GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Phyllobacterium brassicacearum STM 196

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_106710604.1 CU102_RS08100 ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_003010955.1:WP_106710604.1
          Length = 336

 Score =  337 bits (863), Expect = 4e-97
 Identities = 192/354 (54%), Positives = 233/354 (65%), Gaps = 28/354 (7%)

Query: 1   MADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTL 60
           M  L L  V K++G   V+  ++L+I   E +VFVGPSGCGKSTLLR+IAGLE IT GTL
Sbjct: 1   MTALHLNNVRKSFGTFDVIKGVDLEISPSEFMVFVGPSGCGKSTLLRLIAGLEDITSGTL 60

Query: 61  EIDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEK 120
             D  VVN + P+QRGIAMVFQSYALYPHMTV +NM+F LK+AK    EI   V+ AAE 
Sbjct: 61  AFDDKVVNSLTPSQRGIAMVFQSYALYPHMTVFDNMAFGLKLAKGDAGEIKRRVQEAAEM 120

Query: 121 LQLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLK 180
           LQ+  YLDRLPK LSGGQRQRVAIGR+IVRDPKV+LFDEPLSNLDAALRV TRLEIA+L 
Sbjct: 121 LQITAYLDRLPKQLSGGQRQRVAIGRAIVRDPKVFLFDEPLSNLDAALRVQTRLEIAKLH 180

Query: 181 EAMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKM 240
             M E+TM+YVTHDQVEAMTLA RI VL  G + QVG+PLELYEKP++ FVA FIGSPKM
Sbjct: 181 AKMHETTMIYVTHDQVEAMTLADRICVLRDGIVEQVGTPLELYEKPQSIFVAGFIGSPKM 240

Query: 241 NLLPGKIIGTGAQTTVEMTDGGRAVSDYPSDDSLMGAAVNVGVRPEDMVEAAPGGDYVFE 300
           N L  K   T  +T +                        +GVRPE +      G   ++
Sbjct: 241 NFLTEKHADT-YRTHI------------------------LGVRPEHLQIKEKDG--TWD 273

Query: 301 GKVAITEALGEVTLLYFEAPSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVF 354
           GK+ ++E LG  T LY +    +DP + +  G  +   G+   ++     VH F
Sbjct: 274 GKLILSENLGSETYLYIDI-GAKDPLVVRQDGTARQQPGERLYISPINDNVHRF 326


Lambda     K      H
   0.316    0.135    0.379 

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: 390
Number of extensions: 21
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 373
Length of database: 336
Length adjustment: 29
Effective length of query: 344
Effective length of database: 307
Effective search space:   105608
Effective search space used:   105608
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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