Align Branched chain amino acid (Leucine/isoleucine/valine) uptake transporter of 469 aas and 12 TMSs, BcaP or CitA (characterized)
to candidate WP_102938052.1 B1812_RS04230 amino acid permease
Query= TCDB::S6EX81 (469 letters) >NCBI__GCF_002117405.1:WP_102938052.1 Length = 481 Score = 283 bits (725), Expect = 7e-81 Identities = 167/475 (35%), Positives = 256/475 (53%), Gaps = 14/475 (2%) Query: 3 FMRKADFELYRDADKHYN---QVLTTRDFLALGVGTIISTSIFTLPGQVAAQFAGPGVVF 59 F RK+ + + D N + L +A+G+G II IF L GQ AA +AGPGV Sbjct: 10 FSRKSIHLVIAENDAEENGLKRALGWASLMAMGIGGIIGAGIFVLTGQAAADYAGPGVTI 69 Query: 60 SYLLAALVAGFVALAYAEMSTVMPFAGSAYSWISVLFGEGFGWIAGWALLAEYFIAVAFV 119 S+LL+ L FVAL YAE++ ++P AGS Y++ V GE F WI GW L+ EY A V Sbjct: 70 SFLLSGLACTFVALCYAELAALIPAAGSTYTYTYVTLGEIFAWIIGWNLVLEYAAGAATV 129 Query: 120 GSGFSANLQQLLAPLGFHLPKVL-------ANPFGTDGGVVDIISLLVILLSAIIVFRGA 172 G++ +++ LG HLP+ L A+ G GV ++ + +ILL ++ RG Sbjct: 130 AVGWAGYFNRVMQGLGIHLPEALTSAYFANAHSIGGTHGVFNVPAAAIILLLTALLMRGT 189 Query: 173 SDAGRISQILVVLKVAAVIAFIIVGITVIKPANYHPFIPPHNPKTGFGGFSGIWSGVSMI 232 S++ + I+VV+KV V+ I VG + AN+ P IP + G G+SG+ G S++ Sbjct: 190 SESSFFNNIIVVIKVMVVLVVIFVGAAHVDAANWTPLIPENTDHFGHFGWSGVVRGASVV 249 Query: 233 FLAYIGFDSIAANSAEAKNPQKTMPRGIIGSLLIAVVLFAAVTLVLVGMHPYSAYAGNAA 292 F AYIGFD ++ + EA PQ+ +P GI+GSL+I +L+ AV V G+ Y G Sbjct: 250 FFAYIGFDGVSTAAQEAHTPQRDVPIGILGSLVICTILYVAVAAVATGVVSYKE-LGVPD 308 Query: 293 PVGWALQQSGYSVLSEVVTAIALAGMFIALLGMVLAGSRLLYAFGRDGLLPKGLGKMN-A 351 P+ + ++G + LS VV A+AG+ A+L ++ +R+ YA +DGLLPK ++ Sbjct: 309 PMALVMDRTGVAWLSWVVKLGAIAGLTTAILLLLFGQTRIFYAMAQDGLLPKVFAAVHPV 368 Query: 352 RNLPANGVWTLAIVAIVIGAFFPFAFLAQLISAGTLIAFMFVTLGIYSLRRRQGKDLPEA 411 PA + + + FP L +++S GTL AF V + LRR Q D+ Sbjct: 369 WRTPAVSQALVGVFVALAAGLFPINILDEMVSIGTLAAFALVCGAVLHLRRSQ-PDM-HR 426 Query: 412 TYKMPFYPVLPALGFIGSLFVFWGLDVQAKLYSGIWFLIGILIYFAYGNRRSRKS 466 ++ P P +P LG L + L ++ L +W IG+ IYF YG + ++++ Sbjct: 427 PFRAPGIPAMPLLGIASCLALMVALPLETWLRLIVWTAIGMAIYFFYGVKHAKRA 481 Lambda K H 0.328 0.143 0.433 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: 591 Number of extensions: 35 Number of successful extensions: 5 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: 469 Length of database: 481 Length adjustment: 33 Effective length of query: 436 Effective length of database: 448 Effective search space: 195328 Effective search space used: 195328 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.7 bits) S2: 51 (24.3 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