Align 2-isopropylmalate synthase (EC 2.3.3.13) (characterized)
to candidate WP_025274981.1 HALAL_RS0116090 citramalate synthase
Query= BRENDA::Q58595 (518 letters) >NCBI__GCF_000527155.1:WP_025274981.1 Length = 546 Score = 216 bits (549), Expect = 2e-60 Identities = 161/534 (30%), Positives = 265/534 (49%), Gaps = 46/534 (8%) Query: 16 ENLNIPDRVYIFDTTLRDGEQTPGVSLTPEEKIDIAIKLDDLGVDVIEAGFPVSSLGEQE 75 E+ + P +IFDTTLRDG Q G+ + +K+ +A +D+LGVD IE G+P + + E Sbjct: 14 ESPSTPTDFHIFDTTLRDGAQMEGLRYSVADKMSVARLIDELGVDYIEGGWPGALPSDTE 73 Query: 76 AIK-----------KICSLNLDAEICGLARAVKKDIDVAIDCGVDRIHTFIATSPLHRKY 124 + K+ + + G+A A + + ID + + H ++ Sbjct: 74 FFERASEEINFKHAKLVAFGMTRR-AGIAAADDEGLGALIDSRAPTLCLVAKSDIRHVRH 132 Query: 125 KLKKSKEEIIDIAVDAIEYIKEHGIRVEFSAE---DATRTEIDYLIEVYKKAVDAGADII 181 LK S E +++ D+I Y +E+ V E D R DY V K + DAGAD++ Sbjct: 133 ALKASPAENLEMIRDSISYGREYDREVFIDCEHFFDGFRHSPDYATTVVKSSFDAGADVV 192 Query: 182 NVPDTVGVMIPRAMYYLINELKKEIK-------VPISVHCHNDFGLAVANSLAAVEAGAE 234 + DT G IP + +I +L+ + + + +H ND G AVAN+L AVE+G Sbjct: 193 VLCDTNGGSIPSDIARIIGDLRSRLADTMRPEDIRLGIHAQNDTGCAVANTLTAVESGVM 252 Query: 235 QVHCTINGLGERGGNAALEEVVMSLMSIYGVKTNIK--TQKLYEISQLVSKYTEIKVQPN 292 V T NG GER GNA + V+ L + G++ +K+ S ++ + + Sbjct: 253 HVQGTANGYGERPGNADIFSVIGGLQTKMGMRVLPPGGLEKMTHTSHSIAAIANMPPNEH 312 Query: 293 KAIVGENAFAHESGIHAHGVLAHALTYEPIPPELVGQKRKIILGKHTGTHAIEAKLKELG 352 VG AFAH++G+HA + Y I P++VG +I++ + G +IE K ++LG Sbjct: 313 APYVGHAAFAHKAGLHASAIKTDPGLYNHIDPQVVGNDMRILVTEMAGRASIELKSRDLG 372 Query: 353 IEVGKDINKDQFDEIVKRIKALGDKG--KRVTDRDVEAIVEDVVGKLAKKDRVVELEQIA 410 IE+ KD D + KR+K L +G D E +++D +L + +RVV +A Sbjct: 373 IELRG--QKDVLDRVTKRVKDLEAQGWSFEAADASFELLLDD---ELPQANRVVRPFTVA 427 Query: 411 ----VMTGNR---VIPTASVALKIEEEIKKSSAIGVGPVDAAVKAIQKAIGEK------I 457 ++ R V+ A+V L+++ E ++A GPV+A A+++A+ E+ I Sbjct: 428 SYRVIIDHTRDGSVVCEATVRLEVDGEQTITTAQARGPVNALDAALRQALAERFPGLSEI 487 Query: 458 KLKEYHINAITG--GTDALAEVIVTLEGYGREITTKAASEDIVRASVEAVIDGI 509 L +Y + + G GT+A+ V+ TL E TT ++IV AS A+ID + Sbjct: 488 NLSDYKVRILAGTSGTEAITRVLTTLSDGDDEWTTVGVDDNIVEASWRALIDAL 541 Lambda K H 0.316 0.135 0.368 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: 563 Number of extensions: 25 Number of successful extensions: 6 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: 518 Length of database: 546 Length adjustment: 35 Effective length of query: 483 Effective length of database: 511 Effective search space: 246813 Effective search space used: 246813 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: 52 (24.6 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