDQIEAMTMADKIVVMHDGIVEQMGSPLDLYDKPDNQFVAGFIGSPA 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MNF+ G +  +G  +        L L      +   + + G+PVV GVRPE L       
Sbjct: 239 MNFLNGHLKSNGTVYVETDNGAKLPL------LTAPAASNGRPVVYGVRPEHLE------ 286

Query: 301 TTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIHI 360
               D  ++ +V VVE  GSE  +   IG   I+A    RH    G+ + L    +  H+
Sbjct: 287 --LADDGIEAEVVVVEPTGSETQIVARIGTQDIIAVFRDRHEVVPGAKIHLRPRASAAHL 344

Query: 361 FDAET 365
           FD +T
Sbjct: 345 FDKDT 349


Lambda     K      H
   0.321    0.138    0.395 

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: 440
Number of extensions: 26
Number of successful extensions: 4
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: 384
Length of database: 353
Length adjustment: 30
Effective length of query: 354
Effective length of database: 323
Effective search space:   114342
Effective search space used:   114342
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 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