Align 2-oxoglutarate reductase; EC 1.1.1.399; EC 1.1.1.95; EC 3.1.3.3 (characterized, see rationale)
to candidate GFF3804 Psest_3873 Phosphoglycerate dehydrogenase and related dehydrogenases
Query= uniprot:L0G228_ECHVK (630 letters) >lcl|FitnessBrowser__psRCH2:GFF3804 Psest_3873 Phosphoglycerate dehydrogenase and related dehydrogenases Length = 411 Score = 447 bits (1151), Expect = e-130 Identities = 225/405 (55%), Positives = 298/405 (73%), Gaps = 1/405 (0%) Query: 227 SYPKSRINVLLLENVHPIGVEIMKQEGY-NVEVVSSAMSEEELCEKIKNVSIIGIRSKTQ 285 S KS+I LLLE VH V+ +K GY N+E + A+S EEL EKI +V IGIRS+TQ Sbjct: 7 SLDKSKIKFLLLEGVHQNAVDTLKAAGYTNIEYLKGALSTEELKEKIADVHFIGIRSRTQ 66 Query: 286 ITKKVLENANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLM 345 +T++V + A +L+AVG FCIGTNQ++L +E+GIAVFNAP+SNTRSV EL ++E I L+ Sbjct: 67 LTEEVFDAAKKLIAVGCFCIGTNQVNLNAARERGIAVFNAPYSNTRSVAELVLAEAILLL 126 Query: 346 RNLHDKTLKMHQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYDIVE 405 R + +K H+G W KSA+ SFE+RGKKLGIIGYG+IG QLSVLAE +GM VF+YD+V Sbjct: 127 RGIPEKNASCHRGGWIKSAANSFEIRGKKLGIIGYGSIGTQLSVLAEALGMQVFFYDVVT 186 Query: 406 RLALGNATKIDSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVV 465 +L LGNAT+I SL ELL CDI+SLHV + ++ +++I MKKGAIL+N +RG VV Sbjct: 187 KLPLGNATQIGSLYELLGMCDIVSLHVPELPSTQWMIGEKEIRAMKKGAILINAARGTVV 246 Query: 466 DVPALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENI 525 ++ L A++ HL GAA+DVFP EPK+NDE FES L G ILTPHIGGST EAQ NI Sbjct: 247 ELDHLAAAIKDEHLIGAAIDVFPVEPKSNDEEFESPLRGLDRVILTPHIGGSTAEAQANI 306 Query: 526 AQFVPGKIIEYINSGNTFNSVNFPNIQLPFLKDAHRLIHIHQNAPGVLAKINQVLASYKI 585 V K+++Y ++G + +SVNFP + LP HRL+HIHQN PGV+++IN+V A I Sbjct: 307 GLEVAEKLVKYSDNGTSVSSVNFPEVALPSHPGKHRLLHIHQNIPGVMSEINKVFADNGI 366 Query: 586 NIVGQYLKTNEKIGYVITDIDKRYSNDVIDALKEIEGTIRFRILY 630 NI GQ+L+TNEK+GYV+ D+DK YS+ ++ L+ + GTIR R+L+ Sbjct: 367 NICGQFLQTNEKVGYVVIDVDKEYSDLALEKLQHVNGTIRSRVLF 411 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: 642 Number of extensions: 28 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: 630 Length of database: 411 Length adjustment: 34 Effective length of query: 596 Effective length of database: 377 Effective search space: 224692 Effective search space used: 224692 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: 52 (24.6 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 preprint 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