Align D-glycerate 2-kinase (EC 2.7.1.-) (characterized)
to candidate Dsui_3421 Dsui_3421 putative glycerate kinase
Query= reanno::psRCH2:GFF1145 (423 letters) >lcl|FitnessBrowser__PS:Dsui_3421 Dsui_3421 putative glycerate kinase Length = 439 Score = 503 bits (1296), Expect = e-147 Identities = 270/426 (63%), Positives = 314/426 (73%), Gaps = 8/426 (1%) Query: 3 LDPQALLRQLFDSAIEAAHPRHVLADHLPEDRS----GRAIVIGAGKAAAAMAEAIEKVW 58 L P ALL L +A+ AA P ++ HLP+ S GR +V+GAGKAA AMA A+E+ W Sbjct: 9 LAPDALLHNLLQAALAAADPARLVPPHLPDPASLPEGGRLVVVGAGKAAGAMARAVEEHW 68 Query: 59 EGELSGLVVTRYEHHADCKRIEVVEAAHPVPDDAGERVARRVLELVSNLEESDRVIFLLS 118 G LSGLVVTRY H C+RIEVVEAAHPVPD AGE A R+LE V L E DRV+ L+S Sbjct: 69 PGPLSGLVVTRYGHGLPCRRIEVVEAAHPVPDAAGEAAAARILEQVRGLTEKDRVLALIS 128 Query: 119 GGGSSLLALPAEGISLADKQAINKALLRSGAHIGEMNCVRKHLSAIKGGRLAKACWPASV 178 GGGS+L+A PA G+SLA K+A+ +ALL SGA IGE+NCVRKHLSA+KGGRLA A WPA V Sbjct: 129 GGGSALMAAPAPGVSLAQKRALTRALLLSGADIGEINCVRKHLSAVKGGRLAAAAWPAPV 188 Query: 179 YTYAISDVPGDEATVIASGPTVADPTTSEQALEILERYHIEVPANVRAWLEDPRSETLKP 238 T AISDV GD+ +VIASGPTVADPTT AL +L RY IEVP V A L ET KP Sbjct: 189 LTLAISDVAGDDPSVIASGPTVADPTTCADALAVLARYGIEVPPEVAALLHSGALETPKP 248 Query: 239 GDPMLSRSHFRLIATPQQSLDAAAEVARAAGITPLILGD-LEGEAREVAKVHAGIARQVV 297 GDP L RS +RLI PQQSL AAAE ARAAGITPL+LGD +EGE++EVAKV AG+A Sbjct: 249 GDPRLGRSDYRLIGRPQQSLLAAAEAARAAGITPLVLGDRVEGESKEVAKVMAGLALACQ 308 Query: 298 LHGQPIAAPCVILSGGETTVTVRGN---GRGGRNAEFLLALTENLQGLPNVYALAGDTDG 354 HG P+A PCV+LSGGETTV+V GRGGRN+EFLLAL L G P ++ALA DTDG Sbjct: 309 DHGTPLAPPCVLLSGGETTVSVAPGAPLGRGGRNSEFLLALALALGGRPGIHALAADTDG 368 Query: 355 IDGSEDNAGALMMPDSYARAETLGLRAADALANNDGYGYFAALDDLIVTGPTRTNVNDFR 414 IDGSEDNAGA + P + ARA G A LA +D YG+FA L DL++TGPTRTNVNDFR Sbjct: 369 IDGSEDNAGACIGPATLARAAAAGPDAQGHLAGHDAYGFFAGLGDLLLTGPTRTNVNDFR 428 Query: 415 AILILP 420 A+L+LP Sbjct: 429 AVLVLP 434 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: 586 Number of extensions: 32 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: 439 Length adjustment: 32 Effective length of query: 391 Effective length of database: 407 Effective search space: 159137 Effective search space used: 159137 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