GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Alicycliphilus denitrificans K601

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate WP_013518363.1 ALIDE2_RS17025 ABC transporter ATP-binding protein

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



>NCBI__GCF_000204645.1:WP_013518363.1
          Length = 361

 Score =  238 bits (606), Expect = 2e-67
 Identities = 146/359 (40%), Positives = 199/359 (55%), Gaps = 18/359 (5%)

Query: 7   KDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDMFIDGER 66
           + I  SYG   V+  IDL I+ GEF   +GPSG GKSTLLR+IAG  +   G++ +DG+ 
Sbjct: 9   RHISLSYGTTPVLRDIDLRIEPGEFFALLGPSGSGKSTLLRLIAGFNQHQSGELLVDGQD 68

Query: 67  VNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADMLQLTPY 126
           ++ VPP  R I MVFQ+YAL+PHMTV+DN+AFG+   RES++ + R+V    D++ L  Y
Sbjct: 69  ISGVPPHLRNIGMVFQNYALWPHMTVWDNVAFGLVERRESRDAMRRKVGAVLDLVGLAQY 128

Query: 127 LDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLSERMSDT 186
             R P  LSGGQ+QRVA+ R I   P++ L DEPLSNLD  LRV  R E+  L  ++  T
Sbjct: 129 ARRRPAQLSGGQQQRVALARTIVIEPRLLLLDEPLSNLDKQLRVQMREELKNLQRKLGLT 188

Query: 187 TMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAMNVIPAT 246
           T ++VTHDQ EAMT ADR+ VL  G ++QVG    LY+ P N FVA F+G+   N++   
Sbjct: 189 T-VFVTHDQEEAMTTADRMAVLDKGILQQVGTAAGLYDYPHNRFVAGFVGT--ANLLEGE 245

Query: 247 ITATGQQTAVSLAGGKS-VTLDVPTNASENGKTASFGVRPEDLRVTEADD------FLFE 299
           +TA    T    A G   + L  P      G  A+   RP  + +    +         +
Sbjct: 246 VTAVSADTLTFHARGLGPLALARPAEPPAIG-PAALAFRPHQVSMRPRGEPGDGARVWLD 304

Query: 300 GTVSIVEALGEVTLLYIE----GLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFD 354
           G V   E LGE +   +      L  ++P  A   G      G +VR   D A+L   D
Sbjct: 305 GLVESAEFLGEFSRYRVRVGEVALTSDQPHYA---GRGMFAPGAQVRLGLDPAQLRYLD 360


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: 336
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: 362
Length of database: 361
Length adjustment: 29
Effective length of query: 333
Effective length of database: 332
Effective search space:   110556
Effective search space used:   110556
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