Align D-tagatose-1,6-bisphosphate aldolase subunit GatZ (characterized)
to candidate BWI76_RS24875 BWI76_RS24875 tagatose-1,6-bisphosphate aldolase
Query= SwissProt::Q8VS12 (419 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS24875 BWI76_RS24875 tagatose-1,6-bisphosphate aldolase Length = 423 Score = 815 bits (2104), Expect = 0.0 Identities = 409/417 (98%), Positives = 411/417 (98%), Gaps = 1/417 (0%) Query: 1 MKDIISRHKAGEHIGICSVCSAHPLVIEAALSFDLHTNNKVLIEATSNQVNQFGGYTGMS 60 MKDIISRHKAGEHIGICSVCSAHPLVIEAAL FDLHTNNKVLIEATSNQVNQFGGYTGM Sbjct: 1 MKDIISRHKAGEHIGICSVCSAHPLVIEAALRFDLHTNNKVLIEATSNQVNQFGGYTGMQ 60 Query: 61 -CDFRDFVNKIAREVGFPSERIILGGDHLGPNCWQGEPAAEAMEKSVDLIKAYVAAGFSK 119 DFRDFVNKIAREVGFPSERIILGGDHLGPNCWQGEPAAEAMEKSVDLIKAYVAAGFSK Sbjct: 61 PADFRDFVNKIAREVGFPSERIILGGDHLGPNCWQGEPAAEAMEKSVDLIKAYVAAGFSK 120 Query: 120 IHLDASMSCADDPVPLDPAIVAERAARLCQAAEETATDEQKRHLTYVIGTEVPVPGGEAS 179 IHLDASMSCADDPVPLDPAIVAERAARLCQAAEETATDEQKRHLTYVIGTEVPVPGGEAS Sbjct: 121 IHLDASMSCADDPVPLDPAIVAERAARLCQAAEETATDEQKRHLTYVIGTEVPVPGGEAS 180 Query: 180 TIGSVHVTRAQDAAATLETHEAAFRKLGLNAALERVIAIVVQPGVEFDHTQIIHYQPEAA 239 TIGSVHVTRAQDAAATLETHEAAFRKLGLNAALERVIAIVVQPGVEFDHTQIIHYQPEAA Sbjct: 181 TIGSVHVTRAQDAAATLETHEAAFRKLGLNAALERVIAIVVQPGVEFDHTQIIHYQPEAA 240 Query: 240 KALSAWIEGTPMVYEAHSTDYQSRQAYWALVRDHYAILKVGPALTFALREAIFSLAQMEN 299 KALSAWIEGTPMVYEAHSTDYQSRQAY ALVRDHYAILKVGPALTFALREAIF+LAQMEN Sbjct: 241 KALSAWIEGTPMVYEAHSTDYQSRQAYRALVRDHYAILKVGPALTFALREAIFALAQMEN 300 Query: 300 ELVAPESRSRVMEVIDEVMLNEPGYWKKYYRPTWSQAMADIHFSLSDRIRYYWPHPRIRQ 359 ELVAPESRSRVMEVIDEVMLNEPGYWKKYYRPTWSQAM DIHFSLSDRIRYYWPHPRIRQ Sbjct: 301 ELVAPESRSRVMEVIDEVMLNEPGYWKKYYRPTWSQAMVDIHFSLSDRIRYYWPHPRIRQ 360 Query: 360 SVEKLIANLTETKLPLGLISQYIPVQFERLSLNELAAVPHDLILDKIQDVLRAYRYG 416 SVEKLIANLTETKLPLGLISQY+PVQFERLSLNELAAVPHDLILDKIQDVLRAYRYG Sbjct: 361 SVEKLIANLTETKLPLGLISQYMPVQFERLSLNELAAVPHDLILDKIQDVLRAYRYG 417 Lambda K H 0.320 0.134 0.399 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: 740 Number of extensions: 12 Number of successful extensions: 2 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: 419 Length of database: 423 Length adjustment: 32 Effective length of query: 387 Effective length of database: 391 Effective search space: 151317 Effective search space used: 151317 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: 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 preprint 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