Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate GFF3277 PGA1_c33280 putative LL-diaminopimelate aminotransferase
Query= BRENDA::Q9ZEX3 (397 letters) >lcl|FitnessBrowser__Phaeo:GFF3277 PGA1_c33280 putative LL-diaminopimelate aminotransferase Length = 392 Score = 244 bits (624), Expect = 2e-69 Identities = 150/382 (39%), Positives = 211/382 (55%), Gaps = 12/382 (3%) Query: 4 RLDALHPYPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLSVYP 63 R L PY F +LRALL D P D+ ++++IGEPKH PA V I N AG YP Sbjct: 6 RFSNLPPYAFPRLRALL-DHHTPGGDV--VHMTIGEPKHDFPAWVTDVIVDNAAGFQSYP 62 Query: 64 STKGEPALRQAISQWLSRRYSIPAPDPESEVLPVLGSREALFAFAQTVIDPS---AGALV 120 +G LR AIS W+ RRY + DP ++V+ + G+RE L+ A + A +V Sbjct: 63 PNEGSAELRGAISDWIKRRYDVSV-DPMTQVMALNGTREGLYNAAMALCPEQKNGAKPVV 121 Query: 121 VCPNPFYQIYEGAALLAGATPYYVNADPARDFGLRTGRVPDEVWRRTQLVFVCSPGNPAG 180 + PNPFYQ+Y A++ A P +V A D +P EV RT + ++CSP NP G Sbjct: 122 LIPNPFYQVYMVASISVAAEPVFVPATADTDHLPDYVGLPPEVLNRTAVAYICSPANPQG 181 Query: 181 NVMSLEEWRTLFELSDRHGFVIAAYECYSEIYLDEDTPPLGSLQAARRLGRDRYTNLVAF 240 V S W L +L++++ F I A ECYSEIY + P+G+L A+ LG D +V F Sbjct: 182 AVASRAYWTQLIQLAEQYDFRIFADECYSEIY--RASAPVGALSVAQELGADP-ERVVLF 238 Query: 241 SSLSKRSNVPGMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAWS-MRRMCRKT 299 +SLSKRSN+ G+RSG +AG + R R Y G+ + + AA+ W+ + Sbjct: 239 NSLSKRSNLAGLRSGLIAGGPDTMKRVHQLRAYSGAPLPAPLQAAAARVWADEAHVTENR 298 Query: 300 AQYRAKFEAVLPILQNVLDVRAPQASFYLWAGTPGSDTAFARELYGRTGVTVLPGSLLAR 359 A Y+ K+ + + AP+A F+LW + A A +L+ TGV VLPG+ LA+ Sbjct: 299 ALYQEKYRIADQVFDGLDGYMAPEAGFFLWLPVEDGEAA-ALKLWQDTGVRVLPGAYLAQ 357 Query: 360 EAHNANPGQGRIRIALVAPLDQ 381 ANPG+G IR+ALVAP +Q Sbjct: 358 GDGTANPGKGYIRVALVAPAEQ 379 Lambda K H 0.321 0.135 0.412 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: 471 Number of extensions: 23 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: 397 Length of database: 392 Length adjustment: 31 Effective length of query: 366 Effective length of database: 361 Effective search space: 132126 Effective search space used: 132126 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 (21.9 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