Align succinyldiaminopimelate transaminase (EC 2.6.1.17); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate PfGW456L13_4713 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC 2.6.1.17)
Query= BRENDA::Q82IK5 (364 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 Length = 399 Score = 144 bits (362), Expect = 5e-39 Identities = 123/395 (31%), Positives = 181/395 (45%), Gaps = 36/395 (9%) Query: 1 MSAVSDRLPTFPWDKLEPYKARAAAHPDGI-VDLSVGTPVDPVPELIQKALVAAADSPG- 58 M+ +L +P++KL +PD + LS+G P P + +AL + Sbjct: 1 MNNALSQLQPYPFEKLRALLGSVTPNPDKRPIALSIGEPKHRSPSFVAEALAGNLEKMAV 60 Query: 59 YPTVWGTPELRDALTGWVERRLGA-RGVTH--HHVLPIVGSKE-LVAWLPTQLGLGPGDK 114 YPT G PELR+A+ W ERR +G +VLP+ G++E L A+ T + G Sbjct: 61 YPTTLGIPELREAIAAWCERRFDVPKGWIDPARNVLPVNGTREALFAFTQTVVNRGDDAL 120 Query: 115 VAHPRLAYPTYEVGARLARAD--HVVYDDPTELDPT----------GLKLLWLNSPSNPT 162 V P Y YE A LA A ++ D +P ++L+L SP NPT Sbjct: 121 VVSPNPFYQIYEGAAFLAGAKPHYLPCLDENGFNPDFDAVSPDIWKRCQILFLCSPGNPT 180 Query: 163 GKVLSKAELTRIVAWAREHGILVFSDECYLELGWEAD--PVSVLHP--DVCGGSYEGIVS 218 G ++ L +++A A E+ ++ +DECY EL ++ P +L ++ ++ V Sbjct: 181 GALIPVETLKKLIALADEYDFVIAADECYSELYFDEQTPPPGLLSACAELGRKDFKRCVV 240 Query: 219 VHSLSKRSNLAGYRAAFLAGDPAVLGPLLQIRKHGGMMTSAPTQAAVVAALGDDAHVREQ 278 HSLSKRSNL G R+ F+AGD VL L R + G TQ A VAA D+ HVR Sbjct: 241 FHSLSKRSNLPGLRSGFVAGDADVLKGFLLYRTYHGCAMPVQTQLASVAAWNDEVHVRAN 300 Query: 279 RERYAARRTALRDALLSHGFRIEHSEASLYLWATRGESCWDTVAHLADL----GILVAPG 334 R Y + A+ + +LS ++ + S YLW D A DL + V PG Sbjct: 301 RALYREKFDAVLE-ILSPVLDVQRPDGSFYLWP---NVAGDDAAFCRDLFEQEHVTVVPG 356 Query: 335 DFYG------SAGEQFVRVALTATDERVAAAVRRL 363 + + G VR+AL A A R+ Sbjct: 357 SYLSRDVDGVNPGAGRVRMALVAPLAECVEAAERI 391 Lambda K H 0.319 0.135 0.420 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: 432 Number of extensions: 31 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: 364 Length of database: 399 Length adjustment: 30 Effective length of query: 334 Effective length of database: 369 Effective search space: 123246 Effective search space used: 123246 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 (21.7 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