Align Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized)
to candidate AZOBR_RS18740 AZOBR_RS18740 succinyl-diaminopimelate desuccinylase
Query= curated2:B9JZL9 (404 letters) >FitnessBrowser__azobra:AZOBR_RS18740 Length = 427 Score = 115 bits (288), Expect = 2e-30 Identities = 121/401 (30%), Positives = 165/401 (41%), Gaps = 55/401 (13%) Query: 20 LIRCPSVTPAEG---GALSALAAMLEPLGFTVERMVAREEGTPDVENLYARLGT------ 70 LIR P+V P L L GF VE + R +G P + Y R Sbjct: 27 LIRIPTVNPPGDVYTDCAEFLGRRLAGRGFAVEYV--RADGAPGDSDRYPRTNVIARVEG 84 Query: 71 --EGPHLMFAGHTDVVPVGNEADWTYPPFSAEIAGGELYGRGAVDMKGGIACFVAAIARH 128 GP + F GH DVVP G WT PF + G +YGRGA DMKGGIA + A+ Sbjct: 85 REPGPCVHFNGHIDVVPAGQ--GWTVDPFEGVVKDGRVYGRGACDMKGGIAASIIAVEAI 142 Query: 129 IESQGAPKGSISFLITGDEEGPSINGTTKLLEWAAAKGERWDACLVGEPTNPDQLGDMIK 188 +E+ G++ T DEE G L R D ++ EP N D+ + Sbjct: 143 LEAGIPFPGALEISGTVDEESGGYGGVGHLATLGYFSRPRVDHVIIPEPLNVDR----VC 198 Query: 189 IGRRGSLSGEIIVKGVQGHAAYPHLADNPVRGMIKLAE----------ALMHPAFDAGTE 238 IG RG EI KG H + P L + VR M + A A E Sbjct: 199 IGHRGVWWAEIETKGRVAHGSMPFLGNCAVRHMGAVLHRIETELIPRLAAKRTAMPVVPE 258 Query: 239 NFQPSNLEVTTI------DVGNAATNVIPARASAKFNIRFNDTWTAETLRTEIIARLDTA 292 + S L + I D G + ++P R + R+ E +R EI+ L+ Sbjct: 259 GARQSTLNINAIHGGQPEDHGGLPSPMVPDRCRMVIDRRYLIEEDPEEVRAEIVGILED- 317 Query: 293 SADPLLRPGRPPIAYEL--VWADRPSQVFLTRNNA-LISSLSAAIEKMTGKTPALSTTGG 349 LR RP YEL V A P+ LT +A ++ ++ AAIE + G+ A + G Sbjct: 318 -----LRRERPGFDYELREVLAFLPT---LTDADAPVVRAVGAAIETVLGRPAAQVVSPG 369 Query: 350 TSDARFI------KDYCPVVEFGLVGQTMHMVDERVAVSDL 384 T D + I KD C G++ H DE V + D+ Sbjct: 370 TYDQKHIARVGHLKD-CIAYGPGIL-DLAHQPDEYVGIDDM 408 Lambda K H 0.316 0.133 0.399 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: 448 Number of extensions: 30 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: 404 Length of database: 427 Length adjustment: 31 Effective length of query: 373 Effective length of database: 396 Effective search space: 147708 Effective search space used: 147708 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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