Align succinyl-CoA-glutarate CoA-transferase (EC 2.8.3.13) (characterized)
to candidate HSERO_RS18350 HSERO_RS18350 CoA transferase
Query= reanno::pseudo5_N2C3_1:AO356_10845 (406 letters) >lcl|FitnessBrowser__HerbieS:HSERO_RS18350 HSERO_RS18350 CoA transferase Length = 415 Score = 212 bits (540), Expect = 1e-59 Identities = 137/422 (32%), Positives = 216/422 (51%), Gaps = 32/422 (7%) Query: 2 GALSHLRVLDLSRVLAGPWAGQILADLGADVIKVERPGNGDDTRAWGPPFLKDARGENTT 61 G L+ ++VL+L ++AGP+ ++LA+ GADVIKVE PGNGD R W LKD Sbjct: 9 GPLAGIKVLELGTLIAGPFCSRMLAEFGADVIKVEAPGNGDPLRQWR--VLKDGT----- 61 Query: 62 EAAYYLSANRNKQSVTIDFTRPEGQRLVRELAAKSDILIENFKVGGLAAYGLDYDSLKAI 121 + ++ RNK+S+T++ Q + R+LA ++D++IEN++ G L + L Y+ LK + Sbjct: 62 -SLWWSVQARNKKSITLNMKDERAQEIARKLALEADVIIENYRPGVLEKWKLGYEDLKQL 120 Query: 122 NPQLIYCSITGFGQTGPYAKRAGYDFMIQGLGGLMSLTGRPEGDEGAGPVKVGVALTDIL 181 NP I ++G+GQTGP G+ + + +GG+ ++G P+ PV++G+++ D + Sbjct: 121 NPATIMVRLSGYGQTGPLRDLPGFGAIGESMGGIRYVSGHPD----RPPVRIGISIGDSI 176 Query: 182 TGLYSTAAILAALAHRDHVGG--------------GQHIDMALLDVQVACLANQAMNYLT 227 L+ + AL HRD GG GQ +D+AL + + + + Sbjct: 177 AALHGVIGAMMALRHRDVTGGRWNGKQGADCVAGQGQMVDVALYEAVFNMMESMVPEFDF 236 Query: 228 TGNAPKRLGNAHPNIVPYQDFPTADGDFILTVGN-DGQFRKFAEVAGQPQWADDPRFATN 286 G +R G A P IVP + T +G I+ GN D F++ G+ A+DP A N Sbjct: 237 AGVVRERTGGALPGIVPSNTYTTGEGMNIVIAGNGDAIFKRLMSAIGREDMANDPGLARN 296 Query: 287 KVRVANRAVLIPLIRQATVFKTTAEWVTQLEQAGVPCGPINDLAQVFADPQVQARGLAME 346 RV + I+Q +T + L+ A VP G I + + D Q AR + + Sbjct: 297 DGRVPRTEEIDAAIQQWCSTQTIETALATLQAADVPVGKIYSVKDMMNDAQFLARDMFEQ 356 Query: 347 LPHLLAGKVPQVASPI--RLSETPVEYRNAPPLLGEHTLEVLQRVLGLDEAAVMAFREAG 404 H A P I ++SETP + + P LG H+ E+LQ LG DEA + R+ G Sbjct: 357 --HQFADGTPVKLPGITPKMSETPGQTKWLGPELGAHSDEILQS-LGYDEAHIKMLRDQG 413 Query: 405 VL 406 V+ Sbjct: 414 VV 415 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: 472 Number of extensions: 24 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: 406 Length of database: 415 Length adjustment: 31 Effective length of query: 375 Effective length of database: 384 Effective search space: 144000 Effective search space used: 144000 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