Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate GFF3085 PGA1_c31360 putative hydroxypyruvate reductase
Query= BRENDA::O58231 (440 letters) >FitnessBrowser__Phaeo:GFF3085 Length = 424 Score = 229 bits (583), Expect = 2e-64 Identities = 153/437 (35%), Positives = 236/437 (54%), Gaps = 20/437 (4%) Query: 5 DIREIGLRLVGEAIKAADPYRAVLNAVKVSDDKIIVQGKEFEIKGKVYVIALGKAACEMA 64 D+R I R A+ A+P A+ +++ + G G++ ++ALGKAA M Sbjct: 3 DLRSIARRFFAAAVARANPATALAESLRQHPPTLPQPG------GRLILVALGKAAIPMI 56 Query: 65 RAIEDILDVED-GVAVTKYGYGKELKRIKVIEAGHPIPDEKSILGAKEALSILNRAREND 123 R +L D +AVT +L ++V+ HP+P S+ S L+ D Sbjct: 57 RQAMAMLPPPDRAIAVTNPENVADLSDVEVLAGNHPVPHHMSLAAGDALRSALSNLNAKD 116 Query: 124 IVFILISGGGSALFELPEEGISLEDLKLTTDLLLKSGAKIHEINTVRKHISKVKGGKLAK 183 V LISGGGSAL P G++L D TDLLL G I ++N +R+ +S++KGG L + Sbjct: 117 RVIALISGGGSALAVAPAGGLTLADKTAVTDLLLGGGVDITQMNLIRQQLSELKGGGLLR 176 Query: 184 MIKGTGIV-LIISDVVGDNLEAIASGPTVKDPTTFEDAKRILELYDIWEKVPESVRLHIE 242 + + I+SDV+GD+L AIASGPTV + A+ L +++WE +P +V+ H+ Sbjct: 177 AAQPAQVFSYILSDVIGDDLRAIASGPTVAPLGSRAMARDCLLSHNLWEGLPHAVQTHLT 236 Query: 243 RGLRGEVEETLKEDLPNVHNFLIASNSISCEAIAREAQRLGFKAYIMTTTLEGEAKDAGL 302 + + + + H LI SN S A+ +A R G+ A+I++ L G+ + A Sbjct: 237 TPEEPQ-QSPANSSVTSAH--LIGSNRHSLGAVRDQATRDGWSAHIVSDALIGDVEVAAT 293 Query: 303 FIGSIVQEIAERGRPFEPPVVLVFGGETTVTIEGKGGKGGPNQEIALSAT---RKISDLE 359 I + +E E GR P L+FGGETTV + G G+GG NQE+AL R+ Sbjct: 294 EILAATKE-QETGR----PTALIFGGETTVQLTG-SGRGGRNQELALHIARLGRRALKER 347 Query: 360 ALIVAFDTDGTDGPTDAAGGIVDGTTYKKLREKGIDVEKVLKEHNSYEALKKVGGLLFTG 419 ++ TDG DGPTDAAGG+VD T++++ + G + + +L+ ++S ALK G LL TG Sbjct: 348 WTFLSAGTDGRDGPTDAAGGVVDSGTWQRIGDNGGNPDALLRNNDSNAALKLAGDLLITG 407 Query: 420 PTGTNVNSIVIAIVTSK 436 TGTNV + I +++ + Sbjct: 408 GTGTNVADVQIMLLSPR 424 Lambda K H 0.315 0.137 0.376 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: 427 Number of extensions: 17 Number of successful extensions: 6 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: 440 Length of database: 424 Length adjustment: 32 Effective length of query: 408 Effective length of database: 392 Effective search space: 159936 Effective search space used: 159936 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: 42 (22.0 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