GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Marivita geojedonensis DPG-138

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate WP_085635144.1 MGEO_RS02745 ATP-binding cassette domain-containing protein

Query= reanno::Smeli:SMc03065
         (362 letters)



>NCBI__GCF_002115805.1:WP_085635144.1
          Length = 334

 Score =  337 bits (863), Expect = 4e-97
 Identities = 183/357 (51%), Positives = 237/357 (66%), Gaps = 27/357 (7%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  + LK + KS+G + VI  +DL I++GEF VFVGPSGCGKSTLLR+IAGLE+IT G +
Sbjct: 1   MGRIQLKSVTKSFGDIQVIPPLDLTIEDGEFTVFVGPSGCGKSTLLRLIAGLEDITTGTI 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            IDG    ++ P+KRG+AMVFQSYALYPHM+V  N+AF +++A+    EID+R+  AA +
Sbjct: 61  EIDGNDATNLVPAKRGLAMVFQSYALYPHMSVRKNIAFPLKMAKMDPAEIDKRIEAAASV 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           L LT YLDR P  LSGGQRQRVAIGRAI R P  FLFDEPLSNLDAALRV  R+EI++L 
Sbjct: 121 LNLTAYLDRRPGQLSGGQRQRVAIGRAIVREPAAFLFDEPLSNLDAALRVGMRLEISELH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
           +R++ TTMIYVTHDQVEAMT+AD+IVVL AG IEQVG+PLELY+RP N FVA FIGSP M
Sbjct: 181 KRLA-TTMIYVTHDQVEAMTMADKIVVLQAGVIEQVGSPLELYQRPRNTFVAGFIGSPKM 239

Query: 241 NVIPATITATGQQTAVSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLFEG 300
           N+I                             ++    A+ G+RPE + ++E+    ++G
Sbjct: 240 NLISGA-------------------------EAQKHDAATIGIRPEHIDISESSG-AWKG 273

Query: 301 TVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNG 357
            + + E LG  T  +++  V +EP+  +  G      G +V  T     LH F+  G
Sbjct: 274 KIGVSEHLGSDTFFHVQCDVTDEPLTVRATGEVSFKYGSEVYLTPRPEHLHRFNEQG 330


Lambda     K      H
   0.320    0.137    0.387 

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: 355
Number of extensions: 14
Number of successful extensions: 3
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: 362
Length of database: 334
Length adjustment: 29
Effective length of query: 333
Effective length of database: 305
Effective search space:   101565
Effective search space used:   101565
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 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