Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_055437172.1 ASC41_RS13455 sugar ABC transporter ATP-binding protein
Query= uniprot:A0A165KC86 (260 letters) >NCBI__GCF_001418085.1:WP_055437172.1 Length = 507 Score = 130 bits (326), Expect = 7e-35 Identities = 76/233 (32%), Positives = 127/233 (54%), Gaps = 12/233 (5%) Query: 1 MTEKSNEVVLKVAGISKRFGGLQALSDVGITIKRGQVYGLIGPNGAGKTTFFNVITGLYT 60 M NE L+++GISK FG + L DV + +K G+++ L+G NGAGK+T +++G++ Sbjct: 1 MKNSENEYRLEMSGISKSFGVVSVLKDVTLKVKSGEIHALLGENGAGKSTLIKILSGVHH 60 Query: 61 PDAGTFELAGKPYEPTAVHEVAKAGIARTFQNIRLFAEMTALENVMVGRHIRTGSGLFGA 120 D+GT L G+ P HE GI+ +Q + L +++ EN+ + + GA Sbjct: 61 KDSGTVRLNGEEINPKNTHEGQVLGISVVYQELSLVNDLSVAENIYLHK--------LGA 112 Query: 121 VFRTKGFKAEEAAIAKRAQELLDYVGIGKFADYKARTLSYGDQRRLEIARALATDPQLIA 180 F I K AQEL+D +G A K R LS ++ +EIA+AL+ D +++ Sbjct: 113 ----SKFWMNWDKITKDAQELIDSLGFTIDASAKVRNLSIVQKQVVEIAKALSEDTKVLV 168 Query: 181 LDEPAAGMNATEKVQLRELIDRIRNDNRTILLIEHDVKLVMGLCDRVTVLDYG 233 LDEP + T+ +L + + R+R+ +I+ I H + ++ + D +TVL G Sbjct: 169 LDEPTTVFDPTDTKKLFDNLFRLRDQGISIIYISHHLDEIIKIADSITVLRDG 221 Score = 74.3 bits (181), Expect = 5e-18 Identities = 53/213 (24%), Positives = 105/213 (49%), Gaps = 17/213 (7%) Query: 27 DVGITIKRGQVYGLIGPNGAGKTTFFNVITGLYTPDAGTFELAGKPYEP-----TAVHEV 81 DV +++ G+V G+ G G+G+T +I G +GT L GK + A H++ Sbjct: 277 DVSFSVRPGEVLGIAGLGGSGRTETAKLIFGADKKKSGTLILNGKEIKTKSPVDAAAHQI 336 Query: 82 AKAGIARTFQNIRLFAEMTALENVMVGRHIRTGSGLFGAVFRTKGFKAEEAAIAKRAQEL 141 R + + F ++ NV V + ++ SG G + +K + L Sbjct: 337 GFVSEDRKEEGV--FLPLSIRRNVSV-TNFKSISGKLGFINVDNEYK--------KVLGL 385 Query: 142 LDYVGIGK-FADYKARTLSYGDQRRLEIARALATDPQLIALDEPAAGMNATEKVQLRELI 200 +D + I ++ + LS G+Q+++ +A+ L+ D ++I +DEP G++ K+++ LI Sbjct: 386 IDKLNIKTPSSEVDVKNLSGGNQQKVALAKWLSIDSKVIFIDEPTRGVDVGAKIEIYNLI 445 Query: 201 DRIRNDNRTILLIEHDVKLVMGLCDRVTVLDYG 233 + + +++I D+ +MG+ DR+ V+ G Sbjct: 446 NEVAKKGVGVVVISSDMPEIMGISDRILVMHEG 478 Lambda K H 0.319 0.137 0.384 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: 291 Number of extensions: 15 Number of successful extensions: 4 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: 260 Length of database: 507 Length adjustment: 29 Effective length of query: 231 Effective length of database: 478 Effective search space: 110418 Effective search space used: 110418 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 (21.7 bits) S2: 49 (23.5 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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