Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate Synpcc7942_0943 Synpcc7942_0943 acetylornithine aminotransferase
Query= reanno::WCS417:GFF4238 (406 letters) >lcl|FitnessBrowser__SynE:Synpcc7942_0943 Synpcc7942_0943 acetylornithine aminotransferase Length = 422 Score = 323 bits (829), Expect = 4e-93 Identities = 182/405 (44%), Positives = 239/405 (59%), Gaps = 8/405 (1%) Query: 6 APVQRADFDQVMVPNYAPAAFIPVRGEGSRVWDQAGRELIDFAGGIAVNVLGHAHPALVG 65 +P FD ++ Y RGEG RVWD GR +DF GIA LGHAHP LV Sbjct: 16 SPFSTDAFDACVMQTYGRFPLALERGEGCRVWDTQGRSYLDFVAGIATCTLGHAHPELVD 75 Query: 66 ALTEQAHKLWHVSNVFTNEPALRLAHKLIDATFAERVFFCNSGAEANEAAFKLARRVAFD 125 A+++Q KL HVSN++ +LA L + A+RVFFCNSGAEANEAA KLAR+ Sbjct: 76 AISDQIRKLHHVSNLYYIPEQGQLAAWLTANSCADRVFFCNSGAEANEAAIKLARKHGNT 135 Query: 126 RFGSEKYEIIAALNSFHGRTLFTVNVGGQSKYSDGFGPKITGITHVPYNDLDALKA---- 181 +E I+ A SFHGRTL V GQ KY GF P + G +VPYNDL AL+A Sbjct: 136 VLEAENPIILTAQASFHGRTLAAVTATGQPKYHKGFQPLVQGFRYVPYNDLAALEATLAE 195 Query: 182 --AVSDKTCAVVLEPIQGEGGVLPAELAYLQGARDLCDANNALLVFDEVQTGMGRSGHLF 239 A + A++LEP+QGEGGV P + AY Q R LCD LL+ DEVQ GMGRSG L+ Sbjct: 196 LDAAGETVAAILLEPLQGEGGVNPGDRAYFQAVRQLCDQRRMLLILDEVQVGMGRSGQLW 255 Query: 240 AYQHYGVTPDILTSAKSLGGGFPIAAMLTTEALAKHLVVGTHGTTYGGNPLACAVAEAVI 299 Y++ G+ PD T AK LGGG PI A+L +A L G H +T+GGNPLAC A+ Sbjct: 256 GYENLGIEPDAFTVAKGLGGGVPIGALL-VKASCNILQAGEHASTFGGNPLACRAGLAIA 314 Query: 300 DVINTPEVLAGVNAKHDLFKARLEQIGKQY-GIFTEVRGMGLLLGCVLSDAFKGKAKDVF 358 V+ ++LA V A+ + +A L+++ +Y + VRG GL+ G VL + + Sbjct: 315 QVMERDQLLANVQARGEQLRAGLQELVDRYPNLLAGVRGWGLINGLVLRNDPNVTPIALV 374 Query: 359 NAAEKENLMILQAGPDVVRFAPSLVVEDADIKEGLDRFERAVKAL 403 AA ++ L+++ AG +VVRF P L+V A+I E L ERA+ A+ Sbjct: 375 KAAIEQGLLLVPAGAEVVRFVPPLIVSAAEIDEALAMTERALLAI 419 Lambda K H 0.320 0.137 0.400 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: 443 Number of extensions: 20 Number of successful extensions: 4 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: 406 Length of database: 422 Length adjustment: 31 Effective length of query: 375 Effective length of database: 391 Effective search space: 146625 Effective search space used: 146625 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