GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsA in Halomonas desiderata SP1

Align Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate WP_086510781.1 BZY95_RS15410 carbohydrate ABC transporter substrate-binding protein

Query= uniprot:A0A165KPY4
         (416 letters)



>NCBI__GCF_002151265.1:WP_086510781.1
          Length = 422

 Score =  462 bits (1189), Expect = e-135
 Identities = 225/406 (55%), Positives = 293/406 (72%), Gaps = 2/406 (0%)

Query: 9   AVAVGLAAAMSASAGEVEVLHYWTSGGEAKSVAELKKIMQGKGHTWRDFAVAGGGGDSAM 68
           A A   +   S  A EVEVLH+WTSGGEA++   LK++M+ +G+ W DFAVAGGGG++AM
Sbjct: 16  ATAAAASLTFSIQAAEVEVLHWWTSGGEARAANVLKELMEAEGYGWEDFAVAGGGGETAM 75

Query: 69  TVLKSRVISGNPPSAAQTKGPAIQEWASEGVLANMDTLAKAEKWDELLPKVVADVMKYKG 128
           TVLKSR +SGNPPSAAQ KGP IQEW   G+L  +D +A+AE WDELLP  VADVM++ G
Sbjct: 76  TVLKSRAMSGNPPSAAQIKGPEIQEWGELGLLGELDEVAEAEGWDELLPPTVADVMRHNG 135

Query: 129 AYVAAPVNVHRVNWMWGSSEALKKAGVAAMPKTWDEFFAAADKLKAAGLVPVAHGGQNWQ 188
           +YVA PVNVHRVNW+W + + L  AGV  MP T DE FAA + ++ AG +P+AHGGQ WQ
Sbjct: 136 SYVAVPVNVHRVNWLWANPQVLAAAGV-EMPTTLDELFAAGEAIREAGYIPLAHGGQAWQ 194

Query: 189 DFTTFESVVLGVGGAKFYQDALVKLDNTALTSDTMKKSLETFRRIKGYTDPGAPGRDWNL 248
           D T FESV+L  GG +FYQ ALV+LD  AL S+ M ++LETF+R++   D    GRDWN+
Sbjct: 195 DATVFESVLLASGGTEFYQQALVELDPEALGSERMIEALETFKRLRELMDADMSGRDWNI 254

Query: 249 ATAMLIQGKAGFQLMGDWAKGEFLAAGKAPGKDFLCAAAPGSANAFTFNVDSFILFKLKD 308
           AT+M+I+G AG QLMGDWAKGEF AAG   G+++LCAAAPG+ +AFTFN+DS  +F++ +
Sbjct: 255 ATSMVIEGSAGMQLMGDWAKGEFTAAGLTAGEEYLCAAAPGTQDAFTFNIDSLAMFRV-E 313

Query: 309 AAAQKAQSDLASSIMSPAFQEVFNLNKGSIPVRAGQPMDKFDDCAKASAKDFVDTAKSGG 368
              ++AQ  LA  ++ P FQE FNL KGSIP R    M  FD CA+ S  DF  TA+ GG
Sbjct: 314 GEEREAQQALARLVLEPTFQEAFNLAKGSIPARPDLDMSGFDVCAQQSMDDFQRTAEEGG 373

Query: 369 LVPSAAHGMAIAPATEGAIKDVVSQFWNDDKVSVADAMKKIAAAAK 414
           LVPS AHGMA+    +GAI DVV+ ++N   ++  +A +++  AA+
Sbjct: 374 LVPSMAHGMAVRADVQGAIFDVVTNYFNSRDMAAEEAARRMVNAAQ 419


Lambda     K      H
   0.315    0.128    0.383 

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: 560
Number of extensions: 28
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: 416
Length of database: 422
Length adjustment: 32
Effective length of query: 384
Effective length of database: 390
Effective search space:   149760
Effective search space used:   149760
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: 50 (23.9 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