Align mannitol 2-dehydrogenase (EC 1.1.1.67) (characterized)
to candidate WP_156172064.1 AAW01_RS05295 mannitol dehydrogenase family protein
Query= BRENDA::O08355 (493 letters) >NCBI__GCF_001010925.1:WP_156172064.1 Length = 486 Score = 306 bits (785), Expect = 8e-88 Identities = 177/469 (37%), Positives = 257/469 (54%), Gaps = 11/469 (2%) Query: 13 PEVKLPAYTLADTRQGIAHIGVGGFHRAHQAYYTDALMNTGEGLDWSICGVGLRSEDRKA 72 PE + P Y A G+ H+G G FHRAHQA Y DAL++ G W ICG LRS Sbjct: 4 PEARTPCYDRAQPC-GVLHLGTGAFHRAHQATYFDALLSAGHN-GWMICGASLRSP--AV 59 Query: 73 RDDLAGQDYLFTLYELGDTDDTEVRVIGSISDMLLAEDSAQALIDKLASPEIRIVSLTIT 132 + QD LFT+ + D + +V ++GS++++++A ++ AL+ LA ++ +V+LT+T Sbjct: 60 SRQMNPQDGLFTVL-IRDGGEEQVEIVGSVAEVMVAPENPSALVSALAHSDVALVTLTVT 118 Query: 133 EGGYCIDDSNGEFMAHLPQIQHDLAHPSSPKTVFGFICAALTQRRAAGIPAFTVMSCDNL 192 E GYC+D + G + D+A +SP+T GF+ A L R+AAGI FTV+SCDNL Sbjct: 119 EKGYCLDPATGALNLDDEGVAGDIADIASPQTAPGFLVAGLAARKAAGIAPFTVLSCDNL 178 Query: 193 PHNGAVTRKALLAFAALHNAELHDWIKAHVSFPNAMVDRITPMTSTAHRLQLHDEHGIDD 252 P NG TR+A+L A + L WI+ V+FP +MVDRI P T+ G+ D Sbjct: 179 PDNGKRTREAVLTLARAVDPALATWIEDEVAFPCSMVDRIVPATTEEDLDNFESATGLRD 238 Query: 253 AWPVVCEPFVQWVLEDKFVNGRPAWEKVGVQFTDDVTPYEEMKIGLLNGSHLALTYLGFL 312 V EPF QWV+ED F N RP ++VGVQ T+DV +E +K+ LLNG+H AL YLG L Sbjct: 239 EALVKTEPFTQWVVEDDFCNRRPPLDEVGVQMTNDVASWELVKLRLLNGAHSALAYLGGL 298 Query: 313 KGYRFVHETMNDPLFVAYMRAYMDLDVTPNLAPVPGIDLTDYKQTLVDRFSNQAIADQLE 372 G+ +VH+ M P F + A D + L P+ G D +Y+ L RF+N A+ + Sbjct: 299 AGHHYVHQAMAAPGFSRLVEALWD-EAEATLKPIDGFDAKNYRAQLAQRFTNSALEHRTH 357 Query: 373 RVCSDGSSKFPKFTVPTINRLIADGRETERA-ALVVAAWALYLKGVDENGVSYTIPDPRA 431 ++ DGS K P+ + TI R +A + +A W + G ++ G ++ + DP A Sbjct: 358 QIAMDGSQKIPQRWLNTIRAYREADRGVPKALVMALAGWMHWQAGKNDAGETHIVDDPLA 417 Query: 432 EFCQGLVSDDALISQR----LLAVEEIFGTAIPNSPEFVAAFERCYGSL 476 + + A R LL + IFG A+P FV Y S+ Sbjct: 418 ARTAAALREAAGDRMREVANLLGISAIFGEALPADNAFVQHLTEAYCSI 466 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: 596 Number of extensions: 27 Number of successful extensions: 5 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: 486 Length adjustment: 34 Effective length of query: 459 Effective length of database: 452 Effective search space: 207468 Effective search space used: 207468 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