Align mannitol 2-dehydrogenase (EC 1.1.1.67) (characterized)
to candidate WP_007675858.1 BN137_RS06955 fructuronate reductase
Query= BRENDA::O08355 (493 letters) >NCBI__GCF_000319285.1:WP_007675858.1 Length = 488 Score = 351 bits (901), Expect = e-101 Identities = 193/485 (39%), Positives = 278/485 (57%), Gaps = 9/485 (1%) Query: 11 LAPEVKLPAYTLADTRQGIAHIGVGGFHRAHQAYYTDALMNTGEGLDWSICGVGLRSEDR 70 L VK P Y + I H G G FHRAHQA TD ++N G DW IC + L S D Sbjct: 9 LPASVKRPGYDRRALQTRIVHFGFGAFHRAHQALLTDRVLNQNGG-DWGICEISLFSGD- 66 Query: 71 KARDDLAGQDYLFTLYELGDTDDTEVRVIGSISDMLLAE-DSAQALIDKLASPEIRIVSL 129 + L QD+L+T+ E G + + +IG++++ L A+ D +A+I+K P++ IVSL Sbjct: 67 ELMSALRAQDHLYTVLEKGAEGNQPI-IIGAVNECLNAKLDGMEAIIEKFCEPQVAIVSL 125 Query: 130 TITEGGYCIDDSNGEFMAHLPQIQHDLAHPSSPKTVFGFICAALTQRRAAGIPAFTVMSC 189 TITE GYCID + G +I HDL +P +P + G + AL +RRA G AFTV+SC Sbjct: 126 TITEKGYCIDPATGHLDTQNSRIAHDLENPHAPHSAPGLLVEALHRRRARGHAAFTVLSC 185 Query: 190 DNLPHNGAVTRKALLAFAALHNAELHDWIKAHVSFPNAMVDRITPMTSTAHRLQLHDEHG 249 DN+P NG V R+A+L A + L +WI +V+FP MVDRI P + ++ D G Sbjct: 186 DNIPDNGHVVREAVLGMAHQRDPALAEWIAENVTFPGTMVDRIVPAATPESLQEIADTLG 245 Query: 250 IDDAWPVVCEPFVQWVLEDKFVNGRPAWEKVGVQFTDDVTPYEEMKIGLLNGSHLALTYL 309 + D + CEPF+QWV+ED FV GRPAWE GVQ DDV P+E+MK+ +LNGSH L YL Sbjct: 246 VADPCAISCEPFIQWVIEDNFVAGRPAWEDAGVQMVDDVLPWEQMKLRMLNGSHSFLAYL 305 Query: 310 GFLKGYRFVHETMNDPLFVAYMRAYMDLDVTPNLAPVPGIDLTDYKQTLVDRFSNQAIAD 369 G+L GY+ + + MND F R M + P L + G+DLT Y +L+ RF+N ++ Sbjct: 306 GYLAGYQHISDCMNDTHFRDAARQLMLREQAPTLR-ITGVDLTGYADSLIARFANPSLKH 364 Query: 370 QLERVCSDGSSKFPKFTVPTINRLIADGRETERAALVVAAWALYLKGVDENGVSYTIPDP 429 + ++ DGS K P+ + ++ + +G E AL VA W Y+ G+D+NG + DP Sbjct: 365 RTWQIAMDGSQKLPQRMLDSVRWHLQNGGEWSLLALGVAGWMRYVSGLDDNGQPIDVRDP 424 Query: 430 RAEFCQGLV---SDDALISQRLLAVEEIFGTAIPNSPEFVAAFERCYGSLRDNGVTTTLK 486 A+ LV S++ +S LL ++E+FG +P P F+ + SL G + Sbjct: 425 LADKIATLVQSSSEEERVS-ALLTLKEVFGEELPQHPLFIHTLHAAWQSLCRLGAKEAVA 483 Query: 487 HLLKK 491 L ++ Sbjct: 484 RLARR 488 Lambda K H 0.321 0.137 0.414 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: 657 Number of extensions: 28 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: 493 Length of database: 488 Length adjustment: 34 Effective length of query: 459 Effective length of database: 454 Effective search space: 208386 Effective search space used: 208386 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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