GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Rhizobium leguminosarum bv. trifolii WSM1325

Align ABC transporter for D-Mannitol, D-Mannose, and D-Sorbitol, ATPase component (characterized)
to candidate WP_012759619.1 RLEG_RS21560 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::WCS417:GFF2490
         (367 letters)



>NCBI__GCF_000023185.1:WP_012759619.1
          Length = 358

 Score =  387 bits (993), Expect = e-112
 Identities = 200/356 (56%), Positives = 251/356 (70%), Gaps = 6/356 (1%)

Query: 6   IKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSEGTIELDGR 65
           ++ ++K +    +I GIDL ++  EFVVFVGPSGCGKSTLLR+IAGLEE++ G + LD  
Sbjct: 7   LQKVEKRYGSLDVIHGIDLTIDPGEFVVFVGPSGCGKSTLLRMIAGLEEITGGGLLLDNE 66

Query: 66  DITEVTPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVDKKLVESKVSEAARILELGP 125
            + EV PAKR +AMVFQ+YALYPHMSV KN++F L+ AG  K  ++ KV  AA IL++  
Sbjct: 67  RMNEVAPAKRGIAMVFQSYALYPHMSVYKNLAFGLETAGYKKADIQPKVKRAAEILQIEK 126

Query: 126 LLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLHKELQA 185
           LLERKPK LSGGQRQRVAIGRAIVR P+IFLFDEPLSNLDA LRVQMR+E++RLH+ L  
Sbjct: 127 LLERKPKALSGGQRQRVAIGRAIVREPRIFLFDEPLSNLDAELRVQMRVEISRLHRSLGN 186

Query: 186 TMIYVTHDQVEAMTLADKVVVLNSGRIEQVGSPLELYHQPANLFVAGFLGTPKMGFLKGK 245
           TMIYVTHDQVEAMT+ADK+VVLNSGRIEQVG+PL+LY+ PAN FVAGF+G+PKM FLK +
Sbjct: 187 TMIYVTHDQVEAMTMADKIVVLNSGRIEQVGAPLDLYNNPANRFVAGFIGSPKMNFLKAR 246

Query: 246 VTRVESQSCEVQLDAGTLINLP--LSGATLSVGSAVTLGIRPEHLEIASPGQTTLTVTAD 303
           + +V      + +  G  + LP  L G     G  VT GIRPEHL +A       TV  D
Sbjct: 247 IEQVGETETSIHV-CGNSVRLPRRLKG---GAGEEVTFGIRPEHLSLAEGAIALSTVNVD 302

Query: 304 VGERLGSDTFCHVITANGEPLTMRIRGDMASQYGETLHLHLDPAHCHLFDTDGVAV 359
           + E LG  T  +  T + + LT+ + G    + G  +    DPA CH+FD  G  +
Sbjct: 303 LVENLGGATMLYTTTPDNQLLTVALDGQQKVERGANVKASFDPARCHVFDAAGKTI 358


Lambda     K      H
   0.319    0.136    0.384 

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: 388
Number of extensions: 12
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: 358
Length adjustment: 29
Effective length of query: 338
Effective length of database: 329
Effective search space:   111202
Effective search space used:   111202
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