Align 2-isopropylmalate synthase 2; EC 2.3.3.13; Alpha-IPM synthase 2; Alpha-isopropylmalate synthase 2 (uncharacterized)
to candidate WP_010963584.1 CA_RS01455 homocitrate synthase
Query= curated2:Q8RCF9 (384 letters) >NCBI__GCF_000008765.1:WP_010963584.1 Length = 265 Score = 223 bits (569), Expect = 4e-63 Identities = 108/253 (42%), Positives = 169/253 (66%), Gaps = 3/253 (1%) Query: 9 VYIVDTTLRDGEQTAGVVFANNEKIRIAQMLDEIGIDQLEVGIPTMGGDEKETVAKIAKL 68 V +VDTTLRDGEQ AG+ EK IA++LD++GI Q+E G+ MGG EK+++ +I +L Sbjct: 3 VKLVDTTLRDGEQKAGIALGVKEKTEIAKLLDDMGIFQIEAGVAAMGGQEKKSIEEIVRL 62 Query: 69 GLKASIMAWNRAVVKDVQESLECGVDAVAISISTSDIHIEHKLKKTRQWVLDSMTEAVRF 128 GLK+ I ++NR + D+Q S++C VD + IS+ S++ I++ LK +++ V+ +M + + + Sbjct: 63 GLKSKISSFNRMKISDIQHSIDCKVDIIHISVPASNMQIKYNLKTSKEIVISNMKKCIYY 122 Query: 129 AKKEGVYVSVNAEDASRTDMNFLIEFARCAKQAGADRLRFCDTVGFLDPFKTYEMVKAIK 188 A +G V++ EDASR D+ FL+E + A + G R+R+ DTVG L P KT+ + I Sbjct: 123 ALGKGYEVTIGLEDASRADIEFLVELCKEAYKEGIRRVRYADTVGILYPRKTFYNINRII 182 Query: 189 DAVDIEIEMHTHNDFGMATANALAGVKAGAKFVGVTVNGLGERAGNAALEEVVMALKYVY 248 + V +E+E+HTHNDFGMA N+L+ KAGA ++ T+ G+GERAGN + V + + Sbjct: 183 EEVPVEVEIHTHNDFGMAEVNSLSAAKAGANYIDTTIAGIGERAGNC---DFVKFINIIG 239 Query: 249 KMDLGIDTSRFRE 261 K +L ID + +E Sbjct: 240 KTNLRIDDLKLKE 252 Lambda K H 0.318 0.135 0.379 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: 248 Number of extensions: 13 Number of successful extensions: 1 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: 384 Length of database: 265 Length adjustment: 27 Effective length of query: 357 Effective length of database: 238 Effective search space: 84966 Effective search space used: 84966 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: 48 (23.1 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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:
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