Align D-glycerate 2-kinase (EC 2.7.1.-) (characterized)
to candidate GFF1729 PS417_08795 hydroxypyruvate reductase
Query= reanno::psRCH2:GFF1145 (423 letters) >FitnessBrowser__WCS417:GFF1729 Length = 426 Score = 660 bits (1703), Expect = 0.0 Identities = 331/419 (78%), Positives = 377/419 (89%) Query: 1 MTLDPQALLRQLFDSAIEAAHPRHVLADHLPEDRSGRAIVIGAGKAAAAMAEAIEKVWEG 60 M++DPQ LLR+LF +AI+AAHPR VL +LP DRSGR IVIGAGKAAAAMA +E VW+G Sbjct: 1 MSVDPQHLLRELFATAIDAAHPRQVLEPYLPADRSGRVIVIGAGKAAAAMALVVENVWQG 60 Query: 61 ELSGLVVTRYEHHADCKRIEVVEAAHPVPDDAGERVARRVLELVSNLEESDRVIFLLSGG 120 E++GLVVTRY H A C++IEVVEAAHPVPD AG VA+RVL L+SNL E DRVIFLLSGG Sbjct: 61 EVTGLVVTRYGHGAPCQKIEVVEAAHPVPDAAGLAVAQRVLALISNLTEHDRVIFLLSGG 120 Query: 121 GSSLLALPAEGISLADKQAINKALLRSGAHIGEMNCVRKHLSAIKGGRLAKACWPASVYT 180 GS+LLALPAEGI+LADKQAINKALL+SGA IGEMNCVRKHLSAIKGGRLAKA WPA+VYT Sbjct: 121 GSALLALPAEGITLADKQAINKALLKSGATIGEMNCVRKHLSAIKGGRLAKAAWPATVYT 180 Query: 181 YAISDVPGDEATVIASGPTVADPTTSEQALEILERYHIEVPANVRAWLEDPRSETLKPGD 240 YAISDVPGD+ATVIASGPTV DP+TS+QAL IL+RY+I+ PA+VR+WL++P SET+KPGD Sbjct: 181 YAISDVPGDQATVIASGPTVGDPSTSQQALAILKRYNIDAPASVRSWLQNPASETVKPGD 240 Query: 241 PMLSRSHFRLIATPQQSLDAAAEVARAAGITPLILGDLEGEAREVAKVHAGIARQVVLHG 300 P+L+RSHF+LIA PQQSL+A A R AG +PLILGDLEGEAR+VAKVHAGIARQ+V HG Sbjct: 241 PVLARSHFQLIARPQQSLEAVAVKVRQAGFSPLILGDLEGEARDVAKVHAGIARQIVQHG 300 Query: 301 QPIAAPCVILSGGETTVTVRGNGRGGRNAEFLLALTENLQGLPNVYALAGDTDGIDGSED 360 QP+AAPCVILSGGETTVTVRGNGRGGRNAEFLL+LT++L+GLP VYALAGDTDGIDGSED Sbjct: 301 QPLAAPCVILSGGETTVTVRGNGRGGRNAEFLLSLTDSLKGLPGVYALAGDTDGIDGSED 360 Query: 361 NAGALMMPDSYARAETLGLRAADALANNDGYGYFAALDDLIVTGPTRTNVNDFRAILIL 419 NAGA+M P SY+RAE LGL A+D L NN+GYGYFAALD LI+T PTRTNVNDFRAILIL Sbjct: 361 NAGAIMTPCSYSRAEALGLSASDELDNNNGYGYFAALDGLIITEPTRTNVNDFRAILIL 419 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: 572 Number of extensions: 17 Number of successful extensions: 2 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: 426 Length adjustment: 32 Effective length of query: 391 Effective length of database: 394 Effective search space: 154054 Effective search space used: 154054 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