Align succinyl-CoA-glutarate CoA-transferase (EC 2.8.3.13) (characterized)
to candidate Pf6N2E2_3139 L-carnitine dehydratase/bile acid-inducible protein F (EC 2.8.3.16)
Query= reanno::pseudo5_N2C3_1:AO356_10845 (406 letters) >FitnessBrowser__pseudo6_N2E2:Pf6N2E2_3139 Length = 399 Score = 215 bits (548), Expect = 2e-60 Identities = 137/407 (33%), Positives = 217/407 (53%), Gaps = 19/407 (4%) Query: 4 LSHLRVLDLSRVLAGPWAGQILADLGADVIKVERPGNGDDTRAWGPPFLKDARGENTTEA 63 L+ ++V++L ++AGP+A +I + GA+VIKVE P GD R W + T Sbjct: 8 LAGVKVIELGTLIAGPFASRICGEFGAEVIKVESPDGGDPLRKWRKLY-------EGTSL 60 Query: 64 AYYLSANRNKQSVTIDFTRPEGQRLVRELAAKSDILIENFKVGGLAAYGLDYDSLKAINP 123 +++ A RNK+S+T++ PEG ++++L ++DILIENF+ G L GL +D L A+NP Sbjct: 61 WWFVQA-RNKKSLTLNLKHPEGLAILKKLLGEADILIENFRPGVLEKLGLGWDVLHALNP 119 Query: 124 QLIYCSITGFGQTGPYAKRAGYDFMIQGLGGLMSLTGRPEGDEGAGPVKVGVALTDILTG 183 +L+ ++GFGQTGP + G+ + + +GGL +T G E PV+ G+++ D + Sbjct: 120 KLVMVRLSGFGQTGPMKDQPGFGAVGESMGGLRYIT----GFEDRPPVRTGISIGDSIAA 175 Query: 184 LYSTAAILAALAHRDHVGG-GQHIDMALLDVQVACLANQAMNYLTTGNAPKRLGNAHPNI 242 L+ L AL HR+ GG GQ +D+AL + A + + + G +R GN P I Sbjct: 176 LWGVIGALMALRHREINGGTGQVVDVALYEAIFAMMESMVPEFDVFGFIRERTGNIMPGI 235 Query: 243 VPYQDFPTADGDFI-LTVGNDGQFRKFAEVAGQPQWADDPRFATNKVRVANRAVLIPLIR 301 P ++DG + + D F++F ++ G+ A+DP+ A+N R + R L +I Sbjct: 236 TPSSIHTSSDGKHVQIGANGDAIFKRFMQIIGRDDLANDPQLASNDGRDSRRDELYGVID 295 Query: 302 QATVFKTTAEWVTQLEQAGVPCGPINDLAQVFADPQVQARGLAME--LPHLLAGKVPQVA 359 + + QL QAGVP I +F+DPQ AR + ++ LP A K+P + Sbjct: 296 RWVNALPLDSVIDQLNQAGVPASRIFSAEDMFSDPQFLAREMFLQAKLPDGKAFKMPGIV 355 Query: 360 SPIRLSETPVEYRNAPPLLGEHTLEVLQRVLGLDEAAVMAFREAGVL 406 +LS+TP P LGEH +VL LG D + R G + Sbjct: 356 P--KLSDTPGTSEWVGPALGEHNAQVLGE-LGYDAQQIAKLRTEGAI 399 Lambda K H 0.319 0.137 0.408 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: 447 Number of extensions: 26 Number of successful extensions: 7 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: 406 Length of database: 399 Length adjustment: 31 Effective length of query: 375 Effective length of database: 368 Effective search space: 138000 Effective search space used: 138000 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 (21.7 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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