Align phosphogluconate dehydratase (characterized)
to candidate AO356_28760 AO356_28760 dihydroxy-acid dehydratase
Query= CharProtDB::CH_024239 (603 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_28760 Length = 594 Score = 181 bits (458), Expect = 1e-49 Identities = 142/453 (31%), Positives = 210/453 (46%), Gaps = 49/453 (10%) Query: 146 DGALFLGVCDKIVPGLTMAALSFGHLPAVFVPSGPMASGLPNKEKV-------RIRQLYA 198 DG + CDK P MAA + LPA+ + GPM G E + R L A Sbjct: 120 DGVVLTTGCDKTTPACLMAAATTD-LPAIVLSGGPMLDGHHKGELIGSGTVLWHARNLMA 178 Query: 199 EGKVDRMALLESEAASYHAPGTCTFYGTANTNQMVVEFMGMQLPGSSFVHPDSPLRDALT 258 G++D +E A+ + G C GTA + + E +GM LPG + + R + Sbjct: 179 AGEIDYEGFMEMTTAASPSVGHCNTMGTALSMNALAEALGMSLPGCASIPAPYRERGQMA 238 Query: 259 AAAARQVTRMTGNGNEWMPIGKMIDEKVVVNGIVALLATGGSTNHTMHLVAMARAAGIQI 318 A +++ + + +++ + N I A G S+N HL+A+AR G+++ Sbjct: 239 YATGKRICELVLQD---IRPSQIMTRQAFENAIAVASALGASSNCPPHLIAIARHMGVEL 295 Query: 319 NWDDFSDLSDVVPLMARLYPNGPADINHFQAAGGVPVLVRELLKAGLLHEDVNTVAGFGL 378 + DD+ + + VPL+ P G F AGGVP ++ EL KAG LHED TV+G + Sbjct: 296 SLDDWQRIGEDVPLLVNCMPAGKYLGEGFHRAGGVPSVMHELQKAGRLHEDCATVSGRTI 355 Query: 379 SRYTLEPWLNNGELDWREGAEKSLDSN--VIASFEQPFSHHGGTKVLSGN-LGRAVMKTS 435 GE+ SL SN VI F+ P H G VLSGN A+MK S Sbjct: 356 -----------GEI-----VSSSLTSNADVIHPFDTPLKHRAGFIVLSGNFFDSAIMKMS 399 Query: 436 AV-----------PVENQVIEAPAVVFESQHDVMPAFEAGLLDRD--CVVVVRHQGPKA- 481 V P EA A+VFE D + LD D C++V+R G Sbjct: 400 VVGEAFRKTYLSEPGAENSFEARAIVFEGPEDYHARIDDPALDIDERCILVIRGVGTVGY 459 Query: 482 NGMPELHKLMPPLGVLLDRCFKIALVTDGRLSGASGKVPSAIHVTPEAYDGGLLAKVRDG 541 G E+ + PP ++ + + DGR SG S PS ++++PEA GG LA ++ Sbjct: 460 PGSAEVVNMAPPAALIKQGIDSLPCLGDGRQSGTSAS-PSILNMSPEAAVGGGLALLQTN 518 Query: 542 DIIRVNGQTGELTLLVDEAELAARE----PHIP 570 D ++V+ T + LL+D+ E+A R P+IP Sbjct: 519 DRLKVDLNTRTVNLLIDDEEMARRRLEWTPNIP 551 Lambda K H 0.318 0.134 0.392 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: 827 Number of extensions: 42 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: 603 Length of database: 594 Length adjustment: 37 Effective length of query: 566 Effective length of database: 557 Effective search space: 315262 Effective search space used: 315262 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: 53 (25.0 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