Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate WP_092058281.1 BQ4888_RS15490 ABC transporter ATP-binding protein
Query= reanno::acidovorax_3H11:Ac3H11_792 (358 letters) >NCBI__GCF_900111775.1:WP_092058281.1 Length = 596 Score = 85.1 bits (209), Expect = 4e-21 Identities = 67/242 (27%), Positives = 114/242 (47%), Gaps = 33/242 (13%) Query: 23 ALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQER-- 80 AL P+ + G + L+G +G GK+T+ I +G L P G+ F GRD+ ++R Sbjct: 355 ALAPVDLRLRQGEVFGLVGETGSGKSTLAMIAAGALRPDGGRRDFSGRDLEDWLRRDRLS 414 Query: 81 ---NIAQVFQFPVI-----YDTMTVAENLAFPLR-----------NRKVPEGQIKQRVGV 121 I V Q P + +D + +A PLR +V ++ + Sbjct: 415 LARRIGIVQQHPALAVSPRFDVFGI---VAEPLRIQGQTDSADVLRERVTRALVEVHLPT 471 Query: 122 IAEMLE-MSGQLNQRAAGLAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRR 180 E L + QLNQ A Q++ + R L+ + ++ DEP + +DP ++ ++ + Sbjct: 472 APEFLRRLPHQLNQGAL-------QRLCIARALI-TEPLLLIADEPTSALDPSVQAKILK 523 Query: 181 KLKQIHHELKLTLIYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHFI 240 L + E LTL+ VTHD A D++ VM G+ V+VG+A + +RPAH + + Sbjct: 524 LLLDLQIEKGLTLLLVTHDLGLARKVCDRIGVMHAGRLVEVGNAAQVLQRPAHPYTRELL 583 Query: 241 GS 242 + Sbjct: 584 NA 585 Score = 53.1 bits (126), Expect = 2e-11 Identities = 56/233 (24%), Positives = 94/233 (40%), Gaps = 15/233 (6%) Query: 23 ALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPS---HGKVLFDGRDVTRASPQE 79 AL + + E G AL+G SG GKTT+ + GL + G V DG ++T S Sbjct: 20 ALDRVDLRLEPGRVLALVGESGSGKTTLARSLLGLTDKNARIDGVVRLDGEELTGFSEGA 79 Query: 80 RNIAQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQR-VGVIAEMLEMSGQLNQRAAG 138 N + + ++ A N + +V E I+ R +G A + + L Sbjct: 80 WNRVRWARIAMVGQNGAAALNPVLSI-GAQVAEPLIEHRGLGSGAALAQAEMALTAMGLD 138 Query: 139 LAADAKQKISLGRGLVR---------ADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHEL 189 AA + L G ++ D ++ DEP +DP + + ++ Sbjct: 139 PAAARRYPHELSGGQIQRALLAMALILDPQVLILDEPTAALDPPARQFVGEVIRDQRRRG 198 Query: 190 KLTLIYVTHDQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHFIGS 242 K L+ ++HD AD+V V+ G+ ++ A LF P H + + S Sbjct: 199 KAILL-ISHDLDSCRRLADRVAVLYLGRILEELPARDLFANPCHPYTRALVRS 250 Lambda K H 0.320 0.136 0.395 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: 476 Number of extensions: 20 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: 358 Length of database: 596 Length adjustment: 33 Effective length of query: 325 Effective length of database: 563 Effective search space: 182975 Effective search space used: 182975 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: 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