Align putrescine-pyruvate transaminase (EC 2.6.1.113) (characterized)
to candidate SM_b20379 SM_b20379 aminotransferase
Query= BRENDA::Q9I6J2 (456 letters) >FitnessBrowser__Smeli:SM_b20379 Length = 461 Score = 372 bits (955), Expect = e-107 Identities = 197/453 (43%), Positives = 280/453 (61%), Gaps = 9/453 (1%) Query: 7 NAKTREWQALSRDHHLPPFTDYKQLNEKGARIITKAEGVYIWDSEGNKILDAMAGLWCVN 66 N + AL + + P+T+ E G +IT +G+Y+ D EG + ++ +AGL+C Sbjct: 2 NDRPNSLHALDKQSLVHPYTNLAVHQETGPHVITGGDGIYVVDDEGKRYIEGLAGLFCAG 61 Query: 67 VGYGREELVQAATRQMRELPFYNLFFQTAHPPVVELAKAIADVAPEGMNHVFFTGSGSEA 126 +G+ + LV+AATRQ++ +PFY+ F + P + LA+ + +AP M+ VFF GSGSEA Sbjct: 62 LGFSEQRLVEAATRQLKTMPFYHSFAHKSTEPGIRLAEKLLSIAPVPMSKVFFAGSGSEA 121 Query: 127 NDTVLRMVRHYWATKGQPQKKVVIGRWNGYHGSTVAGVSLGGMKALHEQGDFPIPGIVHI 186 NDT ++++ +Y G+P+KK +I R YHG TVA SL G+ H D PI I+H Sbjct: 122 NDTAIKLIWYYNNALGRPEKKKIISRRKAYHGVTVATASLTGLPFNHRDFDLPIANILHT 181 Query: 187 AQP-YW-YGEGGDMSPDEFGVWAAEQLEKKILEVGEENVAAFIAEPIQGAGGVIVPPDTY 244 P YW + E G+ + ++F A LE ILE G E +AAF AEP+ +GGVI PP TY Sbjct: 182 DCPHYWRFAETGE-TEEDFATRMANNLEAIILEEGPETIAAFFAEPVMVSGGVITPPKTY 240 Query: 245 WPKIREILAKYDILFIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGVV 304 + K++ +L KYDIL IADEVICGFGRTG FGS+ YG PD++ AK L++ Y+P+ ++ Sbjct: 241 FEKVQAVLRKYDILLIADEVICGFGRTGNMFGSETYGLKPDMISCAKQLSAAYMPISALM 300 Query: 305 VR----DEIVEVLNQGGEFYHGFTYSGHPVAAAVALENIRILREEKIIEKVKAETAPYLQ 360 + D +V+ + G F HGFTY GHPVAAAVALE + I E I+ V++ AP Q Sbjct: 301 INAKIADALVDQSRKIGTFSHGFTYGGHPVAAAVALEALTIYEEIDIVGHVRS-VAPAFQ 359 Query: 361 KRWQELADHPLVGEARGVGMVAALELVKNKKTRERFTDK-GVGMLCREHCFRNGLIMRAV 419 R ++L +HPL+GEARGVG+VA LE VK+K TRE F V + G++ R + Sbjct: 360 DRVRKLGEHPLIGEARGVGLVAGLEFVKDKATRENFPPAWQVANQAGKFATARGVLTRGL 419 Query: 420 GDTMIISPPLVIDPSQIDELITLARKCLDQTAA 452 GD + + P ++ID QID+L+T LD T A Sbjct: 420 GDMVSLCPAMIIDDEQIDDLMTRMGLALDDTLA 452 Lambda K H 0.320 0.138 0.425 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: 564 Number of extensions: 25 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: 456 Length of database: 461 Length adjustment: 33 Effective length of query: 423 Effective length of database: 428 Effective search space: 181044 Effective search space used: 181044 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