Align putrescine-pyruvate transaminase (EC 2.6.1.113) (characterized)
to candidate AO356_07955 AO356_07955 omega amino acid--pyruvate aminotransferase
Query= BRENDA::Q9I6J2 (456 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_07955 Length = 449 Score = 268 bits (686), Expect = 2e-76 Identities = 163/445 (36%), Positives = 243/445 (54%), Gaps = 23/445 (5%) Query: 16 LSRDHHLPPFTDYKQLNEKGARIITKAEGVYIWDSEGNKILDAMAGLWCVNVGYGREELV 75 L D H P+T + ++ R+I AEG ++ D +G K+ D+++GLW G+ R+E+ Sbjct: 15 LKLDAHWMPYTANRNF-QRDPRLIVAAEGSWLVDDKGRKVYDSLSGLWTCGAGHTRKEIQ 73 Query: 76 QAATRQMRELPFYNLFFQTAHPPVVELAKAIADVAPEGMNHVFFTGSGSEANDTVLRMVR 135 +A +Q+ L Y+ FQ HP +LA+ I + P +NHVFFT SGSE DT ++MVR Sbjct: 74 EAVAKQLGTLD-YSPGFQYGHPLSFQLAEKITSLTPGNLNHVFFTDSGSECADTAVKMVR 132 Query: 136 HYWATKGQPQKKVVIGRWNGYHGSTVAGVSLGGM---KALHEQGDFPIPGIVH-IAQPYW 191 YW KGQ K +IGR GYHG +AG SLGG+ + L Q + + H + Sbjct: 133 AYWRLKGQATKTKMIGRARGYHGVNIAGTSLGGVSGNRKLFGQAMMDVDHLPHTLLASNA 192 Query: 192 YGEGGDMSPDEFGVWAAEQLEKKILEVGEENVAAFIAEPIQGAGGVIVPPDTYWPKIREI 251 Y G P E G+ A++L K I N+AA EP+ G+ GV+VPP+ Y ++REI Sbjct: 193 YSRG---MPKEGGIALADELLKLIELHDASNIAAVFVEPMAGSAGVLVPPEGYLKRLREI 249 Query: 252 LAKYDILFIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGVVVRDEIVE 311 ++ IL + DEVI GFGRTG FG+ +G PDLM IAK +T+G IPMG V+ EI + Sbjct: 250 CDQHSILLVFDEVITGFGRTGSMFGADSFGVTPDLMCIAKQVTNGAIPMGAVIASSEIYQ 309 Query: 312 V-LNQ-----GGEFYHGFTYSGHPVAAAVALENIRILREEKIIEKVKAETAPYLQKRWQE 365 +NQ EF HG+TYS HPVA A L + +L++E +++ V AE AP+ + Sbjct: 310 TFMNQPTPEYAVEFPHGYTYSAHPVACAAGLAALDLLQKENLVQSV-AEIAPHFENALHG 368 Query: 366 LADHPLVGEARGVGMVAALELV-KNKKTRERFTDKGVGMLCREHCFRNGLIMRAVGDTMI 424 L V + R G+ A+++ ++ R + G+ + ++ G +R GDT+ Sbjct: 369 LKGAKNVIDIRNYGLAGAIQIAGRDGDAIVRPFEAGMAL------WKAGFYVRFGGDTLQ 422 Query: 425 ISPPLVIDPSQIDELITLARKCLDQ 449 P P +D L + L++ Sbjct: 423 FGPTFNSKPQDLDRLFDAVGEVLNK 447 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: 537 Number of extensions: 29 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: 456 Length of database: 449 Length adjustment: 33 Effective length of query: 423 Effective length of database: 416 Effective search space: 175968 Effective search space used: 175968 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