Align L-arabinose isomerase (EC 5.3.1.4) (characterized)
to candidate WP_025272425.1 HALAL_RS0102135 L-arabinose isomerase
Query= BRENDA::A0LT86 (501 letters) >NCBI__GCF_000527155.1:WP_025272425.1 Length = 499 Score = 568 bits (1464), Expect = e-166 Identities = 284/475 (59%), Positives = 337/475 (70%), Gaps = 1/475 (0%) Query: 8 EYECWFLTGSQHLYGEDVLSAVARQSQAIVEALNAAGLPVRLVWKPVLTDATGIRRMCSE 67 E E WFLTGSQ LYG++ L VA QS I +N P+ +V KP +T + IRR+ E Sbjct: 12 EPEIWFLTGSQDLYGDETLRIVAEQSAQIAGHINHTN-PINVVSKPTVTSSDAIRRIILE 70 Query: 68 ASATDACIGVIAWMHTFSPAKAWINGLLALRKPLLHLHTQANLTLPWSTIDMDFMNLNQA 127 A+A+D CIG+I WMHTFSPAK WI+GL L+KPLLH HTQ NL LPW IDMDFMNLNQA Sbjct: 71 ANASDQCIGLITWMHTFSPAKMWISGLTKLQKPLLHFHTQFNLDLPWDRIDMDFMNLNQA 130 Query: 128 AHGDREFGYVAARLAIPRKIVTGHFSDPDVVRDIAAWQRAAAGLADLRSTRLVRFGDTMR 187 AHGDREF ++A RL IPRK V GH+ V I W RAAAG A ++ ++ RFGD MR Sbjct: 131 AHGDREFAHIATRLNIPRKTVVGHWEQEYVTDQIETWSRAAAGFAAAQNLKIARFGDNMR 190 Query: 188 NVAVTDGDRVEAQIRLGSAIETYGVHDLGVRVDAVAESDVDALVDRYLADYDMAPELTIG 247 NVAVTDGD+V A+I LG +I YGV+++ RV+A+ S D L++ YL +Y ++PEL Sbjct: 191 NVAVTDGDKVSAEIDLGPSINGYGVNEIAARVEAIPNSATDDLIEIYLNNYSVSPELRPQ 250 Query: 248 GARHESLRYAAKLELALRSFLHDGRFTAFTTNFEDLGPLRQLPGIAVQRLMADGFGFGAE 307 G RH+SLR AAK+E+ALR FL D FT FEDLG L QLPGIAVQRLM +GFGFGAE Sbjct: 251 GNRHQSLRDAAKIEVALREFLRDVGAHGFTDTFEDLGTLPQLPGIAVQRLMNEGFGFGAE 310 Query: 308 GDWKTALLVRAVKTMSRGLPGGTSFMEDYTYHLEPSGRLVLGAHMLEVCPTLTSATPRCE 367 GDWKTA+LVR K M+ GL GGTSFMEDYTY+L +LGAHMLEVCP+L S P CE Sbjct: 311 GDWKTAILVRIAKVMAAGLDGGTSFMEDYTYNLGVEHPQILGAHMLEVCPSLASDVPTCE 370 Query: 368 IHPLLMGGREDPVRLVFTADPAPAVIVGLCDMGDRLRLVANTADLVAPPEPLPRLPVARA 427 IHPL MG + DPVRLVFTA PA +GL D+GDR RLV N D+V P LP LPVARA Sbjct: 371 IHPLAMGAKADPVRLVFTAPTGPAFNIGLTDLGDRFRLVGNEVDVVPPEAELPNLPVARA 430 Query: 428 VWQPHPELKTAATAWIAAGGPHHTALSTAVSAREIRDFARMAGLELVLIDEHTAL 482 VW+P P L T+A AW+ AG PHHT LS A+ DFA MAG+E+ +IDE T L Sbjct: 431 VWEPKPNLATSAAAWMHAGAPHHTLLSQAIGREVWEDFANMAGIEMAVIDERTDL 485 Lambda K H 0.322 0.136 0.421 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: 762 Number of extensions: 21 Number of successful extensions: 2 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: 501 Length of database: 499 Length adjustment: 34 Effective length of query: 467 Effective length of database: 465 Effective search space: 217155 Effective search space used: 217155 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 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:
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