GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK' in Jannaschia aquimarina GSW-M26

Align Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale)
to candidate WP_043917711.1 jaqu_RS04170 ABC transporter ATP-binding protein

Query= uniprot:A8LLL2
         (373 letters)



>NCBI__GCF_000877395.1:WP_043917711.1
          Length = 344

 Score =  316 bits (809), Expect = 7e-91
 Identities = 184/364 (50%), Positives = 236/364 (64%), Gaps = 27/364 (7%)

Query: 2   ADLKLTGVEKAYGDVKVLSNINLDIQQGELIVFVGPSGCGKSTLLRMIAGLEKITGGTLE 61
           A ++L GVEK +GD +V+  ++L +  GE +VFVGPSGCGKSTLLRMIAGLE+ + G + 
Sbjct: 3   AQVELVGVEKWFGDAQVIKGVDLAVAAGEFVVFVGPSGCGKSTLLRMIAGLEETSRGQIL 62

Query: 62  IDGTVVNDVPPAQRGIAMVFQSYALYPHMTVRENMSFALKIAKKSQAEIDAAVEAAAEKL 121
           ++G      PP++RG+AMVFQSYALYPH++VREN+ F LK A  S+ EI A V+ AA  L
Sbjct: 63  VEGRDATAEPPSKRGLAMVFQSYALYPHLSVRENVGFPLKAAGMSKDEISARVDEAARAL 122

Query: 122 QLGQYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRLEIAQLKE 181
           +L  YLDR PK LSGGQRQRVAIGRSIVR+P  +LFDEPLSNLDAALRV  R EIA+L +
Sbjct: 123 RLTDYLDRRPKDLSGGQRQRVAIGRSIVREPVAFLFDEPLSNLDAALRVEMRYEIAKLHQ 182

Query: 182 AMPESTMVYVTHDQVEAMTLATRIVVLAGGGIAQVGSPLELYEKPENEFVAQFIGSPKMN 241
            +  + M+YVTHDQ+EAMTLA RIVVL  G IAQVG+P ELY +P + FVAQFIGSPKMN
Sbjct: 183 QL-GTAMIYVTHDQIEAMTLADRIVVLEAGRIAQVGTPRELYLRPRSLFVAQFIGSPKMN 241

Query: 242 LLPGKIIGTGAQTTVEMTDGGRAVSDYPSDDSLMGAAVNVGVRPEDMVEAAPGGDYVFEG 301
           +     +                    P  D+  GAA  +GVRPED+   AP GD    G
Sbjct: 242 VFTADAV--------------------PDLDAPPGAA-TLGVRPEDL-RIAPQGDGGLSG 279

Query: 302 KVAITEALGEVTLLYFE-APSGEDPTIGKLQGIHKDLKGQVTRLTAEPAKVHVFKD-GVS 359
            V + E LG  T +  +  P+G      ++ G      G+   L  + + +H F + GV+
Sbjct: 280 SVDVLEYLGADTFVIVDCGPAGR--ITARVPGEAGLAPGEAVALEFDRSALHAFDEKGVA 337

Query: 360 LHYP 363
           +  P
Sbjct: 338 VDVP 341


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: 401
Number of extensions: 15
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: 373
Length of database: 344
Length adjustment: 29
Effective length of query: 344
Effective length of database: 315
Effective search space:   108360
Effective search space used:   108360
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