Align putrescine-pyruvate transaminase (EC 2.6.1.113) (characterized)
to candidate GFF3387 PGA1_c34400 aminotransferase class-III
Query= BRENDA::Q9I6J2 (456 letters) >FitnessBrowser__Phaeo:GFF3387 Length = 464 Score = 594 bits (1531), Expect = e-174 Identities = 294/453 (64%), Positives = 348/453 (76%), Gaps = 4/453 (0%) Query: 5 ITN-AKTREWQALSRDHHLPPFTDYKQLNEKGARIITKAEGVYIWDSEGNKILDAMAGLW 63 ITN T E QAL HH+ PFT +L EKGARIIT+A GV + DSEGN+ILDAMAGLW Sbjct: 4 ITNHLPTAELQALDAAHHMHPFTANGELAEKGARIITRARGVTLTDSEGNEILDAMAGLW 63 Query: 64 CVNVGYGREELVQAATRQMRELPFYNLFFQTAHPPVVELAKAIADVAPEGMNHVFFTGSG 123 CVN+GYGR+EL A RQMRELP+YN FFQT H P + LA IA++AP+G+NHVFF GSG Sbjct: 64 CVNIGYGRDELADVAARQMRELPYYNTFFQTTHAPAIALAAKIAELAPDGLNHVFFAGSG 123 Query: 124 SEANDTVLRMVRHYWATKGQPQKKVVIGRWNGYHGSTVAGVSLGGMKALHEQGDFPIPGI 183 SEANDT +RMVRHYWA K +P K V+I R NGYHGS+V SLGGM A+HEQG PIP I Sbjct: 124 SEANDTNIRMVRHYWAMKAKPTKSVIISRKNGYHGSSVGSGSLGGMTAMHEQGGLPIPDI 183 Query: 184 VHIAQPYWYGEGGDMSPDEFGVWAAEQLEKKILEVGEENVAAFIAEPIQGAGGVIVPPDT 243 HI QP W+ EGGDMS ++FG+ A++LE+ ILE+GE+ VAAFIAEP+QGAGGVIVPP T Sbjct: 184 HHINQPNWWAEGGDMSAEDFGLARAQELEQAILELGEDRVAAFIAEPVQGAGGVIVPPAT 243 Query: 244 YWPKIREILAKYDILFIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGV 303 YWP+I+ I KY+IL IADEVICGFGRTG WFGSQ G PD+M IAKGL+SGY P+GG Sbjct: 244 YWPEIQRICDKYEILLIADEVICGFGRTGNWFGSQSVGIRPDIMTIAKGLSSGYAPIGGS 303 Query: 304 VVRDEIVEVLNQGGEFYHGFTYSGHPVAAAVALENIRILREEKIIEKVKAETAPYLQKRW 363 +V DEI V+ GEF HG+TYSGHPVAAAVALEN+RIL EE II V+ APYL+++W Sbjct: 304 IVSDEIASVIG-SGEFNHGYTYSGHPVAAAVALENLRILEEENIIGHVRDVAAPYLKEKW 362 Query: 364 QELADHPLVGEARGVGMVAALELVKNKKTRERFTDKG--VGMLCREHCFRNGLIMRAVGD 421 + LADHPLVGEA+ VGM+ ++ L NK TR F +G VG +CRE CF N L+MR VGD Sbjct: 363 EALADHPLVGEAKIVGMMGSIALTPNKATRAGFAAEGGTVGYICRERCFANNLVMRHVGD 422 Query: 422 TMIISPPLVIDPSQIDELITLARKCLDQTAAAV 454 MIISPPLVI P +ID LI AR+ LD+ AA+ Sbjct: 423 RMIISPPLVITPEEIDTLIARARQSLDECYAAL 455 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: 712 Number of extensions: 26 Number of successful extensions: 3 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: 464 Length adjustment: 33 Effective length of query: 423 Effective length of database: 431 Effective search space: 182313 Effective search space used: 182313 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