Align D-glycerate 2-kinase (EC 2.7.1.-) (characterized)
to candidate Ac3H11_1084 D-glycerate 2-kinase (EC 2.7.1.-)
Query= reanno::psRCH2:GFF1145 (423 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_1084 Length = 465 Score = 459 bits (1180), Expect = e-133 Identities = 258/429 (60%), Positives = 293/429 (68%), Gaps = 18/429 (4%) Query: 9 LRQLFDSAIEAAHPRHVLADHLP----EDRSGRAIVIGAGKAAAAMAEAIEKVWEGE--L 62 L L+ A+ A P H A LP + GR +V+GAGKA AMA+A+E +W + L Sbjct: 37 LEYLYRVAVRRALPLHNTAAFLPAPPSRESGGRTLVLGAGKAGGAMAQAVEALWPADAPL 96 Query: 63 SGLVVTRYEHHADC-----KRIEVVEAAHPVPDDAGERVARRVLELVSNLEESDRVIFLL 117 SGLVVTRY H +RIEVVEAAHPVPD AG A R+L L L E+D V+ L+ Sbjct: 97 SGLVVTRYHHTPPRPDGLPQRIEVVEAAHPVPDAAGLAAAERILALTEGLTENDLVLCLI 156 Query: 118 SGGGSSLLALPAEGISLADKQAINKALLRSGAHIGEMNCVRKHLSAIKGGRLAKACWPAS 177 SGGGS+LL LPA+G++L DKQ INKALL SGA I EMNCVRKHLS IKGGRLA AC PA Sbjct: 157 SGGGSALLTLPADGLTLEDKQRINKALLESGAAIDEMNCVRKHLSRIKGGRLAAACAPAR 216 Query: 178 VYTYAISDVPGDEATVIASGPTVADPTTSEQALEILERYHIEVPANVRAWLEDPRSETLK 237 V T ISDVPGD+ +VIASGPTV D TT AL IL RY IEVP VRA LE ET K Sbjct: 217 VVTLTISDVPGDDPSVIASGPTVPDATTCADALAILARYGIEVPPAVRAALEAGTLETPK 276 Query: 238 PGDPMLSRSHFRLIATPQQSLDAAAEVARAAGITPLILGD-LEGEAREVAKVHAGIARQV 296 PGD + + + ATPQQSL AAAE ARAA + IL D +EGE+REV KVHA +AR V Sbjct: 277 PGDAVFANHVVHMTATPQQSLQAAAEAARAADVAAYILSDEIEGESREVGKVHAALARAV 336 Query: 297 VLHGQPIAAPCVILSGGETTVTVR------GNGRGGRNAEFLLALTENLQGLPNVYALAG 350 HGQP A PCVILSGGETTVT+R GRGGR EF + L + LQG V+ALA Sbjct: 337 ARHGQPFARPCVILSGGETTVTIRPRAPGAAKGRGGRAGEFCMGLAQALQGQAGVWALAA 396 Query: 351 DTDGIDGSEDNAGALMMPDSYARAETLGLRAADALANNDGYGYFAALDDLIVTGPTRTNV 410 DTDGIDG EDNAGA + PD+ ARA GL AD L ND YGYF AL DL++TGPT TNV Sbjct: 397 DTDGIDGVEDNAGARVAPDTLARAAAQGLSIADHLDRNDAYGYFDALGDLVITGPTHTNV 456 Query: 411 NDFRAILIL 419 NDFRAILIL Sbjct: 457 NDFRAILIL 465 Lambda K H 0.316 0.134 0.384 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: 588 Number of extensions: 29 Number of successful extensions: 4 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: 423 Length of database: 465 Length adjustment: 32 Effective length of query: 391 Effective length of database: 433 Effective search space: 169303 Effective search space used: 169303 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 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