Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate AO356_27230 AO356_27230 hypothetical protein
Query= BRENDA::P42588 (459 letters) >FitnessBrowser__pseudo5_N2C3_1:AO356_27230 Length = 871 Score = 264 bits (675), Expect = 8e-75 Identities = 173/433 (39%), Positives = 239/433 (55%), Gaps = 37/433 (8%) Query: 39 IEYFKEHVNPGFLEYRKSVTAGGDYGAVEWQAGSLNTLVDTQGQEFIDCLGGFGIFNVGH 98 I F++HVNP E + V G D V G L D QG+ ++D LG +G GH Sbjct: 7 ISPFEQHVNPAVGELIRRV--GLDKTFVR---GEGCYLYDAQGRAYLDFLGAYGALPFGH 61 Query: 99 RNPVVVSAVQN-QLAKQPLHSQELLDPLRAMLAKTLAALTPGKLKYSFFCNSGTESVEAA 157 +++ + + QL+++P+ Q +LA+ L A+ PG + F NSG E+VEAA Sbjct: 62 SPDALLAELASFQLSREPIFVQPSSLAASGLLAQRLLAIAPGDYRSVTFQNSGAETVEAA 121 Query: 158 LKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATAKSTFRKPFMPLLPGFRHVPFGNIEA 217 LK A G+ ++T +FHGK+LGALSAT +++ F LPGF V +G+I+A Sbjct: 122 LK---ACLIKTGRKRILSTHQSFHGKTLGALSATGSDKYQEGFQAPLPGFDFVDYGDIQA 178 Query: 218 MRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGM 277 + L ++ D AAVI+EP+QGEGG+ LPPP YL +R CD G L+I+DEVQTG+ Sbjct: 179 LEDQL---QRHPDAYAAVIIEPVQGEGGINLPPPEYLQQIRAACDRSGTLLIIDEVQTGL 235 Query: 278 GRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIATEEVFSVLFDNPFLHTTTFGGNP 337 GRTG+MFA VQ D L LAKALGGGVMPIGA + ++ +S F N H++TFGGN Sbjct: 236 GRTGQMFA--SAGVQADCLLLAKALGGGVMPIGACLISKNAYSEDFQNK--HSSTFGGNT 291 Query: 338 LACAAALATINVLLE-QNLPAQAEQKGDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFV 396 LAC L +++L E Q+L G LL+ +LA + ++E RG G L+ IEF Sbjct: 292 LACRIGLKVLDLLDERQDLLDSVRDNGRYLLEQLNELAARHASFIKEVRGAGYLIGIEFD 351 Query: 397 DNEIGY-----NFASEMFRQR---------------VLVAGTLNNAKTIRIEPPLTLTIE 436 + Y F M Q V VA TLN A +R+EPPL Sbjct: 352 LDRSHYPQFYGGFTGIMGEQESLVPILASYLLNVEGVRVAPTLNGANVMRVEPPLIAGRA 411 Query: 437 QCELVIKAARKAL 449 +CE+ I+A + L Sbjct: 412 ECEVFIQALARTL 424 Lambda K H 0.320 0.135 0.393 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: 868 Number of extensions: 41 Number of successful extensions: 8 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: 459 Length of database: 871 Length adjustment: 38 Effective length of query: 421 Effective length of database: 833 Effective search space: 350693 Effective search space used: 350693 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: 54 (25.4 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