GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Methanococcus aeolicus Nankai-3

Align Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized)
to candidate WP_011973701.1 MAEO_RS04980 ABC transporter ATP-binding protein

Query= TCDB::Q72L52
         (376 letters)



>NCBI__GCF_000017185.1:WP_011973701.1
          Length = 258

 Score =  154 bits (388), Expect = 3e-42
 Identities = 84/220 (38%), Positives = 129/220 (58%), Gaps = 9/220 (4%)

Query: 2   AKVRLEHVWKRF----GKVVAVKDFNLETEDGEFVVFVGPSGCGKTTTLRMIAGLEEISE 57
           A + L +V K+F     +VVAV+D N      EF+  VGPSGCGK+T LRMIAGLE+ + 
Sbjct: 3   AVLELRNVGKKFITERKEVVAVEDVNFSVNSNEFLSIVGPSGCGKSTLLRMIAGLEKPTS 62

Query: 58  GNIYIGDRLVNDVPPKDRDIAMVFQNYALYPHMNVYENMAFGLRLRRYPKDEIDRRVKEA 117
           G + +     N +   D +  MVFQ Y L P   V  N+A GL ++   K+E ++  K  
Sbjct: 63  GTLILEG---NKIEKPDAERGMVFQQYTLLPWKTVLGNVALGLEIKGMKKEERNKIAKNF 119

Query: 118 ARILKIEHLLNRKPRELSGGQRQRVAMGRAIVREPKVFLMDEPLSNLDAKLRVEMRAEIA 177
            +++ +E   N  P ELSGG +QRVA+ R +  +PK+ LMDEP   LD + RV ++ E+ 
Sbjct: 120 IKLIGLEEFENSYPYELSGGMQQRVAIARTLANDPKIVLMDEPFGALDTQTRVILQNELL 179

Query: 178 KLQRRLGVTTIYVTHDQVEAMTLGHRIVVM--KDGEIQQV 215
           K+  +   T +++TH   EA+ L  R+++M  + G+I+ +
Sbjct: 180 KIWEKDKKTVVFITHSVEEAVYLSDRVIIMSARPGKIKDI 219


Lambda     K      H
   0.320    0.139    0.400 

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: 231
Number of extensions: 9
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: 376
Length of database: 258
Length adjustment: 27
Effective length of query: 349
Effective length of database: 231
Effective search space:    80619
Effective search space used:    80619
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: 48 (23.1 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