Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_027178119.1 G496_RS0103835 ABC transporter ATP-binding protein
Query= uniprot:B2T9V9 (510 letters) >NCBI__GCF_000429985.1:WP_027178119.1 Length = 513 Score = 229 bits (584), Expect = 2e-64 Identities = 153/493 (31%), Positives = 253/493 (51%), Gaps = 16/493 (3%) Query: 2 NGQMSELTSSVPVVEALEVTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILT 61 +G +E SS P+V +TKRFG A N + + + PG AL+G NGAGKSTL+S+L Sbjct: 12 SGSPAEYASSSPIVSLKGITKRFGKVVANNKIVLDLYPGRIKALLGENGAGKSTLMSMLA 71 Query: 62 GLRKPDTGEVRFSGAAAPSIADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRGGV 121 G +PD G + G + +DA + VYQH ++ ++V EN+ + ++ G Sbjct: 72 GRFQPDEGHIEVDGKRVDFSSSKDAINAGIGMVYQHFMLVDSMTVTENVLLGQE--GGFF 129 Query: 122 IDWQAMRRDARALLDHWKIDVREDARAGDLSVEARQLVEIARALSYGARFIILDEPTAQL 181 ++ + M R + L + +++++ DAR LS+ +Q VEI + L +R +I DEPTA L Sbjct: 130 VNPKEMSRRVKKLAEDYELEIDPDARINQLSMGEKQRVEILKLLYRESRVLIFDEPTAVL 189 Query: 182 DGDEIKRLFRRISELQREGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPREQ 241 E RLF + + R+G + +FISH L+EV I V +LR R V S +PRE+ Sbjct: 190 TPRETFRLFEALWAMTRQGKSIVFISHKLEEVMAIADEVAILR--RGCVD---SEVPREK 244 Query: 242 LIEA--MTGERGGLAVADAAARGALPADTAVALELKELTGADYEGVSFTVKRGEVVGLTG 299 + + G V R + V LE+K L G + ++ V RGEVVG+ G Sbjct: 245 ITSKADLACRMVGKEVLLEIDRNEVEIGDKV-LEVKSLNGLGLKNINIEVHRGEVVGIVG 303 Query: 300 ATSSGRTSVAEAIAGLRAAKRGTISVDGAILPPGDVPASLAHGIGCVPKDRHHEGLVLTQ 359 +G+ ++ E + GLR + ++ + G + H + +P+DR Sbjct: 304 VAGNGQQALVEGVCGLRMPPKDSVFIMGKAWREFFAKMTWNHSLSYIPEDRLDLATAREL 363 Query: 360 SVAENASMTIARVLGKFGIAAPAKKNAFGQKMIDALGIVAQGPEHVVSGLSGGNQQKVVM 419 + +N +T + + K +K+++ + + + LSGGN QK+V+ Sbjct: 364 DLVDNLLLTTRQGFCSGPVLHRDKAAEVAKKLVEDHDVRPGRIQALAWQLSGGNLQKLVL 423 Query: 420 ARALATNPNVLVLIDPTAGVDVKSKEALLSVVDRVREEGK--AVLVVSGELDD-LRTCDR 476 AR L P+++V PT G+D+ + E V +R+ E K VL+V+G+L++ L+ DR Sbjct: 424 ARELYREPHLIVAEQPTQGLDISATE---EVWNRLLEARKMAGVLLVTGDLNEALQLSDR 480 Query: 477 VLVMFRGRVAAEF 489 + VM+RG + +F Sbjct: 481 IAVMYRGEIMDQF 493 Lambda K H 0.318 0.134 0.377 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: 595 Number of extensions: 38 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: 510 Length of database: 513 Length adjustment: 35 Effective length of query: 475 Effective length of database: 478 Effective search space: 227050 Effective search space used: 227050 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 (21.7 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