Align 4-hydroxy-2-oxo-heptane-1,7-dioate aldolase; 2,4-dihydroxyhept-2-ene-1,7-dioic acid aldolase; HHED aldolase; 4-hydroxy-2-ketoheptane-1,7-dioate aldolase; HKHD aldolase; EC 4.1.2.52 (characterized)
to candidate BPHYT_RS28905 BPHYT_RS28905 alpha-dehydro-beta-deoxy-D-glucarate aldolase
Query= SwissProt::Q47098 (262 letters) >FitnessBrowser__BFirm:BPHYT_RS28905 Length = 267 Score = 299 bits (766), Expect = 4e-86 Identities = 152/253 (60%), Positives = 183/253 (72%) Query: 3 NSFKAALKAGRPQIGLWLGLSSSYSAELLAGAGFDWLLIDGEHAPNNVQTVLTQLQAIAP 62 N+FK AL G+PQ GLW L+ +Y ELLA AGFDWLLID EHAPN+V++ L QLQA+A Sbjct: 6 NNFKRALAEGKPQFGLWAALADAYVTELLATAGFDWLLIDNEHAPNDVRSTLAQLQAVAA 65 Query: 63 YPSQPVVRPSWNDPVQIKQLLDVGTQTLLVPMVQNADEAREAVRATRYPPAGIRGVGSAL 122 Y S PVVRP +D IKQLLD+G QTLL+PM+ A++A +AV ATRYPP GIRGVGSAL Sbjct: 66 YASHPVVRPVRSDSALIKQLLDIGAQTLLLPMIDTAEQAADAVAATRYPPQGIRGVGSAL 125 Query: 123 ARASRWNRIPDYLQKANDQMCVLVQIETREAMKNLPQILDVEGVDGVFIGPADLSADMGY 182 ARASRWNRIPDYL A D++CVLVQ+E+ + M+NL I V+GVDGVF GP+DLSA MG Sbjct: 126 ARASRWNRIPDYLNTAADELCVLVQVESVQGMENLSAIAAVDGVDGVFFGPSDLSASMGL 185 Query: 183 AGNPQHPEVQAAIEQAIVQIRESGKAPGILIANEQLAKRYLELGALFVAVGVDTTLLARA 242 G P V+ AI I + +GKA G+L + +A YLE GA FVAVG DT LL+RA Sbjct: 186 LGKPGDASVREAIRNGIQTVLRAGKAAGVLAPDPAIAADYLEAGATFVAVGTDTGLLSRA 245 Query: 243 AEALAARFGAQAT 255 A LAA + AT Sbjct: 246 AADLAASYKKTAT 258 Lambda K H 0.317 0.133 0.387 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: 248 Number of extensions: 3 Number of successful extensions: 1 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: 262 Length of database: 267 Length adjustment: 25 Effective length of query: 237 Effective length of database: 242 Effective search space: 57354 Effective search space used: 57354 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: 47 (22.7 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