Align L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized)
to candidate 15664 b1542 predicted mannonate dehydrogenase (NCBI)
Query= BRENDA::Q9KWR5 (485 letters) >lcl|FitnessBrowser__Keio:15664 b1542 predicted mannonate dehydrogenase (NCBI) Length = 486 Score = 297 bits (761), Expect = 5e-85 Identities = 166/421 (39%), Positives = 242/421 (57%), Gaps = 7/421 (1%) Query: 10 LPANVQAPPYDIDGIKPGIVHFGVGNFFRAHEAFYVEQIL-EHAPDWAIVGVGLTGSDRS 68 L A P YD++ + P IVH G G F RAH+ Y + + EH DW V L G ++ Sbjct: 6 LSAKATLPVYDLNNLAPRIVHLGFGAFHRAHQGVYADILATEHFSDWGYYEVNLIGGEQ- 64 Query: 69 KKKAEEFKAQDCLYSLTETAPSGKSTVRVMGALRDYLLAPADP-EAVLKHLVDPAIRIVS 127 + + + QD LY++ E + + T RV+G ++ L D E VL + +P I IVS Sbjct: 65 --QIADLQQQDNLYTVAEMS-ADVWTARVVGVVKKALHVQIDGLETVLAAMCEPQIAIVS 121 Query: 128 MTITEGGYNINETTGAFDLENAAVKADLKNPEKPSTVFGYVVEALRRRWDAGGKAFTVMS 187 +TITE GY + TG L++ V AD++NP +P T G +VEAL RR AG AFTVMS Sbjct: 122 LTITEKGYFHSPATGQLMLDHPMVAADVQNPHQPKTATGVIVEALARRKAAGLPAFTVMS 181 Query: 188 CDNLRHNGNVARKAFLGYAKARDPELAKWIEENATFPNGMVDRITPTVSAEIAKKLNAAS 247 CDN+ NG+V R YA+A D +LA+WIE+N TFP+ MVDRI P V+ + K+ + Sbjct: 182 CDNMPENGHVMRDVVTSYAQAVDVKLAQWIEDNVTFPSTMVDRIVPAVTEDTLAKIEQLT 241 Query: 248 GLDDDLPLVAEDFHQWVLEDQFADGRPPLEKAGVQMVGDVTDWEYVKIRMLNAGHVMLCF 307 G+ D + E F QWV+ED F GRP EKAG ++V DV +E +K+RMLN H L + Sbjct: 242 GVRDPAGVACEPFRQWVIEDNFVAGRPEWEKAGAELVSDVLPYEEMKLRMLNGSHSFLAY 301 Query: 308 PGILVGYENVDDAIEDSELLGNLKNYLNKDVIPTLKAPSGMTLEGYRDSVISRFSNKAMS 367 G L GY++++D +ED + ++ PTLK G+ L+ Y + +I+R+SN A+ Sbjct: 302 LGYLAGYQHINDCMEDEHYRYAAYGLMLQEQAPTLKV-QGVDLQDYANRLIARYSNPALR 360 Query: 368 DQTLRIASDGCSKVQVFWTETVRRAIEDKRDLSRIAFGIASYLEMLRGRDEKGGTYESSE 427 +T +IA DG K+ ++VR + +A G+A ++ + G DE+G E S+ Sbjct: 361 HRTWQIAMDGSQKLPQRMLDSVRWHLAHDSKFDLLALGVAGWMRYVGGVDEQGNPIEISD 420 Query: 428 P 428 P Sbjct: 421 P 421 Lambda K H 0.317 0.135 0.398 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: 602 Number of extensions: 30 Number of successful extensions: 3 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: 485 Length of database: 486 Length adjustment: 34 Effective length of query: 451 Effective length of database: 452 Effective search space: 203852 Effective search space used: 203852 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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