Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate AO356_13955 AO356_13955 threonine aldolase
Query= reanno::pseudo3_N2E3:AO353_07670 (346 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_13955 Length = 346 Score = 671 bits (1730), Expect = 0.0 Identities = 323/345 (93%), Positives = 334/345 (96%) Query: 1 MTDKSQQFASDNYSGICPEAWAAMEQANQGHQRAYGDDEWTARASDDFRKLFETDCEVFF 60 MTDKSQQFASDNYSGICPEAWAAME+ANQGHQRAYGDDEWT RA+DDFR LFETDCEVFF Sbjct: 1 MTDKSQQFASDNYSGICPEAWAAMEEANQGHQRAYGDDEWTHRAADDFRALFETDCEVFF 60 Query: 61 AFNGTAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLIARTENGKLTPE 120 AFNGTAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLL+ARTENGKLTPE Sbjct: 61 AFNGTAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLLARTENGKLTPE 120 Query: 121 SIREIALKRQDIHYPKPRVVTLTQATEVGSIYTPEEIRAISATCKELGLNLHMDGARFSN 180 +IREIALKRQDIHYPKPRVVTLTQATEVGS+YTP+EIRAIS TCKELGLNLHMDGARFSN Sbjct: 121 AIREIALKRQDIHYPKPRVVTLTQATEVGSVYTPDEIRAISVTCKELGLNLHMDGARFSN 180 Query: 181 ACAFLNCSPADLTWKAGVDVLCFGGTKNGMAVGEAILFFNHKLAEDFDYRCKQAGQLASK 240 ACAFL CSPADLTWK GVDVLCFGGTKNGMAVGEAILFFNH LA DFDYRCKQAGQLASK Sbjct: 181 ACAFLGCSPADLTWKVGVDVLCFGGTKNGMAVGEAILFFNHDLAVDFDYRCKQAGQLASK 240 Query: 241 MRFLSAPWVGLLENDAWLKHARHANYCAQLLAELVSDIPGVELMFPVQANGVFLQLSESA 300 MRFLSAPWVGLL+NDAWLKHARHAN+CAQLLAELV+DIPGVELMFPVQANGVFLQLSE A Sbjct: 241 MRFLSAPWVGLLQNDAWLKHARHANHCAQLLAELVNDIPGVELMFPVQANGVFLQLSEPA 300 Query: 301 VAALTAKSWRFYTFIGKGGARFMCSWDTEVERVRELAADIREVMA 345 +AALTAK WRFYTFIGKGGARFMCSWDTE RVRELAADIREVM+ Sbjct: 301 IAALTAKGWRFYTFIGKGGARFMCSWDTEEARVRELAADIREVMS 345 Lambda K H 0.320 0.132 0.408 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: 550 Number of extensions: 6 Number of successful extensions: 1 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: 346 Length of database: 346 Length adjustment: 29 Effective length of query: 317 Effective length of database: 317 Effective search space: 100489 Effective search space used: 100489 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 (21.9 bits) S2: 49 (23.5 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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