Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate BWI76_RS14020 BWI76_RS14020 aspartate aminotransferase family protein
Query= reanno::Putida:PP_4108 (416 letters) >FitnessBrowser__Koxy:BWI76_RS14020 Length = 461 Score = 198 bits (504), Expect = 2e-55 Identities = 142/426 (33%), Positives = 216/426 (50%), Gaps = 42/426 (9%) Query: 15 PITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNPAVVEAIQAQATR--LTHYAFNAA 72 P+ ++ + D D K+Y+D + G G L LGH +P V+++IQ+ T H Sbjct: 42 PLAITKAEGVWLTDADNKQYLDCLAGAGTLALGHNHPDVLQSIQSVITSGLPLHTLDLTT 101 Query: 73 PHGPYLALMEQLSQFVPVSYPLAG------MLTNSGAEAAENALKVARGATGKRAIIAFD 126 P L ++ S+++ P G SGA+A E ALK+A+ TG+ ++I+F Sbjct: 102 P------LKDRFSEYLLSLLPGEGKEYCLQFTGPSGADAVEAALKLAKKYTGRSSVISFS 155 Query: 127 GGFHGRTLATLNLNGKVAPYKQRVGELPGPVYHLPYPS---ADTGVTCEQALKAMDRLFS 183 GG+HG T L++ G ++P G +P V +PYP G+ E +KA+ F Sbjct: 156 GGYHGMTHGALSVTGNLSPKAAVNGMMP-EVQFMPYPHQYRCPLGIGGEAGVKALTYYFE 214 Query: 184 -----VELAVEDVAAFIFEPVQGEGGFLALDPAFAQALRRFCDERGILIIIDEIQSGFGR 238 VE V AA I E VQGEGG + Q +R+ E GIL+IIDE+Q+GF R Sbjct: 215 NLINDVESGVRKPAAVILEAVQGEGGVNPAPVEWLQRIRKVTQEHGILLIIDEVQAGFAR 274 Query: 239 TGQRFAFPRLGIEPDLLLLAKSIAGGMPLGAVVGRKELMAALPKGGLGGTYSGNPISCAA 298 TG+ FAF GIEPD+++++K++ GG+PL AV+G K+ A G GT+ GN ++ A Sbjct: 275 TGKFFAFEHAGIEPDIIVMSKAVGGGLPL-AVLGIKKQFDAWEPGHHTGTFRGNQLAMAT 333 Query: 299 ALASLAQMTDENL----ATWGERQEQAIVSRYERWKASGLSPYIGRLTGVGAMRGIEFAN 354 L +L + D + A GE + + +R+ P IG + G+G M GIE Sbjct: 334 GLTTLRHLKDNKIADKTAAQGEWLKGKLAEMQKRY------PVIGHVRGLGLMIGIEIVK 387 Query: 355 ADGS-------PAPAQLAKVME-AARARGLLLMPSGKARHIIRLLAPLTIEAEVLEEGLD 406 + + PA +L+ +++ GL+L G+ ++RLL L I LE D Sbjct: 388 PNEAPDHMGCYPADGELSALLQKKCFEAGLILERGGRHGCVLRLLPSLLISNAELEIFFD 447 Query: 407 ILEQCL 412 EQ L Sbjct: 448 KFEQAL 453 Lambda K H 0.320 0.137 0.402 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: 502 Number of extensions: 22 Number of successful extensions: 6 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: 416 Length of database: 461 Length adjustment: 32 Effective length of query: 384 Effective length of database: 429 Effective search space: 164736 Effective search space used: 164736 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: 51 (24.3 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