Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate 16752 b2662 4-aminobutyrate aminotransferase (NCBI)
Query= reanno::pseudo1_N1B4:Pf1N1B4_3440 (406 letters) >lcl|FitnessBrowser__Keio:16752 b2662 4-aminobutyrate aminotransferase (NCBI) Length = 426 Score = 218 bits (556), Expect = 2e-61 Identities = 149/399 (37%), Positives = 203/399 (50%), Gaps = 46/399 (11%) Query: 30 RGAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVS-NVFTNEPALR 88 R RVWD GRE +DFAGGIAV GH HP +VAA+ Q KL H V EP L Sbjct: 29 RAENCRVWDVEGREYLDFAGGIAVLNTGHLHPKVVAAVEAQLKKLSHTCFQVLAYEPYLE 88 Query: 89 LA---HKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEIVAALNSFHGRT 145 L ++ V FA++ +G+EA E A K+AR A R GT +A ++HGRT Sbjct: 89 LCEIMNQKVPGDFAKKTLLVTTGSEAVENAVKIAR-AATKRSGT-----IAFSGAYHGRT 142 Query: 146 LFTVNVGGQ-SKYSDGFG---------------------PKITGITHVPYNDLAALKAAV 183 +T+ + G+ + YS G G I I + ND A Sbjct: 143 HYTLALTGKVNPYSAGMGLMPGHVYRALYPCPLHGISEDDAIASIHRIFKND------AA 196 Query: 184 SDKTCAVVLEPIQGEGGVLPAELSYLQGARELCDAHNALLVFDEVQTGMGRSGKLFAYQH 243 + A+V+EP+QGEGG + +++Q R LCD H +L+ DEVQ+G GR+G LFA + Sbjct: 197 PEDIAAIVIEPVQGEGGFYASSPAFMQRLRALCDEHGIMLIADEVQSGAGRTGTLFAMEQ 256 Query: 244 YGVTPDILTSAKSLGGGFPIAAMLTTEDLAKHLVVGTHGTTYGGNPLACAVAEAVIDVIN 303 GV PD+ T AKS+ GGFP+A + ++ + G G TY GNP+AC A V+ V Sbjct: 257 MGVAPDLTTFAKSIAGGFPLAGVTGRAEVMDAVAPGGLGGTYAGNPIACVAALEVLKVFE 316 Query: 304 TPEVLNGVNAKHDKFKTRLEQIGEKYGLFTEVRGLGLLLGCVL---SDAWKGKAK---DI 357 +L N K K L I EK+ +VRGLG ++ L D K AK +I Sbjct: 317 QENLLQKANDLGQKLKDGLLAIAEKHPEIGDVRGLGAMIAIELFEDGDHNKPDAKLTAEI 376 Query: 358 FNAAEREGLMILQAGP--DVIRFAPSLVVEDADIDAGLD 394 A +GL++L GP +V+R L +EDA I GL+ Sbjct: 377 VARARDKGLILLSCGPYYNVLRILVPLTIEDAQIRQGLE 415 Lambda K H 0.320 0.136 0.400 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: 430 Number of extensions: 20 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: 406 Length of database: 426 Length adjustment: 31 Effective length of query: 375 Effective length of database: 395 Effective search space: 148125 Effective search space used: 148125 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: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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