Align ABC transporter related; Flags: Precursor (characterized, see rationale)
to candidate WP_057507532.1 ABB28_RS04725 ABC transporter ATP-binding protein
Query= uniprot:B2T9V9 (510 letters) >NCBI__GCF_001431535.1:WP_057507532.1 Length = 298 Score = 104 bits (260), Expect = 4e-27 Identities = 80/247 (32%), Positives = 120/247 (48%), Gaps = 19/247 (7%) Query: 13 PVVEALEVTKRFGSTAALNDVSIRVMPGESHALVGRNGAGKSTLVSILTGLRKPDTGEVR 72 P+ +V R+ + AL VS++V PGE AL+GRNGAGK+T +++L GLR PD G+V Sbjct: 7 PLAALHDVQVRYRNAIALAGVSLQVRPGEVLALLGRNGAGKTTAIAVLLGLRLPDAGQVT 66 Query: 73 FSGAAAPSIADRDAWRERVACVYQHSTIIRDLSVAENLFINRQPLRGGVIDWQAMRRDAR 132 G + RE+V + Q + + L V E V ++A R Sbjct: 67 LLGGDPQCRSQ----REQVGVMLQDTALPPKLRVGEL-----------VEQFRASYPRPR 111 Query: 133 ALLDHWKIDVREDARA---GDLSVEARQLVEIARALSYGARFIILDEPTAQLDGDEIKRL 189 L D I +D + G LS ++ V+ A AL G R + LDEPT LD + + + Sbjct: 112 PLADCLAIAGVQDLQQRAYGQLSGGQQRRVQFAIALCGGPRLLFLDEPTTGLDIEARQAM 171 Query: 190 FRRISELQREGVTFLFISHHLQEVYEICQAVTVLRDARHIVSAPVSALPREQLIEAMTGE 249 + I++L+ EG + +H+L+E + V VL R + P++ R QL Sbjct: 172 WHAIAQLRAEGCGIVLTTHYLEEAEALASRVVVLEQGRVLADGPLATF-RPQLAPRRVRC 230 Query: 250 RGGLAVA 256 R GL VA Sbjct: 231 RSGLDVA 237 Score = 77.8 bits (190), Expect = 5e-19 Identities = 58/210 (27%), Positives = 102/210 (48%), Gaps = 23/210 (10%) Query: 284 GVSFTVKRGEVVGLTGATSSGRTSVAEAIAGLRAAKRGTISVDGAILPPGDVPASLAHGI 343 GVS V+ GEV+ L G +G+T+ + GLR G +++ G GD Sbjct: 26 GVSLQVRPGEVLALLGRNGAGKTTAIAVLLGLRLPDAGQVTLLG-----GDPQCR----- 75 Query: 344 GCVPKDRHHEGLVLTQSVAENASMTIARVLGKFGIAAPAKKNAFGQKMIDALGI--VAQG 401 R G++L Q A + + ++ +F + P + + D L I V Sbjct: 76 ----SQREQVGVML-QDTALPPKLRVGELVEQFRASYPRPR-----PLADCLAIAGVQDL 125 Query: 402 PEHVVSGLSGGNQQKVVMARALATNPNVLVLIDPTAGVDVKSKEALLSVVDRVREEGKAV 461 + LSGG Q++V A AL P +L L +PT G+D+++++A+ + ++R EG + Sbjct: 126 QQRAYGQLSGGQQRRVQFAIALCGGPRLLFLDEPTTGLDIEARQAMWHAIAQLRAEGCGI 185 Query: 462 LVVSGELDDLRT-CDRVLVMFRGRVAAEFP 490 ++ + L++ RV+V+ +GRV A+ P Sbjct: 186 VLTTHYLEEAEALASRVVVLEQGRVLADGP 215 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: 340 Number of extensions: 16 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: 510 Length of database: 298 Length adjustment: 30 Effective length of query: 480 Effective length of database: 268 Effective search space: 128640 Effective search space used: 128640 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: 50 (23.9 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