Align acetylornithine/N-succinyldiaminopimelate aminotransferase [EC:2.6.1.11 2.6.1.17] (characterized)
to candidate PfGW456L13_1158 Acetylornithine aminotransferase (EC 2.6.1.11)
Query= reanno::azobra:AZOBR_RS19025 (389 letters) >lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1158 Acetylornithine aminotransferase (EC 2.6.1.11) Length = 427 Score = 247 bits (630), Expect = 5e-70 Identities = 155/384 (40%), Positives = 209/384 (54%), Gaps = 13/384 (3%) Query: 5 VMPTYARADIVFERGEGPYLYATDGRRFLDFAAGVAVNVLGHANPYLVEALTAQAHKLWH 64 +MP+ R VF RG+G +L+ +D R +LDF+ G N LGH+ LV A+TAQA L + Sbjct: 34 LMPSVERPKQVFVRGQGSWLWDSDDRAYLDFSQGGGANSLGHSPSVLVNAITAQAQSLIN 93 Query: 65 TSNLFRVAGQESLAKRLTEATFADTVFFTNSGAEAWECGAKLIRKYHYEKGDKARTRIIT 124 G SLA+ L +T +D + N+G+EA E KL RK+ A +RII Sbjct: 94 PGFGLHNRGMLSLAEHLCASTGSDQAYLLNTGSEACEAAIKLARKWGQRHRGGA-SRIIV 152 Query: 125 FEQAFHGRTLAAVSAAQQEKLIKGFGPLLDGFDLVPFGDLEAVRNAVTDETAGICLEPIQ 184 HGR+LA +SA+ L F P L GF VPF DL A+ AV + T I LEPIQ Sbjct: 153 ANNGCHGRSLATISASDSSTLANRFEPQLPGFSRVPFNDLPALHAAVDERTVAIMLEPIQ 212 Query: 185 GEGGIRAGSVEFLRGLREICDEHGLLLFLDEIQCGMGRTGKLFAHEWAGITPDVMAVAKG 244 E G+ +V +L+G+ +C E G+LL DE+Q G+GR G L A + G+T D++ + KG Sbjct: 213 SEAGVVPATVHYLKGVERLCRELGILLIFDEVQTGIGRCGSLLAEQSCGVTADIVVLGKG 272 Query: 245 IGGGFPLGACLATEKAAS---GMTAGTHGSTYGGNPLATAVGNAVLDKVLEPGFLDHVQR 301 +GGG PL A LA KA G AGTH GN L TA G +VLD V + FL HV Sbjct: 273 LGGGVPLAALLARGKACCFDIGELAGTH----HGNALMTAAGLSVLDTVQDKAFLKHVAE 328 Query: 302 IGGLLQDRLAGLVAENPAVFKGVRGKGLMLGLACGPAVGDVVV--ALRANGLLSVPAGDN 359 G L++ L L + +RG+GL+ GL D VV AL LL+ P D Sbjct: 329 AGQHLREGLGRLA--HRYGHGELRGQGLLWGLTLSDDSADAVVKAALYEGLLLNAPQAD- 385 Query: 360 VVRLLPPLNIGEAEVEEAVAILAK 383 +R P LN+ A ++E + LA+ Sbjct: 386 CLRFTPALNVSNANIDEMLLRLAR 409 Lambda K H 0.321 0.139 0.414 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: 432 Number of extensions: 26 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: 389 Length of database: 427 Length adjustment: 31 Effective length of query: 358 Effective length of database: 396 Effective search space: 141768 Effective search space used: 141768 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 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