GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Bradyrhizobium sp. BTAi1

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate WP_041750694.1 BBTA_RS16625 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3039
         (367 letters)



>NCBI__GCF_000015165.1:WP_041750694.1
          Length = 353

 Score =  338 bits (867), Expect = 1e-97
 Identities = 180/356 (50%), Positives = 243/356 (68%), Gaps = 9/356 (2%)

Query: 1   MANLKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTI 60
           M++++I++++K F GF ++ G+ + + D EFVV VGPSGCGKSTLLR++AGLE ++ GTI
Sbjct: 1   MSSVQIRDVRKSFGGFEVLHGVTIPIEDGEFVVLVGPSGCGKSTLLRMLAGLENITSGTI 60

Query: 61  ELDGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAARI 120
            +  R +  V P +RD+AMVFQ YALYPHM+V  NM F+L L G    +++K V+ AA I
Sbjct: 61  SIGERVVNNVQPKERDIAMVFQNYALYPHMTVADNMGFSLKLRGARPEDIKKGVARAAEI 120

Query: 121 LELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLH 180
           L L P+L+R P+QLSGGQRQRVA+GRAIVR+P++FLFDEPLSNLDA LRV MR E+  LH
Sbjct: 121 LALTPLLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVAMRTEIKELH 180

Query: 181 KELQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMG 240
           + L+ T +YVTHDQ+EAMTMADK+VV++ G +EQ+GSPLDLY +P N FVAGF+G+P M 
Sbjct: 181 QRLKTTTVYVTHDQIEAMTMADKIVVMHDGIVEQMGSPLDLYDKPDNQFVAGFIGSPAMN 240

Query: 241 FLKGKITRVDSQGCEVQLDAGTRVSLPLGGRHLSVGSAVTLGIRPEHLELAKPGDCALQV 300
           FL G +    +    V+ D G ++ L L     S G  V  G+RPEHLELA  G   ++ 
Sbjct: 241 FLNGHLK--SNGTVYVETDNGAKLPL-LTAPAASNGRPVVYGVRPEHLELADDG---IEA 294

Query: 301 TADVSERLGSDTFCHVRTASGEALTM-RVRGDLASRYGETLSLHLDAQHCHLFDAD 355
              V E  GS+T    R  + + + + R R ++    G  + L   A   HLFD D
Sbjct: 295 EVVVVEPTGSETQIVARIGTQDIIAVFRDRHEVVP--GAKIHLRPRASAAHLFDKD 348


Lambda     K      H
   0.320    0.137    0.389 

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: 377
Number of extensions: 14
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: 367
Length of database: 353
Length adjustment: 29
Effective length of query: 338
Effective length of database: 324
Effective search space:   109512
Effective search space used:   109512
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