Align Putative homocitrate synthase AksA; EC 2.3.3.14; (R)-homo(2)citrate synthase; EC 2.3.3.-; (R)-homo(3)citrate synthase; EC 2.3.3.- (uncharacterized)
to candidate 8499505 DvMF_0275 putative alpha-isopropylmalate/homocitrate synthase family transferase (RefSeq)
Query= curated2:Q8TW28 (397 letters) >FitnessBrowser__Miya:8499505 Length = 540 Score = 174 bits (442), Expect = 4e-48 Identities = 128/394 (32%), Positives = 201/394 (51%), Gaps = 23/394 (5%) Query: 21 VYDTTLRDGEQTPGVSFTPEQKLEIAHLLDELGVQQIEAGFPVVSEGERDAVRRIAHEGL 80 +YDTTLRDG Q+ ++ T KL+IA LDE+G+ +IE G+P + + + IA+ L Sbjct: 7 LYDTTLRDGSQSEDINLTAADKLKIALKLDEIGIDRIEGGWPGSNPVDVAFFKEIANYHL 66 Query: 81 -NADILCLARTLRGDVDAALDCDVDGVIT--------FIATSELHLKHKLRMSREEVLER 131 +A I T + A D ++ + F + E+H LR+ LE Sbjct: 67 KHAVISAFGSTHHPNFTADSDPNLRAIAESGARVASIFGKSCEVHAAEALRLDAARNLEI 126 Query: 132 IADTVEYAKDHGLWVAFSAE---DGTRTEFEFLERVYRTAEECGADRVHATDTVGVMIPA 188 I D+V + K V F AE DG R + R A E GAD + DT G +P Sbjct: 127 IGDSVAFLKGKLAEVYFDAEHFFDGYRHNAAYALSALRRAHEAGADVLVLCDTNGGTLPH 186 Query: 189 AMRLFVAKIREVVD-LPIGVHCHDDFGMAVANSLAAVEAGAQAISTTVNGIGERAGNAAL 247 + V ++RE + +G+H H+D +AVANS+AAV+AGA I T+NG+GER GNA L Sbjct: 187 EVARIVTEVREALPGAAVGIHAHNDCELAVANSIAAVQAGAVQIQGTINGVGERCGNANL 246 Query: 248 EEVIMALKELYGID----PGFNTEVLAELSRKVSEYSGIDVPPNKAVVGENAFRHESGIH 303 +I L+ +G + P + L ++ VSE + I + VG +AF H+ G+H Sbjct: 247 CSIIPTLELKFGGEYTCLPEGRLQQLTAVAAYVSEVANIPPFSRQPYVGRSAFAHKGGVH 306 Query: 304 VAAVLEEPRTYEPIDPKEVGMNRKIVLGKHTGRKAVVAKLEELG--VEPEEEIVEEVLKR 361 V+AV + YE I P VG ++I++ + GR +V+ G ++ +E +V+ +L Sbjct: 307 VSAVNRKSSLYEHISPDVVGNRQRILITELAGRSNIVSLARRFGFHLDKDEPVVKGLLTE 366 Query: 362 IK---ALGDRRVRVTDSKLEEIVRNVLESRGDRD 392 +K +LG ++ +E ++ L RG R+ Sbjct: 367 LKKKASLG-YDYAAAEASVELLILRKLARRGVRE 399 Lambda K H 0.317 0.135 0.380 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: 490 Number of extensions: 31 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: 397 Length of database: 540 Length adjustment: 33 Effective length of query: 364 Effective length of database: 507 Effective search space: 184548 Effective search space used: 184548 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 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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