Align 2-oxoglutarate reductase; EC 1.1.1.399; EC 1.1.1.95; EC 3.1.3.3 (characterized, see rationale)
to candidate Synpcc7942_1501 Synpcc7942_1501 D-3-phosphoglycerate dehydrogenase
Query= uniprot:L0G228_ECHVK (630 letters) >FitnessBrowser__SynE:Synpcc7942_1501 Length = 546 Score = 175 bits (444), Expect = 4e-48 Identities = 105/344 (30%), Positives = 184/344 (53%), Gaps = 7/344 (2%) Query: 235 VLLLENVHPIGVEIMKQEGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLENA 294 VL+ + + +G++I+ Q V+V + +S EL + I + +RS T++T +V+E Sbjct: 21 VLVSDPIDQVGLDILSQVA-QVDV-KTGLSPSELAQIIGEYDALMLRSGTRVTAEVIEAG 78 Query: 295 NRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDKTLK 354 +L +G +G + +D+ +GI V N+P NT + E ++ ++ L R++ D Sbjct: 79 QKLRIIGRAGVGVDNVDVPAATRRGIVVVNSPEGNTIAAAEHTLAMMLSLSRHIPDANAS 138 Query: 355 MHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYD--IVERLALGNA 412 G W++ + EV K LG++G G IG+ ++ +A+ MGM + YD I A Sbjct: 139 TKSGGWDRKSFVGTEVYKKTLGVVGLGKIGSHVATVAKAMGMKLLAYDPFISAERAEQIG 198 Query: 413 TKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVVDVPALRD 472 ++ LD L + D I+LH+ E N++N E + KMK ++N +RG V++ AL D Sbjct: 199 ARLVELDILFQEADYITLHIPKTPETANLINAETLAKMKPTTRIINCARGGVINEQALAD 258 Query: 473 ALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENIAQFVPGK 532 A+ +G + GAA+DV+ EP D P + +G N ILTPH+G ST EAQ N+A V + Sbjct: 259 AIAAGKIGGAALDVYDQEPLQADSPLRA--LG-KNLILTPHLGASTTEAQVNVAVDVAEQ 315 Query: 533 IIEYINSGNTFNSVNFPNIQLPFLKDAHRLIHIHQNAPGVLAKI 576 I + + ++VN P + L+ + + + +L+++ Sbjct: 316 IRDVLLGLPARSAVNIPGLYPDILEKLRPYLQLAETLGNLLSQV 359 Score = 28.5 bits (62), Expect = 8e-04 Identities = 13/61 (21%), Positives = 32/61 (52%), Gaps = 6/61 (9%) Query: 566 HQNAPGVLAKINQVLASYKINI----VGQYLKTNEKIGYVITDIDKRYSNDVIDALKEIE 621 H++ PG++ KI +L S+ +NI VG+ + + + ++ +D ++ + ++ Sbjct: 479 HRDMPGIIGKIGSLLGSFNVNIASMQVGRRIVRGDAV--MVLSLDDPLPEGILAEITKVA 536 Query: 622 G 622 G Sbjct: 537 G 537 Lambda K H 0.317 0.136 0.377 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: 626 Number of extensions: 33 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 630 Length of database: 546 Length adjustment: 37 Effective length of query: 593 Effective length of database: 509 Effective search space: 301837 Effective search space used: 301837 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: 53 (25.0 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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