Align D-2-hydroxyglutarate dehydrogenase (EC 1.1.99.39) (characterized)
to candidate WP_066602432.1 V473_RS08145 FAD-binding oxidoreductase
Query= BRENDA::O23240 (559 letters) >NCBI__GCF_001046645.1:WP_066602432.1 Length = 470 Score = 289 bits (739), Expect = 2e-82 Identities = 172/466 (36%), Positives = 256/466 (54%), Gaps = 8/466 (1%) Query: 89 NPLFSSLDSKDVSYFKEILGEKNVVEDKERLETANTDWMHKYKGSSKLMLLPKNTQEVSQ 148 +PL S + F+ IL E V+ + + +M + + ++L P+ T ++SQ Sbjct: 4 DPLAVGPASSLIDQFRAILDEGGVMTGDDVSDRHPGYFMTRVEAD--VLLRPETTDQLSQ 61 Query: 149 ILEYCDSRRLAVVPQGGNTGLVGGSVPVFDEVIVNVGLMNKILSFDEVSGVLVCEAGCIL 208 ++ C + VV QGG +G V + +VI+++ MN+I S D + + +AG IL Sbjct: 62 VMALCHAAGQPVVIQGGMSGWVRATQTRPGDVILSLERMNRIESIDPANRTAIVQAGVIL 121 Query: 209 ENLATFLDTKGFIMPLDLGAKGSCHIGGNVSTNAGGLRLIRYGSLHGTVLGLEAVTANGN 268 E L+ G PLDLG +GSC +GGN +TNAGG+R+IRYG + VLG+E V A+G Sbjct: 122 EKFQDHLEAHGLSFPLDLGGRGSCQLGGNAATNAGGMRVIRYGMMREQVLGMEVVLADGR 181 Query: 269 VLDMLGTLRKDNTGYDLKHLFIGSEGSLGIVTKVSILTQPKLSSVNLAFIACKDYLSCQK 328 VL + + K+NTGYDLK LFIGSEG+LG++T++ + + + S N A + + K Sbjct: 182 VLSSMNQMIKNNTGYDLKQLFIGSEGTLGVITRLVLRLRERPVSSNTALVCADSFDRIAK 241 Query: 329 LLVEAKRNLGEILSAFEFLDNNSMDLVLNHLDGVRNPVSSSENFYILIETTGSDETNDRE 388 LL LG +LSAFE +DNN V + P+ S E +Y +IE GSD DR+ Sbjct: 242 LLRHVDGALGGLLSAFELVDNN-FYRVNTGVGRHPAPLGSDERYYAMIEALGSDHERDRD 300 Query: 389 KLEAFLLKSLEKGLVSDGVIAQDINQASSFWRIREGITEALQKAGAVYKYDLSLPVEEIY 448 EA L + EKGL D +IA+ ++ W IRE + + Y +D+SLPV + Sbjct: 301 LFEAVLTDAAEKGLFDDAIIARSEKDRAAIWGIREDLEHIVHDFQPFYAFDVSLPVGAME 360 Query: 449 NIVNDLRGRLGDL---ANVMGYGHLGDGNLHLNISAAEYNDKLLGLIEPYVYEWTSKHRG 505 + ++ RL + + GH+GDGNLH+ I A D+ +E VYE G Sbjct: 361 AYMGEVTQRLKAIWPDGGIAFLGHVGDGNLHIAIGAGTPQDR--EQVEACVYEPLRPIGG 418 Query: 506 SISAEHGLGVMKANEIFYSKSPETVALMASIKKLLDPKGILNPYKV 551 S+SAEHG+G+ K + ++SP LM IK++ DPK ILNP K+ Sbjct: 419 SVSAEHGIGLEKKPWLSITRSPLERGLMREIKQMFDPKNILNPGKI 464 Lambda K H 0.317 0.136 0.390 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: 637 Number of extensions: 32 Number of successful extensions: 4 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: 559 Length of database: 470 Length adjustment: 35 Effective length of query: 524 Effective length of database: 435 Effective search space: 227940 Effective search space used: 227940 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 Sep 24 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:
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