Align 2-aminoadipate transaminase (2.6.1.39) (characterized)
to candidate PP_4223 PP_4223 diaminobutyrate-2-oxoglutarate transaminase
Query= reanno::Putida:PP_4108 (416 letters) >FitnessBrowser__Putida:PP_4223 Length = 452 Score = 202 bits (513), Expect = 2e-56 Identities = 150/426 (35%), Positives = 210/426 (49%), Gaps = 34/426 (7%) Query: 3 QESISQSIAIVHPITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNPAVVEAIQA--- 59 QES ++S P+ L R V D +G+++ID + G G L LGH +P VVEAIQ Sbjct: 20 QESNARSYPRRIPLALRRARGIHVEDVEGRQFIDCLAGAGTLALGHNHPVVVEAIQRVLA 79 Query: 60 -----QATRLTHYAFNAAPHGPYLALMEQLSQFVPVSYPLAGMLTNSGAEAAENALKVAR 114 LT + + L E L + V + +G +A E ALK+ R Sbjct: 80 DELPLHTLDLTTPVKDRFVQDLFGILPEALRREAKVQF-----CGPTGTDAVEAALKLVR 134 Query: 115 GATGKRAIIAFDGGFHGRTLATLNLNGKVAPYKQRVGELPGP-VYHLPYP---SADTGVT 170 ATG+ ++AF G +HG + LNL G P KQ +G L G V +PYP G+ Sbjct: 135 TATGRSTVLAFQGAYHGMSQGALNLMGSHGP-KQPLGALLGNGVQFMPYPYDYRCPFGLG 193 Query: 171 CEQALKAM-----DRLFSVELAVEDVAAFIFEPVQGEGGFLALDPAFAQALRRFCDERGI 225 E +KA + L E V AA I E VQGEGG + D + + +RR ++ G+ Sbjct: 194 GEAGVKANLHYLENLLLDPESGVPLPAAVILEVVQGEGGVVPADIEWLKGVRRITEQAGV 253 Query: 226 LIIIDEIQSGFGRTGQRFAFPRLGIEPDLLLLAKSIAGGMPLGAVVGRKELMAALPKGGL 285 +I+DEIQSGF RTG+ FAF GI PD++ L+K+I G +PL VV R L P G Sbjct: 254 ALIVDEIQSGFARTGRMFAFEHAGIVPDVVTLSKAIGGSLPLAVVVYRDWLDTWKP-GAH 312 Query: 286 GGTYSGNPISCAAALASLAQMTDENLATWGERQEQAIVSRYERWKASGLSPYIGRLTGVG 345 GT+ GN ++ AA A + + + LA E Q + +R + P +G + G G Sbjct: 313 AGTFRGNQMAMAAGSAVINYLVEHRLAEHAEAMGQRLRGHLQRLQRD--YPQLGDIRGRG 370 Query: 346 AMRGIEFANADGS-------PAPAQLA-KVMEAARARGLLLMPSGKARHIIRLLAPLTIE 397 M G+E + G PA LA KV RGL+L G+ ++R L PL I Sbjct: 371 LMLGVELVDPQGQPDALGHPPANRDLAPKVQRECLKRGLILELGGRHGAVVRFLPPLIIS 430 Query: 398 AEVLEE 403 AE ++E Sbjct: 431 AEQIDE 436 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: 500 Number of extensions: 28 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: 452 Length adjustment: 32 Effective length of query: 384 Effective length of database: 420 Effective search space: 161280 Effective search space used: 161280 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 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