Align D-alanine dehydrogenase (EC 1.4.99.-) (characterized)
to candidate Ac3H11_416 D-amino acid dehydrogenase small subunit (EC 1.4.99.1)
Query= reanno::psRCH2:GFF3724 (432 letters) >lcl|FitnessBrowser__acidovorax_3H11:Ac3H11_416 D-amino acid dehydrogenase small subunit (EC 1.4.99.1) Length = 410 Score = 244 bits (622), Expect = 5e-69 Identities = 150/416 (36%), Positives = 231/416 (55%), Gaps = 16/416 (3%) Query: 1 MRVLVLGSGVVGTASAYYLARAGFEVVVVDRQPAVAMETSFANAGQVSPGYASPWAAPGV 60 M++ ++G+G+VG +AY LA G EV V +++ A A E SFA AG ++P +PWA PG Sbjct: 1 MKIAIVGAGIVGVTTAYELASDGHEVTVFEQRSAAAEEASFATAGLLAPHLLTPWAVPGF 60 Query: 61 PLKAMKWLLQRHAPLAIKLTGDVDQ--YLWMAQMLRNCTAARYAVNKERMVRLSEYSRDC 118 A++ L+ HA L +L+G + + + W+++ R+ T A A + RL++YS+ Sbjct: 61 G-HALR-LMGPHATL--RLSGGLSRANWAWLSRW-RSATHASSAP-AAALERLAQYSQSR 114 Query: 119 LDELRAETGIAYEGRQLGTTQLFRTQAQLDAAAKDIAVLERSGVPYELLDRAAIGRVEPA 178 L L + +E Q G L RT+ + + VL SGV +D ++EP Sbjct: 115 LQALAQRHELDFEASQ-GRLVLLRTEQERAQLQPALQVLRDSGVALREVDADIARQIEPG 173 Query: 179 LAKVAHKLSGALRLPNDQTGDCQMFTSRLAEMALALGVEFRFGQNIQRLEHAGDRIAGVW 238 L+ A L+GA+ LP+ + G+C++F L + GV F F I R+ G GV Sbjct: 174 LSPEA-PLAGAIHLPDARAGNCRLFAQLLRQGTQGSGVHFAFNTRIDRI---GTTPVGVV 229 Query: 239 IDGK--LETADRYVLALGSYSPQMLKPLGIRAPVYPLKGYSLTVPISDPAMAPQSTVLDE 296 + G+ L D VL G+ S +L LG+R P+ + GYS++ P+ + APQ++V+D Sbjct: 230 VQGESDLRRFDAVVLCAGTASAALLPALGMRLPMAAVYGYSVSAPLRESTHAPQASVVDA 289 Query: 297 TYKVAITRFDQRIRVGGMAEIAGHDLSLNPRRRETLEMVVGDLYPQGGDPAEAV-FWTGL 355 +++ITR QR+R+ G AE+AG D + + L + D +P G + V W G Sbjct: 290 AQQISITRLGQRVRIAGGAELAGADAEHHAATLQRLYRTLNDWFPGGAQLSSGVQVWRGA 349 Query: 356 RPATPDGTPIIGATAYRNLYLNTGHGTLGWTMACGSGRVLADLLASKRPQISTDGL 411 RP PDG P++GA+ L+LNTGHG GW +ACGS R LADL+A + P++ DGL Sbjct: 350 RPLLPDGAPVVGASGVPGLWLNTGHGAGGWALACGSARALADLMAQRVPEVPLDGL 405 Lambda K H 0.320 0.135 0.405 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: 508 Number of extensions: 31 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: 432 Length of database: 410 Length adjustment: 32 Effective length of query: 400 Effective length of database: 378 Effective search space: 151200 Effective search space used: 151200 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: 50 (23.9 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 paper from 2022 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