Align succinyldiaminopimelate transaminase (EC 2.6.1.17); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate RR42_RS11930 RR42_RS11930 succinyldiaminopimelate aminotransferase
Query= BRENDA::Q82IK5 (364 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS11930 RR42_RS11930 succinyldiaminopimelate aminotransferase Length = 405 Score = 155 bits (392), Expect = 2e-42 Identities = 138/396 (34%), Positives = 186/396 (46%), Gaps = 42/396 (10%) Query: 6 DRLPTFPWDKLEPYKARAAAHPDGI---VDLSVGTPVDPVPELIQKALVAAADS-PGYPT 61 D L +P++KL A P+G + +G P P PE I+ AL A YPT Sbjct: 6 DLLQPYPFEKLRVLLADVK--PNGALPAISFGIGEPKHPTPEFIKTALSNALQGLANYPT 63 Query: 62 VWGTPELRDALTGWVERRLGARGVTHH-HVLPIVGSKE-LVAWLPTQLGLG-PGDKVAHP 118 G+ LR + W++RR V VLP+ GS+E L A+ T + PG V P Sbjct: 64 TAGSDALRQCMAAWIQRRYNLPAVNATTQVLPVTGSREALFAFAQTVVDASQPGALVLCP 123 Query: 119 RLAYPTYEVGARLARADHVVYD-DPTE-----LDPTG------LKLLWLNSPSNPTGKVL 166 Y YE A LA A V + DP D G ++L+++ SP NPTG VL Sbjct: 124 NPFYQIYEGAALLAGATPVFANSDPARNFAPAFDRIGAETWAKVQLVFVCSPGNPTGAVL 183 Query: 167 SKAELTRIVAWAREHGILVFSDECYLELGWEAD--PVSVLHPDVCGGSYEG------IVS 218 S + + A + HG ++ SDECY E+ ++ P+ L G EG +V Sbjct: 184 SLEDWRELFALSDRHGFVIASDECYSEIYFKEGEPPLGALEAAHKLGRAEGAHPFERLVM 243 Query: 219 VHSLSKRSNLAGYRAAFLAGDPAVLGPLLQIRK-HGGMMTSAPTQAAVVAALGDDAHVRE 277 SLSKRSN+ G R+ F+AGD A+L L R HGG M A Q A VAA D+AHVR Sbjct: 244 FSSLSKRSNVPGLRSGFVAGDAALLKKFLLYRTYHGGAMNPA-VQTASVAAWNDEAHVRN 302 Query: 278 QRERYAARRTALRDALLSHGFRIEHSEASLYLWA---TRGESCWDTVAH-LADLGILVAP 333 R Y AR+ A +L+ + +A YLWA G S + A LA+ + V P Sbjct: 303 NRAAY-ARKFAEVTPMLAEVLDVALPDAGFYLWADVSRTGLSDTEFAARLLAEQNVTVLP 361 Query: 334 GDFYG------SAGEQFVRVALTATDERVAAAVRRL 363 G + + G VR+AL AT E RR+ Sbjct: 362 GSYLAREADGINPGANRVRMALVATPEECLEGARRI 397 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: 407 Number of extensions: 24 Number of successful extensions: 4 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: 405 Length adjustment: 30 Effective length of query: 334 Effective length of database: 375 Effective search space: 125250 Effective search space used: 125250 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