Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate AO356_27515 AO356_27515 4-aminobutyrate aminotransferase
Query= BRENDA::Q88RB9 (425 letters) >lcl|FitnessBrowser__pseudo5_N2C3_1:AO356_27515 AO356_27515 4-aminobutyrate aminotransferase Length = 457 Score = 234 bits (598), Expect = 3e-66 Identities = 151/430 (35%), Positives = 230/430 (53%), Gaps = 23/430 (5%) Query: 3 KTNESL-MQRRVAAVPRGVGQIHPIFVDTAKNSTVIDVEGRELIDFAGGIAVLNTGHLHP 61 +T E+L + R ++ RG G++ P+ +D A +T D + ID + G+ V + G HP Sbjct: 25 RTTEALALSARTESMARGGGRM-PVAMDRAFGATFKDADDNTYIDLSAGVGVSSVGRCHP 83 Query: 62 KVVAAVQEQLTKVSHTCFQVLAYEPYVELCEKINKLVPGDF--DKKTLLVTTGSEAVENA 119 KVV A++EQ + H + EL K++++ P D T +GS+A+E A Sbjct: 84 KVVQAIREQSEVLMHAL--EVNSTRRTELAAKLSEIAPDGLRGDCITFFTQSGSDALEAA 141 Query: 120 VKIARAATGRAGVIAFTGGYHGRTMMTLGLTGKVVPYSAGMGLMPGGIFRALFPSELHGI 179 +K A+ TGR +IAF GGYHG + LT Y G G GG+ A +P + Sbjct: 142 IKFAKRVTGRHQIIAFHGGYHGVWNASGALTTGTA-YRKGYGAQMGGVIHAPYPYA-YRF 199 Query: 180 SVDDAIASVERIFKNDAE---------PRDIAAIILEPVQGEGGFLPAPKELMKRLRALC 230 D S E+I + D+AA+I+EPVQGEGG++P E ++ LR C Sbjct: 200 PFDTTHKSAEQIAGEYVDYLLNTPYTAADDVAAVIVEPVQGEGGYVPPSPEFLQLLRKAC 259 Query: 231 DQHGILLIADEVQTGAGRTGTFFAMEQMGVAPDLTTFAKSIAGGFPLAGVCGKAEYMDAI 290 D+ G LLI DEVQ+GAGRTG +A+E GV PD+ TF K I P+AG+ +++ AI Sbjct: 260 DRSGTLLIVDEVQSGAGRTGKMWAVEHSGVKPDMLTFGKGIGSDLPMAGLIMRSDLAAAI 319 Query: 291 APGGLGGTYAGSPIACAAALAVIEVFEEEK--LLDRSKAVGERLTAGLREIQKKYPIIGD 348 G + T+A + ++ A AL I + ++ + LL+R+ +G +R P++G+ Sbjct: 320 PDGSMPNTFAANSLSAAVALTNISILQDPELDLLNRAHTLGLEAQERIRGFGS--PLVGE 377 Query: 349 VRGLGSMIAVE-VFEKGTHTPNA-AAVGQVVAKAREKGLILLSCGTYGNVLRILVPLTAE 406 VRG G MI +E V + T P A +GQ++ G++++ CG Y NV+R++ LT Sbjct: 378 VRGRGLMIGIELVSDPTTKAPLAPEKIGQLMGYLLSHGVLMIPCGRYSNVMRVMPSLTIS 437 Query: 407 DALLDKGLAI 416 AL K L I Sbjct: 438 RALFFKALDI 447 Lambda K H 0.320 0.138 0.395 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: 528 Number of extensions: 35 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: 425 Length of database: 457 Length adjustment: 32 Effective length of query: 393 Effective length of database: 425 Effective search space: 167025 Effective search space used: 167025 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