Align Inositol transport system ATP-binding protein (characterized)
to candidate WP_027178119.1 G496_RS0103835 ABC transporter ATP-binding protein
Query= reanno::WCS417:GFF2332 (517 letters) >NCBI__GCF_000429985.1:WP_027178119.1 Length = 513 Score = 268 bits (685), Expect = 4e-76 Identities = 165/496 (33%), Positives = 272/496 (54%), Gaps = 10/496 (2%) Query: 23 LLEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDAGEIRL 82 ++ + I+K F VVA + L + PG + AL+GENGAGKSTLM ++AG +QPD G I + Sbjct: 24 IVSLKGITKRFGKVVANNKIVLDLYPGRIKALLGENGAGKSTLMSMLAGRFQPDEGHIEV 83 Query: 83 RGKPIVFETPLAAQKAGIAMIHQELNLMPHMSIAENIWIGREQLNSLHMVNHREMHRCTA 142 GK + F + A AGI M++Q L+ M++ EN+ +G+E VN +EM R Sbjct: 84 DGKRVDFSSSKDAINAGIGMVYQHFMLVDSMTVTENVLLGQE---GGFFVNPKEMSRRVK 140 Query: 143 ELLARLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVAHLFSI 202 +L + +DP+ ++ LS+ E+Q VEI K + +S +LI DEPT+ +T +E LF Sbjct: 141 KLAEDYELEIDPDARINQLSMGEKQRVEILKLLYRESRVLIFDEPTAVLTPRETFRLFEA 200 Query: 203 IADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIG-LQRADSMNSDSLISMMVGREL 261 + + QGK IV+I+HK+ EV AIADEVA+ R G + R + L MVG+E+ Sbjct: 201 LWAMTRQGKSIVFISHKLEEVMAIADEVAILRRGCVDSEVPREKITSKADLACRMVGKEV 260 Query: 262 SQLFPLRETPIGDLLLTVRDLTLDGVFKDVSFDLHAGEILGIAGLMGSGRTNVAETIFGI 321 E IGD +L V+ L G+ K+++ ++H GE++GI G+ G+G+ + E + G+ Sbjct: 261 LLEIDRNEVEIGDKVLEVKSLNGLGL-KNINIEVHRGEVVGIVGVAGNGQQALVEGVCGL 319 Query: 322 TPSSSGQITLDGKAVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVLPHYTG 381 + + GKA R M + + EDR L +++N+ + + Sbjct: 320 RMPPKDSVFIMGKAWREFFAKMTWNHSLSYIPEDRLDLATARELDLVDNLLLTTRQGFCS 379 Query: 382 NGFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTNPRLLILDEP 441 + + + + + + V+ ++ LSGGN QK +LAR L P L++ ++P Sbjct: 380 GPVLHRDKAAEVAKKLVEDHDVRPGRIQALAWQLSGGNLQKLVLARELYREPHLIVAEQP 439 Query: 442 TRGIDVGAKAEIYRLIAFLASEGMA-VIMISSELPEVLGMSDRVMVMHEGELMGTLDRSE 500 T+G+D+ A E++ + L + MA V++++ +L E L +SDR+ VM+ GE+M ++ Sbjct: 440 TQGLDISATEEVWNRL--LEARKMAGVLLVTGDLNEALQLSDRIAVMYRGEIMDQFSVND 497 Query: 501 ATQEKVMQLASGMTAV 516 EKV ++ M V Sbjct: 498 T--EKVDKVGLMMAGV 511 Lambda K H 0.320 0.136 0.381 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: 539 Number of extensions: 35 Number of successful extensions: 8 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: 517 Length of database: 513 Length adjustment: 35 Effective length of query: 482 Effective length of database: 478 Effective search space: 230396 Effective search space used: 230396 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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