Align D-glycerate 2-kinase (EC 2.7.1.-) (characterized)
to candidate SMc04389 SMc04389 hydroxypyruvate reductase
Query= reanno::psRCH2:GFF1145 (423 letters) >FitnessBrowser__Smeli:SMc04389 Length = 455 Score = 381 bits (979), Expect = e-110 Identities = 207/420 (49%), Positives = 273/420 (65%), Gaps = 3/420 (0%) Query: 2 TLDPQALLRQLFDSAIEAAHPRHVLADHLPEDRSGRAIVIGAGKAAAAMAEAIEKVWEGE 61 +++P+ L LF++A+ AA P + HLP GR IV+GAGKAA+ MA A E++W+G Sbjct: 35 SIEPRPFLISLFEAAVAAADPEAAIRAHLPARPKGRTIVVGAGKAASQMAAAFERLWDGP 94 Query: 62 LSGLVVTRYEHHADCKRIEVVEAAHPVPDDAGERVARRVLELVSNLEESDRVIFLLSGGG 121 L+G VV R+ C RI V+++AHPVPD+AG + +LE V L D V+ L+SGGG Sbjct: 95 LAGAVVARHGPVEKCGRIRVLQSAHPVPDEAGLAASAALLETVGGLTADDLVVALISGGG 154 Query: 122 SSLLALPAEGISLADKQAINKALLRSGAHIGEMNCVRKHLSAIKGGRLAKACWPASVYTY 181 S+LL P G++L D+ A+NKALL SGA I MN VRKH+S IKGGRLA A PA V + Sbjct: 155 SALLPAPPGGLTLEDEIAVNKALLASGAPISAMNVVRKHVSRIKGGRLALAAAPARVVSL 214 Query: 182 AISDVPGDEATVIASGPTVADPTTSEQALEILERYHIEVPANVRAWLEDPRSETLKPGDP 241 +SDVPGD +ASGPTVAD ++ E+A EI+ RY I +P V A L + +P D Sbjct: 215 VVSDVPGDNPAFVASGPTVADRSSLEEAREIVARYAIALPERVTAHLASDAARAPRPDDA 274 Query: 242 MLSRSHFRLIATPQQSLDAAAEVARAAGITPLILGD-LEGEAREVAKVHAGIARQVVLHG 300 + + +IA+ SL+AAA AR +GI +IL D +EGEAR++ ++HA +AR+V Sbjct: 275 AFAGNEVHVIASASVSLEAAAARARESGIEAMILSDAIEGEARDIGRMHAALAREVASRN 334 Query: 301 QPIAAPCVILSGGETTVTVRGN--GRGGRNAEFLLALTENLQGLPNVYALAGDTDGIDGS 358 +P + P V+LSGGETTVT+ G G+GGRN+EFLL+L ++ G+ + ALA DTDGIDGS Sbjct: 335 RPFSKPVVLLSGGETTVTISGERYGKGGRNSEFLLSLALDIDGIGGIDALAADTDGIDGS 394 Query: 359 EDNAGALMMPDSYARAETLGLRAADALANNDGYGYFAALDDLIVTGPTRTNVNDFRAILI 418 EDNAGA S R G LA +D + FAA DL V GPT TNVND RAILI Sbjct: 395 EDNAGAFADGASIGRMRAAGADPRSHLAGHDAWTAFAASGDLFVPGPTGTNVNDLRAILI 454 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: 510 Number of extensions: 23 Number of successful extensions: 3 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: 455 Length adjustment: 32 Effective length of query: 391 Effective length of database: 423 Effective search space: 165393 Effective search space used: 165393 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